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49篇 您的检索式：作者名="Roessler E"

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	题名	作者	年代	出处	被引量
1	Reciprocal mouse and human limb phenotypes caused by gainand loss-of-function mutations affecting lmbr1显示文摘	Clark R M Marker P C Roessler E	2001	Genetics2001，159，2：	1
2	Missense substitutions in the GAS1 protein present in holoproseneephaly patients reduce the af-finity for its ligand, SHH 显示文摘	Pineda-Alvarez DE Roessler E Hu P	2012	Hum Genet2012，131，2：	1
3	Genetic transformation of the diatomsCyclotella cryptica andNavicula saprophila显示文摘	Dunahay T G Jarvis E E Roessler P G	1995	Journal of Phycology1995，31，6：	1
4	Genetic transformation of the diatoms Cyclotella cryptica and Navicula saprophila显示文摘	Dunahay T G Jarvis E E Roessler P G	1995	J Phycol1995，31，：	1
5	RAPAd System显示文摘	Anderson R D Haskell R E Xia H Roessler B J Davidson B L	2000	Gene Ther2000，7，：	1
6	Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly显示文摘	Belloni E Muenke M Roessler E	1996	Nat Genet1996，14，3：	1
7	HT29-MTX/Caco-2 cocultures as an in vitro model for the intestinal epithelium: in vitro-in vivo correlation with permeability data from rats and humans显示文摘	Walter E Janich S Roessler BJ	1996	J Pharm Sci1996，85，10：	1
8	Association of adrenal medullar and cortical nodular hyperplasia : a report of two cases with clinical and vaorph-functional considerations 显示文摘	Valdes G Roessler E Salazar I	2006	Endocrine2006，30，3：	1
9	Reciprocal mouse and human limb phenotypes caused by gain- and loss-of-function mutations affecting lmbr1显示文摘	Clark R M Marker P C Roessler E	2001	Genetics2001，159，2：	1
10	Loss-of-functionmutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features显示文摘	ROESSLER E DU Y Z MULLOR J L	2003	Proc Natl Acad Sci USA2003，100，13：	1
11	The genomic structure, chromosomal localization, and analysis of S1L as a candidate gene for holoprosencephaly显示文摘	Karkera JD lzraeli S Roessler E	2002	Cytogenet Genome Res2002，97，：	1
12	Association of adrenal medullar and cortical nodular hyperplasia: a report of two cases with clinical and morpho-functional considerations 显示文摘	Valdes G Roessler E Salazar I	2006	Endocrine2006，30，：	1
13	The genomic structure,chromosome location,and analysis of the human DKK1head inducer gene as a candidate for holoprosencephaly显示文摘	ROESSLER E DU Y GLINKA A	2000	Cytogenet Cell Genet2000，89，34：	1
14	Mutations in the hum an sonic hedgehog gene cause holoprosencephaly显示文摘	Bellonic E Gaudenz K	1996	Nat Genet1996，14，3：	1
15	Human development disorders and the sonic hedgehog pathway显示文摘	Roessler E Muebke M	1998	Mol Med Today1998，4，8：	1
16	Mutation in PATCHED-1,the receptor for SONIC HEDGEHOG,are associated with holoprosencephaly显示文摘	Ming JE Kaupas ME Roessler E		0，，04：	1
17	Human developmental disorders and the sonic hedgehog pathway显示文摘	MING J E ROESSLER E MUENKE M	1998	Mol Med Today1998，4，8：	1
18	Loss-of-function mutations in the EGF-CFC gene CFC1are associated with human left-right laterality defects显示文摘	Bamford RN Roessler E Burdine RD	2000	Nat Genet2000，26，3：	1
19	Loss-of-function mutations in growth differentiation factor-1 (GDF1) are associated with congenital heart defects in humans 显示文摘	Karkera JD Lee JS Roessler E	2007	Am J Hum Genet2007，81，5：	1
20	Induced pluripotent stem cell technology and Direct Conversion:New Possibilities to Study and Treat Parkinson's Disease显示文摘	Roessler R Boddeke E Copray S	2013	Stem Cell Rev and Rep2013，9，4：	1

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