维普期刊资源整合服务平台（V6.5）

45篇 您的检索式：作者名="Knight SW"

选中清除导出查看参考文献查看引证文献引用追踪共3页首页上一页第1页下一页末页 /3 跳转

	题名	作者	年代	出处	被引量
1	Prefrontal cortex regulates inhibition and excitation in distributed neural networks显示文摘	Knight RT Richard SW Swick D	1999	Acta Psychologica1999，101，：	1
2	X-llinked dyskera-tosis congenital is caused by mutations in a highly con-served gene with putative nucleolar nucleolar functions显示文摘	Heiss NS Knight SW Vulliamy TJ		0，，01：	1
3	A link between RNA interference and nonsense-mediated decay in Caenorhabditis elegans显示文摘	Domeier ME Morse DP Knight SW	2000	Science2000，289，5486：	1
4	Fine mapping of the dyskeratosis congenita locus in Xq28显示文摘	Knight SW Vulliamy TJ Forni GL	1996	J Med Genet1996，33，12：	1
5	Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres显示文摘	Knight SJ Horsley SW Regan R	1997	Eur J Hum Genet1997，5，1：	1
6	Xlinked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions显示文摘	Heiss NS Knight SW Vulliamy TJ	1998	Nat Genet1998，19，1：	1
7	A role for the RNase III enzyme DCR-1 in RNA interference and germ line development in Caenorhabditis elegans显示文摘	Knight SW Bass BL	2001	Science2001，293，5538：	1
8	X-linked dyskeratosis congenital is caused by mutations in a highly conserved gene with putative nucleolar functions显示文摘	Knight SW Vulliamy TJ	1998	Nat Genet1998，19，1：	1
9	Identification of novel DKC1 mutations in patients with dyskeratosis congenital:implications for pathophysiology and diagnosis显示文摘	Vulliamy TJ Morgan B	2001	Hum genet2001，108，：	1
10	Unexplained aplastic anaemia,immunodeficiency,and cerebellar hypoplasia (HoyeraalHreidarsson syndrome) due to mutations in the dyskeratosis congenita gene,DKC1显示文摘	Knight SW Heiss NS Vulliamy TJ	1999	Br J Haematol1999，107，2：	1
11	Dyskeratosis congenita caused by a 3 ' deletion:germline and somatic mosaicism in a female carrier显示文摘	Vulliamy TJ Knight SW Heiss NS	1999	Blood1999，94，4：	1
12	X-linked dyskera- tosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions 显示文摘	Heiss NS Knight SW Vulliamy TJ	1998	Nat Genet1998，19，1：	1
13	Identification of novel DKC1 mutations in patients with dyskeratosis congenita:implications for pathophysiology and diagnosis显示文摘	Knight SW Vulliamy TJ Morgan B	2001	Hum Genet2001，108，4：	1
14	A role for the RNase Ⅲ enzyme DCR-1 in RNA interference and germ line development in caenorhabditis elegans显示文摘	Knight SW Bass BL	2001	Science2001，293，5538：	1
15	A role for the RNase Ⅲ enzyme DCR-1 in RNA interference and germ line development in Caenorhabditis elegans显示文摘	Knight SW Bass BL	2001	Science2001，293，5538：	1
16	An Essential rolefor DeltaFosB in the median preoptic nucleus in the sustainedhypertensive effects of chronic intermittent hypoxia 显示文摘	Cunningham JT Knight WD Mifflin SW et at	2012	Hypertension2012，60，1：	1
17	Identification of novel DKC1 mutations in patients with dyskeratosis congenita:implications for pathophysiolngy and diagnosis显示文摘	Knight SW Vulliamy TJ Morgan B	2001	Hum Genet2001，108，4：	1
18	X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions显示文摘	Heiss NS Knight SW Vulliamy TJ	1998	Nat Genet1998，19，1：	1
19	X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene显示文摘	Knight SW Heiss NS Vulliamy TJ	1999	Am J Hum Genet1999，65，1：	1
20	Mutations in dyskerato- sis congenita: their impact on telomere length and the diversity of clinical presentation显示文摘	Vulliamy TJ Marmne A Knight SW	2006	Blood2006，107，7：	1

返回顶部每页显示：

共3页首页上一页第1页下一页末页 /3 跳转

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

用户提示