维普中文期刊产品整合服务
16034篇 您的检索式:期刊名="Nat Genet"
    题名 作者 年代 出处 被引量
1A candidate genetic risk factor for vascular disease : a common mutation in methyllenetetrahydrofolate recductase 显示文摘Frosst P Blom h Milos R 1995Nat Genet1995,10,:2
2A null mutation in the human CNTF gene is not casually related to neurological diseases 显示文摘Takahashi R Yokoji H Misawa H 1994Nat Genet1994,7,:2
3Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease显示文摘Drenth JP de Morsche RH Smink R 2003Nat Genet2003,33,3:2
4Alterations in the PITSLRE protein kinase gene complex on chromosome P36 in childhood neuroblastoma显示文摘Lahit JM Valentine M Xiang J 1994Nat Genet1994,7,:2
5Impaired stress response and reduced anxiety in mice lacking a functional corticotropinreleasing hormone receptor 1显示文摘Timpl P Spanagel R Sillaber I 1998Nat Genet1998,19,2:1
6Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome显示文摘Zimprich A Grabowski M Asmus F 2001Nat Genet2001,29,1:1
7Disruption of a new forkhead/winged protein, scurfin, results in the fatal lympho-proliferatire disorder of the scurfy mouse显示文摘Brunkow M E Jeffery E W Hierrild K A 2001Nat Genet2001,27,1:1
8Positional identification of TNFSF4, encoding OX40 ligand, as a gene that influences atherosclerosis susceptibility显示文摘Wang X Ria M Kelmenson PM 2005Nat Genet2005,4,37:1
9Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease 显示文摘Lohmueller KE Pearce CL Pike M 2003Nat Genet2003,33,2:1
10Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene显示文摘Dittrich B Buiting K Kom B 1996Nat Genet1996,14,2:1
11Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palateectodermal dysplasia 显示文摘Suzuki K Hu D Bustos T 2000Nat Genet2000,25,4:1
12Dysregulation of the TSC-mTOR pathway in human disease 显示文摘Inoki K Corradetti MN Guan KL 2005Nat Genet2005,37,1:1
13Lamrl functional retroposen causes right ventricular dysplasia in mice 显示文摘Asano Y Takashima S Asakura M 2004Nat Genet2004,36,2:1
14A tiling resolution DNA microarray with complete coverage of the human genome显示文摘Ishkanian A S Malloff C A Watson S K 2004Nat Genet2004,36,3:1
15Epigenetic inactivation of SFRP gene allows constitutive WNT signaling in colorectal cancer 显示文摘Suzuki H Watkins DN Jair KW 2004Nat Genet2004,36,4:1
16Minimum information about a microarray experiment (MIAME)-toward standards for microarray data显示文摘BRAZMA A HINGAMP P QUACKENBUSH J 2001Nat Genet2001,29,4:1
17Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible显示文摘Hinkes B Wiggins R C Gbadegesin R Vlangos C N Seelow D Nurnberg G 2006Nat Genet2006,38,:1
18AXINI mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1 显示文摘SATOH S DAIGO Y FURUKAWA Y 2000Nat Genet2000,24,3:1
19Inherited susceptibility to lung cancer may be associated with the T790M drug resistance mutation in EGFR显示文摘Bell DW Gore I Okimoto RA 2005Nat Genet2005,37,12:1
20Human cytogenetics: 46 chromosomes, 46 years and counting 显示文摘Trask BJ 2002Nat Rev Genet2002,3,:1
返回顶部 每页显示:
共802页 首页 上一页 第1页 下一页 末页 /802 跳转

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费