-
1
-
-
0026678490
-
Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
-
Allen RC, Zoghbi HY, Moseley AB, Rosenblatt HM, and Belmont JW. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am J Hum Genet 51: 1229-1239, 1992.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 1229-1239
-
-
Allen, R.C.1
Zoghbi, H.Y.2
Moseley, A.B.3
Rosenblatt, H.M.4
Belmont, J.W.5
-
2
-
-
18244372958
-
Association of human aging with a functional variant of klotho
-
Arking DE, Krebsova A, Macek M Sr, Macek M Jr, Arking A, Mian IS, Fried L, Hamosh A, Dey S, McIntosh I, and Dietz HC. Association of human aging with a functional variant of klotho. Proc Natl Acad Sci USA 99: 856-861, 2002.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 856-861
-
-
Arking, D.E.1
Krebsova, A.2
Macek Sr., M.3
Macek Jr., M.4
Arking, A.5
Mian, I.S.6
Fried, L.7
Hamosh, A.8
Dey, S.9
McIntosh, I.10
Dietz, H.C.11
-
3
-
-
0037623912
-
Cis-acting variation in the expression of a high proportion of genes in human brain
-
Bray NJ, Buckland PR, Owen MJ, and O'Donovan MC. Cis-acting variation in the expression of a high proportion of genes in human brain. Hum Genet 113: 149-153, 2003.
-
(2003)
Hum Genet
, vol.113
, pp. 149-153
-
-
Bray, N.J.1
Buckland, P.R.2
Owen, M.J.3
O'Donovan, M.C.4
-
4
-
-
0032991552
-
Characterization of single-nucleotide polymorphisms in coding regions of human genes
-
Cargill M, Altshuler D, Ireland J, Sklar P, Ardlie K, Patil N, Shaw N, Lane CR, Lim EP, Kalyanaraman N, Nemesh J, Ziaugra L, Friedland L, Rolfe A, Warrington J, Lipshutz R, Daley GQ, and Lander ES. Characterization of single-nucleotide polymorphisms in coding regions of human genes. Nat Genet 22: 231-238, 1999.
-
(1999)
Nat Genet
, vol.22
, pp. 231-238
-
-
Cargill, M.1
Altshuler, D.2
Ireland, J.3
Sklar, P.4
Ardlie, K.5
Patil, N.6
Shaw, N.7
Lane, C.R.8
Lim, E.P.9
Kalyanaraman, N.10
Nemesh, J.11
Ziaugra, L.12
Friedland, L.13
Rolfe, A.14
Warrington, J.15
Lipshutz, R.16
Daley, G.Q.17
Lander, E.S.18
-
5
-
-
0036843938
-
Detection of regulatory variation in mouse genes
-
Cowles CR, Joel NH, Altshuler D, and Lander ES. Detection of regulatory variation in mouse genes. Nat Genet 32: 432-437, 2002.
-
(2002)
Nat Genet
, vol.32
, pp. 432-437
-
-
Cowles, C.R.1
Joel, N.H.2
Altshuler, D.3
Lander, E.S.4
-
6
-
-
0036574913
-
Unravelling heterochromatin: Competition between positive and negative factors regulates accessibility
-
Dillon N and Festenstein R. Unravelling heterochromatin: competition between positive and negative factors regulates accessibility. Trends Genet 18: 252-258, 2002.
-
(2002)
Trends Genet
, vol.18
, pp. 252-258
-
-
Dillon, N.1
Festenstein, R.2
-
7
-
-
0036392059
-
DNA methylation and genomic imprinting: Insights from cancer into epigenetic mechanisms
-
Feinberg AP, Cui H, and Ohlsson R. DNA methylation and genomic imprinting: insights from cancer into epigenetic mechanisms. Semin Cancer Biol 12: 389-398, 2002.
-
(2002)
Semin Cancer Biol
, vol.12
, pp. 389-398
-
-
Feinberg, A.P.1
Cui, H.2
Ohlsson, R.3
-
8
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel SB, Schaffner SF, Nguyen H, Moore JM, Roy J, Blumenstiel B, Higgins J, DeFelice M, Lochner A, Faggart M, Liu-Cordero SN, Rotimi C, Adeyemo A, Cooper R, Ward R, Lander ES, Daly MJ, and Altshuler D. The structure of haplotype blocks in the human genome. Science 296: 2225-2229, 2002.
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
DeFelice, M.8
Lochner, A.9
Faggart, M.10
Liu-Cordero, S.N.11
Rotimi, C.12
Adeyemo, A.13
Cooper, R.14
Ward, R.15
Lander, E.S.16
Daly, M.J.17
Altshuler, D.18
-
9
-
-
0030722935
-
Long human-mouse sequence alignments reveal novel regulatory elements: A reason to sequence the mouse genome
-
Hardison RC, Oeltjen J, and Miller W. Long human-mouse sequence alignments reveal novel regulatory elements: a reason to sequence the mouse genome. Genome Res 7: 959-66, 1997.
-
(1997)
Genome Res
, vol.7
, pp. 959-966
-
-
Hardison, R.C.1
Oeltjen, J.2
Miller, W.3
-
10
-
-
0032495572
-
Hypervariable allelic expression patterns of the imprinted IGF2 gene in tumor cells
-
He L, Cui H, Walsh C, Mattsson R, Lin W, Anneren G, Pfeifer-Ohlsson S, and Ohlsson R. Hypervariable allelic expression patterns of the imprinted IGF2 gene in tumor cells. Oncogene 16: 113-119, 1998.
-
(1998)
Oncogene
, vol.16
, pp. 113-119
-
-
He, L.1
Cui, H.2
Walsh, C.3
Mattsson, R.4
Lin, W.5
Anneren, G.6
Pfeifer-Ohlsson, S.7
Ohlsson, R.8
-
11
-
-
0034858197
-
Universal SNP genotyping assay with fluorescence polarization detection
-
Hsu TM, Chen X, Duan S, Miller RD, and Kwok PY. Universal SNP genotyping assay with fluorescence polarization detection. Biotechniques 31: 560, 562, 564-568, 2001.
-
(2001)
Biotechniques
, vol.31
, pp. 560
-
-
Hsu, T.M.1
Chen, X.2
Duan, S.3
Miller, R.D.4
Kwok, P.Y.5
-
12
-
-
0037381021
-
Wanted: Regulatory SNPs
-
Hudson TJ. Wanted: regulatory SNPs. Nat Genet 33: 439-440, 2003.
-
(2003)
Nat Genet
, vol.33
, pp. 439-440
-
-
Hudson, T.J.1
-
13
-
-
0037372003
-
Epigenetic regulation of gene expression: How the genome integrates intrinsic and environmental signals
-
Jaenisch R and Bird A. Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals. Nat Genet 33: S245-S254, 2003.
-
(2003)
Nat Genet
, vol.33
-
-
Jaenisch, R.1
Bird, A.2
-
14
-
-
0035180561
-
Demonstration of light chain restricted clonal B-lymphoid infiltrates in archival bone marrow trephines by quantitative real-time polymerase chain reaction
-
Lehmann U, Bock O, Langer F, and Kreipe H. Demonstration of light chain restricted clonal B-lymphoid infiltrates in archival bone marrow trephines by quantitative real-time polymerase chain reaction. Am J Pathol 159: 2023-2029, 2001.
-
(2001)
Am J Pathol
, vol.159
, pp. 2023-2029
-
-
Lehmann, U.1
Bock, O.2
Langer, F.3
Kreipe, H.4
-
15
-
-
0017694533
-
The monoclonality of human B-cell lymphomas
-
Levy R, Warnke R, Dorfman J, and Haimovich J. The monoclonality of human B-cell lymphomas. J Exp Med 145: 1014-1028, 1977.
-
(1977)
J Exp Med
, vol.145
, pp. 1014-1028
-
-
Levy, R.1
Warnke, R.2
Dorfman, J.3
Haimovich, J.4
-
16
-
-
0012789869
-
Allelic variation in gene expression is common in the human genome
-
Lo HS, Wang Z, Hu Y, Yang HH, Gere S, Buetow KH, and Lee MP. Allelic variation in gene expression is common in the human genome. Genome Res 13: 1855-1862, 2003.
-
(2003)
Genome Res
, vol.13
, pp. 1855-1862
-
-
Lo, H.S.1
Wang, Z.2
Hu, Y.3
Yang, H.H.4
Gere, S.5
Buetow, K.H.6
Lee, M.P.7
-
17
-
-
0035039122
-
A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome
-
Meguro M, Kashiwagi A, Mitsuya K, Nakao M, Kondo I, Saitoh S, and Oshimura M. A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome. Nat Genet 28: 19-20, 2001.
-
(2001)
Nat Genet
, vol.28
, pp. 19-20
-
-
Meguro, M.1
Kashiwagi, A.2
Mitsuya, K.3
Nakao, M.4
Kondo, I.5
Saitoh, S.6
Oshimura, M.7
-
18
-
-
0037098956
-
Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32
-
Nakabayashi K, Bentley L, Hitchins MP, Mitsuya K, Meguro M, Minagawa S, Bamforth JS, Stanier P, Preece M, Weksberg R, Oshimura M, Moore GE, and Scherer SW. Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32. Hum Mol Genet 11: 1743-1756, 2002.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1743-1756
-
-
Nakabayashi, K.1
Bentley, L.2
Hitchins, M.P.3
Mitsuya, K.4
Meguro, M.5
Minagawa, S.6
Bamforth, J.S.7
Stanier, P.8
Preece, M.9
Weksberg, R.10
Oshimura, M.11
Moore, G.E.12
Scherer, S.W.13
-
19
-
-
0032406475
-
Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human
-
Naumova AK, Olien L, Bird LM, Smith M, Verner AE, Leppert M, Morgan K, and Sapienza C. Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human. Eur J Hum Genet 6: 552-562, 1998.
-
(1998)
Eur J Hum Genet
, vol.6
, pp. 552-562
-
-
Naumova, A.K.1
Olien, L.2
Bird, L.M.3
Smith, M.4
Verner, A.E.5
Leppert, M.6
Morgan, K.7
Sapienza, C.8
-
20
-
-
0030009776
-
Heritability of X chromosome: Inactivation phenotype in a large family
-
Naumova AK, Plenge RM, Bird LM, Leppert M, Morgan K, Willard HF, and Sapienza C. Heritability of X chromosome: inactivation phenotype in a large family. Am J Hum Genet 58: 1111-1119, 1996.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1111-1119
-
-
Naumova, A.K.1
Plenge, R.M.2
Bird, L.M.3
Leppert, M.4
Morgan, K.5
Willard, H.F.6
Sapienza, C.7
-
21
-
-
0035699287
-
Characterization of variability in large-scale gene expression data: Implications for study design
-
Novak JP, Sladek R, and Hudson TJ. Characterization of variability in large-scale gene expression data: implications for study design. Genomics 79: 104-113, 2002.
-
(2002)
Genomics
, vol.79
, pp. 104-113
-
-
Novak, J.P.1
Sladek, R.2
Hudson, T.J.3
-
22
-
-
0036309298
-
Association of klothogene polymorphism with bone density and spondylosis of the lumbar spine in postmenopausal women
-
Ogata N, Matsumura Y, Shiraki M, Kawano K, Koshizuka Y, Hosoi T, Nakamura K, Kuro O, and Kawaguchi H. Association of klotho gene polymorphism with bone density and spondylosis of the lumbar spine in postmenopausal women. Bone 31: 37-42, 2002.
-
(2002)
Bone
, vol.31
, pp. 37-42
-
-
Ogata, N.1
Matsumura, Y.2
Shiraki, M.3
Kawano, K.4
Koshizuka, Y.5
Hosoi, T.6
Nakamura, K.7
Kuro, O.8
Kawaguchi, H.9
-
23
-
-
0031736335
-
Monoallelic expression: "There can only be one"
-
Ohlsson R, Tycko B, and Sapienza C. Monoallelic expression: "there can only be one." Trends Genet 14: 435-438, 1998.
-
(1998)
Trends Genet
, vol.14
, pp. 435-438
-
-
Ohlsson, R.1
Tycko, B.2
Sapienza, C.3
-
24
-
-
0036275126
-
BeadArray technology: Enabling an accurate, cost-effective approach to high-throughput genotyping
-
Oliphant A, Barker DL, Stuelpnagel JR, and Chee MS. BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping. Biotechniques Suppl: 56-61, 2002.
-
(2002)
Biotechniques Suppl
, pp. 56-61
-
-
Oliphant, A.1
Barker, D.L.2
Stuelpnagel, J.R.3
Chee, M.S.4
-
25
-
-
0035870563
-
A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21
-
Ono R, Kobayashi S, Wagatsuma H, Aisaka K, Kohda T, Kaneko-Ishino T, and Ishino F. A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21. Genomics 73: 232-237, 2001.
-
(2001)
Genomics
, vol.73
, pp. 232-237
-
-
Ono, R.1
Kobayashi, S.2
Wagatsuma, H.3
Aisaka, K.4
Kohda, T.5
Kaneko-Ishino, T.6
Ishino, F.7
-
26
-
-
13244277850
-
A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans
-
Prokunina L, Castillejo-Lopez C, Oberg F, Gunnarsson I, Berg L, Magnusson V, Brookes AJ, Tentler D, Kristjansdottir H, Grondal G, Bolstad AI, Svenungsson E, Lundberg I, Sturfelt G, Jonssen A, Truedsson L, Lima G, Alcocer-Varela J, Jonsson R, Gyllensten UB, Harley JB, Alarcon-Segovia D, Steinsson K, and Alarcon-Riquelme ME. A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans. Nat Genet 32: 666-669, 2002.
-
(2002)
Nat Genet
, vol.32
, pp. 666-669
-
-
Prokunina, L.1
Castillejo-Lopez, C.2
Oberg, F.3
Gunnarsson, I.4
Berg, L.5
Magnusson, V.6
Brookes, A.J.7
Tentler, D.8
Kristjansdottir, H.9
Grondal, G.10
Bolstad, A.I.11
Svenungsson, E.12
Lundberg, I.13
Sturfelt, G.14
Jonssen, A.15
Truedsson, L.16
Lima, G.17
Alcocer-Varela, J.18
Jonsson, R.19
Gyllensten, U.B.20
Harley, J.B.21
Alarcon-Segovia, D.22
Steinsson, K.23
Alarcon-Riquelme, M.E.24
more..
-
27
-
-
0037022240
-
Epigenetics: Monoallelic expression in the immune system
-
Rada C and Ferguson-Smith AC. Epigenetics: monoallelic expression in the immune system. Curr Biol 12: R108-R110, 2002.
-
(2002)
Curr Biol
, vol.12
-
-
Rada, C.1
Ferguson-Smith, A.C.2
-
28
-
-
0035234557
-
Genomic imprinting: Parental influence on the genome
-
Reik W and Walter J. Genomic imprinting: parental influence on the genome. Nat Rev Genet 2: 21-32, 2001.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 21-32
-
-
Reik, W.1
Walter, J.2
-
29
-
-
0036855185
-
Abundant raw material for cis-regulatory evolution in humans
-
Rockman MV and Wray GA. Abundant raw material for cis-regulatory evolution in humans. Mol Biol Evol 19: 1991-2004, 2002.
-
(2002)
Mol Biol Evol
, vol.19
, pp. 1991-2004
-
-
Rockman, M.V.1
Wray, G.A.2
-
30
-
-
0037230778
-
Quantitative real-time PCR method for detection of B-lymphocyte monoclonality by comparison of kappa and lambda immunoglobulin light chain expression
-
Stahlberg A, Aman P, Ridell B, Mostad P, and Kubista M. Quantitative real-time PCR method for detection of B-lymphocyte monoclonality by comparison of kappa and lambda immunoglobulin light chain expression. Clin Chem 49: 51-59, 2003.
-
(2003)
Clin Chem
, vol.49
, pp. 51-59
-
-
Stahlberg, A.1
Aman, P.2
Ridell, B.3
Mostad, P.4
Kubista, M.5
-
31
-
-
0035126968
-
A polymorphism in the gene for IGF-I: Functional properties and risk for type 2 diabetes and myocardial infarction
-
Vaessen N, Heutink P, Janssen JA, Witteman JC, Testers L, Hofman A, Lamberts SW, Oostra BA, Pols HA, and van Duijn CM. A polymorphism in the gene for IGF-I: functional properties and risk for type 2 diabetes and myocardial infarction. Diabetes 50: 637-642, 2001.
-
(2001)
Diabetes
, vol.50
, pp. 637-642
-
-
Vaessen, N.1
Heutink, P.2
Janssen, J.A.3
Witteman, J.C.4
Testers, L.5
Hofman, A.6
Lamberts, S.W.7
Oostra, B.A.8
Pols, H.A.9
Van Duijn, C.M.10
-
32
-
-
0035699956
-
Allele specific regulation of cytokine genes: Monoallelic expression of the IL-1A gene
-
Verweij CL, Bayley JP, Bakker A, and Kaijzel EL. Allele specific regulation of cytokine genes: monoallelic expression of the IL-1A gene. Adv Exp Med Biol 495: 129-139, 2001.
-
(2001)
Adv Exp Med Biol
, vol.495
, pp. 129-139
-
-
Verweij, C.L.1
Bayley, J.P.2
Bakker, A.3
Kaijzel, E.L.4
-
33
-
-
0037119584
-
Allelic variation in human gene expression
-
Yan H, Yuan W, Velculescu VE, Vogelstein B, and Kinzler KW. Allelic variation in human gene expression. Science 297: 1143, 2002.
-
(2002)
Science
, vol.297
, pp. 1143
-
-
Yan, H.1
Yuan, W.2
Velculescu, V.E.3
Vogelstein, B.4
Kinzler, K.W.5
-
34
-
-
0036190206
-
Association of the tissue kallikrein gene promoter with ESRD and hypertension
-
Yu H, Song Q, Freedman BI, Chao J, Chao L, Rich SS, and Bowden DW. Association of the tissue kallikrein gene promoter with ESRD and hypertension. Kidney Int 61: 1030-1039, 2002.
-
(2002)
Kidney Int
, vol.61
, pp. 1030-1039
-
-
Yu, H.1
Song, Q.2
Freedman, B.I.3
Chao, J.4
Chao, L.5
Rich, S.S.6
Bowden, D.W.7
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