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58篇 您的检索式：期刊名="Hum Mol Gene"

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	题名	作者	年代	出处	被引量
1	Gene replacement therapy in the retinal degeneration mouse: the effect on retinal degeneration following partial transduction of the retinal显示文摘	Sarra GM Stephens C de Alwis M	2001	Hum Mol Gene2001，10，21：	1
2	Gene replaomaent therapy in the retinal degeneration slow (rds) mouse: the effect on retinal degeneration following partial transduction of the retina 显示文摘	Sarra GM Stephens C de Alwis M Bainbridge JW Smith AJ Thrasher AJ	2001	Hum Mol Gene2001，10，21：	1
3	The complex genetic epidemiology of prostate cancer 显示文摘	Schaid DJ	2004	Hum Mol Gene2004，13，：	1
4	A noval functional VKORC1 promoter polymorphism is associated with in- ter-individual and inter-ethnic differences in warfarin sen- sitivity显示文摘	Yuan HY Chen J J Lee MT	2005	Hum Mol Gene2005，14，13：	1
5	Clinical, biochemicaland molecular genetic ciooelation sin Fried reich'sataxia 显示文摘	Bradley JL Blake JC Chamberlain S	2000	Hum Mol Gene2000，9，2：	1
6	Gene transfer into the mouse retina mediated by an adenoassociated viral vector显示文摘	All RR Reichel MB0 Thrasher AJ Levinsky R J Kinnon C Kanuga N	1996	Hum Mol Gene1996，5，4：	1
7	Structure and sequence variation at the human leptin receptor gene in lean and obese Pima Indians显示文摘	THOMPSON DB RAVUSSIN E BENNET PH	1997	Hum Mol Gene1997，6，5：	1
8	Identifica- tion of SATB2 as the cleft palate gene on 2q32-q33显示文摘	FitzPatrick DR Carr IM McLaren L	2003	Hum Mol Gene2003，12，19：	1
9	Human mesenchymal stem cells ectopically expressing full-length dystrophin can complement Duchenne muscular dystroph myotubes by cell fusion显示文摘	Goncalves MA de Vries AA Holkers M	2006	Hum Mol Gene2006，15，2：	1
10	NOD1 variation, immunoglobulin E and asthma显示文摘	Hysi P Kabesch M Moffatt MF	2005	Hum Mol Gene2005，14，7：	1
11	A genome-wide associationstudy reveals susceptibility variants for non-small cell lung canc- er in the Korean populatiun显示文摘	Yoon KA Park JH Han J	2010	Hum Mol Gene2010，19，24：	1
12	Mutation in Emery-Dreifuss muscular dystrophy and their effects on emerin protein expression显示文摘	Manial S Recan D Sewry CA	1998	Hum Mol Gene1998，7，：	1
13	A novel frameshift mutation of the mtDNA CO III gene leads to the impaired assembly of cytochrome C oxidase in a patient affected by Leigh-like syndrome 显示文摘	Tiranti V Corona P Greco M	2000	Hum Mol Gene2000，9，18：	1
14	Myotilin is mutated in limb girdle muscular dystrophy lA显示文摘	Michael A Hause Stephen K	2000	Hum Mol Gene2000，9，：	1
15	OPA-1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mito- ehondrial morphology, optic nerve structure and visual function 显示文摘	Davies VJ Hollins AJ Piechota MJ	2007	Hum Mol Gene2007，16，13：	1
16	Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate 显示文摘	YUKO O O TOSHIYUKI M KAZUHIRO O	1999	Hum Mol Gene1999，8，6：	1
17	Mild overexpression of MeCP2 causes a progressive neurological disorder in mice 显示文摘	Ann LC Jonathan ML Alexander PV	2004	Hum Mol Gene2004，13，21：	1
18	Emerging functions of mammalian mitochondri- al fusion and fission显示文摘	Chen H Chan DC	2005	Hum Mol Gene2005，14，2：	1
19	Human mesenchy- mal stem cells ectopically expressing full-length dystrophin can complement Duchenne muscular dystroph myotubes by cell fusion 显示文摘	Gonealves MA de Vries AA Holkers M	2006	Hum Mol Gene2006，15，2：	1
20	Molecular and genetics characterization of sarcospan:insight into sarcoglycan-sarcospan inetractions显示文摘	Achell H Crosbie Leland EL	2000	Hum Mol Gene2000，9，：	1

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