维普期刊资源整合服务平台（V6.5）

维普中文期刊产品整合服务

18篇 您的检索式：作者名="Lerer I"

选中清除导出查看参考文献查看引证文献引用追踪共1页首页上一页第1页下一页末页 /1 跳转

		题名	作者	年代	出处	被引量
	1	BDNF Va166Met polymorphism is associated with HPA axis reactivity to psychological stress characterized by genotype and gender interactions显示文摘	Shalev I Lerer E Israel S	2009	Psychoneuroendocrinology2009，34，：	1
	2	Ribosomal protein S6 phosphorylation is a determinant of cell size and glucose homeostasis显示文摘	RUVINSKY I SHARON N LERER T	2005	Genes Dev2005，19，18：	1
	3	Wiedemann-Beckwith syndrome: further prenatal characterization of the condition显示文摘	Reish O Lerer I Amiel A	2002	Am J Med Genet2002，107，3：	1
	4	Ribosomal protein S6 phosphorylation is a determinant of cell size and glucose homeostasis显示文摘	Ruvinsky I Sharon N Lerer T	2005	Genes Dev2005，19，18：	1
	5	Ribosomal protein S6 phosphoryla tion is a determinant of cell size and glucose homeostasis显示文摘	Ruvinsky I Sharon N Lerer T	2005	Genes Dev2005，19，18：	1
	6	A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews显示文摘	Lerer I Sagi M Ben-Neriah Z	2001	Hum Mutat2001，18，5：	1
	7	Machado-Joseph disease:correlationbetween the clinical features,the CAG repeat length and homozygosity for themutation显示文摘	Lerer I Merims D Abeliovich D	1996	Eur J Hum Genet1996，4，1：	1
	8	Contribution of connexin 26mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT显示文摘	Lerer I Sagi M Malamud E	2000	Am J Med Genet2000，95，1：	1
	9	A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: a novel founder mutation in Ashkenazi Jews 显示文摘	LERER I SAQI M BEN-NERIAH Z	2001	Hum Murat2001，18，5：	1
	10	The oxytocin receptor(OXTR)contributes to prosocial fund allocations in the dictator game and thesocial value orientations task显示文摘	Israel S Lerer E Shalev I	2009	PLoS One2009，4，5：	1
	11	Electroconvulsive shock and brain muscarinic receptors: relationship to anterograde amnesia 显示文摘	Lerer B Stanley M Mclntyre I	1984	Life Sci1984，35，：	1
	12	The E148Q mutation in the MEFV gene: is it a disease causing mutation or a sequence variant? 显示文摘	Lerer I Malamud E	2000	Hum Mutat2000，15，：	1
	13	The H syndrome is caused by mutations in the nucleoside transporter h ENT3显示文摘	MOLHO-PESSACH V LERER I ABELIOVICH D	2008	Am J Hum Genet2008，83，4：	1
	14	MachadoJoseph disease:correlation between the clinical features, the CAG repeat length and homozygosity for the mutation显示文摘	Lerer I Merims D Abeliovich D	1996	Eur J Hum Genet1996，4，：	1
	15	A deletion muta- tion in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews 显示文摘	Lerer I Sagi M Ben-Neriah Z	2001	Hum Mutat2001，18，5：	1
	16	Wiedemann-Beckwith syndrome: further prenatal characterization of the condition显示文摘	Reish O Lerer I Amiel A	2002	Am J Med Genet2002，107，3：	1
	17	Riboso- mal protein S6 phosphorylation is a determinant of cell size and glucose homeostasis 显示文摘	RUVINSKY I SHARON N LERER T	2005	Genes Develop- ment2005，19，18：	1
	18	HTR2C (cys23ser) polymor- phism influences early onset in bipolar patients in a large Europe- an multicenter association study 显示文摘	Massat I Lerer B Souery D	2007	Mol Psychiatry2007，12，：	1

返回顶部每页显示：

共1页首页上一页第1页下一页末页 /1 跳转

goolge学术搜索-维普

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