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20篇 您的检索式：作者名="Nishimura DY"

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	题名	作者	年代	出处	被引量
1	Linkage of an autosomal dominant clefting syndrome (Van Der Woude) to loci on chromosome lq显示文摘	Murray JC Nishimura DY Buetow KH	1990	Am J Hunt Genet1990，46，3：	1
2	Linkage of an autosomal dominant clefting syndrome (van Der Woude) to loci on chromosome Iq显示文摘	Murray JC Nishimura DY Buetow KH	1990	Am J Hum Genet1990，46，3：	1
3	Recognition of N-acetylchitooligosaccharide elicitor by rice protoplasts显示文摘	Nishimura N Tanabe S He DY		0，，12：	1
4	The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25 显示文摘	Nishimura DY Swiderski RE Alward WLM	1998	Nat Genet1998，19，7：	1
5	A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye 显示文摘	Nishimura DY Searby CC Alward WL	2001	Am J Hum Genet2001，68，2：	1
6	Reduction of ER stress via a chemical chaperone prevents disease phenotypes in a mouse model of primary open angle glaucoma显示文摘	Zode GS Kuehn MH Nishimura DY	2011	J Clin Invest2011，121，9：	1
7	Reduction of ER stress via a chemical chaperone prevents disease phenotypes in a mouse model of primary open angle glaucoma显示文摘	Zode GS Kuehn MH Nishimura DY	2011	J Clin Invest2011，121，9：	1
8	Optimal procedure for extracting RNA from human ocular tissues and expression profiling of the congenital glaucoma gene FOXC1 using quantitative RT-PCR显示文摘	Wang WH Mcnatt LG Shepard AR Jacobson N Nishimura DY Stone EM	2001	Mol Vis2001，7，：	1
9	Linkage localization of TGFB2 and the human homeobox gene HLX1 to chromosome 1q 显示文摘	Nishimura DY Purchio AF Murray JC	1993	Genetics1993，15，：	1
10	Novel approaches to linkage mapping显示文摘	Sheffield VC Nishimura DY Stone EM	1995	Curr Opin Genet Dev1995，5，3：	1
11	Identification and functional analysis of the vision-specific BBS3 (ARL6) long isoform显示文摘	Pretorius PR Baye LM Nishimura DY	2010	PLoS Genet2010，6，10：	1
12	Linkage local- ization of TGFB2 and the human homeobox gene HLXI to chromosome lq显示文摘	Nishimura DY Purchio AF Murray JC	1993	Genomics1993，15，2：	1
13	Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq显示文摘	Murray JC Nishimura DY Buetow Kid	1990	AmJ Hum Genet1990，46，3：	1
14	Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)显示文摘	Nishimura DY Searby CC Carmi R	2001	Hum Mol Genet2001，10，：	1
15	Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome 显示文摘	Mykytyn K Nishimura DY Searby CC	2002	Nat Genet2002，31，：	1
16	The forkheadtranscription factor gene FKHL7 is responsible for glaucoma pheno-types which map to 6p25显示文摘	Nishimura DY Swiderski RE Alward WL	1998	Nat Genet1998，19，2：	1
17	Comparative genomics and gene expression analysis identifies BBS9,a new Bardet-Biedl syndrome gene显示文摘	Nishimura DY Swiderski RE Searby CC	2005	Am J Hum Genet2005，77，6：	1
18	Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq显示文摘	Murray JC Nishimura DY Buetow KH	1990	Am J Hum Genet1990，46，3：	1
19	Identifica- tion of the gene ( BBS1 ) most commonly involved in Bar- det-Biedl syndrome, a complex human obesity syndrome 显示文摘	Mykytyn K Nishimura DY Searby CC	2002	Nat Genet2002，，4：	1
20	The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25 显示文摘	Nishimura DY Swiderski RE Alward WL	1998	Nat Genet1998，19，2：	1

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