-
1
-
-
79959524146
-
A haplotype map of the human genome
-
doi:10.1038/ nature04226
-
Altshuler, D., Brooks, L. D., Chakravarti, A., Collins, F. S., Daly, M. J. & Donnelly, P. 2005 A haplotype map of the human genome. Nature 437, 1299-1320. (doi:10.1038/ nature04226)
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
Altshuler, D.1
Brooks, L.D.2
Chakravarti, A.3
Collins, F.S.4
Daly, M.J.5
Donnelly, P.6
-
2
-
-
0029974655
-
Connections with connexins: The molecular basis of direct intercellular signaling
-
doi:10.1111/ j.1432-1033.1996.0001q.x
-
Bruzzone, R., White, T. W. & Paul, D. L. 1996 Connections with connexins: the molecular basis of direct intercellular signaling. Eur. J. Biochem. 238, 1-27. (doi:10.1111/ j.1432-1033.1996.0001q.x)
-
(1996)
Eur. J. Biochem
, vol.238
, pp. 1-27
-
-
Bruzzone, R.1
White, T.W.2
Paul, D.L.3
-
3
-
-
18544383003
-
Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract
-
doi:10.1038/ng921
-
Bu, L. et al. 2002 Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract. Nat. Genet. 31, 276-278. (doi:10.1038/ng921)
-
(2002)
Nat. Genet
, vol.31
, pp. 276-278
-
-
Bu, L.1
-
4
-
-
0038375052
-
MRC British Genetics of Hypertension Study. Genome-wide mapping of human loci for essential hypertension
-
doi:10.1016/S0140-6736(03)13722-1
-
Caulfield, M. et al. 2003 MRC British Genetics of Hypertension Study. Genome-wide mapping of human loci for essential hypertension. Lancet 361, 2118-2123. (doi:10.1016/S0140-6736(03)13722-1)
-
(2003)
Lancet
, vol.361
, pp. 2118-2123
-
-
Caulfield, M.1
-
5
-
-
0026507163
-
Occurrence of distinct PML-RAR-alpha fusion gene isoforms in patients with acute promyelocytic leukemia detected by reverse transcriptase/polymerase chain reaction
-
Chen, S. J., Chen, Z., Chen, A., Tong, J. H., Dong, S., Wang, Z. Y., Waxman, S. & Zelent, A. 1992 Occurrence of distinct PML-RAR-alpha fusion gene isoforms in patients with acute promyelocytic leukemia detected by reverse transcriptase/polymerase chain reaction. Oncogene 7, 1223-1232.
-
(1992)
Oncogene
, vol.7
, pp. 1223-1232
-
-
Chen, S.J.1
Chen, Z.2
Chen, A.3
Tong, J.H.4
Dong, S.5
Wang, Z.Y.6
Waxman, S.7
Zelent, A.8
-
6
-
-
0027258363
-
Rearrangements of the retinoic acid receptor alpha and promyelocytic leukemia zinc finger genes resulting from t(11;17)(q23;q21) in a patient with acute promyelocytic leukemia
-
Chen, S. J., Zelent, A., Tong, J. H., Yu, H. Q., Wang, Z. Y., Derre, J., Berger, R., Waxman, S. & Chen, Z. 1993a Rearrangements of the retinoic acid receptor alpha and promyelocytic leukemia zinc finger genes resulting from t(11;17)(q23;q21) in a patient with acute promyelocytic leukemia. J. Clin. Invest. 91, 2260-2267.
-
(1993)
J. Clin. Invest
, vol.91
, pp. 2260-2267
-
-
Chen, S.J.1
Zelent, A.2
Tong, J.H.3
Yu, H.Q.4
Wang, Z.Y.5
Derre, J.6
Berger, R.7
Waxman, S.8
Chen, Z.9
-
7
-
-
0027411688
-
Fusion between a novel Kruppel-like zinc finger gene and the retinoic acid receptor-alpha locus due to a variant t(11;17) translocation associated with acute promyelocytic leukaemia
-
Chen, Z., Brand, N. J., Chen, A., Chen, S. J., Tong, J. H., Wang, Z. Y., Waxman, S. & Zelent, A. 1993b Fusion between a novel Kruppel-like zinc finger gene and the retinoic acid receptor-alpha locus due to a variant t(11;17) translocation associated with acute promyelocytic leukaemia. EMBO J. 12, 1161-1167.
-
(1993)
EMBO J
, vol.12
, pp. 1161-1167
-
-
Chen, Z.1
Brand, N.J.2
Chen, A.3
Chen, S.J.4
Tong, J.H.5
Wang, Z.Y.6
Waxman, S.7
Zelent, A.8
-
8
-
-
33646725529
-
Opportunities and challenges in Human Genome Project
-
Chen, Z., Li, W., Yu, M., Xiong, H. & Chen, S. J. 1998 Opportunities and challenges in Human Genome Project. Chem. Life 18, 5-13.
-
(1998)
Chem. Life
, vol.18
, pp. 5-13
-
-
Chen, Z.1
Li, W.2
Yu, M.3
Xiong, H.4
Chen, S.J.5
-
9
-
-
0041343159
-
Association between genetic variation of CACNA1H and childhood absence epilepsy
-
doi:10.1002/ana.10607
-
Chen, Y. et al. 2003a Association between genetic variation of CACNA1H and childhood absence epilepsy. Ann. Neurol. 54, 239-243. (doi:10.1002/ana.10607)
-
(2003)
Ann. Neurol
, vol.54
, pp. 239-243
-
-
Chen, Y.1
-
10
-
-
0037428218
-
KCNQ1 gain-of-function mutation in familial atrial fibrillation
-
doi:10. 1126/science.1077771
-
Chen, Y. H. et al. 2003b KCNQ1 gain-of-function mutation in familial atrial fibrillation. Science 299, 251-254. (doi:10. 1126/science.1077771)
-
(2003)
Science
, vol.299
, pp. 251-254
-
-
Chen, Y.H.1
-
11
-
-
9744268907
-
Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8
-
doi:10.1093/hmg/ddh322
-
Chen, W. Y., Shi, Y. Y., Zheng, Y. L., Zhao, X. Z., Zhang, G. J., Chen, S. Q., Yang, P. D. & He, L. 2004 Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8. Hum. Mol. Genet. 13, 2991-2995. (doi:10.1093/hmg/ddh322)
-
(2004)
Hum. Mol. Genet
, vol.13
, pp. 2991-2995
-
-
Chen, W.Y.1
Shi, Y.Y.2
Zheng, Y.L.3
Zhao, X.Z.4
Zhang, G.J.5
Chen, S.Q.6
Yang, P.D.7
He, L.8
-
12
-
-
12844251215
-
717A>G polymorphism of human C-reactive protein gene associated with coronary heart disease in ethnic Han Chinese: The Beijing atherosclerosis study
-
doi:10.1007/s00109-004-0585-5
-
Chen, J., Zhao, J., Huang, J., Su, S., Qiang, B. & Gu, D. 2005a - 717A>G polymorphism of human C-reactive protein gene associated with coronary heart disease in ethnic Han Chinese: the Beijing atherosclerosis study. J. Mol. Med. 83, 72-78. (doi:10.1007/s00109-004-0585-5)
-
(2005)
J. Mol. Med
, vol.83
, pp. 72-78
-
-
Chen, J.1
Zhao, J.2
Huang, J.3
Su, S.4
Qiang, B.5
Gu, D.6
-
13
-
-
9644291602
-
A case-control study of the relationship between the metabotropic glutamate receptor 3 gene and schizophrenia in the Chinese population
-
doi:10.1016/j.schres.2004. 07.002
-
Chen, Q., He, G., Chen, Q., Wu, S., Xu, Y., Feng, G., Li, Y., Wang, L. & He, L. 2005b A case-control study of the relationship between the metabotropic glutamate receptor 3 gene and schizophrenia in the Chinese population. Schizophr. Res. 73, 21-26. (doi:10.1016/j.schres.2004. 07.002)
-
(2005)
Schizophr. Res
, vol.73
, pp. 21-26
-
-
Chen, Q.1
He, G.2
Chen, Q.3
Wu, S.4
Xu, Y.5
Feng, G.6
Li, Y.7
Wang, L.8
He, L.9
-
14
-
-
10744220435
-
Nasopharyngeal carcinoma and genetic polymorphisms of NA repair enzymes XRCC1 and hOGG1
-
Cho, E. Y. et al. 2003 Nasopharyngeal carcinoma and genetic polymorphisms of NA repair enzymes XRCC1 and hOGG1. Cancer Epidemiol. Biomarkers Prev. 12, 1100-1104.
-
(2003)
Cancer Epidemiol. Biomarkers Prev
, vol.12
, pp. 1100-1104
-
-
Cho, E.Y.1
-
15
-
-
2442482316
-
RASSF1A is a target tumor suppressor from 3p21.3 in nasopharyngeal carcinoma
-
doi:10.1002/ijc.20079
-
Chow, L. S., Lo, K. W., Kwong, J., To, K. F., Tsang, K. S., Lam, C. W., Dammann, R. & Huang, D. P. 2004 RASSF1A is a target tumor suppressor from 3p21.3 in nasopharyngeal carcinoma. Int. J. Cancer 109, 839-847. (doi:10.1002/ijc.20079)
-
(2004)
Int. J. Cancer
, vol.109
, pp. 839-847
-
-
Chow, L.S.1
Lo, K.W.2
Kwong, J.3
To, K.F.4
Tsang, K.S.5
Lam, C.W.6
Dammann, R.7
Huang, D.P.8
-
16
-
-
0037108758
-
Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia
-
doi:10.1073/pnas. 182412499
-
Chumakov, I. et al. 2002 Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia. Proc. Natl Acad. Sci. USA 99, 13 675-13 680. (doi:10.1073/pnas. 182412499)
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
-
-
Chumakov, I.1
-
17
-
-
0032575085
-
Connexin 26 gene linked to a dominant deafness
-
doi:10.1038/30639
-
Denoyelle, F., Lina-Granade, G., Plauchu, H., Bruzzone, R., Chaib, H., Levi-Acobas, F., Weil, D. & Petit, C. 1998 Connexin 26 gene linked to a dominant deafness. Nature 393, 319-320. (doi:10.1038/30639)
-
(1998)
Nature
, vol.393
, pp. 319-320
-
-
Denoyelle, F.1
Lina-Granade, G.2
Plauchu, H.3
Bruzzone, R.4
Chaib, H.5
Levi-Acobas, F.6
Weil, D.7
Petit, C.8
-
18
-
-
2542608297
-
From proteomic analysis to clinical significance overexpression of cytokeratin 19 correlates with hepatocellular carcinoma metastasis
-
doi:10.1074/mcp.M300094-MCP200
-
Ding, S. J. et al. 2004 From proteomic analysis to clinical significance overexpression of cytokeratin 19 correlates with hepatocellular carcinoma metastasis. Mol. Cell Proteomics 3, 73-81. (doi:10.1074/mcp.M300094-MCP200)
-
(2004)
Mol. Cell Proteomics
, vol.3
, pp. 73-81
-
-
Ding, S.J.1
-
19
-
-
0035436349
-
Confirmation of susceptibility gene loci on chromosome 1 in northern China Han families with type 2 diabetes
-
Du, W. et al. 2001 Confirmation of susceptibility gene loci on chromosome 1 in northern China Han families with type 2 diabetes. Chin. Med. J. 114, 876-878.
-
(2001)
Chin. Med. J
, vol.114
, pp. 876-878
-
-
Du, W.1
-
20
-
-
0023043847
-
A turning point in cancer research: Sequencing the human genome
-
doi:10.1126/science. 3945817
-
Dulbecco, R. 1986 A turning point in cancer research: sequencing the human genome. Science 231, 1055-1056. (doi:10.1126/science. 3945817)
-
(1986)
Science
, vol.231
, pp. 1055-1056
-
-
Dulbecco, R.1
-
21
-
-
0036699967
-
Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4
-
Feng, B. J. et al. 2002 Genome-wide scan for familial nasopharyngeal carcinoma reveals evidence of linkage to chromosome 4. Nat. Genet. 31, 395-399.
-
(2002)
Nat. Genet
, vol.31
, pp. 395-399
-
-
Feng, B.J.1
-
22
-
-
0026022684
-
Allelotype study of primary hepatocellular carcinoma
-
Fujimori, M. et al. 1991 Allelotype study of primary hepatocellular carcinoma. Cancer Res. 51, 89-93.
-
(1991)
Cancer Res
, vol.51
, pp. 89-93
-
-
Fujimori, M.1
-
23
-
-
0034935075
-
Mutations in IHH, encoding Indian hedgehog, cause brachydactyly type A-1
-
doi:10.1038/ng577
-
Gao, B. et al. 2001 Mutations in IHH, encoding Indian hedgehog, cause brachydactyly type A-1. Nat. Genet. 28, 386-388. (doi:10.1038/ng577)
-
(2001)
Nat. Genet
, vol.28
, pp. 386-388
-
-
Gao, B.1
-
24
-
-
0037331534
-
Linkage analysis of 2q14-q23 and 5q32 with blood pressure quantitative traits in Chinese sib pairs
-
doi:10.1097/00004872-200302000-00021
-
Ge, D. et al. 2003 Linkage analysis of 2q14-q23 and 5q32 with blood pressure quantitative traits in Chinese sib pairs. J. Hypertens 21, 305-310. (doi:10.1097/00004872-200302000-00021)
-
(2003)
J. Hypertens
, vol.21
, pp. 305-310
-
-
Ge, D.1
-
25
-
-
0027409955
-
Localization of the chromosome 15 breakpoints and expression of multiple PML-RAR alpha transcripts in acute promyelocytic leukemia: A study of 28 Chinese patients
-
Geng, J. P., Tong, J. H., Dong, S., Wang, Z. Y., Chen, S. J., Chen, Z., Zelent, A., Berger, R. & Larsen, C. J. 1993 Localization of the chromosome 15 breakpoints and expression of multiple PML-RAR alpha transcripts in acute promyelocytic leukemia: a study of 28 Chinese patients. Leukemia 7, 20-26.
-
(1993)
Leukemia
, vol.7
, pp. 20-26
-
-
Geng, J.P.1
Tong, J.H.2
Dong, S.3
Wang, Z.Y.4
Chen, S.J.5
Chen, Z.6
Zelent, A.7
Berger, R.8
Larsen, C.J.9
-
26
-
-
11144357511
-
Association between the FOXP2 gene and autistic disorder in Chinese population
-
doi:10.1002/ ajmg.b.20162
-
Gong, X. et al. 2004 Association between the FOXP2 gene and autistic disorder in Chinese population. Am. J. Med. Genet B Neuropsychiatr. Genet 127, 113-116. (doi:10.1002/ ajmg.b.20162)
-
(2004)
Am. J. Med. Genet B Neuropsychiatr. Genet
, vol.127
, pp. 113-116
-
-
Gong, X.1
-
27
-
-
0030013202
-
Connexins, connexons and intercellular communication
-
doi:10.1146/annurev. bi.65.070196.002355
-
Goodenough, D. A., Goliger, J. A. & Paul, D. L. 1996 Connexins, connexons and intercellular communication. Annu. Rev. Biochem. 65, 475-502. (doi:10.1146/annurev. bi.65.070196.002355)
-
(1996)
Annu. Rev. Biochem
, vol.65
, pp. 475-502
-
-
Goodenough, D.A.1
Goliger, J.A.2
Paul, D.L.3
-
28
-
-
0034585918
-
Gene expression in CD34+ cells from normal bone marrow and leukemic origins
-
doi:10.1038/sj.thj.6200020
-
Gu, J. et al. 2000 Gene expression in CD34+ cells from normal bone marrow and leukemic origins. Hematol J. 1, 206-217. (doi:10.1038/sj.thj.6200020)
-
(2000)
Hematol J
, vol.1
, pp. 206-217
-
-
Gu, J.1
-
29
-
-
0037188535
-
Variant-type PML-RAR(α) fusion transcript in acute promyelocytic leukemia: Use of a cryptic coding sequence from intron 2 of the RAR(α) gene and identification of a new clinical subtype resistant to retinoic acid therapy
-
doi:10.1073/pnas.112194799
-
Gu, B. W. et al. 2002 Variant-type PML-RAR(α) fusion transcript in acute promyelocytic leukemia: use of a cryptic coding sequence from intron 2 of the RAR(α) gene and identification of a new clinical subtype resistant to retinoic acid therapy. Proc. Natl Acad. Sci. USA 99, 7640-7645. (doi:10.1073/pnas.112194799)
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 7640-7645
-
-
Gu, B.W.1
-
30
-
-
0141725587
-
Major form of NUP98/HOXC11 fusion in adult AML with t(11;12)(p15;q13) translocation exhibits aberrant trans-regulatory activity
-
doi:10.1038/sj.leu.2403036
-
Gu, B. W. et al. 2003 Major form of NUP98/HOXC11 fusion in adult AML with t(11;12)(p15;q13) translocation exhibits aberrant trans-regulatory activity. Leukemia 17, 1858-1864. (doi:10.1038/sj.leu.2403036)
-
(2003)
Leukemia
, vol.17
, pp. 1858-1864
-
-
Gu, B.W.1
-
31
-
-
0345860908
-
Transcriptome study in China
-
doi:10.1016/ j.crvi.2003.09.021
-
Han, Z. G., Zhao, G. P. & Chen, Z. 2003 Transcriptome study in China. C. R. Biol. 326, 949-957. (doi:10.1016/ j.crvi.2003.09.021)
-
(2003)
C. R. Biol
, vol.326
, pp. 949-957
-
-
Han, Z.G.1
Zhao, G.P.2
Chen, Z.3
-
32
-
-
0034614637
-
The hallmarks of cancer
-
doi:10.1016/S0092-8674(00)81683-9
-
Hanahan, D. & Weinberg, R. A. 2000 The hallmarks of cancer. Cell 100, 57-70. (doi:10.1016/S0092-8674(00)81683-9)
-
(2000)
Cell
, vol.100
, pp. 57-70
-
-
Hanahan, D.1
Weinberg, R.A.2
-
33
-
-
3042614143
-
Identification of genetic variants in base excision repair pathway and their associations with risk of esophageal squamous cell carcinoma
-
doi:10.1158/0008-5472. CAN-04-0372
-
Hao, B. et al. 2004 Identification of genetic variants in base excision repair pathway and their associations with risk of esophageal squamous cell carcinoma. Cancer Res. 64, 4378-4384. (doi:10.1158/0008-5472. CAN-04-0372)
-
(2004)
Cancer Res
, vol.64
, pp. 4378-4384
-
-
Hao, B.1
-
34
-
-
5644266041
-
Diverse proteomic alterations in gastric adenocarcinoma
-
doi:10.1002/pmic.200300916
-
He, Q. Y., Cheung, Y. H., Leung, S. Y., Yuen, S. T., Chu, K. M. & Chiu, J. F. 2004 Diverse proteomic alterations in gastric adenocarcinoma. Proteomics 4, 3276-3287. (doi:10.1002/pmic.200300916)
-
(2004)
Proteomics
, vol.4
, pp. 3276-3287
-
-
He, Q.Y.1
Cheung, Y.H.2
Leung, S.Y.3
Yuen, S.T.4
Chu, K.M.5
Chiu, J.F.6
-
35
-
-
24944542337
-
Major causes of death among men and women in China
-
He, J. et al. 2005 Major causes of death among men and women in China. J. Med. 353, 1124-1134.
-
(2005)
J. Med
, vol.353
, pp. 1124-1134
-
-
He, J.1
-
36
-
-
0030749790
-
CYP2E1 genetic polymorphisms and risk of nasopharyngeal carcinoma in Taiwan
-
doi:10.1093/jnci/89.16.1207
-
Hildesheim, A. et al. 1997 CYP2E1 genetic polymorphisms and risk of nasopharyngeal carcinoma in Taiwan. J. Natl Cancer Inst. 89, 1207-1212. (doi:10.1093/jnci/89.16.1207)
-
(1997)
J. Natl Cancer Inst
, vol.89
, pp. 1207-1212
-
-
Hildesheim, A.1
-
37
-
-
0037021662
-
Association of HLA class I and II alleles and extended haplotypes with nasopharyngeal carcinoma in Taiwan
-
Hildesheim, A. et al. 2002 Association of HLA class I and II alleles and extended haplotypes with nasopharyngeal carcinoma in Taiwan. J. Natl Cancer Inst. 94, 1780-1789.
-
(2002)
J. Natl Cancer Inst
, vol.94
, pp. 1780-1789
-
-
Hildesheim, A.1
-
38
-
-
12944267044
-
Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning
-
doi:10.1073/pnas.160270997
-
Hu, R. M. et al. 2000 Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning. Proc. Natl Acad. Sci. USA 97, 9543-9548. (doi:10.1073/pnas.160270997)
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 9543-9548
-
-
Hu, R.M.1
-
39
-
-
0037742196
-
A specific splicing variant of SVH, a novel human armadillo repeat protein, is up-regulated in hepatocellular carcinomas
-
Huang, R., Xing, Z., Luan, Z., Wu, T., Wu, X. & Hu, G. 2003 A specific splicing variant of SVH, a novel human armadillo repeat protein, is up-regulated in hepatocellular carcinomas. Cancer Res. 63, 3775-3782.
-
(2003)
Cancer Res
, vol.63
, pp. 3775-3782
-
-
Huang, R.1
Xing, Z.2
Luan, Z.3
Wu, T.4
Wu, X.5
Hu, G.6
-
40
-
-
0032816406
-
-
Hui, A. B. et al. 1999 Detection of recurrent chromosomal gains and losses in primary nasopharyngeal carcinoma by comparative genomic hybridisation. Int. J. Cancer 82, 498-503. (doi:10.1002/(SICI) 1097-0215(19990812) 82:4〈498::AID-IJC5〉3.0.CO;2-S)
-
Hui, A. B. et al. 1999 Detection of recurrent chromosomal gains and losses in primary nasopharyngeal carcinoma by comparative genomic hybridisation. Int. J. Cancer 82, 498-503. (doi:10.1002/(SICI) 1097-0215(19990812) 82:4〈498::AID-IJC5〉3.0.CO;2-S)
-
-
-
-
41
-
-
31544450521
-
A functional variant in the transcriptional regulatory region of gene LOC344967 cosegregates with disease phenotype in familial nasopharyngeal carcinoma
-
doi:10.1158/ 0008-5472.CAN-05-2166
-
Jiang, R. C. et al. 2006 A functional variant in the transcriptional regulatory region of gene LOC344967 cosegregates with disease phenotype in familial nasopharyngeal carcinoma. Cancer Res. 66, 693-700. (doi:10.1158/ 0008-5472.CAN-05-2166)
-
(2006)
Cancer Res
, vol.66
, pp. 693-700
-
-
Jiang, R.C.1
-
42
-
-
0036406845
-
Generic's of myeloid leukemias
-
doi:10.1146/annurev. genom.3.032802.115046
-
Kelly, L. M. & Gilliland, D. G. 2002 Generic's of myeloid leukemias. Annu. Rev. Genomics Hum. Genet. 3, 179-198. (doi:10.1146/annurev. genom.3.032802.115046)
-
(2002)
Annu. Rev. Genomics Hum. Genet
, vol.3
, pp. 179-198
-
-
Kelly, L.M.1
Gilliland, D.G.2
-
43
-
-
0031007349
-
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
-
doi:10.1038/387080a0
-
Kelsell, D. P., Dunlop, J., Stevens, H. P., Lench, N. J., Liang, J. N., Parry, G., Mueller, R. F. & Leigh, I. M. 1997 Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 387, 80-83. (doi:10.1038/387080a0)
-
(1997)
Nature
, vol.387
, pp. 80-83
-
-
Kelsell, D.P.1
Dunlop, J.2
Stevens, H.P.3
Lench, N.J.4
Liang, J.N.5
Parry, G.6
Mueller, R.F.7
Leigh, I.M.8
-
44
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
doi:10.1038/ 35057062
-
Lander, E. S. et al. 2001 Initial sequencing and analysis of the human genome. Nature 409, 860-921. (doi:10.1038/ 35057062)
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
Lander, E.S.1
-
45
-
-
0037226797
-
Mutations in NR4A2 associated with familial Parkinson disease
-
doi:10.1038/ng1066
-
Le, W. D., Xu, P., Jankovic, J., Jiang, H., Appel, S. H., Smith, R. G. & Vassilatis, D. K. 2003 Mutations in NR4A2 associated with familial Parkinson disease. Nat. Genet. 33, 85-89. (doi:10.1038/ng1066)
-
(2003)
Nat. Genet
, vol.33
, pp. 85-89
-
-
Le, W.D.1
Xu, P.2
Jankovic, J.3
Jiang, H.4
Appel, S.H.5
Smith, R.G.6
Vassilatis, D.K.7
-
46
-
-
3242878697
-
Lipoprotein lipase gene polymorphisms and blood pressure levels in the northern Chinese Han population
-
doi:10.1291/ hypres.27.373
-
Li, B., Ge, D., Wang, Y., Zhao, W., Zhou, X., Gu, D. & Chen, R. 2004a Lipoprotein lipase gene polymorphisms and blood pressure levels in the northern Chinese Han population. Hypertens. Res. 27, 373-378. (doi:10.1291/ hypres.27.373)
-
(2004)
Hypertens. Res
, vol.27
, pp. 373-378
-
-
Li, B.1
Ge, D.2
Wang, Y.3
Zhao, W.4
Zhou, X.5
Gu, D.6
Chen, R.7
-
47
-
-
2542564256
-
Accurate qualitative and quantitative proteomic analysis of clinical hepatocellular carcinoma using laser capture microdissection coupled with isotope-coded affinity tag and two-dimensional liquid chromatography mass spectrometry
-
doi:10.1074/mcp.M300133-MCP200
-
Li, C. et al. 2004b Accurate qualitative and quantitative proteomic analysis of clinical hepatocellular carcinoma using laser capture microdissection coupled with isotope-coded affinity tag and two-dimensional liquid chromatography mass spectrometry. Mol. Cell. Proteomics 3, 399-409. (doi:10.1074/mcp.M300133-MCP200)
-
(2004)
Mol. Cell. Proteomics
, vol.3
, pp. 399-409
-
-
Li, C.1
-
48
-
-
0035936780
-
Molecular mechanisms of human hypertension
-
doi:10.1016/S0092-8674(01)00241-0
-
Lifton, R. P., Gharavi, A. G. & Geller, D. S. 2001 Molecular mechanisms of human hypertension. Cell 104, 545-556. (doi:10.1016/S0092-8674(01)00241-0)
-
(2001)
Cell
, vol.104
, pp. 545-556
-
-
Lifton, R.P.1
Gharavi, A.G.2
Geller, D.S.3
-
49
-
-
0344034299
-
Co-inheritance of specific genotypes of HSPG and ApoE gene increases risk of type 2 diabetic nephropathy
-
A:1027364121738, doi:10.1023
-
Liu, L., Xiang, K., Zheng, T., Zhang, R., Li, M. & Li, J. 2003 Co-inheritance of specific genotypes of HSPG and ApoE gene increases risk of type 2 diabetic nephropathy. Mol. Cell. Biochem. 254, 353-358. (doi:10.1023/ A:1027364121738)
-
(2003)
Mol. Cell. Biochem
, vol.254
, pp. 353-358
-
-
Liu, L.1
Xiang, K.2
Zheng, T.3
Zhang, R.4
Li, M.5
Li, J.6
-
50
-
-
2442720107
-
Functional contribution of EEN to leukemogenic transformation by MLL-EEN fusion protein
-
doi:10.1038/sj.onc.1207402
-
Liu, H., Chen, B., Xiong, H., Huang, Q. H., Zhang, Q. H., Wang, Z. G., Li, B. L., Chen, Z. & Chen, S. J. 2004a Functional contribution of EEN to leukemogenic transformation by MLL-EEN fusion protein. Oncogene 23, 3385-3394. (doi:10.1038/sj.onc.1207402)
-
(2004)
Oncogene
, vol.23
, pp. 3385-3394
-
-
Liu, H.1
Chen, B.2
Xiong, H.3
Huang, Q.H.4
Zhang, Q.H.5
Wang, Z.G.6
Li, B.L.7
Chen, Z.8
Chen, S.J.9
-
51
-
-
4644328759
-
Association of DAAO with schizophrenia in the Chinese population
-
doi:10.1016/j.neulet.2004.07.078
-
Liu, X. et al. 2004b Association of DAAO with schizophrenia in the Chinese population. Neurosci. Lett. 369, 228-233. (doi:10.1016/j.neulet.2004.07.078)
-
(2004)
Neurosci. Lett
, vol.369
, pp. 228-233
-
-
Liu, X.1
-
52
-
-
0034235046
-
High resolution allelotype of microdissected primary nasopharyngeal carcinoma
-
Lo, K. W., Teo, P. M., Hui, A. B., To, K. F., Tsang, Y. S., Chan, S. Y., Mak, K. F., Lee, J. C. & Huang, D. P. 2000 High resolution allelotype of microdissected primary nasopharyngeal carcinoma. Cancer Res. 60, 3348-3353.
-
(2000)
Cancer Res
, vol.60
, pp. 3348-3353
-
-
Lo, K.W.1
Teo, P.M.2
Hui, A.B.3
To, K.F.4
Tsang, Y.S.5
Chan, S.Y.6
Mak, K.F.7
Lee, J.C.8
Huang, D.P.9
-
53
-
-
2442540470
-
Focus on nasopharyngeal carcinoma
-
doi:10.1016/S1535-6108(04) 00119-9
-
Lo, K. W., To, K. F. & Huang, D. P. 2004 Focus on nasopharyngeal carcinoma. Cancer Cell 5, 423-428. (doi:10.1016/S1535-6108(04) 00119-9)
-
(2004)
Cancer Cell
, vol.5
, pp. 423-428
-
-
Lo, K.W.1
To, K.F.2
Huang, D.P.3
-
54
-
-
0025698597
-
Linkage of a nasopharyngeal carcinoma susceptibility locus to the HLA region
-
doi:10.1038/346470a0
-
Lu, S. J. et al. 1990 Linkage of a nasopharyngeal carcinoma susceptibility locus to the HLA region. Nature 346, 470-471. (doi:10.1038/346470a0)
-
(1990)
Nature
, vol.346
, pp. 470-471
-
-
Lu, S.J.1
-
55
-
-
0041413308
-
A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads
-
doi:10.1002/ajmg.a.20090
-
Lu, Y. et al. 2003 A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads. Am. J. Med. Genet. A 120, 345-349. (doi:10.1002/ajmg.a.20090)
-
(2003)
Am. J. Med. Genet. A
, vol.120
, pp. 345-349
-
-
Lu, Y.1
-
56
-
-
16244383220
-
Genetic polymorphisms of interleukin (IL)-1B, IL-1RN, IL-8, IL-10 and tumor necrosis factor a and risk of gastric cancer in a Chinese population
-
doi:10.1093/carcin/bgh349
-
Lu, W., Pan, K., Zhang, L., Lin, D., Miao, X. & You, W. 2005 Genetic polymorphisms of interleukin (IL)-1B, IL-1RN, IL-8, IL-10 and tumor necrosis factor a and risk of gastric cancer in a Chinese population. Carcinogenesis 26, 631-636. (doi:10.1093/carcin/bgh349)
-
(2005)
Carcinogenesis
, vol.26
, pp. 631-636
-
-
Lu, W.1
Pan, K.2
Zhang, L.3
Lin, D.4
Miao, X.5
You, W.6
-
57
-
-
0035058351
-
A genome-wide search for type II diabetes susceptibility genes in Chinese Hans
-
doi:10.1007/s001250051649
-
Luo, T. H., Zhao, Y., Li, G., Yuan, W. T., Zhao, J. J., Chen, J. L., Huang, W & Luo, M. 2001 A genome-wide search for type II diabetes susceptibility genes in Chinese Hans. Diabetologia 44, 501-506. (doi:10.1007/s001250051649)
-
(2001)
Diabetologia
, vol.44
, pp. 501-506
-
-
Luo, T.H.1
Zhao, Y.2
Li, G.3
Yuan, W.T.4
Zhao, J.J.5
Chen, J.L.6
Huang, W.7
Luo, M.8
-
58
-
-
1442351994
-
(2+)-relevant and differentiation-associated genes downregulated in esophageal squamous cell carcinoma using cDNA microarray
-
doi:10.1038/sj.onc. 1207218
-
(2+)-relevant and differentiation-associated genes downregulated in esophageal squamous cell carcinoma using cDNA microarray. Oncogene 23, 1291-1299. (doi:10.1038/sj.onc. 1207218)
-
(2004)
Oncogene
, vol.23
, pp. 1291-1299
-
-
Luo, A.1
-
59
-
-
13144302844
-
Identification of genes expressed in human CD34(+) hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning
-
doi:10.1073/pnas.95.14.8175
-
Mao, M. et al. 1998 Identification of genes expressed in human CD34(+) hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning. Proc. Natl Acad. Sci. USA 95, 8175-8180. (doi:10.1073/pnas.95.14.8175)
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 8175-8180
-
-
Mao, M.1
-
60
-
-
1842612033
-
Genetics of essential hypertension
-
doi:10.1093/hmg/ddh078
-
Mein, C. A., Caulfield, M. J., Dobson, R. J. & Munroe, P. B. 2004 Genetics of essential hypertension. Hum. Mol. Genet. 13, R169-R175. (doi:10.1093/hmg/ddh078)
-
(2004)
Hum. Mol. Genet
, vol.13
-
-
Mein, C.A.1
Caulfield, M.J.2
Dobson, R.J.3
Munroe, P.B.4
-
61
-
-
0043175420
-
A functional polymorphism in the matrix metalloproteinase-2 gene promoter (-1306C/T) is associated with risk of development but not metastasis of gastric cardia adenocarcinoma
-
Miao, X., Yu, C., Tan, W., Xiong, P., Liang, G., Lu, W. & Lin, D. 2003 A functional polymorphism in the matrix metalloproteinase-2 gene promoter (-1306C/T) is associated with risk of development but not metastasis of gastric cardia adenocarcinoma. Cancer Res. 63, 3987-3990.
-
(2003)
Cancer Res
, vol.63
, pp. 3987-3990
-
-
Miao, X.1
Yu, C.2
Tan, W.3
Xiong, P.4
Liang, G.5
Lu, W.6
Lin, D.7
-
62
-
-
8444221622
-
Functional STK15 Phe31Ile polymorphism is associated with the occurrence and advanced disease status of esophageal squamous cell carcinoma
-
doi:10.1158/0008-5472.CAN-04-0651
-
Miao, X., Sun, T., Wang, Y., Zhang, X., Tan, W. & Lin, D. 2004 Functional STK15 Phe31Ile polymorphism is associated with the occurrence and advanced disease status of esophageal squamous cell carcinoma. Cancer Res. 64, 2680-2683. (doi:10.1158/0008-5472.CAN-04-0651)
-
(2004)
Cancer Res
, vol.64
, pp. 2680-2683
-
-
Miao, X.1
Sun, T.2
Wang, Y.3
Zhang, X.4
Tan, W.5
Lin, D.6
-
63
-
-
9044241254
-
Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia
-
doi:10.1038/ng0296-154
-
Nakamura, T et al. 1996 Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia. Nat. Genet. 12, 154-158. (doi:10.1038/ng0296-154)
-
(1996)
Nat. Genet
, vol.12
, pp. 154-158
-
-
Nakamura, T.1
-
64
-
-
0033048354
-
Glutathione S-transferase M1 and susceptibility to nasopharyngeal carcinoma
-
Nazar-Stewart, V., Vaughan, T. L., Burt, R. D., Chen, C., Berwick, M. & Swanson, G. M. 1999 Glutathione S-transferase M1 and susceptibility to nasopharyngeal carcinoma. Cancer Epidemiol. Biomarkers Prev. 8, 547-551.
-
(1999)
Cancer Epidemiol. Biomarkers Prev
, vol.8
, pp. 547-551
-
-
Nazar-Stewart, V.1
Vaughan, T.L.2
Burt, R.D.3
Chen, C.4
Berwick, M.5
Swanson, G.M.6
-
65
-
-
10744219678
-
A deletion mutation in the beta-A1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family
-
doi:10.1007/s00439-003-1049-7
-
Qi, Y et al. 2004 A deletion mutation in the beta-A1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family. Hum. Genet. 114, 192-197. (doi:10.1007/s00439-003-1049-7)
-
(2004)
Hum. Genet
, vol.114
, pp. 192-197
-
-
Qi, Y.1
-
66
-
-
2142662138
-
Human genome research in China
-
doi:10.1007/s00109-003-0515-y
-
Qiang, B. 2004 Human genome research in China. J. Mol. Med. 82, 214-222. (doi:10.1007/s00109-003-0515-y)
-
(2004)
J. Mol. Med
, vol.82
, pp. 214-222
-
-
Qiang, B.1
-
67
-
-
0033571783
-
The association of chromosome 8p deletion and tumor metastasis in human hepatocellular carcinoma
-
Qin, L. X., Tang, Z. Y., Sham, J. S., Ma, Z. C., Ye, S. L., Zhou, X. D., Wu, Z. Q., Trent, J. M. & Guan, X. Y. 1999 The association of chromosome 8p deletion and tumor metastasis in human hepatocellular carcinoma. Cancer Res. 59, 5662-5665.
-
(1999)
Cancer Res
, vol.59
, pp. 5662-5665
-
-
Qin, L.X.1
Tang, Z.Y.2
Sham, J.S.3
Ma, Z.C.4
Ye, S.L.5
Zhou, X.D.6
Wu, Z.Q.7
Trent, J.M.8
Guan, X.Y.9
-
68
-
-
0031796918
-
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis
-
doi:10.1038/3840
-
Richard, G., Smith, L. E., Bailey, R. A., Itin, P., Hohl, D., Epstein Jr, E. H., DiGiovanna, J. J., Compton, J. G. & Bale, S. J. 1998 Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis. Nat. Genet. 20, 366-369. (doi:10.1038/3840)
-
(1998)
Nat. Genet
, vol.20
, pp. 366-369
-
-
Richard, G.1
Smith, L.E.2
Bailey, R.A.3
Itin, P.4
Hohl, D.5
Epstein Jr, E.H.6
DiGiovanna, J.J.7
Compton, J.G.8
Bale, S.J.9
-
69
-
-
18044400336
-
A history of the Human Genome Project
-
doi:10.1126/science.291.5507.1195
-
Roberts, L., Davenport, R. J., Pennisi, E. & Marshall, E. 2001 A history of the Human Genome Project. Science 291, 1195. (doi:10.1126/science.291.5507.1195)
-
(2001)
Science
, vol.291
, pp. 1195
-
-
Roberts, L.1
Davenport, R.J.2
Pennisi, E.3
Marshall, E.4
-
70
-
-
10644285689
-
Complexities in psychiatric genetics
-
doi:10.1080/09540260400014393
-
Sanders, A. R., Duan, J. & Gejman, P. V. 2004 Complexities in psychiatric genetics. Int. Rev. Psychiatry 16, 284-293. (doi:10.1080/09540260400014393)
-
(2004)
Int. Rev. Psychiatry
, vol.16
, pp. 284-293
-
-
Sanders, A.R.1
Duan, J.2
Gejman, P.V.3
-
71
-
-
10744232028
-
Examination of G72 and D-amino acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder
-
doi:10.1038/sj.mp.4001421
-
Schumacher, J. et al. 2004 Examination of G72 and D-amino acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder. Mol. Psychiatry 9, 203-207. (doi:10.1038/sj.mp.4001421)
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 203-207
-
-
Schumacher, J.1
-
72
-
-
0028263741
-
Association between a deletion polymorphism of the angiotensin-converting enzyme and left ventricular hypertrophy
-
doi:10.1056/ NEJM199406093302302
-
Schunkert, H., Hense, H. W., Holmer, S. R., Stender, M., Perz, S., Keil, U., Lorell, B. H. & Riegger, G. 1994 Association between a deletion polymorphism of the angiotensin-converting enzyme and left ventricular hypertrophy. N. Engl. J. Med. 330, 1634-1638. (doi:10.1056/ NEJM199406093302302)
-
(1994)
N. Engl. J. Med
, vol.330
, pp. 1634-1638
-
-
Schunkert, H.1
Hense, H.W.2
Holmer, S.R.3
Stender, M.4
Perz, S.5
Keil, U.6
Lorell, B.H.7
Riegger, G.8
-
73
-
-
16244390251
-
Methylenetetrahydrofolate reductase polymorphisms/haplotypes and risk of gastric cancer: A case-control analysis in China
-
Shen, H. et al. 2005 Methylenetetrahydrofolate reductase polymorphisms/haplotypes and risk of gastric cancer: a case-control analysis in China. Oncol. Rep. 13, 355-360.
-
(2005)
Oncol. Rep
, vol.13
, pp. 355-360
-
-
Shen, H.1
-
74
-
-
0000778884
-
EEN encodes for a member of a new family of proteins containing an Src homology 3 domain and is the third gene located on chromosome 19p13 that fuses to MLL in human leukaemia
-
doi:10.1073/pnas.94.6.2563
-
So, C. W., Caldas, C., Liu, M. M., Chen, S. J., Huang, Q. H., Gu, L. J., Sham, M. H., Wiedemann, L. M. & Chan, L. C. 1997 EEN encodes for a member of a new family of proteins containing an Src homology 3 domain and is the third gene located on chromosome 19p13 that fuses to MLL in human leukaemia. Proc. Natl Acad. Sci. USA 94, 2563-2568. (doi:10.1073/pnas.94.6.2563)
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 2563-2568
-
-
So, C.W.1
Caldas, C.2
Liu, M.M.3
Chen, S.J.4
Huang, Q.H.5
Gu, L.J.6
Sham, M.H.7
Wiedemann, L.M.8
Chan, L.C.9
-
75
-
-
0035870245
-
Methylenetetrahydrofolate reductase polymorphisms increase risk of esophageal squamous cell carcinoma in a Chinese population
-
Song, C., Xing, D., Tan, W., Wei, Q. & Lin, D. 2001 Methylenetetrahydrofolate reductase polymorphisms increase risk of esophageal squamous cell carcinoma in a Chinese population. Cancer Res. 61, 3272-3275.
-
(2001)
Cancer Res
, vol.61
, pp. 3272-3275
-
-
Song, C.1
Xing, D.2
Tan, W.3
Wei, Q.4
Lin, D.5
-
76
-
-
0031772251
-
One connexin, two diseases
-
doi:10.1038/3781
-
Steel, K. P. 1998 One connexin, two diseases. Nat. Genet. 20, 319-320. (doi:10.1038/3781)
-
(1998)
Nat. Genet
, vol.20
, pp. 319-320
-
-
Steel, K.P.1
-
77
-
-
0035916969
-
-
Tan, W., Chen, G. F., Xing, D. Y., Song, C. Y., Kadlubar, F. F. & Lin, D. X. 2001 Frequency of CYP2A6 gene deletion and its relation to risk of lung and esophageal cancer in the Chinese population. Int. J. Cancer 95, 96-101. (doi:10.1002/1097-0215(20010320)95:2〈96:: AID-IJC1017〉3.0.CO;2-2)
-
Tan, W., Chen, G. F., Xing, D. Y., Song, C. Y., Kadlubar, F. F. & Lin, D. X. 2001 Frequency of CYP2A6 gene deletion and its relation to risk of lung and esophageal cancer in the Chinese population. Int. J. Cancer 95, 96-101. (doi:10.1002/1097-0215(20010320)95:2〈96:: AID-IJC1017〉3.0.CO;2-2)
-
-
-
-
78
-
-
2642549716
-
A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family
-
doi:10.1016/j. jns.2004.03.001
-
Tang, B., Li, H., Xia, K., Jiang, H., Pan, Q., Shen, L., Long, Z., Zhao, G. & Cai, F 2004 A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family. J. Neurol. Sci. 221, 31-34. (doi:10.1016/j. jns.2004.03.001)
-
(2004)
J. Neurol. Sci
, vol.221
, pp. 31-34
-
-
Tang, B.1
Li, H.2
Xia, K.3
Jiang, H.4
Pan, Q.5
Shen, L.6
Long, Z.7
Zhao, G.8
Cai, F.9
-
79
-
-
0026608058
-
Molecular rearrangements of the MYL gene in acute promyelocytic leukemia (APL, M3) define a breakpoint cluster region as well as some molecular variants
-
Tong, J. H. et al. 1992 Molecular rearrangements of the MYL gene in acute promyelocytic leukemia (APL, M3) define a breakpoint cluster region as well as some molecular variants. Oncogene 7, 311-316.
-
(1992)
Oncogene
, vol.7
, pp. 311-316
-
-
Tong, J.H.1
-
80
-
-
8144227590
-
Large-scale cDNA transfection screening for genes related to cancer development and progression
-
doi:10. 1073/pnas.0404089101
-
Wan, D. et al. 2004 Large-scale cDNA transfection screening for genes related to cancer development and progression. Proc. Nad Acad. Sci. USA 101, 15 724-15 729. (doi:10. 1073/pnas.0404089101)
-
(2004)
Proc. Nad Acad. Sci. USA
, vol.101
-
-
Wan, D.1
-
81
-
-
9044240040
-
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
-
doi:10.1038/ng0196-17
-
Wang, Q. et al. 1996 Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat. Genet. 12, 17-23. (doi:10.1038/ng0196-17)
-
(1996)
Nat. Genet
, vol.12
, pp. 17-23
-
-
Wang, Q.1
-
82
-
-
19944431253
-
AML1-ETO and c-KIT mutation/overexpression in t(8;21) leukemia: Implication in stepwise leukemogenesis and response to Gleevec
-
doi:10.1073/pnas.0408831102
-
Wang, Y. Y. et al. 2005 AML1-ETO and c-KIT mutation/overexpression in t(8;21) leukemia: implication in stepwise leukemogenesis and response to Gleevec. Proc. Nad Acad. Sci. USA 102, 1104-1109. (doi:10.1073/pnas.0408831102)
-
(2005)
Proc. Nad Acad. Sci. USA
, vol.102
, pp. 1104-1109
-
-
Wang, Y.Y.1
-
83
-
-
3042700201
-
Confirmation and refinement of a genetic locus for disseminated superficial actinic porokeratosis (DSAP1) at 12q23.2-24.1
-
doi:10.1111/j.1365- 2133.2004.05912.x
-
Wu, L. Q. et al. 2004 Confirmation and refinement of a genetic locus for disseminated superficial actinic porokeratosis (DSAP1) at 12q23.2-24.1. Br. J. Dermatol. 150, 999-1004. (doi:10.1111/j.1365- 2133.2004.05912.x)
-
(2004)
Br. J. Dermatol
, vol.150
, pp. 999-1004
-
-
Wu, L.Q.1
-
84
-
-
30144433414
-
Hypomethylation-linked activation of PAX2 mediates tamoxifen-stimulated endometrial carcinogenesis
-
doi:10.1038/nature04225
-
Wu, H. et al. 2005 Hypomethylation-linked activation of PAX2 mediates tamoxifen-stimulated endometrial carcinogenesis. Nature 438, 981-987. (doi:10.1038/nature04225)
-
(2005)
Nature
, vol.438
, pp. 981-987
-
-
Wu, H.1
-
85
-
-
7944225101
-
Transmission disequilibrium analysis of the GSN gene in a cohort of family trios with schizophrenia
-
doi:10.1016/j.neulet.2004.09.041
-
Xi, Z. R., Qin, W., Yang, Y. F., He, G., Gao, S. H., Ren, M. S., Peng, Y. W., Zhang, Z. & He, L. 2004 Transmission disequilibrium analysis of the GSN gene in a cohort of family trios with schizophrenia. Neurosci. Lett. 372, 200-203. (doi:10.1016/j.neulet.2004.09.041)
-
(2004)
Neurosci. Lett
, vol.372
, pp. 200-203
-
-
Xi, Z.R.1
Qin, W.2
Yang, Y.F.3
He, G.4
Gao, S.H.5
Ren, M.S.6
Peng, Y.W.7
Zhang, Z.8
He, L.9
-
86
-
-
17344373747
-
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment
-
doi:10.1038/3845
-
Xia, J. H. et al. 1998 Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment. Nat. Genet. 20, 370-373. (doi:10.1038/3845)
-
(1998)
Nat. Genet
, vol.20
, pp. 370-373
-
-
Xia, J.H.1
-
87
-
-
0034130869
-
Identification of a locus for disseminated superficial actinic porokeratosis (DSAP) at Chromosome 12q23.2-24.1
-
doi:10.1046/j.1523-1747.2000.00978.x
-
Xia, J. H. 2000 Identification of a locus for disseminated superficial actinic porokeratosis (DSAP) at Chromosome 12q23.2-24.1. J. Invest. Dermatol. 114, 1071-1074. (doi:10.1046/j.1523-1747.2000.00978.x)
-
(2000)
J. Invest. Dermatol
, vol.114
, pp. 1071-1074
-
-
Xia, J.H.1
-
88
-
-
0036408582
-
A novel locus (DSAP2) for disseminated superficial actinic porokeratosis maps to chromosome 15q25.1-26.1
-
doi:10. 1046/j.1365-2133.2002.05058.x
-
Xia, K. et al. 2002 A novel locus (DSAP2) for disseminated superficial actinic porokeratosis maps to chromosome 15q25.1-26.1. Br. J. Dermatol. 147, 650-654. (doi:10. 1046/j.1365-2133.2002.05058.x)
-
(2002)
Br. J. Dermatol
, vol.147
, pp. 650-654
-
-
Xia, K.1
-
89
-
-
0035136682
-
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP
-
doi:10. 1038/84848
-
Xiao, S. et al. 2001 Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP. Nat. Genet. 27, 201-204. (doi:10. 1038/84848)
-
(2001)
Nat. Genet
, vol.27
, pp. 201-204
-
-
Xiao, S.1
-
90
-
-
0035918562
-
-
Xing, D. Y., Tan, W., Song, N. & Lin, D. X. 2001 Ser326Cys polymorphism in hOGG1 gene and risk of esophageal cancer in Chinese population. Int. J. Cancer 95, 140-143. (doi:10.1002/1097-0215(20010520)95: 3〈140::AID-IJC 1024〉3.0.CO;2-2)
-
Xing, D. Y., Tan, W., Song, N. & Lin, D. X. 2001 Ser326Cys polymorphism in hOGG1 gene and risk of esophageal cancer in Chinese population. Int. J. Cancer 95, 140-143. (doi:10.1002/1097-0215(20010520)95: 3〈140::AID-IJC 1024〉3.0.CO;2-2)
-
-
-
-
91
-
-
0042242613
-
A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2
-
doi:10.1086/377007
-
Xing, Q. H. et al. 2003 A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2. Am. J. Hum. Genet. 73, 377-382. (doi:10.1086/377007)
-
(2003)
Am. J. Hum. Genet
, vol.73
, pp. 377-382
-
-
Xing, Q.H.1
-
92
-
-
12144289414
-
A susceptibility locus at chromosome 3p21 linked to familial nasopharyngeal carcinoma
-
doi:10.1158/0008-5472.CAN-03-3253
-
Xiong, W. et al. 2004 A susceptibility locus at chromosome 3p21 linked to familial nasopharyngeal carcinoma. Cancer Res. 64, 1972-1974. (doi:10.1158/0008-5472.CAN-03-3253)
-
(2004)
Cancer Res
, vol.64
, pp. 1972-1974
-
-
Xiong, W.1
-
93
-
-
0035300430
-
Expression profiling suggested a regulatory role of liver-enriched transcription factors in human hepatocellular carcinoma
-
Xu, L. et al. 2001a Expression profiling suggested a regulatory role of liver-enriched transcription factors in human hepatocellular carcinoma. Cancer Res. 61, 3176-3181.
-
(2001)
Cancer Res
, vol.61
, pp. 3176-3181
-
-
Xu, L.1
-
94
-
-
0035910064
-
Insight into hepatocellular carcinogenesis at transcriptome level by comparing gene expression profiles of hepatocellular carcinoma with those of corresponding noncancerous liver
-
doi:10.1073/pnas. 241522398
-
Xu, X. R. et al. 2001b Insight into hepatocellular carcinogenesis at transcriptome level by comparing gene expression profiles of hepatocellular carcinoma with those of corresponding noncancerous liver. Proc. Nad Acad. Sci. USA 98, 15 089-15 094. (doi:10.1073/pnas. 241522398)
-
(2001)
Proc. Nad Acad. Sci. USA
, vol.98
-
-
Xu, X.R.1
-
95
-
-
0041321377
-
A novel liver-specific zona pellucida domain containing protein that is expressed rarely in hepatocellular carcinoma
-
doi:10.1053/jhep.2003.50340
-
Xu, Z. G. et al. 2003 A novel liver-specific zona pellucida domain containing protein that is expressed rarely in hepatocellular carcinoma. Hepatology 38, 735-744. (doi:10.1053/jhep.2003.50340)
-
(2003)
Hepatology
, vol.38
, pp. 735-744
-
-
Xu, Z.G.1
-
96
-
-
3142555952
-
Association study of an SNP combination pattern in the dopaminergic pathway in paranoid schizophrenia: A novel strategy for complex disorders
-
doi:10.1038/sj.mp.4001472
-
Xu, Q. et al. 2004a Association study of an SNP combination pattern in the dopaminergic pathway in paranoid schizophrenia: a novel strategy for complex disorders. Mol. Psychiatry 9, 510-521. (doi:10.1038/sj.mp.4001472)
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 510-521
-
-
Xu, Q.1
-
97
-
-
4243185856
-
Interaction and relationship between angiotensin converting enzyme gene and environmental factors predisposing to essential hypertension in Mongolian population of China
-
Xu, Q. et al. 2004b Interaction and relationship between angiotensin converting enzyme gene and environmental factors predisposing to essential hypertension in Mongolian population of China. Biomed. Environ. Sci. 17, 177-186.
-
(2004)
Biomed. Environ. Sci
, vol.17
, pp. 177-186
-
-
Xu, Q.1
-
98
-
-
4544318732
-
Negative regulation of hepatocellular carcinoma cell growth by signal regulatory protein alpha1
-
doi:10.1002/hep.20360
-
Yan, H. X. et al. 2004 Negative regulation of hepatocellular carcinoma cell growth by signal regulatory protein alpha1. Hepatology 40, 618-628. (doi:10.1002/hep.20360)
-
(2004)
Hepatology
, vol.40
, pp. 618-628
-
-
Yan, H.X.1
-
99
-
-
0033912596
-
A locus for brachydactyly type A-1 maps to chromosome 2q35-q36
-
doi:10.1086/302806
-
Yang, X., She, C., Guo, J., Yu, A. C., Lu, Y., Shi, X., Feng, G. & He, L. 2000 A locus for brachydactyly type A-1 maps to chromosome 2q35-q36. Am. J. Hum. Genet. 66, 892-903. (doi:10.1086/302806)
-
(2000)
Am. J. Hum. Genet
, vol.66
, pp. 892-903
-
-
Yang, X.1
She, C.2
Guo, J.3
Yu, A.C.4
Lu, Y.5
Shi, X.6
Feng, G.7
He, L.8
-
100
-
-
0043280886
-
Evidence for linkage and association of the markers near the LPL gene with hypertension in Chinese families
-
doi:10.1136/jmg.40.5.e57
-
Yang, W. J. et al. 2003 Evidence for linkage and association of the markers near the LPL gene with hypertension in Chinese families. J. Med. Genet. 40, e57. (doi:10.1136/jmg.40.5.e57)
-
(2003)
J. Med. Genet
, vol.40
-
-
Yang, W.J.1
-
101
-
-
12144288410
-
Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia
-
doi:10.1136/jmg. 2003.012153
-
Yang, Y. 2004a Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia. J. Med. Genet. 41, 171-174. (doi:10.1136/jmg. 2003.012153)
-
(2004)
J. Med. Genet
, vol.41
, pp. 171-174
-
-
Yang, Y.1
-
102
-
-
6344292572
-
Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation
-
doi:10. 1086/425342
-
Yang, Y. et al. 2004b Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation. Am. J. Hum. Genet. 75, 899-905. (doi:10. 1086/425342)
-
(2004)
Am. J. Hum. Genet
, vol.75
, pp. 899-905
-
-
Yang, Y.1
-
103
-
-
0037391756
-
Predicting hepatitis B virus-positive metastatic hepatocellular carcinomas using gene expression profiling and supervised machine learning
-
doi:10.1038/nm843
-
Ye, Q. H. et al. 2003 Predicting hepatitis B virus-positive metastatic hepatocellular carcinomas using gene expression profiling and supervised machine learning. Nat. Med. 9, 416-423. (doi:10.1038/nm843)
-
(2003)
Nat. Med
, vol.9
, pp. 416-423
-
-
Ye, Q.H.1
-
104
-
-
0034883257
-
Gene expression profiling in human fetal liver and identification of tissue- and developmental-stage-specific genes through compiled expression profiles and efficient cloning of full-length cDNAs
-
doi:10.1101/gr.175501
-
Yu, Y. et al. 2001 Gene expression profiling in human fetal liver and identification of tissue- and developmental-stage-specific genes through compiled expression profiles and efficient cloning of full-length cDNAs. Genome Res. 11, 1392-1403. (doi:10.1101/gr.175501)
-
(2001)
Genome Res
, vol.11
, pp. 1392-1403
-
-
Yu, Y.1
-
105
-
-
5644232084
-
Functional haplotypes in the promoter of matrix metalloproteinase-2 predict risk of the occurrence and metastasis of esophageal cancer
-
doi:10. 1158/0008-5472.CAN-04-1521
-
Yu, C., Zhou, Y., Miao, X., Xiong, P., Tan, W. & Lin, D. 2004 Functional haplotypes in the promoter of matrix metalloproteinase-2 predict risk of the occurrence and metastasis of esophageal cancer. Cancer Res. 64, 7622-7628. (doi:10. 1158/0008-5472.CAN-04-1521)
-
(2004)
Cancer Res
, vol.64
, pp. 7622-7628
-
-
Yu, C.1
Zhou, Y.2
Miao, X.3
Xiong, P.4
Tan, W.5
Lin, D.6
-
106
-
-
0346752004
-
Short esophageal cancer-related tandem repeat polymorphism in a novel gene (ECRG2) implicates susceptibility to esophageal cancer in Chinese population
-
doi:10.1002/ijc.11560
-
Yue, C. M., Bi, M. X., Tan, W., Deng, D. J., Zhang, X. Y., Guo, L. P., Lin, D. X. & Lu, S. H. 2004 Short esophageal cancer-related tandem repeat polymorphism in a novel gene (ECRG2) implicates susceptibility to esophageal cancer in Chinese population. Int. J. Cancer 108, 232-236. (doi:10.1002/ijc.11560)
-
(2004)
Int. J. Cancer
, vol.108
, pp. 232-236
-
-
Yue, C.M.1
Bi, M.X.2
Tan, W.3
Deng, D.J.4
Zhang, X.Y.5
Guo, L.P.6
Lin, D.X.7
Lu, S.H.8
-
107
-
-
13944250989
-
-
Zelent, A., Petrie, K., Chen, Z., Lotan, R., Lubbert, M., Tallman, M. S., Ohno, R., Degos, L. & Waxman, S. 2005 Molecular target-based treatment of human cancer: summary of the 10th International Conference on Differentiation Therapy. Cancer Res. 65, 1117-1123. (doi:10.1158/0008-5472.CAN-04- 3603)
-
Zelent, A., Petrie, K., Chen, Z., Lotan, R., Lubbert, M., Tallman, M. S., Ohno, R., Degos, L. & Waxman, S. 2005 Molecular target-based treatment of human cancer: summary of the 10th International Conference on Differentiation Therapy. Cancer Res. 65, 1117-1123. (doi:10.1158/0008-5472.CAN-04- 3603)
-
-
-
-
108
-
-
13044286010
-
Genomic sequence, structural organization, molecular evolution, and aberrant rearrangement of promyelocytic leukemia zinc finger gene
-
doi:10.1073/pnas.96.20.11422
-
Zhang, T. et al. 1999 Genomic sequence, structural organization, molecular evolution, and aberrant rearrangement of promyelocytic leukemia zinc finger gene. Proc. Natl Acad. Sci. USA 96, 11 422-11 427. (doi:10.1073/pnas.96.20.11422)
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
-
-
Zhang, T.1
-
109
-
-
0033782920
-
Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells
-
doi:10. 1101/gr.140200
-
Zhang, Q. H. et al. 2000a Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells. Genome Res. 10, 1546-1560. (doi:10. 1101/gr.140200)
-
(2000)
Genome Res
, vol.10
, pp. 1546-1560
-
-
Zhang, Q.H.1
-
110
-
-
0033910916
-
20006 Segregation analysis of esophageal cancer in a moderately high-incidence area of northern China
-
doi:10.1086/302970
-
Zhang, W., Bailey-Wilson, J. E., Li, W., Wang, X., Zhang, C., Mao, X., Liu, Z., Zhou, C. & Wu, M. 20006 Segregation analysis of esophageal cancer in a moderately high-incidence area of northern China. Am. J. Hum. Genet. 67, 110-119. (doi:10.1086/302970)
-
Am. J. Hum. Genet
, vol.67
, pp. 110-119
-
-
Zhang, W.1
Bailey-Wilson, J.E.2
Li, W.3
Wang, X.4
Zhang, C.5
Mao, X.6
Liu, Z.7
Zhou, C.8
Wu, M.9
-
111
-
-
0035134329
-
DSPP mutation in dentinogenesis imperfecta Shields type II
-
doi:10.1038/84765
-
Zhang, X. et al. 2001 DSPP mutation in dentinogenesis imperfecta Shields type II. Nat. Genet. 27, 151-152. (doi:10.1038/84765)
-
(2001)
Nat. Genet
, vol.27
, pp. 151-152
-
-
Zhang, X.1
-
112
-
-
3342964099
-
Positive association of the human frizzled 3 (FZD3) gene haplotype with schizophrenia in Chinese Han population
-
Zhang, Y. et al. 2004 Positive association of the human frizzled 3 (FZD3) gene haplotype with schizophrenia in Chinese Han population. Am. J. Med. Genet. B Neuropsychiatr. Genet. 129, 16-19.
-
(2004)
Am. J. Med. Genet. B Neuropsychiatr. Genet
, vol.129
, pp. 16-19
-
-
Zhang, Y.1
-
113
-
-
20244383447
-
A mutation in SART3 gene in a Chinese pedigree with disseminated superficial actinic porokeratosis
-
doi:10. 1111/j.1365-2133.2005.06443.x
-
Zhang, Z. H. et al. 2005 A mutation in SART3 gene in a Chinese pedigree with disseminated superficial actinic porokeratosis. Br. J. Dermatol. 152, 658-663. (doi:10. 1111/j.1365-2133.2005.06443.x)
-
(2005)
Br. J. Dermatol
, vol.152
, pp. 658-663
-
-
Zhang, Z.H.1
-
114
-
-
20144389794
-
An autosomal genomic scan for loci linked to type 2 diabetes in northern Han Chinese
-
doi:10.1007/s00109-004-0587-3
-
Zhao, J. Y. 2005 An autosomal genomic scan for loci linked to type 2 diabetes in northern Han Chinese. J. Mol. Med. 83, 209-215. (doi:10.1007/s00109-004-0587-3)
-
(2005)
J. Mol. Med
, vol.83
, pp. 209-215
-
-
Zhao, J.Y.1
-
115
-
-
2342647586
-
CYLD mutation causes multiple familial trichoepithelioma in three Chinese families
-
doi:10.1002/humu.9231
-
Zheng, G. et al. 2004 CYLD mutation causes multiple familial trichoepithelioma in three Chinese families. Hum. Mutat. 23, 400. (doi:10.1002/humu.9231)
-
(2004)
Hum. Mutat
, vol.23
, pp. 400
-
-
Zheng, G.1
-
116
-
-
0036782183
-
A novel gene, NMES1, downregulated in human esophageal squamous cell carcinoma
-
doi:10.1002/ijc.10600
-
Zhou, J. et al. 2002 A novel gene, NMES1, downregulated in human esophageal squamous cell carcinoma. Int. J. Cancer 101, 311-316. (doi:10.1002/ijc.10600)
-
(2002)
Int. J. Cancer
, vol.101
, pp. 311-316
-
-
Zhou, J.1
-
117
-
-
11844282202
-
Overexpression of human pituitary tumor transforming gene (hPTTG), is regulated by beta-catenin/TCF pathway in human esophageal squamous cell carcinoma
-
doi:10.1002/ ijc.20642
-
Zhou, C. et al. 2005 Overexpression of human pituitary tumor transforming gene (hPTTG), is regulated by beta-catenin/TCF pathway in human esophageal squamous cell carcinoma. Int. J. Cancer 113, 891-898. (doi:10.1002/ ijc.20642)
-
(2005)
Int. J. Cancer
, vol.113
, pp. 891-898
-
-
Zhou, C.1
-
118
-
-
0035139750
-
Linkage of hypertension to chromosome 2q14-q23 in Chinese families
-
doi:10.1097/00004872-200101000-00008
-
Zhu, D. L. et al. 2001 Linkage of hypertension to chromosome 2q14-q23 in Chinese families. J. Hypertens 19, 55-61. (doi:10.1097/00004872-200101000-00008)
-
(2001)
J. Hypertens
, vol.19
, pp. 55-61
-
-
Zhu, D.L.1
|