vgainullin/citation_classifier
Text Classification • Updated • 5
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
0 | DISCUSSION | 0 | null | null | 17,342,250 | null | Pain during labor is usually defined as an unpleasant sensory and emotional experience. | null | 87 | 0 | 0 | false | null | null | Pain during labor is usually defined as an unpleasant sensory and emotional experience. | true | true | true | true | true | 0 |
0 | DISCUSSION | 0 | null | null | 17,342,250 | null | Electro-acupuncture is a method which now is increasingly being used in China and some other countries. | null | 103 | 1 | 0 | false | null | null | Electro-acupuncture is a method which now is increasingly being used in China and some other countries. | true | true | true | true | true | 0 |
0 | DISCUSSION | 0 | null | null | 17,342,250 | null | No undesirable side-effect has been observed and it is thought that electro-acupuncture could be an alternative to other methods of pain relief during labor. | null | 157 | 2 | 0 | false | null | null | No undesirable side-effect has been observed and it is thought that electro-acupuncture could be an alternative to other methods of pain relief during labor. | true | true | true | true | true | 0 |
1 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B7",
"B7",
"B8",
"B10",
"B9",
"B10",
"B9 B10 B11 B12 B13 B14 B15"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | In ancient acupuncture practice, Hegu (LI-4) and Sanyinjiao (SP-6) were listed as forbidden acupoints for pregnant women due to their oxytocic effects[7]. | [
"7",
"7",
"7",
"7",
"8",
"10",
"9",
"10",
"9–15"
] | 154 | 3 | 1 | false | In ancient acupuncture practice, Hegu (LI-4) and Sanyinjiao (SP-6) were listed as forbidden acupoints for pregnant women due to their oxytocic effects. | [
"7"
] | In ancient acupuncture practice, Hegu (LI-4) and Sanyinjiao (SP-6) were listed as forbidden acupoints for pregnant women due to their oxytocic effects. | true | true | true | true | true | 1 |
1 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B7",
"B7",
"B8",
"B10",
"B9",
"B10",
"B9 B10 B11 B12 B13 B14 B15"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | The forbidden acupoints for pregnant women were indicated even in the most ancient extant book on acupuncture[7], the Su Wen (Essential Questions) of the Huang Di Nei Jing (The Yellow emperor's Internal Medicine) in which an entire chapter is devoted to this topic. | [
"7",
"7",
"7",
"7",
"8",
"10",
"9",
"10",
"9–15"
] | 265 | 4 | 1 | false | The forbidden acupoints for pregnant women were indicated even in the most ancient extant book on acupuncture, the Su Wen (Essential Questions) of the Huang Di Nei Jing (The Yellow emperor's Internal Medicine) in which an entire chapter is devoted to this topic. | [
"7"
] | The forbidden acupoints for pregnant women were indicated even in the most ancient extant book on acupuncture, the Su Wen (Essential Questions) of the Huang Di Nei Jing (The Yellow emperor's Internal Medicine) in which an entire chapter is devoted to this topic. | true | true | true | true | true | 1 |
1 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B7",
"B7",
"B8",
"B10",
"B9",
"B10",
"B9 B10 B11 B12 B13 B14 B15"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Huang Fu Mi's Zhen Jiu Jia Yi Jing (The systematic Canon of Acupuncture and Moxibustion), 3rd century AD lists 24 points of forbidden to acupuncture and moxibustion, and Yang Ji-Zhou's Zhen Jiu Da Chen (The Great Compendium of Acupuncture and moxibustion) | [
"7",
"7",
"7",
"7",
"8",
"10",
"9",
"10",
"9–15"
] | 255 | 5 | 0 | false | Huang Fu Mi's Zhen Jiu Jia Yi Jing (The systematic Canon of Acupuncture and Moxibustion), 3rd century AD lists 24 points of forbidden to acupuncture and moxibustion, and Yang Ji-Zhou's Zhen Jiu Da Chen (The Great Compendium of Acupuncture and moxibustion) | [] | Huang Fu Mi's Zhen Jiu Jia Yi Jing (The systematic Canon of Acupuncture and Moxibustion), 3rd century AD lists 24 points of forbidden to acupuncture and moxibustion, and Yang Ji-Zhou's Zhen Jiu Da Chen (The Great Compendium of Acupuncture and moxibustion) | true | true | false | true | false | 1 |
1 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B7",
"B7",
"B8",
"B10",
"B9",
"B10",
"B9 B10 B11 B12 B13 B14 B15"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | [7] was published in 1602 AD. | [
"7",
"7",
"7",
"7",
"8",
"10",
"9",
"10",
"9–15"
] | 29 | 6 | 1 | false | was published in 1602 AD. | [
"7"
] | was published in 1602 AD. | false | true | true | true | false | 1 |
1 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B7",
"B7",
"B8",
"B10",
"B9",
"B10",
"B9 B10 B11 B12 B13 B14 B15"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Yang Ji-Zhou summarized the forbidden points in two odes[7]. | [
"7",
"7",
"7",
"7",
"8",
"10",
"9",
"10",
"9–15"
] | 60 | 7 | 1 | false | Yang Ji-Zhou summarized the forbidden points in two odes. | [
"7"
] | Yang Ji-Zhou summarized the forbidden points in two odes. | true | true | true | true | true | 1 |
1 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B7",
"B7",
"B8",
"B10",
"B9",
"B10",
"B9 B10 B11 B12 B13 B14 B15"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | :Jin Jiu Xue Ge (Ode to the Forbidden Points for Moxibustion) which lists 45 points, and Jin Zhen Xue Ge (Ode to the Forbidden Points for Needling) which lists 32 points. | [
"7",
"7",
"7",
"7",
"8",
"10",
"9",
"10",
"9–15"
] | 170 | 8 | 0 | false | :Jin Jiu Xue Ge (Ode to the Forbidden Points for Moxibustion) which lists 45 points, and Jin Zhen Xue Ge (Ode to the Forbidden Points for Needling) which lists 32 points. | [] | :Jin Jiu Xue Ge (Ode to the Forbidden Points for Moxibustion) which lists 45 points, and Jin Zhen Xue Ge (Ode to the Forbidden Points for Needling) which lists 32 points. | false | false | true | true | false | 1 |
1 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B7",
"B7",
"B8",
"B10",
"B9",
"B10",
"B9 B10 B11 B12 B13 B14 B15"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Modern experiments[8-10] have shown that Hegu (LI-4) has a dual effect on the uterine smooth muscle through the regulation of the CNS. | [
"7",
"7",
"7",
"7",
"8",
"10",
"9",
"10",
"9–15"
] | 134 | 9 | 0 | false | Modern experiments have shown that Hegu (LI-4) has a dual effect on the uterine smooth muscle through the regulation of the CNS. | [
"8-10"
] | Modern experiments have shown that Hegu (LI-4) has a dual effect on the uterine smooth muscle through the regulation of the CNS. | true | true | true | true | true | 1 |
1 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B7",
"B7",
"B8",
"B10",
"B9",
"B10",
"B9 B10 B11 B12 B13 B14 B15"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Acupuncture on Sanyinjiao (SP-6) which lies within the innervation of L4, can excite the spinal central nerves by stimulating the somatic sensory nerve fibers and by exciting the pelvic neuroplex through sympathetic nerves, resulting in contraction of uterus [9,10]. | [
"7",
"7",
"7",
"7",
"8",
"10",
"9",
"10",
"9–15"
] | 266 | 10 | 0 | false | Acupuncture on Sanyinjiao (SP-6) which lies within the innervation of L4, can excite the spinal central nerves by stimulating the somatic sensory nerve fibers and by exciting the pelvic neuroplex through sympathetic nerves, resulting in contraction of uterus. | [
"9,10"
] | Acupuncture on Sanyinjiao (SP-6) which lies within the innervation of L4, can excite the spinal central nerves by stimulating the somatic sensory nerve fibers and by exciting the pelvic neuroplex through sympathetic nerves, resulting in contraction of uterus. | true | true | true | true | true | 1 |
1 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B7",
"B7",
"B8",
"B10",
"B9",
"B10",
"B9 B10 B11 B12 B13 B14 B15"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | The pain during labor is mainly caused by uterine contractions. | [
"7",
"7",
"7",
"7",
"8",
"10",
"9",
"10",
"9–15"
] | 63 | 11 | 0 | false | The pain during labor is mainly caused by uterine contractions. | [] | The pain during labor is mainly caused by uterine contractions. | true | true | true | true | true | 1 |
1 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B7",
"B7",
"B8",
"B10",
"B9",
"B10",
"B9 B10 B11 B12 B13 B14 B15"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Both Hegu (LI-4) and Sanyinjiao (SP-6) have an effect on the contraction of uterus. | [
"7",
"7",
"7",
"7",
"8",
"10",
"9",
"10",
"9–15"
] | 83 | 12 | 0 | false | Both Hegu (LI-4) and Sanyinjiao (SP-6) have an effect on the contraction of uterus. | [] | Both Hegu (LI-4) and Sanyinjiao (SP-6) have an effect on the contraction of uterus. | true | true | true | true | true | 1 |
1 | DISCUSSION | 1 | 9–15 | [
"B7",
"B7",
"B7",
"B7",
"B8",
"B10",
"B9",
"B10",
"B9 B10 B11 B12 B13 B14 B15"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA|NA | Needling the two points can produce the rhythmic coordination of the uterus muscles during the oxytocic process and neuroendocrine alteration[9–15]. | [
"7",
"7",
"7",
"7",
"8",
"10",
"9",
"10",
"9–15"
] | 148 | 13 | 1 | false | Needling the two points can produce the rhythmic coordination of the uterus muscles during the oxytocic process and neuroendocrine alteration. | [
"9–15"
] | Needling the two points can produce the rhythmic coordination of the uterus muscles during the oxytocic process and neuroendocrine alteration. | true | true | true | true | true | 1 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | According to the thousand years of experience in acupuncture practice, it is known that different manners of needle manipulation may produce different therapeutic effects, though the scientific mechanisms remain unknown | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 219 | 14 | 0 | false | According to the thousand years of experience in acupuncture practice, it is known that different manners of needle manipulation may produce different therapeutic effects, though the scientific mechanisms remain unknown | [] | According to the thousand years of experience in acupuncture practice, it is known that different manners of needle manipulation may produce different therapeutic effects, though the scientific mechanisms remain unknown | true | true | false | true | false | 2 |
2 | DISCUSSION | 1 | 16–25 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | Some studies[16–25] have indicated that analgesia produced by electro-acupuncture of different frequencies are mediated by different varieties of opioids in the spinal cord: low frequency (2Hz) electro-acupuncture analgesia is mediated by enkephalin and high frequency (100Hz) electro-acupuncture analgesia by dynorphin. | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 320 | 15 | 1 | false | Some studies have indicated that analgesia produced by electro-acupuncture of different frequencies are mediated by different varieties of opioids in the spinal cord: low frequency (2Hz) electro-acupuncture analgesia is mediated by enkephalin and high frequency (100Hz) electro-acupuncture analgesia by dynorphin. | [
"16–25"
] | Some studies have indicated that analgesia produced by electro-acupuncture of different frequencies are mediated by different varieties of opioids in the spinal cord: low frequency electro-acupuncture analgesia is mediated by enkephalin and high frequency electro-acupuncture analgesia by dynorphin. | true | true | true | true | true | 2 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | Enkephalin and β-EP were mixed μ and δ opioid receptor agonists as the endomorphin was considered as the pure μ opioid receptor agonist | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 135 | 16 | 0 | false | Enkephalin and β-EP were mixed μ and δ opioid receptor agonists as the endomorphin was considered as the pure μ opioid receptor agonist | [] | Enkephalin and β-EP were mixed μ and δ opioid receptor agonists as the endomorphin was considered as the pure μ opioid receptor agonist | true | true | false | true | false | 2 |
2 | DISCUSSION | 1 | 17 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | [17] and dynorphin the relatively pure κ opioid agonist [18]. | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 61 | 17 | 1 | false | and dynorphin the relatively pure κ opioid agonist. | [
"17",
"18"
] | and dynorphin the relatively pure κ opioid agonist. | false | true | true | true | false | 2 |
2 | DISCUSSION | 1 | 19 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | Study [19] has suggested that the analgesia induced by 2 Hz electro-acupuncture was mediated by the μ receptor and that of 100 Hz electro-acupuncture by κ opioid receptors. | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 172 | 18 | 1 | false | Study has suggested that the analgesia induced by 2 Hz electro-acupuncture was mediated by the μ receptor and that of 100 Hz electro-acupuncture by κ opioid receptors. | [
"19"
] | Study has suggested that the analgesia induced by 2 Hz electro-acupuncture was mediated by the μ receptor and that of 100 Hz electro-acupuncture by κ opioid receptors. | true | true | true | true | true | 2 |
2 | DISCUSSION | 1 | 20 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | This conclusion was verified later by the use of subtype specific opioid receptor antagonists[20]. | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 98 | 19 | 1 | false | This conclusion was verified later by the use of subtype specific opioid receptor antagonists. | [
"20"
] | This conclusion was verified later by the use of subtype specific opioid receptor antagonists. | true | true | true | true | true | 2 |
2 | DISCUSSION | 1 | 21 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | The direct evidence [21]was obtained by measuring the neuropeptide release in the CNS triggered by electro-acupuncture of different frequencies. | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 144 | 20 | 1 | false | The direct evidence was obtained by measuring the neuropeptide release in the CNS triggered by electro-acupuncture of different frequencies. | [
"21"
] | The direct evidence was obtained by measuring the neuropeptide release in the CNS triggered by electro-acupuncture of different frequencies. | true | true | true | true | true | 2 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | Results have shown that 2 Hz electro-acupuncture produced a 7 fold increase in enkephalin but not dynorphin. | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 108 | 21 | 0 | false | Results have shown that 2 Hz electro-acupuncture produced a 7 fold increase in enkephalin but not dynorphin. | [] | Results have shown that 2 Hz electro-acupuncture produced a 7 fold increase in enkephalin but not dynorphin. | true | true | true | true | true | 2 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | In contrast, 100 Hz electro-acupuncture produced a 2 fold increase in the release of dynorphin but not enkephalin. | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 114 | 22 | 0 | false | In contrast, 100 Hz electro-acupuncture produced a 2 fold increase in the release of dynorphin but not enkephalin. | [] | In contrast, 100 Hz electro-acupuncture produced a 2 fold increase in the release of dynorphin but not enkephalin. | true | true | true | true | true | 2 |
2 | DISCUSSION | 1 | 22 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | Further studies have shown that β-EP [22] and endomorphin [23] share similar characteristics of a stimulation-induced release profile as enkephalin, i.e. | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 153 | 23 | 1 | false | Further studies have shown that β-EP and endomorphin share similar characteristics of a stimulation-induced release profile as enkephalin, i.e. | [
"22",
"23"
] | Further studies have shown that β-EP and endomorphin share similar characteristics of a stimulation-induced release profile as enkephalin, i.e. | true | true | true | true | true | 2 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | preferable to 2 Hz stimulation, leaving dynorphin as the only opioid peptide responsive to high-frequency stimulation and there was a general consensus that μ and κ opioid receptor agonists possess an analgesic effect [24,25]. | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 226 | 24 | 0 | false | preferable to 2 Hz stimulation, leaving dynorphin as the only opioid peptide responsive to high-frequency stimulation and there was a general consensus that μ and κ opioid receptor agonists possess an analgesic effect. | [
"24,25"
] | preferable to 2 Hz stimulation, leaving dynorphin as the only opioid peptide responsive to high-frequency stimulation and there was a general consensus that μ and κ opioid receptor agonists possess an analgesic effect. | false | true | true | true | false | 2 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | These results were primarily obtained in animals and recently verified in humans. | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 81 | 25 | 0 | false | These results were primarily obtained in animals and recently verified in humans. | [] | These results were primarily obtained in animals and recently verified in humans. | true | true | true | true | true | 2 |
2 | DISCUSSION | 1 | 7 | [
"B7",
"B16 B17 B18 B19 B20 B21 B22 B23 B24 B25",
"B17",
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24",
"B25"
] | 17,342,250 | NA|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA|NA|NA|NA|NA|NA|NA|NA|pmid-6130439|NA | One could thus anticipate that if low-frequency stimulation appears alternately with high-frequency stimulation, both enkephalin and dynorphin will be released successively or simultaneously to produce a more potent analgesic effect via a synergistic interaction between the opioid peptides. | [
"7",
"16–25",
"17",
"18",
"19",
"20",
"21",
"22",
"23",
"24",
"25"
] | 291 | 26 | 0 | false | One could thus anticipate that if low-frequency stimulation appears alternately with high-frequency stimulation, both enkephalin and dynorphin will be released successively or simultaneously to produce a more potent analgesic effect via a synergistic interaction between the opioid peptides. | [] | One could thus anticipate that if low-frequency stimulation appears alternately with high-frequency stimulation, both enkephalin and dynorphin will be released successively or simultaneously to produce a more potent analgesic effect via a synergistic interaction between the opioid peptides. | true | true | true | true | true | 2 |
3 | DISCUSSION | 0 | null | null | 17,342,250 | null | β-EP and 5-HT are both neurotransmitters of CNS, which interact with each other and have relationship with the transmission of peripheral pain and contraction of the uterus. | null | 173 | 27 | 0 | false | null | null | β-EP and 5-HT are both neurotransmitters of CNS, which interact with each other and have relationship with the transmission of peripheral pain and contraction of the uterus. | false | true | true | true | false | 3 |
3 | DISCUSSION | 0 | null | null | 17,342,250 | null | Selection of them is based on observed indexes. | null | 47 | 28 | 0 | false | null | null | Selection of them is based on observed indexes. | true | true | true | true | true | 3 |
4 | DISCUSSION | 1 | 26 | [
"B26",
"B27"
] | 17,342,250 | pmid-6305238|pmid-6279134 | β-EP is derived from proopiocortin, in the anterior pituitary gland and is released into the circulation under conditions of pain and stress. | [
"26",
"27"
] | 141 | 29 | 0 | false | β-EP is derived from proopiocortin, in the anterior pituitary gland and is released into the circulation under conditions of pain and stress. | [] | β-EP is derived from proopiocortin, in the anterior pituitary gland and is released into the circulation under conditions of pain and stress. | false | true | true | true | false | 4 |
4 | DISCUSSION | 1 | 26 | [
"B26",
"B27"
] | 17,342,250 | pmid-6305238|pmid-6279134 | The concentration of this increases during unmedicated labor. | [
"26",
"27"
] | 61 | 30 | 0 | false | The concentration of this increases during unmedicated labor. | [] | The concentration of this increases during unmedicated labor. | true | true | true | true | true | 4 |
4 | DISCUSSION | 1 | 26 | [
"B26",
"B27"
] | 17,342,250 | pmid-6305238|pmid-6279134 | Abboud et al. | [
"26",
"27"
] | 13 | 31 | 0 | false | Abboud et al. | [] | Abboud et al. | true | true | true | true | true | 4 |
4 | DISCUSSION | 1 | 26 | [
"B26",
"B27"
] | 17,342,250 | pmid-6305238|pmid-6279134 | [26] measured concentrations of β-EP in non-pregnant healthy women, and among two groups of women in established labor: one prior to and after epidural analgesia, and the other before and after saline. | [
"26",
"27"
] | 201 | 32 | 1 | false | measured concentrations of β-EP in non-pregnant healthy women, and among two groups of women in established labor: one prior to and after epidural analgesia, and the other before and after saline. | [
"26"
] | measured concentrations of β-EP in non-pregnant healthy women, and among two groups of women in established labor: one prior to and after epidural analgesia, and the other before and after saline. | false | true | true | true | false | 4 |
4 | DISCUSSION | 1 | 26 | [
"B26",
"B27"
] | 17,342,250 | pmid-6305238|pmid-6279134 | β-EP concentration decreased by 50% in those who received epidural analgesia whereas there was no significant change in those who received saline. | [
"26",
"27"
] | 146 | 33 | 0 | false | β-EP concentration decreased by 50% in those who received epidural analgesia whereas there was no significant change in those who received saline. | [] | β-EP concentration decreased by 50% in those who received epidural analgesia whereas there was no significant change in those who received saline. | false | true | true | true | false | 4 |
4 | DISCUSSION | 1 | 26 | [
"B26",
"B27"
] | 17,342,250 | pmid-6305238|pmid-6279134 | The finding suggests that labor pain is an important factor in causing β-EP release during labor. | [
"26",
"27"
] | 97 | 34 | 0 | false | The finding suggests that labor pain is an important factor in causing β-EP release during labor. | [] | The finding suggests that labor pain is an important factor in causing β-EP release during labor. | true | true | true | true | true | 4 |
4 | DISCUSSION | 1 | 27 | [
"B26",
"B27"
] | 17,342,250 | pmid-6305238|pmid-6279134 | Thomas [27] et al also found that serum β-EP concentration increased during labor and the increase was significantly greater among women who received nitrous oxide than those who received intramuscular pethidine or epidural analgesia. | [
"26",
"27"
] | 234 | 35 | 1 | false | Thomas et al also found that serum β-EP concentration increased during labor and the increase was significantly greater among women who received nitrous oxide than those who received intramuscular pethidine or epidural analgesia. | [
"27"
] | Thomas et al also found that serum β-EP concentration increased during labor and the increase was significantly greater among women who received nitrous oxide than those who received intramuscular pethidine or epidural analgesia. | true | true | true | true | true | 4 |
5 | DISCUSSION | 1 | 28–30 | [
"B28 B29 B30",
"B31 B32 B33",
"B34",
"B35",
"B36",
"B31",
"B33",
"B37",
"B38",
"B48"
] | 17,342,250 | NA|NA|NA|pmid-14622832|pmid-15312783|pmid-15312782|pmid-7116141|pmid-1422859|pmid-8420635|pmid-14622832|pmid-15312782|pmid-3485785|pmid-187888|pmid-920207 | Studies have demonstrated that acupuncture-mediated analgesia is modulated through a central mechanism involving neurohumoral pathways. | [
"28–30",
"31–33",
"34",
"35",
"36",
"31",
"33",
"37",
"38",
"48"
] | 135 | 36 | 0 | false | Studies have demonstrated that acupuncture-mediated analgesia is modulated through a central mechanism involving neurohumoral pathways. | [] | Studies have demonstrated that acupuncture-mediated analgesia is modulated through a central mechanism involving neurohumoral pathways. | true | true | true | true | true | 5 |
5 | DISCUSSION | 1 | 28–30 | [
"B28 B29 B30",
"B31 B32 B33",
"B34",
"B35",
"B36",
"B31",
"B33",
"B37",
"B38",
"B48"
] | 17,342,250 | NA|NA|NA|pmid-14622832|pmid-15312783|pmid-15312782|pmid-7116141|pmid-1422859|pmid-8420635|pmid-14622832|pmid-15312782|pmid-3485785|pmid-187888|pmid-920207 | The stimulation of the acupuncture point by needling, selectively activates myelinated nerve fibers | [
"28–30",
"31–33",
"34",
"35",
"36",
"31",
"33",
"37",
"38",
"48"
] | 99 | 37 | 0 | false | The stimulation of the acupuncture point by needling, selectively activates myelinated nerve fibers | [] | The stimulation of the acupuncture point by needling, selectively activates myelinated nerve fibers | true | true | false | true | false | 5 |
5 | DISCUSSION | 1 | 31–33 | [
"B28 B29 B30",
"B31 B32 B33",
"B34",
"B35",
"B36",
"B31",
"B33",
"B37",
"B38",
"B48"
] | 17,342,250 | NA|NA|NA|pmid-14622832|pmid-15312783|pmid-15312782|pmid-7116141|pmid-1422859|pmid-8420635|pmid-14622832|pmid-15312782|pmid-3485785|pmid-187888|pmid-920207 | This subsequently results in the activation of certain neurons in the spinal cord and supraspinal regions, including neurons in the deep layers of spinal dorsal horn, [31–33] the nucleus raphe magnus in the brain stem,[34] and the hypothalamus and thalamus [35,36]. | [
"28–30",
"31–33",
"34",
"35",
"36",
"31",
"33",
"37",
"38",
"48"
] | 265 | 38 | 1 | false | This subsequently results in the activation of certain neurons in the spinal cord and supraspinal regions, including neurons in the deep layers of spinal dorsal horn, the nucleus raphe magnus in the brain stem, and the hypothalamus and thalamus. | [
"31–33",
"34",
"35,36"
] | This subsequently results in the activation of certain neurons in the spinal cord and supraspinal regions, including neurons in the deep layers of spinal dorsal horn, the nucleus raphe magnus in the brain stem, and the hypothalamus and thalamus. | true | true | true | true | true | 5 |
5 | DISCUSSION | 1 | 28–30 | [
"B28 B29 B30",
"B31 B32 B33",
"B34",
"B35",
"B36",
"B31",
"B33",
"B37",
"B38",
"B48"
] | 17,342,250 | NA|NA|NA|pmid-14622832|pmid-15312783|pmid-15312782|pmid-7116141|pmid-1422859|pmid-8420635|pmid-14622832|pmid-15312782|pmid-3485785|pmid-187888|pmid-920207 | These neurons modulate pain by inhibiting neurons located at the superficial layer of the dorsal horn and small unmyelinated fibers [31,33,37] as well as releasing neurotransmitters, such as β-EP and 5-HT [38-48]. | [
"28–30",
"31–33",
"34",
"35",
"36",
"31",
"33",
"37",
"38",
"48"
] | 213 | 39 | 0 | false | These neurons modulate pain by inhibiting neurons located at the superficial layer of the dorsal horn and small unmyelinated fibers as well as releasing neurotransmitters, such as β-EP and 5-HT. | [
"31,33,37",
"38-48"
] | These neurons modulate pain by inhibiting neurons located at the superficial layer of the dorsal horn and small unmyelinated fibers as well as releasing neurotransmitters, such as β-EP and 5-HT. | true | true | true | true | true | 5 |
6 | DISCUSSION | 1 | 49 | [
"B49",
"B50 B51 B52 B53 B54 B55 B56 B57 B58",
"B59"
] | 17,342,250 | NA|pmid-1840089|NA|NA|NA|pmid-9201546|NA|NA|NA|NA|pmid-7053025 | Opioid peptides bind to their receptors on central neurons and produce analgesic effects [49]. | [
"49",
"50–58",
"59"
] | 94 | 40 | 1 | false | Opioid peptides bind to their receptors on central neurons and produce analgesic effects. | [
"49"
] | Opioid peptides bind to their receptors on central neurons and produce analgesic effects. | true | true | true | true | true | 6 |
6 | DISCUSSION | 1 | 49 | [
"B49",
"B50 B51 B52 B53 B54 B55 B56 B57 B58",
"B59"
] | 17,342,250 | NA|pmid-1840089|NA|NA|NA|pmid-9201546|NA|NA|NA|NA|pmid-7053025 | However, whether, and to what extent, the peripheral release of opioids plays a role in acupuncture analgesia has not been investigated. | [
"49",
"50–58",
"59"
] | 136 | 41 | 0 | false | However, whether, and to what extent, the peripheral release of opioids plays a role in acupuncture analgesia has not been investigated. | [] | However, whether, and to what extent, the peripheral release of opioids plays a role in acupuncture analgesia has not been investigated. | true | true | true | true | true | 6 |
6 | DISCUSSION | 1 | 49 | [
"B49",
"B50 B51 B52 B53 B54 B55 B56 B57 B58",
"B59"
] | 17,342,250 | NA|pmid-1840089|NA|NA|NA|pmid-9201546|NA|NA|NA|NA|pmid-7053025 | Two lines of evidence suggest that acupuncture-induced peripheral opioid release is possible. | [
"49",
"50–58",
"59"
] | 93 | 42 | 0 | false | Two lines of evidence suggest that acupuncture-induced peripheral opioid release is possible. | [] | Two lines of evidence suggest that acupuncture-induced peripheral opioid release is possible. | true | true | true | true | true | 6 |
6 | DISCUSSION | 1 | 50–58 | [
"B49",
"B50 B51 B52 B53 B54 B55 B56 B57 B58",
"B59"
] | 17,342,250 | NA|pmid-1840089|NA|NA|NA|pmid-9201546|NA|NA|NA|NA|pmid-7053025 | First, acupuncture has been shown to modulate immunological activities,[50–58] and immune cells are a key component of the peripheral opioid system. | [
"49",
"50–58",
"59"
] | 148 | 43 | 1 | false | First, acupuncture has been shown to modulate immunological activities, and immune cells are a key component of the peripheral opioid system. | [
"50–58"
] | First, acupuncture has been shown to modulate immunological activities, and immune cells are a key component of the peripheral opioid system. | true | true | true | true | true | 6 |
6 | DISCUSSION | 1 | 49 | [
"B49",
"B50 B51 B52 B53 B54 B55 B56 B57 B58",
"B59"
] | 17,342,250 | NA|pmid-1840089|NA|NA|NA|pmid-9201546|NA|NA|NA|NA|pmid-7053025 | Second, central opioid mechanisms do not explain why needling an acupuncture point adjacent to a painful area, a common clinical practice, is generally more effective in relieving pain than needling remote areas, a phenomenon that is consonant with the presence of a localized analgesic mechanism. | [
"49",
"50–58",
"59"
] | 297 | 44 | 0 | false | Second, central opioid mechanisms do not explain why needling an acupuncture point adjacent to a painful area, a common clinical practice, is generally more effective in relieving pain than needling remote areas, a phenomenon that is consonant with the presence of a localized analgesic mechanism. | [] | Second, central opioid mechanisms do not explain why needling an acupuncture point adjacent to a painful area, a common clinical practice, is generally more effective in relieving pain than needling remote areas, a phenomenon that is consonant with the presence of a localized analgesic mechanism. | true | true | true | true | true | 6 |
6 | DISCUSSION | 1 | 59 | [
"B49",
"B50 B51 B52 B53 B54 B55 B56 B57 B58",
"B59"
] | 17,342,250 | NA|pmid-1840089|NA|NA|NA|pmid-9201546|NA|NA|NA|NA|pmid-7053025 | Endogenous morphine release has been described as a possible mechanism of acupuncture-mediated analgesia [59]. | [
"49",
"50–58",
"59"
] | 110 | 45 | 1 | false | Endogenous morphine release has been described as a possible mechanism of acupuncture-mediated analgesia. | [
"59"
] | Endogenous morphine release has been described as a possible mechanism of acupuncture-mediated analgesia. | true | true | true | true | true | 6 |
6 | DISCUSSION | 1 | 49 | [
"B49",
"B50 B51 B52 B53 B54 B55 B56 B57 B58",
"B59"
] | 17,342,250 | NA|pmid-1840089|NA|NA|NA|pmid-9201546|NA|NA|NA|NA|pmid-7053025 | This is confirmed by our data. | [
"49",
"50–58",
"59"
] | 30 | 46 | 0 | false | This is confirmed by our data. | [] | This is confirmed by our data. | true | true | true | true | true | 6 |
7 | DISCUSSION | 0 | null | null | 17,342,250 | null | Clinical research has shown that after electro-acupuncture, the release of β-EP into the peripheral blood improved and patients' labor pain was alleviated. | null | 155 | 47 | 0 | false | null | null | Clinical research has shown that after electro-acupuncture, the release of β-EP into the peripheral blood improved and patients' labor pain was alleviated. | true | true | true | true | true | 7 |
7 | DISCUSSION | 0 | null | null | 17,342,250 | null | The release of β-EP represents a natural mechanism for the modulation of stress. | null | 80 | 48 | 0 | false | null | null | The release of β-EP represents a natural mechanism for the modulation of stress. | true | true | true | true | true | 7 |
7 | DISCUSSION | 0 | null | null | 17,342,250 | null | β-EP can antagonize and coordinate contraction of uterus caused by oxytocin. | null | 76 | 49 | 0 | false | null | null | β-EP can antagonize and coordinate contraction of uterus caused by oxytocin. | false | true | true | true | false | 7 |
7 | DISCUSSION | 0 | null | null | 17,342,250 | null | The increased release of β-EP into the peripheral blood after electro-acupuncture, which is greater than natural vaginal delivery, activates an endogenous analgesia system and lessens the afferent sign of labor pain and increases the tolerance to labor pain. | null | 258 | 50 | 0 | false | null | null | The increased release of β-EP into the peripheral blood after electro-acupuncture, which is greater than natural vaginal delivery, activates an endogenous analgesia system and lessens the afferent sign of labor pain and increases the tolerance to labor pain. | true | true | true | true | true | 7 |
7 | DISCUSSION | 0 | null | null | 17,342,250 | null | One might then believe that increasing the release of β-EP into the peripheral blood is one mechanism of the electro-acupuncture in relieving labor pain. | null | 153 | 51 | 0 | false | null | null | One might then believe that increasing the release of β-EP into the peripheral blood is one mechanism of the electro-acupuncture in relieving labor pain. | true | true | true | true | true | 7 |
7 | DISCUSSION | 0 | null | null | 17,342,250 | null | It is through regulating the CNS and the contraction of uterus that β-EP plays a significant role in relieving labor pain with electro-acupuncture. | null | 147 | 52 | 0 | false | null | null | It is through regulating the CNS and the contraction of uterus that β-EP plays a significant role in relieving labor pain with electro-acupuncture. | true | true | true | true | true | 7 |
8 | DISCUSSION | 1 | 60 | [
"B60",
"B61",
"B62",
"B63"
] | 17,342,250 | NA|pmid-10447217|pmid-11203736|NA | Prior to the discovery of endogenous opioids, Han [60] focused on various candidate neurotransmitters including monoamines, and found that 5-HT was most important among classical neurotransmitters for the mediation of acupuncture analgesia. | [
"60",
"61",
"62",
"63"
] | 240 | 53 | 1 | false | Prior to the discovery of endogenous opioids, Han focused on various candidate neurotransmitters including monoamines, and found that 5-HT was most important among classical neurotransmitters for the mediation of acupuncture analgesia. | [
"60"
] | Prior to the discovery of endogenous opioids, Han focused on various candidate neurotransmitters including monoamines, and found that 5-HT was most important among classical neurotransmitters for the mediation of acupuncture analgesia. | true | true | true | true | true | 8 |
8 | DISCUSSION | 1 | 60 | [
"B60",
"B61",
"B62",
"B63"
] | 17,342,250 | NA|pmid-10447217|pmid-11203736|NA | 5-HT is released from platelets due to tissue damage or ischemia and participates in pain mediation via the 5-HT3 receptor. | [
"60",
"61",
"62",
"63"
] | 123 | 54 | 0 | false | 5-HT is released from platelets due to tissue damage or ischemia and participates in pain mediation via the 5-HT3 receptor. | [] | 5-HT is released from platelets due to tissue damage or ischemia and participates in pain mediation via the 5-HT3 receptor. | false | false | true | true | false | 8 |
8 | DISCUSSION | 1 | 61 | [
"B60",
"B61",
"B62",
"B63"
] | 17,342,250 | NA|pmid-10447217|pmid-11203736|NA | A previous study [61] has shown that high levels of 5-HT in the masseter muscle was associated with pain and allodynia/hyperalgesia in patients with chronic myalgia. | [
"60",
"61",
"62",
"63"
] | 165 | 55 | 1 | false | A previous study has shown that high levels of 5-HT in the masseter muscle was associated with pain and allodynia/hyperalgesia in patients with chronic myalgia. | [
"61"
] | A previous study has shown that high levels of 5-HT in the masseter muscle was associated with pain and allodynia/hyperalgesia in patients with chronic myalgia. | true | true | true | true | true | 8 |
8 | DISCUSSION | 1 | 62 | [
"B60",
"B61",
"B62",
"B63"
] | 17,342,250 | NA|pmid-10447217|pmid-11203736|NA | It also seems that circulating 5-HT may be involved in determining the mechanical pain threshold over healthy muscles, since a high level of 5-HT was associated with a low pressure pain threshold (PPT) in healthy subjects [62]. | [
"60",
"61",
"62",
"63"
] | 227 | 56 | 1 | false | It also seems that circulating 5-HT may be involved in determining the mechanical pain threshold over healthy muscles, since a high level of 5-HT was associated with a low pressure pain threshold (PPT) in healthy subjects. | [
"62"
] | It also seems that circulating 5-HT may be involved in determining the mechanical pain threshold over healthy muscles, since a high level of 5-HT was associated with a low pressure pain threshold (PPT) in healthy subjects. | true | true | true | true | true | 8 |
8 | DISCUSSION | 1 | 60 | [
"B60",
"B61",
"B62",
"B63"
] | 17,342,250 | NA|pmid-10447217|pmid-11203736|NA | Electro-acupuncture can increase the concentration of 5-HT in peripheral blood and the CNS, as electro-acupuncture can improve the concentration of tryptophane in blood which is a necessary precursor to combine 5-HT. | [
"60",
"61",
"62",
"63"
] | 216 | 57 | 0 | false | Electro-acupuncture can increase the concentration of 5-HT in peripheral blood and the CNS, as electro-acupuncture can improve the concentration of tryptophane in blood which is a necessary precursor to combine 5-HT. | [] | Electro-acupuncture can increase the concentration of 5-HT in peripheral blood and the CNS, as electro-acupuncture can improve the concentration of tryptophane in blood which is a necessary precursor to combine 5-HT. | true | true | true | true | true | 8 |
8 | DISCUSSION | 1 | 63 | [
"B60",
"B61",
"B62",
"B63"
] | 17,342,250 | NA|pmid-10447217|pmid-11203736|NA | As a consequence, this improves the permeability of blood-brain barrier [63]. | [
"60",
"61",
"62",
"63"
] | 77 | 58 | 1 | false | As a consequence, this improves the permeability of blood-brain barrier. | [
"63"
] | As a consequence, this improves the permeability of blood-brain barrier. | true | true | true | true | true | 8 |
8 | DISCUSSION | 1 | 60 | [
"B60",
"B61",
"B62",
"B63"
] | 17,342,250 | NA|pmid-10447217|pmid-11203736|NA | The study has shown that it is through the CNS that 5-HT functions in relieving labor pain with electro-acupuncture. | [
"60",
"61",
"62",
"63"
] | 116 | 59 | 0 | false | The study has shown that it is through the CNS that 5-HT functions in relieving labor pain with electro-acupuncture. | [] | The study has shown that it is through the CNS that 5-HT functions in relieving labor pain with electro-acupuncture. | true | true | true | true | true | 8 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3"
] | 17,426,135 | pmid-15809261|pmid-10508687|NA | Eukaryotes contain thousands of genes that are expressed in unique patterns to ensure the correct establishment of cellular identities. | [
"1–3"
] | 135 | 60 | 0 | false | Eukaryotes contain thousands of genes that are expressed in unique patterns to ensure the correct establishment of cellular identities. | [] | Eukaryotes contain thousands of genes that are expressed in unique patterns to ensure the correct establishment of cellular identities. | true | true | true | true | true | 9 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3"
] | 17,426,135 | pmid-15809261|pmid-10508687|NA | This process requires the coordinate transcriptional regulation of hundreds of genes. | [
"1–3"
] | 85 | 61 | 0 | false | This process requires the coordinate transcriptional regulation of hundreds of genes. | [] | This process requires the coordinate transcriptional regulation of hundreds of genes. | true | true | true | true | true | 9 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3"
] | 17,426,135 | pmid-15809261|pmid-10508687|NA | Gene expression is controlled by promoter sequences located immediately upstream of the transcriptional start sites of genes as well as additional regulatory sequences present close to or within the genes themselves. | [
"1–3"
] | 216 | 62 | 0 | false | Gene expression is controlled by promoter sequences located immediately upstream of the transcriptional start sites of genes as well as additional regulatory sequences present close to or within the genes themselves. | [] | Gene expression is controlled by promoter sequences located immediately upstream of the transcriptional start sites of genes as well as additional regulatory sequences present close to or within the genes themselves. | true | true | true | true | true | 9 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3"
] | 17,426,135 | pmid-15809261|pmid-10508687|NA | These cis-regulatory elements, which can act as enhancers or silencers of gene expression, are stretches of DNA that usually span a few hundred base pairs, even while being able to exert long-range effects regardless of their position or orientation (1–3). | [
"1–3"
] | 256 | 63 | 1 | false | These cis-regulatory elements, which can act as enhancers or silencers of gene expression, are stretches of DNA that usually span a few hundred base pairs, even while being able to exert long-range effects regardless of their position or orientation. | [
"1–3"
] | These cis-regulatory elements, which can act as enhancers or silencers of gene expression, are stretches of DNA that usually span a few hundred base pairs, even while being able to exert long-range effects regardless of their position or orientation. | true | true | true | true | true | 9 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3"
] | 17,426,135 | pmid-15809261|pmid-10508687|NA | At the same time, neighbouring genes which should theoretically be influenced by the same enhancer often display independent transcription profiles. | [
"1–3"
] | 148 | 64 | 0 | false | At the same time, neighbouring genes which should theoretically be influenced by the same enhancer often display independent transcription profiles. | [] | At the same time, neighbouring genes which should theoretically be influenced by the same enhancer often display independent transcription profiles. | true | true | true | true | true | 9 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3"
] | 17,426,135 | pmid-15809261|pmid-10508687|NA | This raises the fundamental question of how the range of enhancer action can be restricted. | [
"1–3"
] | 91 | 65 | 0 | false | This raises the fundamental question of how the range of enhancer action can be restricted. | [] | This raises the fundamental question of how the range of enhancer action can be restricted. | true | true | true | true | true | 9 |
1 | INTRODUCTION | 1 | 3–5 | [
"B3 B4 B5"
] | 17,426,135 | NA|pmid-12971721|pmid-14517543|pmid-11700282|pmid-12787766|pmid-12067651|pmid-11865056|pmid-12700350 | Evidence suggests that the control of specific expression patterns may be correlated with the spatial positioning of genes within the nucleus. | [
"3–5"
] | 142 | 66 | 0 | false | Evidence suggests that the control of specific expression patterns may be correlated with the spatial positioning of genes within the nucleus. | [] | Evidence suggests that the control of specific expression patterns may be correlated with the spatial positioning of genes within the nucleus. | true | true | true | true | true | 10 |
1 | INTRODUCTION | 1 | 3–5 | [
"B3 B4 B5"
] | 17,426,135 | NA|pmid-12971721|pmid-14517543|pmid-11700282|pmid-12787766|pmid-12067651|pmid-11865056|pmid-12700350 | Indeed, recent data have shown that enhancers and their target promoters are in close proximity to each other within the nuclear space. | [
"3–5"
] | 135 | 67 | 0 | false | Indeed, recent data have shown that enhancers and their target promoters are in close proximity to each other within the nuclear space. | [] | Indeed, recent data have shown that enhancers and their target promoters are in close proximity to each other within the nuclear space. | true | true | true | true | true | 10 |
1 | INTRODUCTION | 1 | 3–5 | [
"B3 B4 B5"
] | 17,426,135 | NA|pmid-12971721|pmid-14517543|pmid-11700282|pmid-12787766|pmid-12067651|pmid-11865056|pmid-12700350 | These interactions persist during transcription, suggesting that the direct interactions of enhancers with their target genes may be important for activation (3–5). | [
"3–5"
] | 164 | 68 | 1 | false | These interactions persist during transcription, suggesting that the direct interactions of enhancers with their target genes may be important for activation. | [
"3–5"
] | These interactions persist during transcription, suggesting that the direct interactions of enhancers with their target genes may be important for activation. | true | true | true | true | true | 10 |
1 | INTRODUCTION | 1 | 3–5 | [
"B3 B4 B5"
] | 17,426,135 | NA|pmid-12971721|pmid-14517543|pmid-11700282|pmid-12787766|pmid-12067651|pmid-11865056|pmid-12700350 | These specific interactions are at least partly mediated by enhancers and by specific promoter-bound proteins. | [
"3–5"
] | 110 | 69 | 0 | false | These specific interactions are at least partly mediated by enhancers and by specific promoter-bound proteins. | [] | These specific interactions are at least partly mediated by enhancers and by specific promoter-bound proteins. | true | true | true | true | true | 10 |
2 | INTRODUCTION | 1 | 6 | [
"B6",
"B7"
] | 17,426,135 | pmid-1848159|pmid-1569958|pmid-14996934|pmid-11106742|pmid-12925706 | Distant enhancer and promoter interactions can also be limited by DNA elements called insulators. | [
"6",
"7"
] | 97 | 70 | 0 | false | Distant enhancer and promoter interactions can also be limited by DNA elements called insulators. | [] | Distant enhancer and promoter interactions can also be limited by DNA elements called insulators. | true | true | true | true | true | 11 |
2 | INTRODUCTION | 1 | 6 | [
"B6",
"B7"
] | 17,426,135 | pmid-1848159|pmid-1569958|pmid-14996934|pmid-11106742|pmid-12925706 | Insulators possess two functional properties. | [
"6",
"7"
] | 45 | 71 | 0 | false | Insulators possess two functional properties. | [] | Insulators possess two functional properties. | true | true | true | true | true | 11 |
2 | INTRODUCTION | 1 | 6 | [
"B6",
"B7"
] | 17,426,135 | pmid-1848159|pmid-1569958|pmid-14996934|pmid-11106742|pmid-12925706 | First, insulators positioned between enhancers and promoters can block their interaction. | [
"6",
"7"
] | 89 | 72 | 0 | false | First, insulators positioned between enhancers and promoters can block their interaction. | [] | First, insulators positioned between enhancers and promoters can block their interaction. | true | true | true | true | true | 11 |
2 | INTRODUCTION | 1 | 6 | [
"B6",
"B7"
] | 17,426,135 | pmid-1848159|pmid-1569958|pmid-14996934|pmid-11106742|pmid-12925706 | Second, insulators (also called boundaries) prevent the advance of nearby condensed chromatin and thereby protect gene expression from positive or negative chromatin effects (6,7). | [
"6",
"7"
] | 180 | 73 | 0 | false | Second, insulators (also called boundaries) prevent the advance of nearby condensed chromatin and thereby protect gene expression from positive or negative chromatin effects. | [
"6,7"
] | Second, insulators (also called boundaries) prevent the advance of nearby condensed chromatin and thereby protect gene expression from positive or negative chromatin effects. | true | true | true | true | true | 11 |
2 | INTRODUCTION | 1 | 6 | [
"B6",
"B7"
] | 17,426,135 | pmid-1848159|pmid-1569958|pmid-14996934|pmid-11106742|pmid-12925706 | Insulators have been identified in most eukaryotic genomes, suggesting that they have a conserved role in defining domains of gene function. | [
"6",
"7"
] | 140 | 74 | 0 | false | Insulators have been identified in most eukaryotic genomes, suggesting that they have a conserved role in defining domains of gene function. | [] | Insulators have been identified in most eukaryotic genomes, suggesting that they have a conserved role in defining domains of gene function. | true | true | true | true | true | 11 |
2 | INTRODUCTION | 1 | 6 | [
"B6",
"B7"
] | 17,426,135 | pmid-1848159|pmid-1569958|pmid-14996934|pmid-11106742|pmid-12925706 | They have also been shown to play critical roles in many developmental processes, such as imprinting and mammalian dosage compensation. | [
"6",
"7"
] | 135 | 75 | 0 | false | They have also been shown to play critical roles in many developmental processes, such as imprinting and mammalian dosage compensation. | [] | They have also been shown to play critical roles in many developmental processes, such as imprinting and mammalian dosage compensation. | true | true | true | true | true | 11 |
3 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B12"
] | 17,426,135 | pmid-15815711|pmid-11161205|pmid-11161206|pmid-16227580|pmid-11106742 | The Drosophila genome contains many sequences with insulator function (8). | [
"8",
"9",
"10",
"11",
"12"
] | 74 | 76 | 1 | false | The Drosophila genome contains many sequences with insulator function. | [
"8"
] | The Drosophila genome contains many sequences with insulator function. | true | true | true | true | true | 12 |
3 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B12"
] | 17,426,135 | pmid-15815711|pmid-11161205|pmid-11161206|pmid-16227580|pmid-11106742 | The first insulators to be identified were scs and scs′, which correspond to regions of unusual chromatin structure flanking the decondensed domain produced by the transcription of two heat-shock (hs) genes. | [
"8",
"9",
"10",
"11",
"12"
] | 207 | 77 | 0 | false | The first insulators to be identified were scs and scs′, which correspond to regions of unusual chromatin structure flanking the decondensed domain produced by the transcription of two heat-shock (hs) genes. | [] | The first insulators to be identified were scs and scs′, which correspond to regions of unusual chromatin structure flanking the decondensed domain produced by the transcription of two heat-shock (hs) genes. | true | true | true | true | true | 12 |
3 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B12"
] | 17,426,135 | pmid-15815711|pmid-11161205|pmid-11161206|pmid-16227580|pmid-11106742 | Another Drosophila insulator is the gypsy insulator. | [
"8",
"9",
"10",
"11",
"12"
] | 52 | 78 | 0 | false | Another Drosophila insulator is the gypsy insulator. | [] | Another Drosophila insulator is the gypsy insulator. | true | true | true | true | true | 12 |
3 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B12"
] | 17,426,135 | pmid-15815711|pmid-11161205|pmid-11161206|pmid-16227580|pmid-11106742 | This element was identified as the region within the gypsy retrotransposon that is responsible for the induction of tissue-specific mutations in many genes. | [
"8",
"9",
"10",
"11",
"12"
] | 156 | 79 | 0 | false | This element was identified as the region within the gypsy retrotransposon that is responsible for the induction of tissue-specific mutations in many genes. | [] | This element was identified as the region within the gypsy retrotransposon that is responsible for the induction of tissue-specific mutations in many genes. | true | true | true | true | true | 12 |
3 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B12"
] | 17,426,135 | pmid-15815711|pmid-11161205|pmid-11161206|pmid-16227580|pmid-11106742 | Although the gypsy insulator acts as an enhancer blocker when present as a single copy, when two gypsy insulators are present between an enhancer and a promoter they lose their enhancer-blocking activity (9,10); in other words, the presence of two gypsy insulators results in an insulator bypass. | [
"8",
"9",
"10",
"11",
"12"
] | 296 | 80 | 0 | false | Although the gypsy insulator acts as an enhancer blocker when present as a single copy, when two gypsy insulators are present between an enhancer and a promoter they lose their enhancer-blocking activity ; in other words, the presence of two gypsy insulators results in an insulator bypass. | [
"9,10"
] | Although the gypsy insulator acts as an enhancer blocker when present as a single copy, when two gypsy insulators are present between an enhancer and a promoter they lose their enhancer-blocking activity ; in other words, the presence of two gypsy insulators results in an insulator bypass. | true | true | true | true | true | 12 |
3 | INTRODUCTION | 1 | 11 | [
"B8",
"B9",
"B10",
"B11",
"B12"
] | 17,426,135 | pmid-15815711|pmid-11161205|pmid-11161206|pmid-16227580|pmid-11106742 | Gypsy insulators have also been shown to stabilize trans activation between distantly located enhancers and promoters (11). | [
"8",
"9",
"10",
"11",
"12"
] | 123 | 81 | 1 | false | Gypsy insulators have also been shown to stabilize trans activation between distantly located enhancers and promoters. | [
"11"
] | Gypsy insulators have also been shown to stabilize trans activation between distantly located enhancers and promoters. | true | true | true | true | true | 12 |
3 | INTRODUCTION | 1 | 12 | [
"B8",
"B9",
"B10",
"B11",
"B12"
] | 17,426,135 | pmid-15815711|pmid-11161205|pmid-11161206|pmid-16227580|pmid-11106742 | While the proteins bound to the gypsy insulator are uniformly distributed along polytene chromosomes, in interphase nuclei of diploid cells they coalesce into large foci called insulator bodies (12). | [
"8",
"9",
"10",
"11",
"12"
] | 199 | 82 | 1 | false | While the proteins bound to the gypsy insulator are uniformly distributed along polytene chromosomes, in interphase nuclei of diploid cells they coalesce into large foci called insulator bodies. | [
"12"
] | While the proteins bound to the gypsy insulator are uniformly distributed along polytene chromosomes, in interphase nuclei of diploid cells they coalesce into large foci called insulator bodies. | true | true | true | true | true | 12 |
4 | INTRODUCTION | 1 | 13 | [
"B13",
"B14",
"B12"
] | 17,426,135 | pmid-7637789|pmid-8557045|pmid-11106742 | The enhancer-blocking effects of insulators are accomplished without affecting the intrinsic properties of any of the regulatory elements, implying that insulators somehow disrupt the signalling between enhancers, silencers and promoters (13,14). | [
"13",
"14",
"12"
] | 246 | 83 | 0 | false | The enhancer-blocking effects of insulators are accomplished without affecting the intrinsic properties of any of the regulatory elements, implying that insulators somehow disrupt the signalling between enhancers, silencers and promoters. | [
"13,14"
] | The enhancer-blocking effects of insulators are accomplished without affecting the intrinsic properties of any of the regulatory elements, implying that insulators somehow disrupt the signalling between enhancers, silencers and promoters. | true | true | true | true | true | 13 |
4 | INTRODUCTION | 1 | 12 | [
"B13",
"B14",
"B12"
] | 17,426,135 | pmid-7637789|pmid-8557045|pmid-11106742 | While the mechanism whereby insulators establish independent functional domains is unclear, it might involve interactions between insulators and/or nuclear substructures to form loop domains that limit the action of transcriptional regulatory elements (12). | [
"13",
"14",
"12"
] | 257 | 84 | 1 | false | While the mechanism whereby insulators establish independent functional domains is unclear, it might involve interactions between insulators and/or nuclear substructures to form loop domains that limit the action of transcriptional regulatory elements. | [
"12"
] | While the mechanism whereby insulators establish independent functional domains is unclear, it might involve interactions between insulators and/or nuclear substructures to form loop domains that limit the action of transcriptional regulatory elements. | true | true | true | true | true | 13 |
5 | INTRODUCTION | 1 | 15 | [
"B15",
"B16",
"B15"
] | 17,426,135 | pmid-10331252|pmid-11865056|pmid-10331252|pmid-11106742|pmid-9286681|pmid-12629048|pmid-12062099|pmid-14996934 | Some years ago, we reported the identification of alleles of the Drosophila melanogaster white gene that were caused by the successive insertion of two LTR retrotransposons called ZAM and Idefix (15). | [
"15",
"16",
"15"
] | 200 | 85 | 1 | false | Some years ago, we reported the identification of alleles of the Drosophila melanogaster white gene that were caused by the successive insertion of two LTR retrotransposons called ZAM and Idefix. | [
"15"
] | Some years ago, we reported the identification of alleles of the Drosophila melanogaster white gene that were caused by the successive insertion of two LTR retrotransposons called ZAM and Idefix. | true | true | true | true | true | 14 |
5 | INTRODUCTION | 1 | 15 | [
"B15",
"B16",
"B15"
] | 17,426,135 | pmid-10331252|pmid-11865056|pmid-10331252|pmid-11106742|pmid-9286681|pmid-12629048|pmid-12062099|pmid-14996934 | Subsequent analysis of the molecular mechanisms by which ZAM and Idefix interfere with white gene regulation revealed that the 5′ untranslated region (5′ UTR) of ZAM bears cis-acting regulatory sequences that can enhance the transcription of white in the eyes of a line called RevI. | [
"15",
"16",
"15"
] | 282 | 86 | 0 | false | Subsequent analysis of the molecular mechanisms by which ZAM and Idefix interfere with white gene regulation revealed that the 5′ untranslated region (5′ UTR) of ZAM bears cis-acting regulatory sequences that can enhance the transcription of white in the eyes of a line called RevI. | [] | Subsequent analysis of the molecular mechanisms by which ZAM and Idefix interfere with white gene regulation revealed that the 5′ untranslated region of ZAM bears cis-acting regulatory sequences that can enhance the transcription of white in the eyes of a line called RevI. | true | true | true | true | true | 14 |
5 | INTRODUCTION | 1 | 16 | [
"B15",
"B16",
"B15"
] | 17,426,135 | pmid-10331252|pmid-11865056|pmid-10331252|pmid-11106742|pmid-9286681|pmid-12629048|pmid-12062099|pmid-14996934 | In another line, called RevII, this activation can be counteracted by the long terminal repeat (LTR) of Idefix, which acts as an insulator in the flies’ eyes to isolate the white gene from the upstream ZAM enhancer (16). | [
"15",
"16",
"15"
] | 220 | 87 | 1 | false | In another line, called RevII, this activation can be counteracted by the long terminal repeat (LTR) of Idefix, which acts as an insulator in the flies’ eyes to isolate the white gene from the upstream ZAM enhancer. | [
"16"
] | In another line, called RevII, this activation can be counteracted by the long terminal repeat (LTR) of Idefix, which acts as an insulator in the flies’ eyes to isolate the white gene from the upstream ZAM enhancer. | true | true | true | true | true | 14 |
5 | INTRODUCTION | 1 | 15 | [
"B15",
"B16",
"B15"
] | 17,426,135 | pmid-10331252|pmid-11865056|pmid-10331252|pmid-11106742|pmid-9286681|pmid-12629048|pmid-12062099|pmid-14996934 | We also reported the surprising discovery that an additional copy of Idefix inserted between the ZAM enhancer and the white gene in a line called RevIV leads to the full reversion of the orange eye colour phenotype that is caused by the presence of a single Idefix element: in the presence of both copies of Idefix, the eyes became brick red. | [
"15",
"16",
"15"
] | 342 | 88 | 0 | false | We also reported the surprising discovery that an additional copy of Idefix inserted between the ZAM enhancer and the white gene in a line called RevIV leads to the full reversion of the orange eye colour phenotype that is caused by the presence of a single Idefix element: in the presence of both copies of Idefix, the eyes became brick red. | [] | We also reported the surprising discovery that an additional copy of Idefix inserted between the ZAM enhancer and the white gene in a line called RevIV leads to the full reversion of the orange eye colour phenotype that is caused by the presence of a single Idefix element: in the presence of both copies of Idefix, the eyes became brick red. | true | true | true | true | true | 14 |
5 | INTRODUCTION | 1 | 15 | [
"B15",
"B16",
"B15"
] | 17,426,135 | pmid-10331252|pmid-11865056|pmid-10331252|pmid-11106742|pmid-9286681|pmid-12629048|pmid-12062099|pmid-14996934 | This reversion occurred through a mechanism that remained unelucidated (15). | [
"15",
"16",
"15"
] | 76 | 89 | 1 | false | This reversion occurred through a mechanism that remained unelucidated. | [
"15"
] | This reversion occurred through a mechanism that remained unelucidated. | true | true | true | true | true | 14 |
6 | INTRODUCTION | 0 | null | null | 17,426,135 | pmid-3002631 | In this study, we sought to advance our understanding of the insulator properties of Idefix and of its potential impact on nearby genes. | null | 136 | 90 | 0 | false | null | null | In this study, we sought to advance our understanding of the insulator properties of Idefix and of its potential impact on nearby genes. | true | true | true | true | true | 15 |
6 | INTRODUCTION | 0 | null | null | 17,426,135 | pmid-3002631 | We combined transgenic experiments with 3D fluorescent in situ hybridization (3D FISH)-immunoassays to further dissect its enhancer-blocker properties. | null | 151 | 91 | 0 | false | null | null | We combined transgenic experiments with 3D fluorescent in situ hybridization (3D FISH)-immunoassays to further dissect its enhancer-blocker properties. | true | true | true | true | true | 15 |
6 | INTRODUCTION | 0 | null | null | 17,426,135 | pmid-3002631 | We demonstrate that the ability of the Idefix insulator to protect genes from enhancer effects in cis is increased when two copies of the insulator are present. | null | 160 | 92 | 0 | false | null | null | We demonstrate that the ability of the Idefix insulator to protect genes from enhancer effects in cis is increased when two copies of the insulator are present. | true | true | true | true | true | 15 |
6 | INTRODUCTION | 0 | null | null | 17,426,135 | pmid-3002631 | This is similar to data reported for tandem repeats of scs/scs′ elements. | null | 73 | 93 | 0 | false | null | null | This is similar to data reported for tandem repeats of scs/scs′ elements. | true | true | true | true | true | 15 |
6 | INTRODUCTION | 0 | null | null | 17,426,135 | pmid-3002631 | We also show that when an additional DNA fragment from the 5′ UTR of Idefix is fused to the insulator domain, the enhancer-blocking activity of the Idefix LTR is neutralized. | null | 174 | 94 | 0 | false | null | null | We also show that when an additional DNA fragment from the 5′ UTR of Idefix is fused to the insulator domain, the enhancer-blocking activity of the Idefix LTR is neutralized. | true | true | true | true | true | 15 |
6 | INTRODUCTION | 0 | null | null | 17,426,135 | pmid-3002631 | This novel functional module promotes insulator bypass, as has been observed with pairs of gypsy insulators. | null | 108 | 95 | 0 | false | null | null | This novel functional module promotes insulator bypass, as has been observed with pairs of gypsy insulators. | true | true | true | true | true | 15 |
6 | INTRODUCTION | 0 | null | null | 17,426,135 | pmid-3002631 | We further show that this loss of insulator function is correlated with a displacement of the tested sequence from the interior of the nucleus towards the nuclear periphery. | null | 173 | 96 | 0 | false | null | null | We further show that this loss of insulator function is correlated with a displacement of the tested sequence from the interior of the nucleus towards the nuclear periphery. | true | true | true | true | true | 15 |
0 | DISCUSSION | 0 | null | null | 17,426,135 | pmid-15809261|pmid-10508687|NA | In this study, we show that the enhancer-blocker activity mediated by the chromatin insulator found within the Idefix retrotransposon is stronger when two copies of the insulator are present than when only one is present. | null | 221 | 97 | 0 | false | null | null | In this study, we show that the enhancer-blocker activity mediated by the chromatin insulator found within the Idefix retrotransposon is stronger when two copies of the insulator are present than when only one is present. | true | true | true | true | true | 16 |
0 | DISCUSSION | 0 | null | null | 17,426,135 | pmid-15809261|pmid-10508687|NA | The activity can be abolished, however, when the 5′ UTR region of Idefix is associated with the insulator. | null | 106 | 98 | 0 | false | null | null | The activity can be abolished, however, when the 5′ UTR region of Idefix is associated with the insulator. | true | true | true | true | true | 16 |
0 | DISCUSSION | 0 | null | null | 17,426,135 | pmid-15809261|pmid-10508687|NA | We further show that the 5′ UTR causes flanking genomic sequences to be displaced to the nuclear periphery, | null | 107 | 99 | 0 | false | null | null | We further show that the 5′ UTR causes flanking genomic sequences to be displaced to the nuclear periphery, | true | true | false | true | false | 16 |
No dataset card yet