id
stringlengths
30
30
corpus
stringclasses
3 values
sentence
stringlengths
10
1.38k
token
stringlengths
1
16
complexity
float64
0
0.86
difficulty
stringclasses
5 values
3YO4AH2FPDK1PZHZAT8WAEBL70T0Q4
biomed
Mice also appear to have independent CO versus NCO recombination pathways [46].
NCO
0.5375
neutral
3TC2K6WK9G22F5KH3MVA7BJ0ATO82K
biomed
Another possibility is that TRIP13 is required for disassembly of NCO recombinational repair complexes [51] containing those proteins that persist abnormally on Trip13Gt/Gt pachytene chromosomes.
NCO
0.673077
difficult
3RHLQY6EDT4OZEVVO8PEMIUZ5YI4DJ
biomed
Cells in the stratum germinativum of the neopallial cortex, which surrounds the lateral ventricle, show at E13 and E15 a staining for Annexin A7 mainly in the cytosol.
stratum
0.538462
neutral
36U4VBVNQODHHM8FLFBG4B9XJBYUR1
biomed
Alterations in XPD resulting in defective TFIIH function are associated with UV-sensitive, multisystem disorders including xeroderma pigmentosum (XP), XP combined with Cockayne syndrome (CS), and trichothiodystrophy (TTD) [8-10].
CS
0.625
difficult
3A9LA2FRWSEW9WO7UFA9AE6VQLEXHY
biomed
Using an isoform-specific null mouse we show that Rb drives SAC differentiation through E2f3a.
SAC
0.543478
neutral
38O9DZ0A62NFBR1TA7YCNXN94YY26S
biomed
Myosin Va is enriched in the PSD [43], and DNCL1 binds to a variety of PSD proteins including guanylate kinase domain-associated protein [44] and neuronal nitric oxide synthase [45].
oxide
0.546875
neutral
3THR0FZ95PTB1JT5K92BJT89VXQOLX
biomed
Mutation of Smad3 or expression of dominant negative transforming growth factor β (TGF-β) type II receptor also disrupts normal articular cartilage maintenance (Serra et al. 1997; Yang et al. 2001).
Serra
0.55
neutral
302OLP89DZ7TWB5YXD4UFFYHC79CA7
biomed
Our genetically modified mouse strain has the potential to be a useful and sensitive tools for detailed investigation of ADAM proteins' functions in the nervous system.
ADAM
0.55
neutral
31YWE12TE0CZG7IVH6OXJ1H1CHR7XD
biomed
The roles of PAX6 in brain development have mainly been studied in homozygous mutant mice or rats and include arealisation of the cerebral cortex [7], formation of the prosencephalon-mesencephalon boundary [8], axon guidance [8], differentiation of neurons from glia [9] and neuronal migration in the cerebellum [10].
cerebellum
0.552632
neutral
30OITAWPBQ368069RZ4VUBKDJHQ9HS
biomed
Therefore, electrophyological studies to enable analysis of synaptic transmission and plasticity in the hippocampus and cerebellum of ADAM11-deficient mice will be needed.
cerebellum
0.6
difficult
3HKIF5DF6YXS84BY7TMD9B8C4HIG95
biomed
Other defects included absence or hypoplasia of the pineal gland, cortical polymicrogyria, white matter changes in the corpus callosum and grey matter changes in the cerebellum [11-13].
cerebellum
0.602273
difficult
3G5RUKN2EC3YIWSKUXZ8ZVH95T4N9K
biomed
Mutations in Crx have been associated with several human diseases that lead to blindness, including cone-rod dystrophy 2 [6,13,14], retinitis pigmentosa [14], and LCA [14-16].
dystrophy
0.552632
neutral
3Q9SPIIRWJM2A9B3E44VR95K4NQAWD
biomed
In contrast to TEL, ph does not contain an obvious sequence-specific DNA binding motif (16).
motif
0.553571
neutral
3FTID4TN8LYNVXX7QWB9LK6B97PLY5
biomed
The former motif is thought to be involved in protein-protein interactions in chromatin [7], and the latter is a feature of chromatin-remodelling proteins, and the presence of disease-causing mutations indicates the functional importance of these domains.
motif
0.75
difficult
3HEADTGN2PSHU1XFQ5LL0XBGXICRVS
biomed
However, the repressive effect was more significant when DBD-tail, which does not contain SAM domain, was co-introduced with the 5xGAL4-pGL3 reporter plasmid.
SAM
0.556818
neutral
3UY4PIS8QRLGTRPPQKKFKPZQ7I8N15
biomed
Previous reports suggested that the SAM domain is a protein-protein interaction module.
SAM
0.558824
neutral
3BKZLF990ZZYMUDKI1J52655JDCYQ7
biomed
Bmp2 and Bmp4 are also expressed in the AER, where Prx1::cre is inactive, and these domains of expression are not affected (Figure 1A–1D, black arrows).
cre
0.558824
neutral
3126F2F5F83FGDVEINSMVYNFW5GPEN
biomed
This transgene expresses cre very early in limb development, resulting in complete recombination of floxed alleles at early limb bud stages.
cre
0.65
difficult
3SV8KD29L4SCGHPU1I1RKR2YQ1IZK1
biomed
These expression domains are completely lost by E10.5 in the presence of the Prx1::cre transgene (Figure 1D).
cre
0.683333
difficult
3T2EL38U0MK9MPNAD5X3JSYWH7DXQV
biomed
While it is possible that dox acts in some other way to slow amyloid clearance, data from multiple studies demonstrate that microglial responses are normally weak in the mouse AD models [37–40], and thus it is doubtful that dox-mediated microglial inhibition affected the outcome of our study.
AD
0.558824
neutral
3A520CCNWN08T9PCT4AP53YKXJGEAW
biomed
However, the development of safe and effective secretase inhibitors will ultimately be required to determine whether the human brain has the capacity to repair amyloid-associated damage of AD once the progression of pathology is arrested.
AD
0.583333
neutral
3ZFRE2BDQ9EI0HO101GGALA0MAXZXQ
biomed
It is possible that a combination of therapies to limit Aβ production, increase Aβ degradation, and enhance phagocytosis of deposited amyloid may be required to reverse damage associated with AD.
AD
0.590909
neutral
3EKZL9T8Y8M86YDC3JEMW1LLP2ZCHI
biomed
Early support for this hypothesis came from genetic studies linking early-onset AD to mutations in the amyloid precursor protein (APP), from which Aβ is derived, and presenilins 1 and 2, which are interchangeable components of a endoprotease complex that releases Aβ from APP (for review see [2,3]).
AD
0.602941
difficult
3E6L1VR4XWMZCLD5Y2DJ7GHYD156FG
biomed
The lack of clearance in both models of AD pathology comes as a stark contrast to the rapid removal of protein aggregates found in similar tet-off mouse models of Huntington [32] and prion disease [62].
AD
0.671875
difficult
3EHVO81VN5LOJV3ENMP2F52UL52H1R
biomed
Pericentric domains from different chromosomes form clusters, which are revealed by FISH as large spots that coincide with DAPI-dense foci in the interphase nucleus (Figure 4A).
interphase
0.559524
neutral
3EPG8DX9LKQFKU2L7MZJR4H2JCM5P7
biomed
AlphaB, expressed in transfected CHO cells, has been shown to ectopically localize to interphase nuclei, suggesting a regulatory role for this protein in the nucleus [19].
interphase
0.75
difficult
32TZXEA1OLKU7JFJ8F5JLGTQG0H14Q
biomed
Several quantitative trait loci (QTL) have been identified that influence two-bottle intake of bitter stimuli in the mouse, including loci for quinine (Qui) [12,16,26], cyclohexamide (Cyx) [13] and sucrose octaacetate (Soa) [14,15,17] sensitivity.
Qui
0.5625
neutral
3RDTX9JRTY19FB0XEQIJ3YVJ5E097W
biomed
XY and SI drafted the manuscript.
SI
0.5625
neutral
3CKVGCS3PG5D2FWC2XX15EQMPODS0K
biomed
Annexin A7 is thought to have a role in vesicle fusion and in regulating and stabilizing membrane domains [1].
vesicle
0.5625
neutral
32XN26MTXZJQY21MIO00TSCRXUAL04
biomed
Having excluded a direct role in vesicle formation and membrane fusion, annexin A7 might act by its property as Ca2+-binding protein [17].
vesicle
0.734375
difficult
3N7PQ0KLI5P89OQRKPVFIVKER9P3EQ
biomed
Since the possible new locus of potential interest on chromosome 1 was of suggestive significance, and since the locus identified on chromosome 13 probably is Cia28, we are now paying special attention to the significant QTL for CIA incidence detected at 60–70 cM on chromosome 11 (denoted Cia40).
cM
0.565789
neutral
304QEQWKZPKY4N4JVGGSL9GLSZAO0J
biomed
Erythroid progenitor cells in mon mutants are initially present, but fail to express normal levels of hematopoietic transcription factors and undergo apoptosis.
mon
0.565789
neutral
36818Z1KV3D5JB9F4KTTMCUN6UV3AZ
biomed
The primary genetic defect (>80% disease chromosomes) leading to JNCL is a 1.02 kb genomic DNA deletion in the CLN3 gene, which eliminates exons 7 and 8 and surrounding intronic DNA, predicting a non-functional protein product [2].
kb
0.566667
neutral
3511RHPADVEEYWLLC1JFDODE6K5LRY
biomed
Using PCR primers T3F and C11R, which should be more than 200 kb apart, we were able to amplify a fragment 953 bp in size using DNA from each of the three affected family members as template.
kb
0.569444
neutral
3GVPRXWRPHU2QCT0IKOWGRUMO4HI7I
biomed
The human ADAM22 gene is relatively large, at 300 kb in length, and is comprised of more than 30 exons.
kb
0.617647
difficult
3SSN80MU8CONBMPF00D6N6MNI1LXK3
biomed
However, using homologous recombination in ES cells to generate mutant mice is an inefficient, slow and expensive method because (i) homologous recombination typically occurs at low frequency in ES cells, requiring sophisticated selection schemes and screening of hundreds of clones to identify the desired mutant; (ii) large (15-20 kb) plasmids, often difficult to clone, are required to increase targeting efficiency and (iii) breeding mice to homozygosity and housing a mouse colony generate further delays and costs.
kb
0.625
difficult
3P520RYKCH6SCZAHO8YD1A41RT95UY
biomed
Cln3Δex7/8 knock-in mice harbor the ~1 kb common JNCL mutation and express a non-truncated mutant battenin isoform that is detectable with antibodies recognizing C-terminal epitopes.
kb
0.75
difficult
38VTL6WC4AD9T8UMY9V24VAENHL5YX
biomed
Overexpression of Shh in the distal lung epithelium resulted in the absence of functional alveoli and an increase in interstitial tissue caused by an increased proliferation of both epithelial and mesenchyme cells [26].
Shh
0.568182
neutral
3VIVIU06FKCLBF0NMQQLZ9RCJTCMIX
biomed
These structures defined a novel family of enzymes, now called sedolisins or serine-carboxyl peptidases, that is characterized by the utilization of a fully conserved catalytic triad (Ser, Glu, Asp) and by the presence of an Asp in the oxyanion hole [8].
Ser
0.569444
neutral
371DNNCG442WZ4EUM1F68YSQA538TC
biomed
Congenital diaphragmatic defects are a heterogeneous group of disorders of unknown etiology.
etiology
0.569444
neutral
3EAWOID6MTXTU7DGWS26G1ATOSCV0X
biomed
The use of mouse models has provided valuable insight into the etiology of monogenic syndromes caused by single gene mutations.
etiology
0.583333
neutral
3VCK0Q0PO5EGM247U1GF6KGG2P60NH
biomed
Glaucoma is a leading cause of blindness but its molecular etiology is poorly understood.
etiology
0.592105
neutral
3XBXDSS888JYVS7XL0P726Z271QLXU
biomed
Whereas genetic-based studies have provided novel insights into the pathways that regulate bone development [12–14], relatively little is known about the etiology of age-related bone loss.
etiology
0.6
difficult
3ZQX1VYFTD5GMC9MQKT7EOM3BXRO8B
biomed
In particular, in the absence of Er81, achieved by mutation in the gene or by deprivation of peripheral neurotrophin signaling, group Ia proprioceptive afferents fail to invade the ventral spinal cord and to make effective synaptic connections with motor neurons [9,14].
Ia
0.571429
neutral
3ZXV7Q5FJBOOS2M68TQMTG989NGCFE
biomed
PST domain, proline-, serine- and threonine-rich domain; PSD, post-synaptic density; PCR, polymerase chain reaction.
PST
0.573529
neutral
3MQKOF1EE2O08GEFYEVXHADQPQNWD1
biomed
None of the mutations affected the interaction with TRIM11, suggesting that they do not alter the conformation of the more N-terminal part of the PST domain.
PST
0.6
difficult
38EHZ67RIMS7FOUSW2QIEXEW4HIGMZ
biomed
In addition to the paired domain, PAX6 also contains a DNA-binding homeodomain and a proline, serine and threonine-rich (PST) domain at the C-terminus [1,6].
PST
0.638889
difficult
3BVS8WK9Q0VPSOWQV10CLTGI7UDIB9
biomed
The PST domain, which encompasses the C-terminal 145 amino acids of PAX6, has been shown to act as a transcriptional activator [6].
PST
0.765625
difficult
3VADEH0UHCXGQW0WJICRKFRUXWUSPW
biomed
All our data are consistent with the hypothesis that TRIM11 does not interact with the C-terminal peptide, but interacts with the PST domain between the homeodomain and the C-terminal peptide.
PST
0.84375
very difficult
3GMLHYZ0LEXQENK1ZA3AC72UMYIYUC
biomed
We discovered that in Alk5/Wnt1-Cre mutants, pharyngeal organs (thymus and parathyroid) fail to migrate appropriately.
pharyngeal
0.576087
neutral
34R3P23QHS1HKWJHKAEN8VSOHIGWHA
biomed
Our data suggest that ALK5 is required cell autonomously in the NC to mediate non-redundant signaling events that are essential for appropriate patterning of the pharyngeal organs and cardiac OFT.
pharyngeal
0.609375
difficult
3VDVA3ILIDFAJZ833G7KU5QT66NG1R
biomed
Subsequently cardiac neural crest cells (CNCCs) delaminate, undergo a phenotypic transformation from an epithelial to mesenchymal cell type, and migrate latero-ventrally into the 3rd, 4th and 6th pharyngeal arch arteries (PAAs), where they contribute to the formation of the smooth muscle cell layer of endothelial structures derived from the aortic arch arteries [1-3].
pharyngeal
0.734375
difficult
31YWE12TE0CZG7IVH6OXJ1H1CHL7X7
biomed
TN supervised the project.
TN
0.578125
neutral
3K3IX1W4S6RCQ0E22IQ0ZFXOBQNPAX
biomed
TN conducted the in silico analysis of the quinine taste QTL, analyzed the Tas2r genes, participated in the design of the study and drafted the manuscript.
TN
0.65625
difficult
3CZH926SICETRK9VK30YS0CK59K4EB
biomed
TN and JK supervised the project.
TN
0.722222
difficult
3V7ICJJAZAGVKHXBACY8RS6Z2CCB4N
biomed
In all animals harboring amyloid deposits, we found that the vast majority of Aβ (>99%) was extracted into the SDS and FA fractions (Figure 5A and 5B).
SDS
0.583333
neutral
3OWZNK3RYLP0D2RU6PWF331P7JI2UU
biomed
To further ensure we could detect any such insoluble aggregates that might bias our measure of changes in peptide synthesis, we performed a sequential three-step extraction with PBS, 2% SDS, and 70% FA that would separate peptides by solubility.
SDS
0.625
difficult
3D06DR5225J65XHPA2Y8IB3T6L7MAT
biomed
Consistent with the filter trap results presented above, there were no significant differences in SDS- or FA-soluble Aβ between the 6 mo untreated cohort and either the 6 mo + 3 mo treated or 6 mo + 6 mo treated cohorts.
SDS
0.777778
difficult
3G9UA71JVVUYLND6029WSS9M1J6J7V
biomed
Cortical homogenates were sequentially extracted to separate peptide into PBS-, SDS-, and FA-soluble fractions, then transgene-derived Aβ40 and Aβ42 were measured by human-specific ELISA [23].
SDS
0.825
very difficult
3D1TUISJWI04ON5WVSH7QJ86WGDUIX
biomed
Ovaries of Dmrt4 mutant females have polyovular follicles (follicles containing multiple oocytes), but it is unknown whether this reflects a defect in the germ line or the soma.
soma
0.5875
neutral
3ZQA3IO31BRYBCP1RZKSZEZVXRLO1R
biomed
This system, commonly known as the tet-off system, can be regulated by analogs of tetracycline administered in food or water [12,13].
tetracycline
0.588235
neutral
322ZSN9Z5GKVG3RSAYPTRMCL8J74T1
biomed
The transgenic approach that was used to create the intermediate MSUD model was based on the tetracycline regulated gene switch system that has been used with great success in other studies, for example [34].
tetracycline
0.642857
difficult
3OZ4VAIBEXF0WDE2I0CCY6PPN2BJVN
biomed
This work demonstrated that the CF inflammatory phenotype is much less severe in mice with a small contribution of 129/Sv alleles.
CF
0.588235
neutral
3EPG8DX9LKQFKU2L7MZJR4H2JDFP5M
biomed
Previous work using human patients and genetically altered mice has identified some modifier genes and have advanced our understanding of CF pathophysiology [4].
CF
0.607143
difficult
3M93N4X8HKNK4LXYO577NJ5IOXJJSI
biomed
6 was strongly associated with lung inflammation, consisting of mononuclear cell interstitial infiltration and fibrosis in CF mouse airways; and other loci on chr.
CF
0.642857
difficult
3EQVJH0T40LPSFFNP59CLBLPDOYTHH
biomed
Mucus is involved in obstruction of the gut which occurs frequently in CF infants (called meconium ileus, MI) and adults (called distal intestinal obstruction syndrome, DIOS) [11,13].
CF
0.65625
difficult
3AFT28WXLF29BILZZ65YRDGHETWOIJ
biomed
However, mice on the mixed background seemed more robust than CF mice on the B6 background which prompted us to characterize them in greater detail.
CF
0.725
difficult
335HHSX8CD5IBQJQ3F9XG733A25HDH
biomed
RM, ÅA, RH and ML designed the study.
RM
0.589286
neutral
3FK4G712NX0D3OGOBZGLFKW5KGWSS7
biomed
ML is responsible for genotyping, phenotyping, analyses and, together with RM, for interpretation and for writing the manuscript.
RM
0.7
difficult
3N5YJ55YXG3CNF2PM3D8VQSTBBHANH
biomed
From this screen, we identified a line of mice carrying a recessive mutation that results in primary pulmonary hypoplasia and abnormal diaphragmatic and cardiac development.
diaphragmatic
0.589286
neutral
3D17ECOUOEV9PNWF8100BB1K20Q13A
biomed
This region contains several genes, including those encoding FcγRII, the complement receptor CR1/2 (CD35/CD21), and the decay-accelerating factor CD55 (Prodeus et al. 1998; Bolland and Ravetch 2000; Miwa et al. 2002; Wu et al. 2002), which have each been implicated in the causation of SLE when inactivated by gene-targeting in 129 embryonic stem cells.
causation
0.59375
neutral
3X878VYTIEIIGLRAHCIBDUHU8DN7FG
biomed
CA = chronic arthritis; CIA = collagen-induced arthritis; CV = coefficiant of variation; GO = Gene Ontology; LN = lymph node; LOD = logarithm of the odds; MAPK = mitogen-activated protein kinase; NC = naive control; OA = onset of arthritis; PI = post-immunisation; QTG = quantitative trait gene; QTL = quantitative trait loci; RA = rheumatoid arthritis.
LN
0.59375
neutral
35A1YQPVFEGN38FHUR9ZI7GQXZKI53
biomed
In this assay, serial dilutions of protein homogenate are passed through a cellulose acetate filter; particles larger than the pore size of the filter become trapped in the membrane and are revealed by immunoblotting [22].
acetate
0.594828
neutral
38EHZ67RIMS7FOUSW2QIEXEW4GKMG5
biomed
Nuclei were incubated in buffers with different salt concentrations ranging from 100 mM NaCl to 1 M NaCl.
mM
0.597222
neutral
38Z7YZ2SB32CWUYFEJX2GIBHTV7IQG
biomed
The μ and m designations derive from the levels of Ca2+ required in vitro for optimal activation; 10–50 μM Ca2+ for μ-calpain and 0.3–0.35 mM Ca2+ for m-calpain.
mM
0.602941
difficult
34F34TZU7WZRZMG0UQS1W1SEQ4I2JY
biomed
As significant differences between phenotypes from targeted p53 mutants in vivo and transfection data were observed [e.g. Refs (1–5)], more targeted mutations need to be generated and analyzed in multiple tissues to formulate more accurate models of p53 regulation.
Refs
0.597826
neutral
388CL5C1RJN1927IGW7LZKB8JBCLH6
biomed
JMW, TC, PH-M and MEM drafted the manuscript and RC contributed to its finalization.
MEM
0.6
difficult
367O8HRHKG8U13EDLYK3HHGZ60T4SC
biomed
MEM co-conceived of the study and assisted on drafting of the manuscript.
MEM
0.703125
difficult
3VMV5CHJZ8FBSJKC5ZRU0B9OYOLGT5
biomed
Seventy-three percent of retrogradely labeled gastrocnemius muscle afferents were reported to be expressing TrkC RNA in the adult rat DRG, although some of these (about 10%) may represent cutaneous innervation (McMahon et al. 1994).
gastrocnemius
0.602941
difficult
3538U0YQ1FU0F2QNF0FL0D5E3B1F3J
biomed
Superficial and deep anterior cortical staining was grossly different between alphaA/BKO (Figure 3A,3D,3F and 3I) and wild type lenses (Figure 3K,3N,3P and 3S).
N
0.602941
difficult
3TTPFEFXCTKJQH4BTS1JA1TBTGIH6P
biomed
Peptide Aβ is released from APP by the action of two enzymes, the β-APP cleaving enzyme 1 (BACE1) and γ-secretase, which cleave the holoprotein at the N- and C-termini of Aβ, respectively.
N
0.75
difficult
3R5LWXWHR08I90TWA9SRPEUUBK9GXO
biomed
CA = chronic arthritis; CIA = collagen-induced arthritis; CV = coefficiant of variation; GO = Gene Ontology; LN = lymph node; LOD = logarithm of the odds; MAPK = mitogen-activated protein kinase; NC = naive control; OA = onset of arthritis; PI = post-immunisation; QTG = quantitative trait gene; QTL = quantitative trait loci; RA = rheumatoid arthritis.
logarithm
0.602941
difficult
3RZS0FBRWKA0JFB0MWMR5ANCBT3PCU
biomed
MR, SIRG, and CSC planned and carried out the experiments, evaluated the results, and drafted the manuscript.
MR
0.602941
difficult
32L724R85LKRWIX0E6IDGDL7OZLPIW
biomed
Glaucoma involves retinal ganglion cell death and optic nerve damage that is often associated with elevated intraocular pressure (IOP) [1-5].
ganglion
0.607143
difficult
3MDWE879UH2WHN3NR7UZ80HFO5J9BC
biomed
Previously noted chemoattractant action of the embryonic mouse maxillary process on trigeminal ganglion neurons (Lumsden and Davies 1986) is now attributed to NT-3 and brain-derived neurotrophic factor (BDNF) (O'Connor et al. 1999).
ganglion
0.631579
difficult
39KV3A5D187RKQWWNWIAKT09X2JS7K
biomed
Rb knockout (KO) RTCs continue to proliferate inappropriately and some (rod, ganglion, and bipolar cells) die by apoptosis [2,3].
ganglion
0.673077
difficult
30F94FBDNRKF12C1PDZGZ0IRIBTTB1
biomed
Cone photoreceptors, ganglion cells, horizontal cells and amacrine cells are generated earlier, while Müller glia and bipolar cells are generated later.
ganglion
0.6875
difficult
3YGE63DIN8X69WDLM27223T7V1F0WD
biomed
Consistent with an apparent absence of mature hair cells, initial work suggested that all vestibular and most spiral ganglion cells are lost by postnatal day 14 (P14; [1]).
ganglion
0.7
difficult
3JGHED38EDROGC85M2AZ2FOAENF7YD
biomed
The muscle phenotypes described here are remarkably similar to those of transgenic mice expressing either calcineurin, calmodulin-dependent kinase, or PGC-1α (Naya et al. 2000; Lin et al. 2002; Wu et al. 2002), indicating that PPARδ could be one of the hypothetical downstream transcription factors of these pathways.
Lin
0.607143
difficult
3R4QIDVOJPCBJM6O99CB1MOBIYJEEW
biomed
The best-studied strains of mice that spontaneously develop a lupus-like pathology are the New Zealand Black/New Zealand White hybrid strain (NZB/WF1); the MRL/Mp lpr/lpr strain, which carries the lpr mutation of the FAS receptor gene; and the BXSB strain, which carries the Y chromosome autoimmune accelerator (Yaa) gene (Theofilopoulos and Dixon 1985).
FAS
0.608696
difficult
3X4Q1O9UBHMCMY43GF110OQ80DM7O8
biomed
In MD rat, early death is caused by the dysfunction of the brain stem which is essential for autonomic control of respiration during hypoxia [24].
MD
0.609375
difficult
3ZLW647WALVGE8EBR50EGUBPU6Z32O
biomed
A recent report estimates that the carrier frequency of MLIV in the Ashkenazi Jewish population is 1 in 100, and mutations have been reported in Jewish and non-Jewish families [6-9].
Ashkenazi
0.611111
difficult
3QO7EE372ON29MK9895LUV74Y4UBQ5
biomed
However, we were unable to consistently turn off the human E2 expression cassette by the potent tetracycline analogue, doxycycline in either of the two transgenic lines tested (data not shown).
doxycycline
0.611111
difficult
3SBX2M1TKDNIONZ0TUVYMH1YOCE4QT
biomed
The reason these two lines were unresponsive to doxycycline is unknown.
doxycycline
0.75
difficult
39O0SQZVJN7FJBWJ87I5UJVDB05R70
biomed
cDNA identification and RACE data have been used to determine gene structure for about 30 genes, see, for example, [19,23].
RACE
0.611111
difficult
3MG8450X2OAW59S08N7RZG9IIU7UP8
biomed
The high SNP frequency (0.312%; 295 SNP in 94.492 kbp) in CAST genes may lead to a higher rate of false positives using DNA microarrays or quantitative real-time PCR assays, most of which are based on B6 sequence.
CAST
0.617647
difficult
3UQVX1UPFSHKXGFE8IIVEWDIRUE20R
biomed
Due to the paucity of experimental evidence of the olfactory function of most genes in the family and suggestions of extra-olfactory roles, we embarked on an olfactory receptor expressed sequence tag (EST) project to confirm olfactory epithelial expression of hundreds of mouse odorant receptor genes.
paucity
0.625
difficult
3EKZL9T8Y8M86YDC3JEMW1LLP2THCH
biomed
The SAM domain of the mr-s protein is closely related to that of ph and TEL, whose SAM domains can form a helical, head-to-tail polymeric structure and mediate the formation of a higher order chromatin structure.
TEL
0.625
difficult
36FFXPMST9O9FNAFTONDR1F2EGIHOK
biomed
Crx, cone-rod homeobox; Otx2, orthodenticle-related homeobox 2; TRβ2, thyroid hormone receptor beta 2; Nrl, neural retina leucine zipper; Nr2e3, nuclear receptor subfamily 2 group E member 3; EST, expressed sequence tag; EphB2, ephrin receptor B2; EphA4, ephrin receptor A4; TEL, translocation ETS leukemia.
TEL
0.625
difficult
3TY2U1TEB7AR5IE81BYTVIEVSEBJJ7
biomed
The cause of goiter appears to be an impairment of iodide fixation in the follicular lumen due to a reduced rate of iodide transport across the apical membrane of thyroid gland epithelial cells [4].
lumen
0.625
difficult