paragraph_index int64 | sec string | p_has_citation int64 | cites string | citeids list | pmid int64 | cited_id string | sentences string | all_sent_cites list | sent_len int64 | sentence_batch_index int64 | sent_has_citation float64 | qc_fail bool | cited_sentence string | cites_in_sentence list | cln_sentence string | is_cap bool | is_alpha bool | ends_wp bool | cit_qc bool | lgtm bool | __index_level_0__ int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | DISCUSSION | 1 | 10 | [
"B10",
"B12",
"B22",
"B23",
"B24",
"B25",
"B11"
] | 15,716,603 | pmid-7525417|pmid-9679948|pmid-9102204|pmid-9744541|pmid-7574932|pmid-3395818|pmid-9395230|pmid-10910963|pmid-14684572|pmid-8804119|pmid-9679948|pmid-9744541|pmid-7525094|pmid-8640931|pmid-11606502|pmid-11731407|pmid-9102204 | Therefore, it may be useful in clarifying the biological role of iNOS expression on Barrett's esophagus-associated adenocarcinoma to study the effect of iNOS inhibitor on animal esophageal adenocarcinoma model. | [
"10",
"12",
"22",
"23",
"24",
"25",
"11"
] | 210 | 42,619 | 0 | false | Therefore, it may be useful in clarifying the biological role of iNOS expression on Barrett's esophagus-associated adenocarcinoma to study the effect of iNOS inhibitor on animal esophageal adenocarcinoma model. | [] | Therefore, it may be useful in clarifying the biological role of iNOS expression on Barrett's esophagus-associated adenocarcinoma to study the effect of iNOS inhibitor on animal esophageal adenocarcinoma model. | true | true | true | true | true | 7,386 |
2 | DISCUSSION | 1 | 18 | [
"B18",
"B26",
"B27",
"B28",
"B29",
"B10",
"B12",
"B11"
] | 15,716,603 | pmid-14684572|pmid-14648704|pmid-7688473|pmid-7514189|pmid-11910360|pmid-9679948|pmid-9744541|pmid-9102204 | We have observed over-expression of COX-2, microsomal prostaglandin synthase-1 and EP receptors in this model (18). | [
"18",
"26",
"27",
"28",
"29",
"10",
"12",
"11"
] | 115 | 42,620 | 1 | false | We have observed over-expression of COX-2, microsomal prostaglandin synthase-1 and EP receptors in this model. | [
"18"
] | We have observed over-expression of COX-2, microsomal prostaglandin synthase-1 and EP receptors in this model. | true | true | true | true | true | 7,387 |
2 | DISCUSSION | 1 | 26 | [
"B18",
"B26",
"B27",
"B28",
"B29",
"B10",
"B12",
"B11"
] | 15,716,603 | pmid-14684572|pmid-14648704|pmid-7688473|pmid-7514189|pmid-11910360|pmid-9679948|pmid-9744541|pmid-9102204 | Recently, PGE2 mediates up-regulation of iNOS in murine breast cancer cell line through EP4 receptors activation (26). | [
"18",
"26",
"27",
"28",
"29",
"10",
"12",
"11"
] | 118 | 42,621 | 1 | false | Recently, PGE2 mediates up-regulation of iNOS in murine breast cancer cell line through EP4 receptors activation. | [
"26"
] | Recently, PGE2 mediates up-regulation of iNOS in murine breast cancer cell line through EP4 receptors activation. | true | true | true | true | true | 7,387 |
2 | DISCUSSION | 1 | 18 | [
"B18",
"B26",
"B27",
"B28",
"B29",
"B10",
"B12",
"B11"
] | 15,716,603 | pmid-14684572|pmid-14648704|pmid-7688473|pmid-7514189|pmid-11910360|pmid-9679948|pmid-9744541|pmid-9102204 | NO has been also found to enhance the activity and expression of COX-2 (27, 28). | [
"18",
"26",
"27",
"28",
"29",
"10",
"12",
"11"
] | 80 | 42,622 | 0 | false | NO has been also found to enhance the activity and expression of COX-2. | [
"27, 28"
] | NO has been also found to enhance the activity and expression of COX-2. | true | true | true | true | true | 7,387 |
2 | DISCUSSION | 1 | 29 | [
"B18",
"B26",
"B27",
"B28",
"B29",
"B10",
"B12",
"B11"
] | 15,716,603 | pmid-14684572|pmid-14648704|pmid-7688473|pmid-7514189|pmid-11910360|pmid-9679948|pmid-9744541|pmid-9102204 | Use of COX-2 inhibitors resulted in a reduction of the development of esophageal adenocarcinoma induced by duodenal reflux (29). | [
"18",
"26",
"27",
"28",
"29",
"10",
"12",
"11"
] | 128 | 42,623 | 1 | false | Use of COX-2 inhibitors resulted in a reduction of the development of esophageal adenocarcinoma induced by duodenal reflux. | [
"29"
] | Use of COX-2 inhibitors resulted in a reduction of the development of esophageal adenocarcinoma induced by duodenal reflux. | true | true | true | true | true | 7,387 |
2 | DISCUSSION | 1 | 18 | [
"B18",
"B26",
"B27",
"B28",
"B29",
"B10",
"B12",
"B11"
] | 15,716,603 | pmid-14684572|pmid-14648704|pmid-7688473|pmid-7514189|pmid-11910360|pmid-9679948|pmid-9744541|pmid-9102204 | These findings suggest that cross talk between NO and COX pathway may play an important role in Barrett's esophagus-associated neoplastic progression. | [
"18",
"26",
"27",
"28",
"29",
"10",
"12",
"11"
] | 150 | 42,624 | 0 | false | These findings suggest that cross talk between NO and COX pathway may play an important role in Barrett's esophagus-associated neoplastic progression. | [] | These findings suggest that cross talk between NO and COX pathway may play an important role in Barrett's esophagus-associated neoplastic progression. | true | true | true | true | true | 7,387 |
2 | DISCUSSION | 1 | 18 | [
"B18",
"B26",
"B27",
"B28",
"B29",
"B10",
"B12",
"B11"
] | 15,716,603 | pmid-14684572|pmid-14648704|pmid-7688473|pmid-7514189|pmid-11910360|pmid-9679948|pmid-9744541|pmid-9102204 | In Barrett's esophagus, iNOS expression was observed at the cytoplasmic area of stromal and epithelial cells (10, 12). | [
"18",
"26",
"27",
"28",
"29",
"10",
"12",
"11"
] | 118 | 42,625 | 0 | false | In Barrett's esophagus, iNOS expression was observed at the cytoplasmic area of stromal and epithelial cells. | [
"10, 12"
] | In Barrett's esophagus, iNOS expression was observed at the cytoplasmic area of stromal and epithelial cells. | true | true | true | true | true | 7,387 |
2 | DISCUSSION | 1 | 18 | [
"B18",
"B26",
"B27",
"B28",
"B29",
"B10",
"B12",
"B11"
] | 15,716,603 | pmid-14684572|pmid-14648704|pmid-7688473|pmid-7514189|pmid-11910360|pmid-9679948|pmid-9744541|pmid-9102204 | In contrast, our study revealed characteristic localization at the apical surface of epithelial cells. | [
"18",
"26",
"27",
"28",
"29",
"10",
"12",
"11"
] | 102 | 42,626 | 0 | false | In contrast, our study revealed characteristic localization at the apical surface of epithelial cells. | [] | In contrast, our study revealed characteristic localization at the apical surface of epithelial cells. | true | true | true | true | true | 7,387 |
2 | DISCUSSION | 1 | 11 | [
"B18",
"B26",
"B27",
"B28",
"B29",
"B10",
"B12",
"B11"
] | 15,716,603 | pmid-14684572|pmid-14648704|pmid-7688473|pmid-7514189|pmid-11910360|pmid-9679948|pmid-9744541|pmid-9102204 | This result is in agreement with immunolocalization of iNOS in rat colon tumors induced by azoxymethane (11). | [
"18",
"26",
"27",
"28",
"29",
"10",
"12",
"11"
] | 109 | 42,627 | 1 | false | This result is in agreement with immunolocalization of iNOS in rat colon tumors induced by azoxymethane. | [
"11"
] | This result is in agreement with immunolocalization of iNOS in rat colon tumors induced by azoxymethane. | true | true | true | true | true | 7,387 |
2 | DISCUSSION | 1 | 18 | [
"B18",
"B26",
"B27",
"B28",
"B29",
"B10",
"B12",
"B11"
] | 15,716,603 | pmid-14684572|pmid-14648704|pmid-7688473|pmid-7514189|pmid-11910360|pmid-9679948|pmid-9744541|pmid-9102204 | Its significance remains to be determined. | [
"18",
"26",
"27",
"28",
"29",
"10",
"12",
"11"
] | 42 | 42,628 | 0 | false | Its significance remains to be determined. | [] | Its significance remains to be determined. | true | true | true | true | true | 7,387 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B1"
] | 20,733,961 | pmid-9598491|pmid-9598491|pmid-16939474|pmid-7816861|pmid-2357567 | Selective serotonin reuptake inhibitors (SSRIs) have previously been used as a treatment for premature ejaculation. | [
"1",
"1"
] | 115 | 42,629 | 0 | false | Selective serotonin reuptake inhibitors (SSRIs) have previously been used as a treatment for premature ejaculation. | [] | Selective serotonin reuptake inhibitors (SSRIs) have previously been used as a treatment for premature ejaculation. | true | true | true | true | true | 7,388 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B1"
] | 20,733,961 | pmid-9598491|pmid-9598491|pmid-16939474|pmid-7816861|pmid-2357567 | The use of SSRIs for the treatment of premature ejaculation began after it was discovered that treatment of depression in males with SSRIs resulted in a side effect of delayed ejaculation [1]. | [
"1",
"1"
] | 192 | 42,630 | 1 | false | The use of SSRIs for the treatment of premature ejaculation began after it was discovered that treatment of depression in males with SSRIs resulted in a side effect of delayed ejaculation. | [
"1"
] | The use of SSRIs for the treatment of premature ejaculation began after it was discovered that treatment of depression in males with SSRIs resulted in a side effect of delayed ejaculation. | true | true | true | true | true | 7,388 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B1"
] | 20,733,961 | pmid-9598491|pmid-9598491|pmid-16939474|pmid-7816861|pmid-2357567 | Sertraline is an SSRI, and its treatment efficacy for premature ejaculation has also been reported | [
"1",
"1"
] | 98 | 42,631 | 0 | false | Sertraline is an SSRI, and its treatment efficacy for premature ejaculation has also been reported | [] | Sertraline is an SSRI, and its treatment efficacy for premature ejaculation has also been reported | true | true | false | true | false | 7,388 |
1 | INTRODUCTION | 1 | 2 | [
"B2"
] | 20,733,961 | pmid-7876038|pmid-18194183 | Current-source analysis of electroencephalography (EEG) is an electrographic and functional imaging method that is used to find the current source of neuronal activity of the brain. | [
"2"
] | 181 | 42,632 | 0 | false | Current-source analysis of electroencephalography (EEG) is an electrographic and functional imaging method that is used to find the current source of neuronal activity of the brain. | [] | Current-source analysis of electroencephalography (EEG) is an electrographic and functional imaging method that is used to find the current source of neuronal activity of the brain. | true | true | true | true | true | 7,389 |
1 | INTRODUCTION | 1 | 2 | [
"B2"
] | 20,733,961 | pmid-7876038|pmid-18194183 | It involves a computational and mathematical algorithm that analyzes digital EEG data. | [
"2"
] | 86 | 42,633 | 0 | false | It involves a computational and mathematical algorithm that analyzes digital EEG data. | [] | It involves a computational and mathematical algorithm that analyzes digital EEG data. | true | true | true | true | true | 7,389 |
1 | INTRODUCTION | 1 | 2 | [
"B2"
] | 20,733,961 | pmid-7876038|pmid-18194183 | The discrete model of current-source analysis provides information about location, strength, and orientation of current-source dipoles. | [
"2"
] | 135 | 42,634 | 0 | false | The discrete model of current-source analysis provides information about location, strength, and orientation of current-source dipoles. | [] | The discrete model of current-source analysis provides information about location, strength, and orientation of current-source dipoles. | true | true | true | true | true | 7,389 |
1 | INTRODUCTION | 1 | 2 | [
"B2"
] | 20,733,961 | pmid-7876038|pmid-18194183 | The distributed model is a method used to find the location and extent of the current source distribution. | [
"2"
] | 106 | 42,635 | 0 | false | The distributed model is a method used to find the location and extent of the current source distribution. | [] | The distributed model is a method used to find the location and extent of the current source distribution. | true | true | true | true | true | 7,389 |
1 | INTRODUCTION | 1 | 2 | [
"B2"
] | 20,733,961 | pmid-7876038|pmid-18194183 | Low-resolution electromagnetic tomography (LORETA) is a distributed model of current-source analysis [2]. | [
"2"
] | 105 | 42,636 | 1 | false | Low-resolution electromagnetic tomography (LORETA) is a distributed model of current-source analysis. | [
"2"
] | Low-resolution electromagnetic tomography (LORETA) is a distributed model of current-source analysis. | true | true | true | true | true | 7,389 |
2 | INTRODUCTION | 1 | 3 | [
"B3",
"B4",
"B5"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | Studies of neurocognitive function using EEG data have focused on the frequency band above 20 Hz. | [
"3",
"4",
"5"
] | 97 | 42,637 | 0 | false | Studies of neurocognitive function using EEG data have focused on the frequency band above 20 Hz. | [] | Studies of neurocognitive function using EEG data have focused on the frequency band above 20 Hz. | true | true | true | true | true | 7,390 |
2 | INTRODUCTION | 1 | 3 | [
"B3",
"B4",
"B5"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | It has been shown in human EEG studies that cortical high-frequency activity is topically enhanced in various cognitive processes [3]. | [
"3",
"4",
"5"
] | 134 | 42,638 | 1 | false | It has been shown in human EEG studies that cortical high-frequency activity is topically enhanced in various cognitive processes. | [
"3"
] | It has been shown in human EEG studies that cortical high-frequency activity is topically enhanced in various cognitive processes. | true | true | true | true | true | 7,390 |
2 | INTRODUCTION | 1 | 3 | [
"B3",
"B4",
"B5"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | Complex cognitive tasks ignite neuronal cell assemblies and activate loops of neuronal networks. | [
"3",
"4",
"5"
] | 96 | 42,639 | 0 | false | Complex cognitive tasks ignite neuronal cell assemblies and activate loops of neuronal networks. | [] | Complex cognitive tasks ignite neuronal cell assemblies and activate loops of neuronal networks. | true | true | true | true | true | 7,390 |
2 | INTRODUCTION | 1 | 4 | [
"B3",
"B4",
"B5"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | In the case of language processing, a loop between Broca's and Wernicke's regions is activated [4]. | [
"3",
"4",
"5"
] | 99 | 42,640 | 1 | false | In the case of language processing, a loop between Broca's and Wernicke's regions is activated. | [
"4"
] | In the case of language processing, a loop between Broca's and Wernicke's regions is activated. | true | true | true | true | true | 7,390 |
2 | INTRODUCTION | 1 | 3 | [
"B3",
"B4",
"B5"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | The neuronal oscillations have a circulation frequency of 25 to 30 Hz. | [
"3",
"4",
"5"
] | 70 | 42,641 | 0 | false | The neuronal oscillations have a circulation frequency of 25 to 30 Hz. | [] | The neuronal oscillations have a circulation frequency of 25 to 30 Hz. | true | true | true | true | true | 7,390 |
2 | INTRODUCTION | 1 | 5 | [
"B3",
"B4",
"B5"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | In contrast, higher-frequency oscillatory cortical activity, in the range of 40 to 60 Hz, is observed in less widely dispersed cell assemblies [5]. | [
"3",
"4",
"5"
] | 147 | 42,642 | 1 | false | In contrast, higher-frequency oscillatory cortical activity, in the range of 40 to 60 Hz, is observed in less widely dispersed cell assemblies. | [
"5"
] | In contrast, higher-frequency oscillatory cortical activity, in the range of 40 to 60 Hz, is observed in less widely dispersed cell assemblies. | true | true | true | true | true | 7,390 |
2 | INTRODUCTION | 1 | 3 | [
"B3",
"B4",
"B5"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | The highest frequency band that can be analyzed by LORETA is the high beta frequency band (22-30 Hz). | [
"3",
"4",
"5"
] | 101 | 42,643 | 0 | false | The highest frequency band that can be analyzed by LORETA is the high beta frequency band. | [
"22-30 Hz"
] | The highest frequency band that can be analyzed by LORETA is the high beta frequency band. | true | true | true | true | true | 7,390 |
2 | INTRODUCTION | 1 | 3 | [
"B3",
"B4",
"B5"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | The analysis of this frequency band may be helpful for evaluating neurocognitive functions in various situations. | [
"3",
"4",
"5"
] | 113 | 42,644 | 0 | false | The analysis of this frequency band may be helpful for evaluating neurocognitive functions in various situations. | [] | The analysis of this frequency band may be helpful for evaluating neurocognitive functions in various situations. | true | true | true | true | true | 7,390 |
3 | INTRODUCTION | 1 | 6 | [
"B6"
] | 20,733,961 | pmid-18194183 | Little is known about the cerebral control mechanisms of ejaculation. | [
"6"
] | 69 | 42,645 | 0 | false | Little is known about the cerebral control mechanisms of ejaculation. | [] | Little is known about the cerebral control mechanisms of ejaculation. | true | true | true | true | true | 7,391 |
3 | INTRODUCTION | 1 | 6 | [
"B6"
] | 20,733,961 | pmid-18194183 | According to our previous study using EEG recordings from patients with premature ejaculation (PE) [6], we observed decreased neuronal activity in the precentral gyrus and the insula of the right cerebral hemisphere and in both superior parietal lobules during sexual arousal induced by erotic videos. | [
"6"
] | 301 | 42,646 | 1 | false | According to our previous study using EEG recordings from patients with premature ejaculation (PE), we observed decreased neuronal activity in the precentral gyrus and the insula of the right cerebral hemisphere and in both superior parietal lobules during sexual arousal induced by erotic videos. | [
"6"
] | According to our previous study using EEG recordings from patients with premature ejaculation (PE), we observed decreased neuronal activity in the precentral gyrus and the insula of the right cerebral hemisphere and in both superior parietal lobules during sexual arousal induced by erotic videos. | true | true | true | true | true | 7,391 |
3 | INTRODUCTION | 1 | 6 | [
"B6"
] | 20,733,961 | pmid-18194183 | In addition, the neuronal activity of PE patients decreased in the right parahippocampal gyrus and in the left middle temporal gyrus compared with normal controls. | [
"6"
] | 163 | 42,647 | 0 | false | In addition, the neuronal activity of PE patients decreased in the right parahippocampal gyrus and in the left middle temporal gyrus compared with normal controls. | [] | In addition, the neuronal activity of PE patients decreased in the right parahippocampal gyrus and in the left middle temporal gyrus compared with normal controls. | true | true | true | true | true | 7,391 |
3 | INTRODUCTION | 1 | 6 | [
"B6"
] | 20,733,961 | pmid-18194183 | These findings suggest that the inhibitory control of ejaculation in the central nervous system may be impaired in PE patients. | [
"6"
] | 127 | 42,648 | 0 | false | These findings suggest that the inhibitory control of ejaculation in the central nervous system may be impaired in PE patients. | [] | These findings suggest that the inhibitory control of ejaculation in the central nervous system may be impaired in PE patients. | true | true | true | true | true | 7,391 |
3 | INTRODUCTION | 1 | 6 | [
"B6"
] | 20,733,961 | pmid-18194183 | The purpose of this study was to examine the changes in the brain current-source density of the high beta frequency band (22-30 Hz) induced by sertraline administration and erotic stimuli in healthy adult males. | [
"6"
] | 211 | 42,649 | 0 | false | The purpose of this study was to examine the changes in the brain current-source density of the high beta frequency band (22-30 Hz) induced by sertraline administration and erotic stimuli in healthy adult males. | [] | The purpose of this study was to examine the changes in the brain current-source density of the high beta frequency band (22-30 Hz) induced by sertraline administration and erotic stimuli in healthy adult males. | true | true | true | true | true | 7,391 |
0 | DISCUSSION | 1 | 12 | [
"B12",
"B14",
"B13"
] | 20,733,961 | pmid-9598491|pmid-9598491|pmid-16939474|pmid-7816861|pmid-2357567 | It is known that the serotonin pathway plays a role in the mechanism of ejaculation in males. | [
"12",
"14",
"13"
] | 93 | 42,650 | 0 | false | It is known that the serotonin pathway plays a role in the mechanism of ejaculation in males. | [] | It is known that the serotonin pathway plays a role in the mechanism of ejaculation in males. | true | true | true | true | true | 7,392 |
0 | DISCUSSION | 1 | 12 | [
"B12",
"B14",
"B13"
] | 20,733,961 | pmid-9598491|pmid-9598491|pmid-16939474|pmid-7816861|pmid-2357567 | In the central nervous system, the medial preoptic area, nucleus paragigantocellularis, stria terminalis, amygdala, and thalamus may be the anatomical locations associated with this mechanism [12-14]. | [
"12",
"14",
"13"
] | 200 | 42,651 | 0 | false | In the central nervous system, the medial preoptic area, nucleus paragigantocellularis, stria terminalis, amygdala, and thalamus may be the anatomical locations associated with this mechanism. | [
"12-14"
] | In the central nervous system, the medial preoptic area, nucleus paragigantocellularis, stria terminalis, amygdala, and thalamus may be the anatomical locations associated with this mechanism. | true | true | true | true | true | 7,392 |
0 | DISCUSSION | 1 | 12 | [
"B12",
"B14",
"B13"
] | 20,733,961 | pmid-9598491|pmid-9598491|pmid-16939474|pmid-7816861|pmid-2357567 | Serotonergic pathways descending from the nucleus paragigantocellularis to the lumbosacral motor nuclei tonically inhibit ejaculation. | [
"12",
"14",
"13"
] | 134 | 42,652 | 0 | false | Serotonergic pathways descending from the nucleus paragigantocellularis to the lumbosacral motor nuclei tonically inhibit ejaculation. | [] | Serotonergic pathways descending from the nucleus paragigantocellularis to the lumbosacral motor nuclei tonically inhibit ejaculation. | true | true | true | true | true | 7,392 |
0 | DISCUSSION | 1 | 13 | [
"B12",
"B14",
"B13"
] | 20,733,961 | pmid-9598491|pmid-9598491|pmid-16939474|pmid-7816861|pmid-2357567 | When the signal from the medial preoptic area inhibits the nucleus paragigantocellularis, the motor nuclei in the lumbosacral spinal area are released from the tonic inhibition of the nucleus paragigantocellularis, which allows ejaculation [13]. | [
"12",
"14",
"13"
] | 245 | 42,653 | 1 | false | When the signal from the medial preoptic area inhibits the nucleus paragigantocellularis, the motor nuclei in the lumbosacral spinal area are released from the tonic inhibition of the nucleus paragigantocellularis, which allows ejaculation. | [
"13"
] | When the signal from the medial preoptic area inhibits the nucleus paragigantocellularis, the motor nuclei in the lumbosacral spinal area are released from the tonic inhibition of the nucleus paragigantocellularis, which allows ejaculation. | true | true | true | true | true | 7,392 |
1 | DISCUSSION | 1 | 6 | [
"B6"
] | 20,733,961 | pmid-7876038|pmid-18194183 | In our previous study, we found that the neuronal activity of PE patients decreased in the precentral gyrus and the insula of the right cerebral hemisphere and in both of the superior parietal lobules during sexual arousal induced by erotic videos [6]. | [
"6"
] | 252 | 42,654 | 1 | false | In our previous study, we found that the neuronal activity of PE patients decreased in the precentral gyrus and the insula of the right cerebral hemisphere and in both of the superior parietal lobules during sexual arousal induced by erotic videos. | [
"6"
] | In our previous study, we found that the neuronal activity of PE patients decreased in the precentral gyrus and the insula of the right cerebral hemisphere and in both of the superior parietal lobules during sexual arousal induced by erotic videos. | true | true | true | true | true | 7,393 |
1 | DISCUSSION | 1 | 6 | [
"B6"
] | 20,733,961 | pmid-7876038|pmid-18194183 | In addition, the activity decreased in the right parahippocampal gyrus and in the left middle temporal gyrus compared with the normal controls. | [
"6"
] | 143 | 42,655 | 0 | false | In addition, the activity decreased in the right parahippocampal gyrus and in the left middle temporal gyrus compared with the normal controls. | [] | In addition, the activity decreased in the right parahippocampal gyrus and in the left middle temporal gyrus compared with the normal controls. | true | true | true | true | true | 7,393 |
1 | DISCUSSION | 1 | 6 | [
"B6"
] | 20,733,961 | pmid-7876038|pmid-18194183 | These results suggested that the debasement of inhibitory control in the central nervous system located above the medial preoptic area may be a cause of premature ejaculation. | [
"6"
] | 175 | 42,656 | 0 | false | These results suggested that the debasement of inhibitory control in the central nervous system located above the medial preoptic area may be a cause of premature ejaculation. | [] | These results suggested that the debasement of inhibitory control in the central nervous system located above the medial preoptic area may be a cause of premature ejaculation. | true | true | true | true | true | 7,393 |
2 | DISCUSSION | 1 | 15 | [
"B15"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | When SSRIs are administered to patients for the treatment of depression, the brain activity measured by functional magnetic resonance imaging (fMRI) decreases in the cingulate gyrus and the caudate nucleus | [
"15"
] | 205 | 42,657 | 0 | false | When SSRIs are administered to patients for the treatment of depression, the brain activity measured by functional magnetic resonance imaging (fMRI) decreases in the cingulate gyrus and the caudate nucleus | [] | When SSRIs are administered to patients for the treatment of depression, the brain activity measured by functional magnetic resonance imaging (fMRI) decreases in the cingulate gyrus and the caudate nucleus | true | true | false | true | false | 7,394 |
2 | DISCUSSION | 1 | 15 | [
"B15"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | Positron emission tomography (PET) and fMRI are methods used to evaluate neural activity indirectly by observing local cerebral blood flow or metabolism without observing neuronal activity directly. | [
"15"
] | 198 | 42,658 | 0 | false | Positron emission tomography (PET) and fMRI are methods used to evaluate neural activity indirectly by observing local cerebral blood flow or metabolism without observing neuronal activity directly. | [] | Positron emission tomography (PET) and fMRI are methods used to evaluate neural activity indirectly by observing local cerebral blood flow or metabolism without observing neuronal activity directly. | true | true | true | true | true | 7,394 |
2 | DISCUSSION | 1 | 15 | [
"B15"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | In contrast, the current-source analysis of EEGs observes the electric activity of neurons directly. | [
"15"
] | 100 | 42,659 | 0 | false | In contrast, the current-source analysis of EEGs observes the electric activity of neurons directly. | [] | In contrast, the current-source analysis of EEGs observes the electric activity of neurons directly. | true | true | true | true | true | 7,394 |
2 | DISCUSSION | 1 | 15 | [
"B15"
] | 20,733,961 | pmid-20331719|pmid-8753932|pmid-7577330|NA | Therefore, results from the current-source analysis of EEGs may differ from the results of studies using PET or fMRI. | [
"15"
] | 117 | 42,660 | 0 | false | Therefore, results from the current-source analysis of EEGs may differ from the results of studies using PET or fMRI. | [] | Therefore, results from the current-source analysis of EEGs may differ from the results of studies using PET or fMRI. | true | true | true | true | true | 7,394 |
3 | DISCUSSION | 0 | null | null | 20,733,961 | pmid-18194183 | We recorded EEGs before and 4 hours after sertraline intake in healthy, right-handed young males under erotic stimulation using sexual video excerpts and analyzed the current source of the high beta frequency band by using a distributed model. | null | 243 | 42,661 | 0 | false | null | null | We recorded EEGs before and 4 hours after sertraline intake in healthy, right-handed young males under erotic stimulation using sexual video excerpts and analyzed the current source of the high beta frequency band by using a distributed model. | true | true | true | true | true | 7,395 |
3 | DISCUSSION | 0 | null | null | 20,733,961 | pmid-18194183 | Erotic stimuli decreased the current source density of the high beta frequency band in the middle frontal gyrus, the precentral gyrus, the postcentral gyrus, and the supramarginal gyrus of the left cerebral hemisphere in the baseline EEGs (p<0.05) (Table 1, Fig. | null | 262 | 42,662 | 0 | false | null | null | Erotic stimuli decreased the current source density of the high beta frequency band in the middle frontal gyrus, the precentral gyrus, the postcentral gyrus, and the supramarginal gyrus of the left cerebral hemisphere in the baseline EEGs (p<0.05) (Table 1, Fig. | true | true | true | true | true | 7,395 |
3 | DISCUSSION | 0 | null | null | 20,733,961 | pmid-18194183 | These changes were not observed 4 hours after sertraline was administered. | null | 74 | 42,663 | 0 | false | null | null | These changes were not observed 4 hours after sertraline was administered. | true | true | true | true | true | 7,395 |
3 | DISCUSSION | 0 | null | null | 20,733,961 | pmid-18194183 | In addition, we also observed that sertraline increased the current-source density in the superior, middle, and inferior frontal gyri and the precentral gyrus of the left cerebral hemisphere (p<0.05) (Table 2, Fig 2). | null | 217 | 42,664 | 0 | false | null | null | In addition, we also observed that sertraline increased the current-source density in the superior, middle, and inferior frontal gyri and the precentral gyrus of the left cerebral hemisphere (p<0.05) (Table 2, Fig 2). | true | true | true | true | true | 7,395 |
3 | DISCUSSION | 0 | null | null | 20,733,961 | pmid-18194183 | According to these results, the erotic stimuli may trigger a functional debasement of inhibitory controls in the middle frontal gyrus, the postcentral gyrus, the precentral gyrus, and the supramarginal gyrus of the left cerebral hemisphere, which may lead to the sexually excited state. | null | 286 | 42,665 | 0 | false | null | null | According to these results, the erotic stimuli may trigger a functional debasement of inhibitory controls in the middle frontal gyrus, the postcentral gyrus, the precentral gyrus, and the supramarginal gyrus of the left cerebral hemisphere, which may lead to the sexually excited state. | true | true | true | true | true | 7,395 |
3 | DISCUSSION | 0 | null | null | 20,733,961 | pmid-18194183 | It is also possible that sertraline may suppress these cerebral changes and decrease sexual excitement. | null | 103 | 42,666 | 0 | false | null | null | It is also possible that sertraline may suppress these cerebral changes and decrease sexual excitement. | true | true | true | true | true | 7,395 |
3 | DISCUSSION | 0 | null | null | 20,733,961 | pmid-18194183 | In addition, sertraline may reduce the excessive sexual excitement in the brain, prolong the duration of an erection, and suppress ejaculation. | null | 143 | 42,667 | 0 | false | null | null | In addition, sertraline may reduce the excessive sexual excitement in the brain, prolong the duration of an erection, and suppress ejaculation. | true | true | true | true | true | 7,395 |
4 | DISCUSSION | 1 | 16 | [
"B16",
"B17",
"B18",
"B19"
] | 20,733,961 | pmid-19818382|pmid-19407204|pmid-17823419|pmid-16399686 | The prefrontal cortex is known to be a crucial area for cognitive control [16], and the dorsolateral prefrontal cortex (DLPFC) is involved in self-control | [
"16",
"17",
"18",
"19"
] | 154 | 42,668 | 1 | false | The prefrontal cortex is known to be a crucial area for cognitive control, and the dorsolateral prefrontal cortex (DLPFC) is involved in self-control | [
"16"
] | The prefrontal cortex is known to be a crucial area for cognitive control, and the dorsolateral prefrontal cortex (DLPFC) is involved in self-control | true | true | false | true | false | 7,396 |
4 | DISCUSSION | 1 | 18 | [
"B16",
"B17",
"B18",
"B19"
] | 20,733,961 | pmid-19818382|pmid-19407204|pmid-17823419|pmid-16399686 | In a study observing the reaction of the cerebral cortex to meals in right-handed females, the decreased activity of the left DLPFC was associated with poor control of appetite and resulting obesity [18]. | [
"16",
"17",
"18",
"19"
] | 204 | 42,669 | 1 | false | In a study observing the reaction of the cerebral cortex to meals in right-handed females, the decreased activity of the left DLPFC was associated with poor control of appetite and resulting obesity. | [
"18"
] | In a study observing the reaction of the cerebral cortex to meals in right-handed females, the decreased activity of the left DLPFC was associated with poor control of appetite and resulting obesity. | true | true | true | true | true | 7,396 |
4 | DISCUSSION | 1 | 19 | [
"B16",
"B17",
"B18",
"B19"
] | 20,733,961 | pmid-19818382|pmid-19407204|pmid-17823419|pmid-16399686 | In another study investigating the association between the stop-signal task and response inhibition, the precentral gyrus of the left cerebral hemisphere was activated during response inhibition, and this activation was associated with the stop-signal reaction time [19]. | [
"16",
"17",
"18",
"19"
] | 271 | 42,670 | 1 | false | In another study investigating the association between the stop-signal task and response inhibition, the precentral gyrus of the left cerebral hemisphere was activated during response inhibition, and this activation was associated with the stop-signal reaction time. | [
"19"
] | In another study investigating the association between the stop-signal task and response inhibition, the precentral gyrus of the left cerebral hemisphere was activated during response inhibition, and this activation was associated with the stop-signal reaction time. | true | true | true | true | true | 7,396 |
4 | DISCUSSION | 1 | 16 | [
"B16",
"B17",
"B18",
"B19"
] | 20,733,961 | pmid-19818382|pmid-19407204|pmid-17823419|pmid-16399686 | Our results are similar to these reports in showing that the activity of the middle frontal gyrus and the precentral gyrus of the left cerebral hemisphere decreased during sexual arousal in right-handed healthy young males. | [
"16",
"17",
"18",
"19"
] | 223 | 42,671 | 0 | false | Our results are similar to these reports in showing that the activity of the middle frontal gyrus and the precentral gyrus of the left cerebral hemisphere decreased during sexual arousal in right-handed healthy young males. | [] | Our results are similar to these reports in showing that the activity of the middle frontal gyrus and the precentral gyrus of the left cerebral hemisphere decreased during sexual arousal in right-handed healthy young males. | true | true | true | true | true | 7,396 |
4 | DISCUSSION | 1 | 16 | [
"B16",
"B17",
"B18",
"B19"
] | 20,733,961 | pmid-19818382|pmid-19407204|pmid-17823419|pmid-16399686 | These changes recovered after administration of sertraline. | [
"16",
"17",
"18",
"19"
] | 59 | 42,672 | 0 | false | These changes recovered after administration of sertraline. | [] | These changes recovered after administration of sertraline. | true | true | true | true | true | 7,396 |
4 | DISCUSSION | 1 | 16 | [
"B16",
"B17",
"B18",
"B19"
] | 20,733,961 | pmid-19818382|pmid-19407204|pmid-17823419|pmid-16399686 | Taken together, these findings suggest that the debasement of inhibitory control by erotic stimuli in the middle frontal gyrus and the precentral gyrus of the left cerebral hemisphere may lead healthy young males to be excited sexually. | [
"16",
"17",
"18",
"19"
] | 236 | 42,673 | 0 | false | Taken together, these findings suggest that the debasement of inhibitory control by erotic stimuli in the middle frontal gyrus and the precentral gyrus of the left cerebral hemisphere may lead healthy young males to be excited sexually. | [] | Taken together, these findings suggest that the debasement of inhibitory control by erotic stimuli in the middle frontal gyrus and the precentral gyrus of the left cerebral hemisphere may lead healthy young males to be excited sexually. | true | true | true | true | true | 7,396 |
4 | DISCUSSION | 1 | 16 | [
"B16",
"B17",
"B18",
"B19"
] | 20,733,961 | pmid-19818382|pmid-19407204|pmid-17823419|pmid-16399686 | These results also suggest that inhibitory control may be recovered by the effects of sertraline. | [
"16",
"17",
"18",
"19"
] | 97 | 42,674 | 0 | false | These results also suggest that inhibitory control may be recovered by the effects of sertraline. | [] | These results also suggest that inhibitory control may be recovered by the effects of sertraline. | true | true | true | true | true | 7,396 |
5 | DISCUSSION | 1 | 20 | [
"B20",
"B21"
] | 20,733,961 | pmid-9918735|pmid-12382157 | The supramarginal gyrus of the left cerebral hemisphere is responsible for the detection of changes in phonological units [20]. | [
"20",
"21"
] | 127 | 42,675 | 1 | false | The supramarginal gyrus of the left cerebral hemisphere is responsible for the detection of changes in phonological units. | [
"20"
] | The supramarginal gyrus of the left cerebral hemisphere is responsible for the detection of changes in phonological units. | true | true | true | true | true | 7,397 |
5 | DISCUSSION | 1 | 21 | [
"B20",
"B21"
] | 20,733,961 | pmid-9918735|pmid-12382157 | The postcentral gyrus is a somatosensory area, and lesions in the left postcentral gyrus induce sensory changes in the contralateral face and body [21]. | [
"20",
"21"
] | 152 | 42,676 | 1 | false | The postcentral gyrus is a somatosensory area, and lesions in the left postcentral gyrus induce sensory changes in the contralateral face and body. | [
"21"
] | The postcentral gyrus is a somatosensory area, and lesions in the left postcentral gyrus induce sensory changes in the contralateral face and body. | true | true | true | true | true | 7,397 |
5 | DISCUSSION | 1 | 20 | [
"B20",
"B21"
] | 20,733,961 | pmid-9918735|pmid-12382157 | Even though it is difficult to interpret the changes induced by erotic stimuli in those areas, the aforementioned structures may also be a part of the cerebral inhibitory center that controls sexual excitement in males. | [
"20",
"21"
] | 219 | 42,677 | 0 | false | Even though it is difficult to interpret the changes induced by erotic stimuli in those areas, the aforementioned structures may also be a part of the cerebral inhibitory center that controls sexual excitement in males. | [] | Even though it is difficult to interpret the changes induced by erotic stimuli in those areas, the aforementioned structures may also be a part of the cerebral inhibitory center that controls sexual excitement in males. | true | true | true | true | true | 7,397 |
6 | DISCUSSION | 1 | 22 | [
"B22",
"B22",
"B24",
"B25",
"B26",
"B27"
] | 20,733,961 | pmid-10348329|pmid-10348329|pmid-11738201|pmid-15351361|pmid-16253551|pmid-17029950 | We used the small number of 25 available channels, which could have resulted in some localization errors, particularly in the basal aspects of the brain [22]. | [
"22",
"22",
"24",
"25",
"26",
"27"
] | 158 | 42,678 | 1 | false | We used the small number of 25 available channels, which could have resulted in some localization errors, particularly in the basal aspects of the brain. | [
"22"
] | We used the small number of 25 available channels, which could have resulted in some localization errors, particularly in the basal aspects of the brain. | true | true | true | true | true | 7,398 |
6 | DISCUSSION | 1 | 22 | [
"B22",
"B22",
"B24",
"B25",
"B26",
"B27"
] | 20,733,961 | pmid-10348329|pmid-10348329|pmid-11738201|pmid-15351361|pmid-16253551|pmid-17029950 | The errors associated with using a spherical model with the small number of electrodes range from 10 to 20mm [22-24]. | [
"22",
"22",
"24",
"25",
"26",
"27"
] | 117 | 42,679 | 0 | false | The errors associated with using a spherical model with the small number of electrodes range from 10 to 20mm. | [
"22-24"
] | The errors associated with using a spherical model with the small number of electrodes range from 10 to 20mm. | true | true | true | true | true | 7,398 |
6 | DISCUSSION | 1 | 25 | [
"B22",
"B22",
"B24",
"B25",
"B26",
"B27"
] | 20,733,961 | pmid-10348329|pmid-10348329|pmid-11738201|pmid-15351361|pmid-16253551|pmid-17029950 | The localization accuracy for LORETA has been shown to increase using 25 to 89 electrodes and to plateau thereafter [25]. | [
"22",
"22",
"24",
"25",
"26",
"27"
] | 121 | 42,680 | 1 | false | The localization accuracy for LORETA has been shown to increase using 25 to 89 electrodes and to plateau thereafter. | [
"25"
] | The localization accuracy for LORETA has been shown to increase using 25 to 89 electrodes and to plateau thereafter. | true | true | true | true | true | 7,398 |
6 | DISCUSSION | 1 | 22 | [
"B22",
"B22",
"B24",
"B25",
"B26",
"B27"
] | 20,733,961 | pmid-10348329|pmid-10348329|pmid-11738201|pmid-15351361|pmid-16253551|pmid-17029950 | However, to localize the areas of increased activity, the small number of electrodes may be sufficient for the SnPM method of LORETA [26,27]. | [
"22",
"22",
"24",
"25",
"26",
"27"
] | 141 | 42,681 | 0 | false | However, to localize the areas of increased activity, the small number of electrodes may be sufficient for the SnPM method of LORETA. | [
"26,27"
] | However, to localize the areas of increased activity, the small number of electrodes may be sufficient for the SnPM method of LORETA. | true | true | true | true | true | 7,398 |
6 | DISCUSSION | 1 | 22 | [
"B22",
"B22",
"B24",
"B25",
"B26",
"B27"
] | 20,733,961 | pmid-10348329|pmid-10348329|pmid-11738201|pmid-15351361|pmid-16253551|pmid-17029950 | It has also been observed that current source estimation using LORETA in a three-shell head model is similar when using between 19 and 46 scalp electrodes when the electrodes are evenly distributed. | [
"22",
"22",
"24",
"25",
"26",
"27"
] | 198 | 42,682 | 0 | false | It has also been observed that current source estimation using LORETA in a three-shell head model is similar when using between 19 and 46 scalp electrodes when the electrodes are evenly distributed. | [] | It has also been observed that current source estimation using LORETA in a three-shell head model is similar when using between 19 and 46 scalp electrodes when the electrodes are evenly distributed. | true | true | true | true | true | 7,398 |
6 | DISCUSSION | 1 | 22 | [
"B22",
"B22",
"B24",
"B25",
"B26",
"B27"
] | 20,733,961 | pmid-10348329|pmid-10348329|pmid-11738201|pmid-15351361|pmid-16253551|pmid-17029950 | To investigate cognitive function, lobar-level information may provide useful information, which is not the case for the current-source analysis of epilepsy. | [
"22",
"22",
"24",
"25",
"26",
"27"
] | 157 | 42,683 | 0 | false | To investigate cognitive function, lobar-level information may provide useful information, which is not the case for the current-source analysis of epilepsy. | [] | To investigate cognitive function, lobar-level information may provide useful information, which is not the case for the current-source analysis of epilepsy. | true | true | true | true | true | 7,398 |
7 | DISCUSSION | 1 | 28 | [
"B28"
] | 20,733,961 | pmid-16467858 | The changes in cerebral activity in response to erotic stimuli may differ depending on subject age [28]. | [
"28"
] | 104 | 42,684 | 1 | false | The changes in cerebral activity in response to erotic stimuli may differ depending on subject age. | [
"28"
] | The changes in cerebral activity in response to erotic stimuli may differ depending on subject age. | true | true | true | true | true | 7,399 |
7 | DISCUSSION | 1 | 28 | [
"B28"
] | 20,733,961 | pmid-16467858 | If the subjects were older, the results of this study could be different. | [
"28"
] | 73 | 42,685 | 0 | false | If the subjects were older, the results of this study could be different. | [] | If the subjects were older, the results of this study could be different. | true | true | true | true | true | 7,399 |
7 | DISCUSSION | 1 | 28 | [
"B28"
] | 20,733,961 | pmid-16467858 | The results and interpretation of this study may be limited to young males. | [
"28"
] | 75 | 42,686 | 0 | false | The results and interpretation of this study may be limited to young males. | [] | The results and interpretation of this study may be limited to young males. | true | true | true | true | true | 7,399 |
7 | DISCUSSION | 1 | 28 | [
"B28"
] | 20,733,961 | pmid-16467858 | Another limitation of this study is that we did not assess the objective level of sexual excitement by using penile erection status or other measures. | [
"28"
] | 150 | 42,687 | 0 | false | Another limitation of this study is that we did not assess the objective level of sexual excitement by using penile erection status or other measures. | [] | Another limitation of this study is that we did not assess the objective level of sexual excitement by using penile erection status or other measures. | true | true | true | true | true | 7,399 |
7 | DISCUSSION | 1 | 28 | [
"B28"
] | 20,733,961 | pmid-16467858 | We addressed this limitation by using a self-report questionnaire to evaluate the status of sexual excitement, and all subjects reported that they experienced penile erection with sexual excitement. | [
"28"
] | 198 | 42,688 | 0 | false | We addressed this limitation by using a self-report questionnaire to evaluate the status of sexual excitement, and all subjects reported that they experienced penile erection with sexual excitement. | [] | We addressed this limitation by using a self-report questionnaire to evaluate the status of sexual excitement, and all subjects reported that they experienced penile erection with sexual excitement. | true | true | true | true | true | 7,399 |
7 | DISCUSSION | 1 | 28 | [
"B28"
] | 20,733,961 | pmid-16467858 | Even though the repetitive exposures to erotic video could reduce the sexual arousal, the results of this study may still be reliable. | [
"28"
] | 134 | 42,689 | 0 | false | Even though the repetitive exposures to erotic video could reduce the sexual arousal, the results of this study may still be reliable. | [] | Even though the repetitive exposures to erotic video could reduce the sexual arousal, the results of this study may still be reliable. | true | true | true | true | true | 7,399 |
7 | DISCUSSION | 1 | 28 | [
"B28"
] | 20,733,961 | pmid-16467858 | Because the refractory period of young adults may be short, the re-exposure to the same erotic video after 4 hours may not reduce the sexual arousal that much. | [
"28"
] | 159 | 42,690 | 0 | false | Because the refractory period of young adults may be short, the re-exposure to the same erotic video after 4 hours may not reduce the sexual arousal that much. | [] | Because the refractory period of young adults may be short, the re-exposure to the same erotic video after 4 hours may not reduce the sexual arousal that much. | true | true | true | true | true | 7,399 |
7 | DISCUSSION | 1 | 28 | [
"B28"
] | 20,733,961 | pmid-16467858 | In addition, all attendants also reported the penile erection with sexual arousal in the questionnaires taken after the 2nd EEG sessions. | [
"28"
] | 137 | 42,691 | 0 | false | In addition, all attendants also reported the penile erection with sexual arousal in the questionnaires taken after the 2nd EEG sessions. | [] | In addition, all attendants also reported the penile erection with sexual arousal in the questionnaires taken after the 2nd EEG sessions. | true | true | true | true | true | 7,399 |
8 | DISCUSSION | 0 | null | null | 20,733,961 | null | More advanced studies can be based on the results presented here. | null | 65 | 42,692 | 0 | false | null | null | More advanced studies can be based on the results presented here. | true | true | true | true | true | 7,400 |
8 | DISCUSSION | 0 | null | null | 20,733,961 | null | Similar research designs could be adapted for future studies including healthy people or patients with sexual dysfunction in a range of age groups. | null | 147 | 42,693 | 0 | false | null | null | Similar research designs could be adapted for future studies including healthy people or patients with sexual dysfunction in a range of age groups. | true | true | true | true | true | 7,400 |
8 | DISCUSSION | 0 | null | null | 20,733,961 | null | The reliability of information could also be improved in a variety of ways in future studies. | null | 93 | 42,694 | 0 | false | null | null | The reliability of information could also be improved in a variety of ways in future studies. | true | true | true | true | true | 7,400 |
8 | DISCUSSION | 0 | null | null | 20,733,961 | null | We could use more objective monitoring, by measuring, for example, penile tumescence, and could conduct placebo-controlled studies. | null | 131 | 42,695 | 0 | false | null | null | We could use more objective monitoring, by measuring, for example, penile tumescence, and could conduct placebo-controlled studies. | true | true | true | true | true | 7,400 |
8 | DISCUSSION | 0 | null | null | 20,733,961 | null | Such research designs may be useful for pharmacological studies of many other drugs for sexual dysfunction. | null | 107 | 42,696 | 0 | false | null | null | Such research designs may be useful for pharmacological studies of many other drugs for sexual dysfunction. | true | true | true | true | true | 7,400 |
0 | DISCUSSION | 1 | 16 | [
"r16",
"r18",
"r30",
"r31",
"r21",
"r31",
"r32",
"r17",
"r33",
"r2",
"r3",
"r20",
"r21",
"r34",
"r35",
"r2",
"r3",
"r20",
"r21"
] | 18,443,205 | pmid-10723801|pmid-14597638|pmid-17303919|pmid-10195896|pmid-11489937|pmid-10195896|pmid-10195897|pmid-10823818|pmid-9346485|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937|pmid-15951441|pmid-16505240|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937 | IKKβ is a core component of the oligomeric IKK complex, which consists of two catalytic subunits, IKKα and IKKβ, and a regulatory subunit IKKγ, or NEMO (16,18,30,31). | [
"16",
"18",
"30",
"31",
"21",
"31",
"32",
"17",
"33",
"2",
"3",
"20",
"21",
"34",
"35",
"2",
"3",
"20",
"21"
] | 166 | 42,697 | 0 | false | IKKβ is a core component of the oligomeric IKK complex, which consists of two catalytic subunits, IKKα and IKKβ, and a regulatory subunit IKKγ, or NEMO. | [
"16,18,30,31"
] | IKKβ is a core component of the oligomeric IKK complex, which consists of two catalytic subunits, IKKα and IKKβ, and a regulatory subunit IKKγ, or NEMO. | true | true | true | true | true | 7,401 |
0 | DISCUSSION | 1 | 21 | [
"r16",
"r18",
"r30",
"r31",
"r21",
"r31",
"r32",
"r17",
"r33",
"r2",
"r3",
"r20",
"r21",
"r34",
"r35",
"r2",
"r3",
"r20",
"r21"
] | 18,443,205 | pmid-10723801|pmid-14597638|pmid-17303919|pmid-10195896|pmid-11489937|pmid-10195896|pmid-10195897|pmid-10823818|pmid-9346485|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937|pmid-15951441|pmid-16505240|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937 | The two catalytic subunits share ∼50% amino acid sequence homology, whereas the regulatory subunit does not contain a recognizable catalytic domain (21). | [
"16",
"18",
"30",
"31",
"21",
"31",
"32",
"17",
"33",
"2",
"3",
"20",
"21",
"34",
"35",
"2",
"3",
"20",
"21"
] | 153 | 42,698 | 1 | false | The two catalytic subunits share ∼50% amino acid sequence homology, whereas the regulatory subunit does not contain a recognizable catalytic domain. | [
"21"
] | The two catalytic subunits share ∼50% amino acid sequence homology, whereas the regulatory subunit does not contain a recognizable catalytic domain. | true | true | true | true | true | 7,401 |
0 | DISCUSSION | 1 | 16 | [
"r16",
"r18",
"r30",
"r31",
"r21",
"r31",
"r32",
"r17",
"r33",
"r2",
"r3",
"r20",
"r21",
"r34",
"r35",
"r2",
"r3",
"r20",
"r21"
] | 18,443,205 | pmid-10723801|pmid-14597638|pmid-17303919|pmid-10195896|pmid-11489937|pmid-10195896|pmid-10195897|pmid-10823818|pmid-9346485|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937|pmid-15951441|pmid-16505240|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937 | Despite the overall sequence identity between IKKα and IKKβ, these subunits have specialized roles as mediators of cellular stress. | [
"16",
"18",
"30",
"31",
"21",
"31",
"32",
"17",
"33",
"2",
"3",
"20",
"21",
"34",
"35",
"2",
"3",
"20",
"21"
] | 131 | 42,699 | 0 | false | Despite the overall sequence identity between IKKα and IKKβ, these subunits have specialized roles as mediators of cellular stress. | [] | Despite the overall sequence identity between IKKα and IKKβ, these subunits have specialized roles as mediators of cellular stress. | true | true | true | true | true | 7,401 |
0 | DISCUSSION | 1 | 31 | [
"r16",
"r18",
"r30",
"r31",
"r21",
"r31",
"r32",
"r17",
"r33",
"r2",
"r3",
"r20",
"r21",
"r34",
"r35",
"r2",
"r3",
"r20",
"r21"
] | 18,443,205 | pmid-10723801|pmid-14597638|pmid-17303919|pmid-10195896|pmid-11489937|pmid-10195896|pmid-10195897|pmid-10823818|pmid-9346485|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937|pmid-15951441|pmid-16505240|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937 | For example, deletion of IKKα (IKKα−/−) causes limb deformities (31), whereas deletion of IKKβ (IKKβ−/−) is lethal in mouse embryos (32). | [
"16",
"18",
"30",
"31",
"21",
"31",
"32",
"17",
"33",
"2",
"3",
"20",
"21",
"34",
"35",
"2",
"3",
"20",
"21"
] | 137 | 42,700 | 1 | false | For example, deletion of IKKα (IKKα−/−) causes limb deformities, whereas deletion of IKKβ (IKKβ−/−) is lethal in mouse embryos. | [
"31",
"32"
] | For example, deletion of IKKα (IKKα−/−) causes limb deformities, whereas deletion of IKKβ (IKKβ−/−) is lethal in mouse embryos. | true | true | true | true | true | 7,401 |
0 | DISCUSSION | 1 | 16 | [
"r16",
"r18",
"r30",
"r31",
"r21",
"r31",
"r32",
"r17",
"r33",
"r2",
"r3",
"r20",
"r21",
"r34",
"r35",
"r2",
"r3",
"r20",
"r21"
] | 18,443,205 | pmid-10723801|pmid-14597638|pmid-17303919|pmid-10195896|pmid-11489937|pmid-10195896|pmid-10195897|pmid-10823818|pmid-9346485|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937|pmid-15951441|pmid-16505240|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937 | Of the two catalytic subunits, IKKβ is considered to be the main regulator of NF-κB function because of its higher activity (∼30-fold) toward IκBα (17,33). | [
"16",
"18",
"30",
"31",
"21",
"31",
"32",
"17",
"33",
"2",
"3",
"20",
"21",
"34",
"35",
"2",
"3",
"20",
"21"
] | 155 | 42,701 | 0 | false | Of the two catalytic subunits, IKKβ is considered to be the main regulator of NF-κB function because of its higher activity toward IκBα. | [
"∼30-fold",
"17,33"
] | Of the two catalytic subunits, IKKβ is considered to be the main regulator of NF-κB function because of its higher activity toward IκBα. | true | true | true | true | true | 7,401 |
0 | DISCUSSION | 1 | 16 | [
"r16",
"r18",
"r30",
"r31",
"r21",
"r31",
"r32",
"r17",
"r33",
"r2",
"r3",
"r20",
"r21",
"r34",
"r35",
"r2",
"r3",
"r20",
"r21"
] | 18,443,205 | pmid-10723801|pmid-14597638|pmid-17303919|pmid-10195896|pmid-11489937|pmid-10195896|pmid-10195897|pmid-10823818|pmid-9346485|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937|pmid-15951441|pmid-16505240|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937 | Recent evidence underscores a central role of IKKβ in insulin sensitivity and type 2 diabetes pathogenesis (2,3,20,21,34,35). | [
"16",
"18",
"30",
"31",
"21",
"31",
"32",
"17",
"33",
"2",
"3",
"20",
"21",
"34",
"35",
"2",
"3",
"20",
"21"
] | 125 | 42,702 | 0 | false | Recent evidence underscores a central role of IKKβ in insulin sensitivity and type 2 diabetes pathogenesis. | [
"2,3,20,21,34,35"
] | Recent evidence underscores a central role of IKKβ in insulin sensitivity and type 2 diabetes pathogenesis. | true | true | true | true | true | 7,401 |
0 | DISCUSSION | 1 | 16 | [
"r16",
"r18",
"r30",
"r31",
"r21",
"r31",
"r32",
"r17",
"r33",
"r2",
"r3",
"r20",
"r21",
"r34",
"r35",
"r2",
"r3",
"r20",
"r21"
] | 18,443,205 | pmid-10723801|pmid-14597638|pmid-17303919|pmid-10195896|pmid-11489937|pmid-10195896|pmid-10195897|pmid-10823818|pmid-9346485|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937|pmid-15951441|pmid-16505240|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937 | High doses of salicylates, which repress IKKβ activity, reverse hyperglycemia, hyperinsulinemia, and dyslipidemia in obese rodents by increasing insulin sensitivity (2,3,20,21). | [
"16",
"18",
"30",
"31",
"21",
"31",
"32",
"17",
"33",
"2",
"3",
"20",
"21",
"34",
"35",
"2",
"3",
"20",
"21"
] | 177 | 42,703 | 0 | false | High doses of salicylates, which repress IKKβ activity, reverse hyperglycemia, hyperinsulinemia, and dyslipidemia in obese rodents by increasing insulin sensitivity. | [
"2,3,20,21"
] | High doses of salicylates, which repress IKKβ activity, reverse hyperglycemia, hyperinsulinemia, and dyslipidemia in obese rodents by increasing insulin sensitivity. | true | true | true | true | true | 7,401 |
0 | DISCUSSION | 1 | 16 | [
"r16",
"r18",
"r30",
"r31",
"r21",
"r31",
"r32",
"r17",
"r33",
"r2",
"r3",
"r20",
"r21",
"r34",
"r35",
"r2",
"r3",
"r20",
"r21"
] | 18,443,205 | pmid-10723801|pmid-14597638|pmid-17303919|pmid-10195896|pmid-11489937|pmid-10195896|pmid-10195897|pmid-10823818|pmid-9346485|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937|pmid-15951441|pmid-16505240|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937 | Consequently, we determined the role of IKKβ in insulin action on glucose uptake using siRNA-mediated gene silencing. | [
"16",
"18",
"30",
"31",
"21",
"31",
"32",
"17",
"33",
"2",
"3",
"20",
"21",
"34",
"35",
"2",
"3",
"20",
"21"
] | 117 | 42,704 | 0 | false | Consequently, we determined the role of IKKβ in insulin action on glucose uptake using siRNA-mediated gene silencing. | [] | Consequently, we determined the role of IKKβ in insulin action on glucose uptake using siRNA-mediated gene silencing. | true | true | true | true | true | 7,401 |
0 | DISCUSSION | 1 | 16 | [
"r16",
"r18",
"r30",
"r31",
"r21",
"r31",
"r32",
"r17",
"r33",
"r2",
"r3",
"r20",
"r21",
"r34",
"r35",
"r2",
"r3",
"r20",
"r21"
] | 18,443,205 | pmid-10723801|pmid-14597638|pmid-17303919|pmid-10195896|pmid-11489937|pmid-10195896|pmid-10195897|pmid-10823818|pmid-9346485|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937|pmid-15951441|pmid-16505240|pmid-9817203|pmid-11533494|pmid-12021247|pmid-11489937 | We provide evidence that IKKβ plays a role in TNF-α–induced impairments in insulin action on Akt signaling and glucose uptake and metabolism in human skeletal muscle. | [
"16",
"18",
"30",
"31",
"21",
"31",
"32",
"17",
"33",
"2",
"3",
"20",
"21",
"34",
"35",
"2",
"3",
"20",
"21"
] | 166 | 42,705 | 0 | false | We provide evidence that IKKβ plays a role in TNF-α–induced impairments in insulin action on Akt signaling and glucose uptake and metabolism in human skeletal muscle. | [] | We provide evidence that IKKβ plays a role in TNF-α–induced impairments in insulin action on Akt signaling and glucose uptake and metabolism in human skeletal muscle. | true | true | true | true | true | 7,401 |
1 | DISCUSSION | 1 | 36 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | TNF-α has a biphasic response to NF-κB, which is required for cytokine-induced skeletal muscle damage and wasting/cachexia (36,37). | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 131 | 42,706 | 0 | false | TNF-α has a biphasic response to NF-κB, which is required for cytokine-induced skeletal muscle damage and wasting/cachexia. | [
"36,37"
] | TNF-α has a biphasic response to NF-κB, which is required for cytokine-induced skeletal muscle damage and wasting/cachexia. | true | true | true | true | true | 7,402 |
1 | DISCUSSION | 1 | 36 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | Cytokines activate the IKK complex, leading to phosphorylation of IκBα on Ser32 and Ser36. | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 90 | 42,707 | 0 | false | Cytokines activate the IKK complex, leading to phosphorylation of IκBα on Ser32 and Ser36. | [] | Cytokines activate the IKK complex, leading to phosphorylation of IκBα on Ser32 and Ser36. | true | true | true | true | true | 7,402 |
1 | DISCUSSION | 1 | 16 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | Phosphorylation of these residues causes polyubiquitination and subsequent degradation of IκBα by proteosomes (16). | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 115 | 42,708 | 1 | false | Phosphorylation of these residues causes polyubiquitination and subsequent degradation of IκBα by proteosomes. | [
"16"
] | Phosphorylation of these residues causes polyubiquitination and subsequent degradation of IκBα by proteosomes. | true | true | true | true | true | 7,402 |
1 | DISCUSSION | 1 | 38 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | The breakdown of IκBα leads to the release and nuclear translocation of NF-κB, where it binds to target genes and drives the expression of cytokines, including TNF-α, interleukin-6, and interleukin-1β (38). | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 206 | 42,709 | 1 | false | The breakdown of IκBα leads to the release and nuclear translocation of NF-κB, where it binds to target genes and drives the expression of cytokines, including TNF-α, interleukin-6, and interleukin-1β. | [
"38"
] | The breakdown of IκBα leads to the release and nuclear translocation of NF-κB, where it binds to target genes and drives the expression of cytokines, including TNF-α, interleukin-6, and interleukin-1β. | true | true | true | true | true | 7,402 |
1 | DISCUSSION | 1 | 36 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | Here, we report that a 2-h TNF-α exposure of cultured myotubes decreased Iκβα protein content, indicating that Iκβα is targeted for degradation after cytokine exposure. | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 168 | 42,710 | 0 | false | Here, we report that a 2-h TNF-α exposure of cultured myotubes decreased Iκβα protein content, indicating that Iκβα is targeted for degradation after cytokine exposure. | [] | Here, we report that a 2-h TNF-α exposure of cultured myotubes decreased Iκβα protein content, indicating that Iκβα is targeted for degradation after cytokine exposure. | true | true | true | true | true | 7,402 |
1 | DISCUSSION | 1 | 37 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | This finding is consistent with the first transient phase of TNF-α–mediated activation of NF-κB (37). | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 101 | 42,711 | 1 | false | This finding is consistent with the first transient phase of TNF-α–mediated activation of NF-κB. | [
"37"
] | This finding is consistent with the first transient phase of TNF-α–mediated activation of NF-κB. | true | true | true | true | true | 7,402 |
1 | DISCUSSION | 1 | 36 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | The siRNA-mediated reduction of IKKβ prevented the TNF-α effect on Iκβα degradation. | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 84 | 42,712 | 0 | false | The siRNA-mediated reduction of IKKβ prevented the TNF-α effect on Iκβα degradation. | [] | The siRNA-mediated reduction of IKKβ prevented the TNF-α effect on Iκβα degradation. | true | true | true | true | true | 7,402 |
1 | DISCUSSION | 1 | 36 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | Skeletal muscle wasting/cachexia, due to accelerated protein degradation through ubiquitin-dependent proteolysis, occurs in a manner analogous to IKKβ-mediated degradation of IκBα. | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 180 | 42,713 | 0 | false | Skeletal muscle wasting/cachexia, due to accelerated protein degradation through ubiquitin-dependent proteolysis, occurs in a manner analogous to IKKβ-mediated degradation of IκBα. | [] | Skeletal muscle wasting/cachexia, due to accelerated protein degradation through ubiquitin-dependent proteolysis, occurs in a manner analogous to IKKβ-mediated degradation of IκBα. | true | true | true | true | true | 7,402 |
1 | DISCUSSION | 1 | 36 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | Genetic inhibition of the IKKβ/NF-κB/MuRF1 pathway or through pharmacological therapeutics, such as salicylates to inhibit IKKβ activity, rescues the skeletal muscle-wasting phenotype (37,39,40). | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 195 | 42,714 | 0 | false | Genetic inhibition of the IKKβ/NF-κB/MuRF1 pathway or through pharmacological therapeutics, such as salicylates to inhibit IKKβ activity, rescues the skeletal muscle-wasting phenotype. | [
"37,39,40"
] | Genetic inhibition of the IKKβ/NF-κB/MuRF1 pathway or through pharmacological therapeutics, such as salicylates to inhibit IKKβ activity, rescues the skeletal muscle-wasting phenotype. | true | true | true | true | true | 7,402 |
1 | DISCUSSION | 1 | 36 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | In the current study, skeletal muscle morphology was not altered by either TNF-α exposure or siRNA-mediated gene silencing of IKKβ. | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 131 | 42,715 | 0 | false | In the current study, skeletal muscle morphology was not altered by either TNF-α exposure or siRNA-mediated gene silencing of IKKβ. | [] | In the current study, skeletal muscle morphology was not altered by either TNF-α exposure or siRNA-mediated gene silencing of IKKβ. | true | true | true | true | true | 7,402 |
1 | DISCUSSION | 1 | 36 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | However, our experiments were limited to a short-term (first phase) TNF-α exposure, and we did not directly test whether IKKβ siRNA would modify culture growth in the presence of a long-term (second phase) | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 205 | 42,716 | 0 | false | However, our experiments were limited to a short-term (first phase) TNF-α exposure, and we did not directly test whether IKKβ siRNA would modify culture growth in the presence of a long-term (second phase) | [] | However, our experiments were limited to a short-term (first phase) TNF-α exposure, and we did not directly test whether IKKβ siRNA would modify culture growth in the presence of a long-term (second phase) | true | true | false | true | false | 7,402 |
1 | DISCUSSION | 1 | 36 | [
"r36",
"r37",
"r16",
"r38",
"r37",
"r37",
"r39",
"r40"
] | 18,443,205 | pmid-15685173|pmid-12431991|pmid-10723801|pmid-11134171|pmid-12431991|pmid-12431991|pmid-17303713|pmid-15479644 | TNF-α exposure. | [
"36",
"37",
"16",
"38",
"37",
"37",
"39",
"40"
] | 15 | 42,717 | 0 | false | TNF-α exposure. | [] | TNF-α exposure. | true | true | true | true | true | 7,402 |
2 | DISCUSSION | 1 | 1 | [
"r1",
"r41",
"r42",
"r22",
"r5",
"r6",
"r35",
"r20",
"r21",
"r3",
"r20",
"r21",
"r43",
"r44"
] | 18,443,205 | pmid-16186396|pmid-9832430|pmid-17141630|pmid-17227768|pmid-16823477|pmid-12606524|pmid-16505240|pmid-12021247|pmid-11489937|pmid-11533494|pmid-12021247|pmid-11489937|pmid-17959861|pmid-17317777 | TNF-α directly induces skeletal muscle insulin resistance in vivo in healthy humans (1) and rodents (41,42) and in vitro in cultured myotubes (22). | [
"1",
"41",
"42",
"22",
"5",
"6",
"35",
"20",
"21",
"3",
"20",
"21",
"43",
"44"
] | 147 | 42,718 | 1 | false | TNF-α directly induces skeletal muscle insulin resistance in vivo in healthy humans and rodents and in vitro in cultured myotubes. | [
"1",
"41,42",
"22"
] | TNF-α directly induces skeletal muscle insulin resistance in vivo in healthy humans and rodents and in vitro in cultured myotubes. | true | true | true | true | true | 7,403 |
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