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27篇 您的检索式：作者名="SEMINA EV"

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	题名	作者	年代	出处	被引量
1	A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD显示文摘	Semina EV Ferrell RE Mintz-Hittner HA	1998	Nat Genet1998，19，：	1
2	Antagonistic signals between BMP4 and FGF8 define the expression of Pitxl and Pitx2 in mouse tooth - forming anlage显示文摘	AMAND TR ZHANG Y SEMINA EV	2000	Dev Biol2000，15，：	1
3	A novel home- obox gene PITX3 is mutatedin families with autosomal-dominant cataracts and ASMD显示文摘	Semina EV Ferrell RE Mintz-Hittner HA	1998	Nat Genet1998，19，：	1
4	MIP/Aquaporin 0 represents a direct transcriptional target of PITX3 in the devel- oping lens显示文摘	Sorokina EA Muheisen S Mlodik N Semina EV	2011	PLoS One2011，6，21：	1
5	A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD显示文摘	Semina EV Ferrell RE Mintz-Hittner HA	1998	Nat Genet1998，19，：	1
6	Cloning and characterization of a novel bicoid-related homeobox transcription factor gene,RIEG,involved in Rieger syndrome显示文摘	Semina EV Reiter R Leysens NJ	1996	Nat Genet1996，14，：	1
7	Cloning and characterization of a novel bicoid-related homeobox transcription factor gene,RIEG,involved in Rieger syndrome显示文摘	Semina EV Reiter R Leysens NJ		0，，04：	1
8	Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome 显示文摘	Semina EV Reiter R Leysens N J Alward WL Small KW Datson NA	1996	Nat Genet1996，14，4：	1
9	Current molecular understanding of Axenfeld Rieger syndrome 显示文摘	Hjah TA Semina EV	2005	Expert Rev Mol Med2005，7，25：	1
10	Cloning and character- ization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in rieger syndrome 显示文摘	Semina EV Reiter R Leysens N J	1996	Nat Genet1996，14，4：	1
11	Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene 显示文摘	El-Shanti H Murray JC Semina EV	1998	Eur J Hum Genet1998，6，3：	1
12	A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD显示文摘	Semina EV Ferrell RE Mintz-Hittner HA	1998	Nature Genet1998，19，：	1
13	Analysis of FOXD3 sequence variation in hu- man ocular disease 显示文摘	KLOSS BA REIS LM BREMOND-GIGNAC D GLASER T SEMINA EV	2012	Mol Vis2012，18，：	1
14	Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia 显示文摘	BREMOND-GIGNAC D BITOUN P REIS LM COPIN H MUR- RAY JC SEMINA EV	2010	Mol Vis2010，16，：	1
15	Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/ PITX2 ) gene显示文摘	ALWARD WL SEMINA EV KALENAK JW HI'ON E SHETH BP STONE EM	1998	Am J Ophthalmol1998，125，1：	1
16	Current molecular understanding of Axenfeld-Rieger syndrome显示文摘	Hjalt TA Semina EV	2005	Expert Rev Mol Med2005，7，25：	1
17	pitx2 Deficiency results in abnormal ocular and craniofacial development in zebrafish显示文摘	Liu Y Semina EV		0，，01：	1
18	Current molecular understanding of Axenfeld- Rieger syndrome 显示文摘	Hjalt TA Semina EV	2005	Expert Rev Mol Med2005，7，25：	1
19	Assignment of gene re- sponsible for progressive pseudorheumatoid dysplasia to chromo- some 6 and examination of COL10A1 as candidate gene显示文摘	el-Shanti H Murray JC Semina EV	1998	Eur J Hum Genet1998，6，3：	1
20	Peculiarities of transfer of acetylene and methane through films based on sulfonate-containing poly - m - phenylisophalamides显示文摘	Kirsh Yu E Vorob' ev A V Semina N V	1997	Russian Journal of Physical Chemistry1997，71，5：	1

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