-
1
-
-
0025183708
-
Basic local alignment search tool
-
DOI 10.1006/jmbi.1990.9999
-
Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. 1990. Basic local alignment search tool. J Mol Biol 215: 403-410. (Pubitemid 20364473)
-
(1990)
Journal of Molecular Biology
, vol.215
, Issue.3
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
2
-
-
77954092701
-
Genetic evidence that the differential expression of the ligand-independent isoform of CTLA-4 is the molecular basis of the Idd5.1 type 1 diabetes region in nonobese diabetic mice
-
Araki M, Chung D, Liu S, Rainbow DB, Chamberlain G, Garner V, Hunter KM, Vijayakrishnan L, Peterson LB, Oukka M, et al. 2009. Genetic evidence that the differential expression of the ligand-independent isoform of CTLA-4 is the molecular basis of the Idd5.1 type 1 diabetes region in nonobese diabetic mice. J Immunol 183: 5146-5157.
-
(2009)
J Immunol
, vol.183
, pp. 5146-5157
-
-
Araki, M.1
Chung, D.2
Liu, S.3
Rainbow, D.B.4
Chamberlain, G.5
Garner, V.6
Hunter, K.M.7
Vijayakrishnan, L.8
Peterson, L.B.9
Oukka, M.10
-
3
-
-
0035928391
-
Type 1 diabetes: New perspectives on disease pathogenesis and treatment
-
DOI 10.1016/S0140-6736(01)05415-0
-
Atkinson MA, Eisenbarth GS. 2001. Type 1 diabetes: New perspectives on disease pathogenesis and treatment. Lancet 358: 221-229. (Pubitemid 32718550)
-
(2001)
Lancet
, vol.358
, Issue.9277
, pp. 221-229
-
-
Atkinson, M.A.1
Eisenbarth, G.S.2
-
4
-
-
0033001488
-
The NOD mouse model of type 1 diabetes: As good as it gets?
-
Atkinson MA, Leiter EH. 1999. The NOD mouse model of type 1 diabetes: As good as it gets? Nat Med 5: 601-604.
-
(1999)
Nat Med
, vol.5
, pp. 601-604
-
-
Atkinson, M.A.1
Leiter, E.H.2
-
5
-
-
67349199566
-
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
-
Barrett JC, Clayton DG, Concannon P, Akolkar B, Cooper JD, Erlich HA, Julier C, Morahan G, Nerup J, Nierras C, et al. 2009. Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. Nat Genet 41: 703-707.
-
(2009)
Nat Genet
, vol.41
, pp. 703-707
-
-
Barrett, J.C.1
Clayton, D.G.2
Concannon, P.3
Akolkar, B.4
Cooper, J.D.5
Erlich, H.A.6
Julier, C.7
Morahan, G.8
Nerup, J.9
Nierras, C.10
-
6
-
-
0033989159
-
Genealogies of mouse inbred strains
-
Beck JA, Lloyd S, Hafezparast M, Lennon-Pierce M, Eppig JT, Festing MF, Fisher EM. 2000. Genealogies of mouse inbred strains. Nat Genet 24: 23-25.
-
(2000)
Nat Genet
, vol.24
, pp. 23-25
-
-
Beck, J.A.1
Lloyd, S.2
Hafezparast, M.3
Lennon-Pierce, M.4
Eppig, J.T.5
Festing, M.F.6
Fisher, E.M.7
-
7
-
-
0033555906
-
Tandem repeats finder: A program to analyze DNA sequences
-
DOI 10.1093/nar/27.2.573
-
Benson G. 1999. Tandem repeats finder: A program to analyze DNA sequences. Nucleic Acids Res 27: 573-580. (Pubitemid 29210025)
-
(1999)
Nucleic Acids Research
, vol.27
, Issue.2
, pp. 573-580
-
-
Benson, G.1
-
8
-
-
0013394889
-
Mechanisms of alternative pre-messenger RNA splicing
-
Black DL. 2003. Mechanisms of alternative pre-messenger RNA splicing. Annu Rev Biochem 72: 291-336.
-
(2003)
Annu Rev Biochem
, vol.72
, pp. 291-336
-
-
Black, D.L.1
-
9
-
-
35148822185
-
A highly polymorphic meiotic recombination mouse hot spot exhibits incomplete repair
-
Bois PR. 2007. A highly polymorphic meiotic recombination mouse hot spot exhibits incomplete repair. Mol Cell Biol 27: 7053-7062.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 7053-7062
-
-
Bois, P.R.1
-
10
-
-
0034014761
-
Localization of Idd11 using NOD congenic mouse strains: Elimination of Slc9a1 as a candidate gene
-
Brodnicki TC, McClive P, Couper S, Morahan G. 2000. Localization of Idd11 using NOD congenic mouse strains: Elimination of Slc9a1 as a candidate gene. Immunogenetics 51: 37-41.
-
(2000)
Immunogenetics
, vol.51
, pp. 37-41
-
-
Brodnicki, T.C.1
McClive, P.2
Couper, S.3
Morahan, G.4
-
11
-
-
30744446294
-
Localization of Idd11 is not associated with thymus and NKTcell abnormalities in NOD mice
-
Brodnicki TC, Fletcher AL, Pellicci DG, Berzins SP, McClive P, Quirk F, Webster KE, Scott HS, Boyd RL, Godfrey DI, et al. 2005. Localization of Idd11 is not associated with thymus and NKTcell abnormalities in NOD mice. Diabetes 54: 3453-3457.
-
(2005)
Diabetes
, vol.54
, pp. 3453-3457
-
-
Brodnicki, T.C.1
Fletcher, A.L.2
Pellicci, D.G.3
Berzins, S.P.4
McClive, P.5
Quirk, F.6
Webster, K.E.7
Scott, H.S.8
Boyd, R.L.9
Godfrey, D.I.10
-
12
-
-
42449129287
-
Searching for splicing motifs
-
Chasin LA. 2007. Searching for splicing motifs. Adv Exp Med Biol 623: 85-106.
-
(2007)
Adv Exp Med Biol
, vol.623
, pp. 85-106
-
-
Chasin, L.A.1
-
13
-
-
34548743476
-
Gene conversion: Mechanisms, evolution and human disease
-
Chen JM, Cooper DN, Chuzhanova N, Ferec C, Patrinos GP. 2007. Gene conversion: Mechanisms, evolution and human disease. Nat Rev Genet 8: 762-775.
-
(2007)
Nat Rev Genet
, vol.8
, pp. 762-775
-
-
Chen, J.M.1
Cooper, D.N.2
Chuzhanova, N.3
Ferec, C.4
Patrinos, G.P.5
-
14
-
-
64649096894
-
Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium
-
Concannon, P., Chen, W.M., Julier, C., Morahan, G., Akolkar, B., Erlich, H.A., Hilner, J.E., Nerup, J., Nierras, C., Pociot, F. et al. 2009a. Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium. Diabetes 58: 1018-1022.
-
(2009)
Diabetes
, vol.58
, pp. 1018-1022
-
-
Concannon, P.1
Chen, W.M.2
Julier, C.3
Morahan, G.4
Akolkar, B.5
Erlich, H.A.6
Hilner, J.E.7
Nerup, J.8
Nierras, C.9
Pociot, F.10
-
16
-
-
77950461601
-
Origins and functional impact of copy number variation in the human genome
-
Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, Zhang Y, Aerts J, Andrews TD, Barnes C, Campbell P, et al. 2009. Origins and functional impact of copy number variation in the human genome. Nature 464: 704-712.
-
(2009)
Nature
, vol.464
, pp. 704-712
-
-
Conrad, D.F.1
Pinto, D.2
Redon, R.3
Feuk, L.4
Gokcumen, O.5
Zhang, Y.6
Aerts, J.7
Andrews, T.D.8
Barnes, C.9
Campbell, P.10
-
17
-
-
43249119095
-
Defining the role of the MHC in autoimmunity: A review and pooled analysis
-
doi: 10.1371/journal.pgen.1000024
-
Fernando MM, Stevens CR, Walsh EC, De Jager PL, Goyette P, Plenge RM, Vyse TJ, Rioux JD. 2008. Defining the role of the MHC in autoimmunity: A review and pooled analysis. PLoS Genet 4: e1000024. doi: 10.1371/journal.pgen.1000024.
-
(2008)
PLoS Genet
, vol.4
-
-
Fernando, M.M.1
Stevens, C.R.2
Walsh, E.C.3
De Jager, P.L.4
Goyette, P.5
Plenge, R.M.6
Vyse, T.J.7
Rioux, J.D.8
-
18
-
-
38549146894
-
The Pfam protein families database
-
Finn RD, Tate J, Mistry J, Coggill PC, Sammut SJ, Hotz HR, Ceric G, Forslund K, Eddy SR, Sonnhammer EL, et al. 2008. The Pfam protein families database. Nucleic Acids Res 36: D281-D288.
-
(2008)
Nucleic Acids Res
, vol.36
-
-
Finn, R.D.1
Tate, J.2
Mistry, J.3
Coggill, P.C.4
Sammut, S.J.5
Hotz, H.R.6
Ceric, G.7
Forslund, K.8
Eddy, S.R.9
Sonnhammer, E.L.10
-
19
-
-
58149191274
-
Rfam: Updates to the RNA families database
-
Gardner PP, Daub J, Tate JG, Nawrocki EP, Kolbe DL, Lindgreen S, Wilkinson AC, Finn RD, Griffiths-Jones S, Eddy SR, et al. 2009. Rfam: Updates to the RNA families database. Nucleic Acids Res 37: D136-D140.
-
(2009)
Nucleic Acids Res
, vol.37
-
-
Gardner, P.P.1
Daub, J.2
Tate, J.G.3
Nawrocki, E.P.4
Kolbe, D.L.5
Lindgreen, S.6
Wilkinson, A.C.7
Finn, R.D.8
Griffiths-Jones, S.9
Eddy, S.R.10
-
20
-
-
65949107547
-
Common genetic variation and human traits
-
Goldstein DB. 2009. Common genetic variation and human traits. N Engl J Med 360: 1696-1698.
-
(2009)
N Engl J Med
, vol.360
, pp. 1696-1698
-
-
Goldstein, D.B.1
-
21
-
-
33644750115
-
MiRBase: MicroRNA sequences, targets and gene nomenclature
-
Griffiths-Jones S, Grocock RJ, van Dongen S, Bateman A, Enright AJ. 2006. miRBase: MicroRNA sequences, targets and gene nomenclature. Nucleic Acids Res 34: D140-D144.
-
(2006)
Nucleic Acids Res
, vol.34
-
-
Griffiths-Jones, S.1
Grocock, R.J.2
Van Dongen, S.3
Bateman, A.4
Enright, A.J.5
-
22
-
-
0036787813
-
An initiation site formeiotic crossing-over and gene conversion in the mouse
-
Guillon H, deMassy B. 2002. An initiation site formeiotic crossing-over and gene conversion in the mouse. Nat Genet 32: 296-299.
-
(2002)
Nat Genet
, vol.32
, pp. 296-299
-
-
Guillon, H.1
DeMassy, B.2
-
23
-
-
62249133709
-
Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals
-
Guttman M, Amit I, Garber M, French C, Lin MF, Feldser D, Huarte M, Zuk O, Carey BW, Cassady JP, et al. 2009. Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals. Nature 458: 223-227.
-
(2009)
Nature
, vol.458
, pp. 223-227
-
-
Guttman, M.1
Amit, I.2
Garber, M.3
French, C.4
Lin, M.F.5
Feldser, D.6
Huarte, M.7
Zuk, O.8
Carey, B.W.9
Cassady, J.P.10
-
24
-
-
34547621758
-
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
-
DOI 10.1038/nature06010, PII NATURE06010
-
Hakonarson H, Grant SF, Bradfield JP, Marchand L, Kim CE, Glessner JT, Grabs R, Casalunovo T, Taback SP, Frackelton EC, et al. 2007. A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. Nature 448: 591-594. (Pubitemid 47206935)
-
(2007)
Nature
, vol.448
, Issue.7153
, pp. 591-594
-
-
Hakonarson, H.1
Grant, S.F.A.2
Bradfield, J.P.3
Marchand, L.4
Kim, C.E.5
Glessner, J.T.6
Grabs, R.7
Casalunovo, T.8
Taback, S.P.9
Frackelton, E.C.10
Lawson, M.L.11
Robinson, L.J.12
Skraban, R.13
Lu, Y.14
Chiavacci, R.M.15
Stanley, C.A.16
Kirsch, S.E.17
Rappaport, E.F.18
Orange, J.S.19
Monos, D.S.20
Devoto, M.21
Qu, H.-Q.22
Polychronakos, C.23
more..
-
26
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA. 2009. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci 106: 9362-9367.
-
(2009)
Proc Natl Acad Sci
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
Sethupathy, P.2
Junkins, H.A.3
Ramos, E.M.4
Mehta, J.P.5
Collins, F.S.6
Manolio, T.A.7
-
27
-
-
0141739796
-
Haplotypes and the systematic analysis of genetic variation in genes and genomes
-
DOI 10.1517/phgs.4.5.547.23791
-
Hoehe MR. 2003. Haplotypes and the systematic analysis of genetic variation in genes and genomes. Pharmacogenomics 4: 547-570. (Pubitemid 37120944)
-
(2003)
Pharmacogenomics
, vol.4
, Issue.5
, pp. 547-570
-
-
Hoehe, M.R.1
-
28
-
-
0002294347
-
A simple sequentially rejective multiple test procedure
-
Holm S. 1979. A simple sequentially rejective multiple test procedure. Scand J Stat 6: 65-70.
-
(1979)
Scand J Stat
, vol.6
, pp. 65-70
-
-
Holm, S.1
-
29
-
-
33748748734
-
Identification of the transcription factor ARNTL2 as a candidate gene for the type 1 diabetes locus Idd6
-
DOI 10.1093/hmg/ddl209
-
Hung MS, Avner P, Rogner UC. 2006. Identification of the transcription factor Arntl2 as a candidate gene for the type 1 diabetes locus Idd6. Hum Mol Genet 15: 2732-2742. (Pubitemid 44400400)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.18
, pp. 2732-2742
-
-
Hung, M.-S.1
Avner, P.2
Rogner, U.C.3
-
30
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
The International HapMap Consortium
-
The International HapMap Consortium. 2007. A second generation human haplotype map of over 3.1 million SNPs. Nature 449: 851-861.
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
-
31
-
-
0842310835
-
Intense and highly localized gene conversion activity in human meiotic crossover hot spots
-
Jeffreys AJ, May CA. 2004. Intense and highly localized gene conversion activity in human meiotic crossover hot spots. Nat Genet 36: 151-156.
-
(2004)
Nat Genet
, vol.36
, pp. 151-156
-
-
Jeffreys, A.J.1
May, C.A.2
-
32
-
-
40349095438
-
Type 1 diabetes: Global epidemiology
-
(ed. J.M. Ekoe et al.), John Wiley & Sons, West Sussex
-
Karvonen M, Sekikawa A, LaPorte R, Tuomilehto J, Tuomilehto-Wolf E. 2001. Type 1 diabetes: Global epidemiology. In The epidemiology of diabetes mellitus (ed. J.M. Ekoe et al.), pp. 71-102. John Wiley & Sons, West Sussex.
-
(2001)
The Epidemiology of Diabetes Mellitus
, pp. 71-102
-
-
Karvonen, M.1
Sekikawa, A.2
LaPorte, R.3
Tuomilehto, J.4
Tuomilehto-Wolf, E.5
-
33
-
-
3042742130
-
Where the crossovers are: Recombination distributions in mammals
-
DOI 10.1038/nrg1346
-
Kauppi L, Jeffreys AJ, Keeney S. 2004. Where the crossovers are: Recombination distributions in mammals. Nat Rev Genet 5: 413-424. (Pubitemid 38915408)
-
(2004)
Nature Reviews Genetics
, vol.5
, Issue.6
, pp. 413-424
-
-
Kauppi, L.1
Jeffreys, A.J.2
Keeney, S.3
-
34
-
-
34548103252
-
Meiotic crossover hotspots contained in haplotype block boundaries of the mouse genome
-
Kauppi L, Jasin M, Keeney S. 2007. Meiotic crossover hotspots contained in haplotype block boundaries of the mouse genome. Proc Natl Acad Sci 104: 13396-13401.
-
(2007)
Proc Natl Acad Sci
, vol.104
, pp. 13396-13401
-
-
Kauppi, L.1
Jasin, M.2
Keeney, S.3
-
35
-
-
0041853625
-
MATCH: A tool for searching transcription factor binding sites in DNA sequences
-
Kel AE, Gossling E, Reuter I, Cheremushkin E, Kel-Margoulis OV, Wingender E. 2003. MATCH: A tool for searching transcription factor binding sites in DNA sequences. Nucleic Acids Res 31: 3576-3579.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 3576-3579
-
-
Kel, A.E.1
Gossling, E.2
Reuter, I.3
Cheremushkin, E.4
Kel-Margoulis, O.V.5
Wingender, E.6
-
36
-
-
33645395980
-
In vivo RNA interference demonstrates a role for Nramp1 in modifying susceptibility to type 1 diabetes
-
Kissler S, Stern P, Takahashi K, Hunter K, Peterson LB, Wicker L. 2006. In vivo RNA interference demonstrates a role for Nramp1 in modifying susceptibility to type 1 diabetes. Nat Genet 38: 479-483.
-
(2006)
Nat Genet
, vol.38
, pp. 479-483
-
-
Kissler, S.1
Stern, P.2
Takahashi, K.3
Hunter, K.4
Peterson, L.B.5
Wicker, L.6
-
37
-
-
58149178565
-
The UCSC Genome Browser Database: Update 2009
-
Kuhn RM, Karolchik D, Zweig AS, Wang T, Smith KE, Rosenbloom KR, Rhead B, Raney BJ, Pohl A, Pheasant M, et al. 2009. The UCSC Genome Browser Database: Update 2009. Nucleic Acids Res 37: D755-D761.
-
(2009)
Nucleic Acids Res
, vol.37
-
-
Kuhn, R.M.1
Karolchik, D.2
Zweig, A.S.3
Wang, T.4
Smith, K.E.5
Rosenbloom, K.R.6
Rhead, B.7
Raney, B.J.8
Pohl, A.9
Pheasant, M.10
-
38
-
-
33644754665
-
Impaired Crkl expression contributes to the defective DNA binding of Stat5b in nonobese diabetic mice
-
Laloraya M, Davoodi-Semiromi A, Kumar GP, McDuffie M, She JX. 2006. Impaired Crkl expression contributes to the defective DNA binding of Stat5b in nonobese diabetic mice. Diabetes 55: 734-741.
-
(2006)
Diabetes
, vol.55
, pp. 734-741
-
-
Laloraya, M.1
Davoodi-Semiromi, A.2
Kumar, G.P.3
McDuffie, M.4
She, J.X.5
-
39
-
-
67650224471
-
NOD 3 129.H2g7 backcross delineates 129S1/SvImJ-derived genomic regions modulating type 1 diabetes (T1D) development in mice
-
Leiter EH, Reifsnyder PC, Wallace R, Li R, King B, Churchill GC. 2009. NOD 3 129.H2g7 backcross delineates 129S1/SvImJ-derived genomic regions modulating type 1 diabetes (T1D) development in mice. Diabetes 58: 1700-1703.
-
(2009)
Diabetes
, vol.58
, pp. 1700-1703
-
-
Leiter, E.H.1
Reifsnyder, P.C.2
Wallace, R.3
Li, R.4
King, B.5
Churchill, G.C.6
-
40
-
-
34547664096
-
Genomic disorders: Molecular mechanisms for rearrangements and conveyed phenotypes
-
doi: 10.1371/journal.pgen.0010049
-
Lupski JR, Stankiewicz P. 2005. Genomic disorders: Molecular mechanisms for rearrangements and conveyed phenotypes. PLoS Genet 1: e49. doi: 10.1371/journal.pgen.0010049.
-
(2005)
PLoS Genet
, vol.1
-
-
Lupski, J.R.1
Stankiewicz, P.2
-
41
-
-
0033711184
-
The NOD Idd9 genetic interval influences the pathogenicity of insulitis and contains molecular variants of Cd30, Tnfr2, and Cd137
-
Lyons PA, Hancock WW, Denny P, Lord CJ, Hill NJ, Armitage N, Siegmund T, Todd JA, Phillips MS, Hess JF, et al. 2000. The NOD Idd9 genetic interval influences the pathogenicity of insulitis and contains molecular variants of Cd30, Tnfr2, and Cd137. Immunity 13: 107-115.
-
(2000)
Immunity
, vol.13
, pp. 107-115
-
-
Lyons, P.A.1
Hancock, W.W.2
Denny, P.3
Lord, C.J.4
Hill, N.J.5
Armitage, N.6
Siegmund, T.7
Todd, J.A.8
Phillips, M.S.9
Hess, J.F.10
-
42
-
-
0018841766
-
Breeding of a non-obese, diabetic strain of mice
-
Makino S, Kunimoto K, Muraoka Y, Mizushima Y, Katagiri K, Tochino Y. 1980. Breeding of a non-obese, diabetic strain of mice. Jikken Dobutsu 29: 1-13.
-
(1980)
Jikken Dobutsu
, vol.29
, pp. 1-13
-
-
Makino, S.1
Kunimoto, K.2
Muraoka, Y.3
Mizushima, Y.4
Katagiri, K.5
Tochino, Y.6
-
43
-
-
33644876958
-
TRANSFAC and its module TRANSCompel: Transcriptional gene regulation in eukaryotes
-
Matys V, Kel-Margoulis OV, Fricke E, Liebich I, Land S, Barre-Dirrie A, Reuter I, Chekmenev D, Krull M, Hornischer K, et al. 2006. TRANSFAC and its module TRANSCompel: Transcriptional gene regulation in eukaryotes. Nucleic Acids Res 34: D108-D110.
-
(2006)
Nucleic Acids Res
, vol.34
-
-
Matys, V.1
Kel-Margoulis, O.V.2
Fricke, E.3
Liebich, I.4
Land, S.5
Barre-Dirrie, A.6
Reuter, I.7
Chekmenev, D.8
Krull, M.9
Hornischer, K.10
-
44
-
-
0029021388
-
Crosses of NOD mice with the related NON strain. A polygenic model for IDDM
-
McAleer MA, Reifsnyder P, Palmer SM, Prochazka M, Love JM, Copeman JB, Powell EE, Rodrigues NR, Prins JB, Serreze DV, et al. 1995. Crosses of NOD mice with the related NON strain. A polygenic model for IDDM. Diabetes 44: 1186-1195.
-
(1995)
Diabetes
, vol.44
, pp. 1186-1195
-
-
McAleer, M.A.1
Reifsnyder, P.2
Palmer, S.M.3
Prochazka, M.4
Love, J.M.5
Copeman, J.B.6
Powell, E.E.7
Rodrigues, N.R.8
Prins, J.B.9
Serreze, D.V.10
-
45
-
-
0033853488
-
Derivation of diabetes-resistant congenic lines from the nonobese diabetic mouse
-
DOI 10.1006/clim.2000.4893
-
McDuffie M. 2000. Derivation of diabetes-resistant congenic lines from the nonobese diabetic mouse. Clin Immunol 96: 119-130. (Pubitemid 30612779)
-
(2000)
Clinical Immunology
, vol.96
, Issue.2
, pp. 119-130
-
-
McDuffie, M.1
-
46
-
-
73349091581
-
Loss of parity between IL-2 and IL-21 in the NOD Idd3 locus
-
McGuire HM, Vogelzang A, Hill N, Flodstrom-Tullberg M, Sprent J, King C. 2009. Loss of parity between IL-2 and IL-21 in the NOD Idd3 locus. Proc Natl Acad Sci 106: 19438-19443.
-
(2009)
Proc Natl Acad Sci
, vol.106
, pp. 19438-19443
-
-
McGuire, H.M.1
Vogelzang, A.2
Hill, N.3
Flodstrom-Tullberg, M.4
Sprent, J.5
King, C.6
-
48
-
-
34547624303
-
Genome-wide maps of chromatin state in pluripotent and lineage-committed cells
-
Mikkelsen TS, Ku M, Jaffe DB, Issac B, Lieberman E, Giannoukos G, Alvarez P, Brockman W, Kim TK, Koche RP, et al. 2007. Genome-wide maps of chromatin state in pluripotent and lineage-committed cells. Nature 448: 553-560.
-
(2007)
Nature
, vol.448
, pp. 553-560
-
-
Mikkelsen, T.S.1
Ku, M.2
Jaffe, D.B.3
Issac, B.4
Lieberman, E.5
Giannoukos, G.6
Alvarez, P.7
Brockman, W.8
Kim, T.K.9
Koche, R.P.10
-
50
-
-
77949716888
-
A recombination hotspot in a schizophrenia-associated region of GABRB2
-
doi: 10.1371/journal.pone.0009547
-
Ng SK, Lo WS, Pun FW, Zhao C, Yu Z, Chen J, Tong KL, Xu Z, Tsang SY, Yang Q, et al. 2010. A recombination hotspot in a schizophrenia-associated region of GABRB2. PLoS ONE 5: e9547. doi: 10.1371/journal.pone.0009547.
-
(2010)
PLoS ONE
, vol.5
-
-
Ng, S.K.1
Lo, W.S.2
Pun, F.W.3
Zhao, C.4
Yu, Z.5
Chen, J.6
Tong, K.L.7
Xu, Z.8
Tsang, S.Y.9
Yang, Q.10
-
51
-
-
67650432118
-
Validated germline-competent embryonic stem cell lines from nonobese diabetic mice
-
Nichols J, Jones K, Phillips JM, Newland SA, Roode M, Mansfield W, Smith A, Cooke A. 2009. Validated germline-competent embryonic stem cell lines from nonobese diabetic mice. Nat Med 15: 814-818.
-
(2009)
Nat Med
, vol.15
, pp. 814-818
-
-
Nichols, J.1
Jones, K.2
Phillips, J.M.3
Newland, S.A.4
Roode, M.5
Mansfield, W.6
Smith, A.7
Cooke, A.8
-
52
-
-
48249120009
-
The recombinational anatomy of a mouse chromosome
-
doi: 10.1371/journal.pgen.1000119
-
Paigen K, Szatkiewicz JP, Sawyer K, Leahy N, Parvanov ED, Ng SH, Graber JH, Broman KW, Petkov PM. 2008. The recombinational anatomy of a mouse chromosome. PLoS Genet 4: e1000119. doi: 10.1371/journal.pgen.1000119.
-
(2008)
PLoS Genet
, vol.4
-
-
Paigen, K.1
Szatkiewicz, J.P.2
Sawyer, K.3
Leahy, N.4
Parvanov, E.D.5
Ng, S.H.6
Graber, J.H.7
Broman, K.W.8
Petkov, P.M.9
-
53
-
-
0035345013
-
Meiotic recombination hot spots and cold spots
-
Petes TD. 2001. Meiotic recombination hot spots and cold spots. Nat Rev Genet 2: 360-369.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 360-369
-
-
Petes, T.D.1
-
54
-
-
60149099385
-
Evolution and functions of long noncoding RNAs
-
Ponting CP, Oliver PL, Reik W. 2009. Evolution and functions of long noncoding RNAs. Cell 136: 629-641.
-
(2009)
Cell
, vol.136
, pp. 629-641
-
-
Ponting, C.P.1
Oliver, P.L.2
Reik, W.3
-
55
-
-
0026580530
-
NOR/Lt mice: MHC-matched diabetes-resistant control strain for NOD mice
-
Prochazka M, Serreze DV, Frankel WN, Leiter EH. 1992. NOR/Lt mice: MHC-matched diabetes-resistant control strain for NOD mice. Diabetes 41: 98-106.
-
(1992)
Diabetes
, vol.41
, pp. 98-106
-
-
Prochazka, M.1
Serreze, D.V.2
Frankel, W.N.3
Leiter, E.H.4
-
56
-
-
33845382786
-
TRPV1+ sensory neurons control β cell stress and islet inflammation in autoimmune disease
-
Razavi R, Chan Y, Afifiyan FN, Liu XJ, Wan X, Yantha J, Tsui H, Tang L, Tsai S, Santamaria P, et al. 2006. TRPV1+ sensory neurons control β cell stress and islet inflammation in autoimmune disease. Cell 127: 1123-1135.
-
(2006)
Cell
, vol.127
, pp. 1123-1135
-
-
Razavi, R.1
Chan, Y.2
Afifiyan, F.N.3
Liu, X.J.4
Wan, X.5
Yantha, J.6
Tsui, H.7
Tang, L.8
Tsai, S.9
Santamaria, P.10
-
57
-
-
26944502773
-
Conditioning the genome identifies additional diabetes resistance loci in Type I diabetes resistant NOR/Lt mice
-
Reifsnyder PC, Li R, Silveira PA, Churchill G, Serreze DV, Leiter EH. 2005. Conditioning the genome identifies additional diabetes resistance loci in Type I diabetes resistant NOR/Lt mice. Genes Immun 6: 528-538.
-
(2005)
Genes Immun
, vol.6
, pp. 528-538
-
-
Reifsnyder, P.C.1
Li, R.2
Silveira, P.A.3
Churchill, G.4
Serreze, D.V.5
Leiter, E.H.6
-
58
-
-
57749208427
-
Gene-gene interactions in the NOD mouse model of type 1 diabetes
-
Ridgway WM, Peterson LB, Todd JA, Rainbow DB, Healy B, Burren OS, Wicker LS. 2008. Gene-gene interactions in the NOD mouse model of type 1 diabetes. Adv Immunol 100: 151-175.
-
(2008)
Adv Immunol
, vol.100
, pp. 151-175
-
-
Ridgway, W.M.1
Peterson, L.B.2
Todd, J.A.3
Rainbow, D.B.4
Healy, B.5
Burren, O.S.6
Wicker, L.S.7
-
59
-
-
0034785352
-
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
-
Rioux JD, Daly MJ, Silverberg MS, Lindblad K, Steinhart H, Cohen Z, Delmonte T, Kocher K, Miller K, Guschwan S, et al. 2001. Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nat Genet 29: 223-228.
-
(2001)
Nat Genet
, vol.29
, pp. 223-228
-
-
Rioux, J.D.1
Daly, M.J.2
Silverberg, M.S.3
Lindblad, K.4
Steinhart, H.5
Cohen, Z.6
Delmonte, T.7
Kocher, K.8
Miller, K.9
Guschwan, S.10
-
60
-
-
0028385769
-
Mapping of an insulin-dependent diabetes locus, Idd9, in NOD mice to chromosome 4
-
Rodrigues NR, Cornall RJ, Chandler P, Simpson E, Wicker LS, Peterson LB, Todd JA. 1994. Mapping of an insulin-dependent diabetes locus, Idd9, in NOD mice to chromosome 4. Mamm Genome 5: 167-170.
-
(1994)
Mamm Genome
, vol.5
, pp. 167-170
-
-
Rodrigues, N.R.1
Cornall, R.J.2
Chandler, P.3
Simpson, E.4
Wicker, L.S.5
Peterson, L.B.6
Todd, J.A.7
-
61
-
-
0037363496
-
Congenic mice: Cutting tools for complex immune disorders
-
DOI 10.1038/nri1031
-
Rogner UC, Avner P. 2003. Congenic mice: Cutting tools for complex immune disorders. Nat Rev Immunol 3: 243-252. (Pubitemid 37323209)
-
(2003)
Nature Reviews Immunology
, vol.3
, Issue.3
, pp. 243-252
-
-
Rogner, U.C.1
Avner, P.2
-
62
-
-
0035237619
-
Genes and cellular requirements for autoimmune diabetes susceptibility in nonobese diabetic mice
-
Serreze DV, Leiter EH. 2001. Genes and cellular requirements for autoimmune diabetes susceptibility in nonobese diabetic mice. Curr Dir Autoimmun 4: 31-67.
-
(2001)
Curr Dir Autoimmun
, vol.4
, pp. 31-67
-
-
Serreze, D.V.1
Leiter, E.H.2
-
63
-
-
0028949751
-
Hotspots of homologous recombination in mouse meiosis
-
Shiroishi T, Koide T, Yoshino M, Sagai T, Moriwaki K. 1995. Hotspots of homologous recombination in mouse meiosis. Adv Biophys 31: 119-132.
-
(1995)
Adv Biophys
, vol.31
, pp. 119-132
-
-
Shiroishi, T.1
Koide, T.2
Yoshino, M.3
Sagai, T.4
Moriwaki, K.5
-
64
-
-
34347341846
-
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
-
Todd JA, Walker NM, Cooper JD, Smyth DJ, Downes K, Plagnol V, Bailey R, Nejentsev S, Field SF, Payne F, et al. 2007. Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. Nat Genet 39: 857-864.
-
(2007)
Nat Genet
, vol.39
, pp. 857-864
-
-
Todd, J.A.1
Walker, N.M.2
Cooper, J.D.3
Smyth, D.J.4
Downes, K.5
Plagnol, V.6
Bailey, R.7
Nejentsev, S.8
Field, S.F.9
Payne, F.10
-
65
-
-
37549018501
-
Germline rates of de novo meiotic deletions and duplications causing several genomic disorders
-
Turner DJ, Miretti M, Rajan D, Fiegler H, Carter NP, Blayney ML, Beck S, Hurles ME. 2008. Germline rates of de novo meiotic deletions and duplications causing several genomic disorders. Nat Genet 40: 90-95.
-
(2008)
Nat Genet
, vol.40
, pp. 90-95
-
-
Turner, D.J.1
Miretti, M.2
Rajan, D.3
Fiegler, H.4
Carter, N.P.5
Blayney, M.L.6
Beck, S.7
Hurles, M.E.8
-
66
-
-
10344252778
-
Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupus
-
Wandstrat AE, Nguyen C, Limaye N, Chan AY, Subramanian S, Tian XH, Yim YS, Pertsemlidis A, Garner HR Jr, Morel L, et al. 2004. Association of extensive polymorphisms in the SLAM/CD2 gene cluster with murine lupus. Immunity 21: 769-780.
-
(2004)
Immunity
, vol.21
, pp. 769-780
-
-
Wandstrat, A.E.1
Nguyen, C.2
Limaye, N.3
Chan, A.Y.4
Subramanian, S.5
Tian, X.H.6
Yim, Y.S.7
Pertsemlidis, A.8
Garner Jr., H.R.9
Morel, L.10
-
67
-
-
42449098125
-
Splicing regulation: From a parts list of regulatory elements to an integrated splicing code
-
Wang Z, Burge CB. 2008. Splicing regulation: From a parts list of regulatory elements to an integrated splicing code. RNA 14: 802-813.
-
(2008)
RNA
, vol.14
, pp. 802-813
-
-
Wang, Z.1
Burge, C.B.2
-
68
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
The Wellcome Trust Case Control Consortium
-
The Wellcome Trust Case Control Consortium. 2007. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447: 661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
69
-
-
77950405093
-
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
-
The Wellcome Trust Case Control Consortium
-
The Wellcome Trust Case Control Consortium. 2010. Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature 464: 713-720.
-
(2010)
Nature
, vol.464
, pp. 713-720
-
-
-
70
-
-
33847246293
-
Interleukin-2 gene variation impairs regulatory T cell function and causes autoimmunity
-
Yamanouchi J, Rainbow D, Serra P, Howlett S, Hunter K, Garner VE, Gonzalez-Munoz A, Clark J, Veijola R, Cubbon R, et al. 2007. Interleukin-2 gene variation impairs regulatory T cell function and causes autoimmunity. Nat Genet 39: 329-337.
-
(2007)
Nat Genet
, vol.39
, pp. 329-337
-
-
Yamanouchi, J.1
Rainbow, D.2
Serra, P.3
Howlett, S.4
Hunter, K.5
Garner, V.E.6
Gonzalez-Munoz, A.7
Clark, J.8
Veijola, R.9
Cubbon, R.10
-
71
-
-
0037451351
-
High-resolution sperm typing of meiotic recombination in the mouse MHC Eb gene
-
Yauk CL, Bois PR, Jeffreys AJ. 2003. High-resolution sperm typing of meiotic recombination in the mouse MHC Eb gene. EMBO J 22: 1389-1397.
-
(2003)
EMBO J
, vol.22
, pp. 1389-1397
-
-
Yauk, C.L.1
Bois, P.R.2
Jeffreys, A.J.3
|