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

19篇 您的检索式：作者名="OOSTRA B"

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	The hemochromatosis N144H mutation of SLC11A3 gene in patients with type 2 diabetes显示文摘	NJAJOU O T VAESSEN N OOSTRA B	2002	Mol Genet Metab2002，75，：	1
	2	FMRP detection assay for the diagnosis of the Fragile X syndrome 显示文摘	Willemsen R Oostra B	2000	Am J Med Genet2000，97，4：	1
	3	ACE polymor- phisms 显示文摘	F A Sayed-Tabatabaei B A Oostra A Isaacs	2006	Circ Res2006，98，9：	1
	4	CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder显示文摘	Mathews C A Joosse M Eussen B H J Heutink P Oostra B A	2003	Genomics2003，82，：	1
	5	FMR1:a gene with three faces显示文摘	Oostra B A Willemsen R	2009	Biochim Biophys Acta2009，1790，6：	1
	6	Understanding fragile X syndrome:insights from animal models显示文摘	BAKKER C E OOSTRA B A	2003	Cytogenet Genome Res2003，100，14：	1
	7	FMR1: a gene with three faces 显示文摘	Oostra B A Willemsen R	2009	Biochim Biophys Acta2009，1790，6：	1
	8	FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway显示文摘	XUE Y OOSTRA A B	2007	EMBO J2007，26，：	1
	9	FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome显示文摘	A Di Fonzo M C.J. Dekker P Montagna A Baruzzi E H. Yonova L Correia Guedes A Szczerbinska T Zhao L O.M. Dubbel-Hulsman C H. Wouters E de Graaff W J.G. Oyen E J. Simons G J. Breedveld B A. Oostra M W. Horstink V Bonifati	2009	Neurology2009，，3：	1
	10	Studying the genetics of Hischsprung, s disease: unraveling an oligogenic disorder 显示文摘	Brooks A S Oostra B A Hofstra R M	2005	Clin Genet2005，67，1：	1
	11	Understanding fragile X syndrome:insights from animal models显示文摘	Bakker C E Oostra B A	2003	Cytogenet Genome Res2003，100，：	1
	12	Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's disease显示文摘	Bonifati V Oostra B A Heutink P	2004	J Mol Med2004，82，3：	1
	13	Association of os- teoprotegerin and bone loss after adjuvant chemotherapy in early-stage breast cancer显示文摘	DREW R OOSTRA MARYAM B	2015	Molecular and Cellular En- docrinology2015，402，：	1
	14	The Fragile X Syndrome:From Molecular Genetics to Neurobiology显示文摘	Willemsen R Oostra B Bassell G	2004	Mental Retardation and Developmental Disabilities Research Reviews2004，10，：	1
	15	Deletion of FMR1 in Purkinje ceils enhances parallel fiber LTD,en- larges spines ,and attenuates cerebellar eyelid conditioning in Fragile X syndrome 显示文摘	KOEKKOEK S K NELSON D L OOSTRA B A	2005	Neuron2005，47，3：	1
	16	Fragile X Syndrome at the Turn of the Century显示文摘	Kooy R F Willemsen R Oostra B A	2000	Mol Med Today2000，6，5：	1
	17	The Fragile X Gene and Its Function显示文摘	Oostra B A Chiurazzi P	2001	Clin Genet2001，60，：	1
	18	Microsatellite repeat instability and neurological disease显示文摘	Brouwer J R Willemsen R Oostra B A	2009	Bioessays2009，31，1：	1
	19	Studying the genetics of Hirsehsprung's disease: unraveling an oligogenie disorder显示文摘	Brooks A S Oostra B A Hofstra R M	2005	Clin Genet2005，67，1：	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