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Experimental Eye Research
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October 17, 2012
Zebrafish hmx1 promotes retinogenesis
Gaëlle Boisset, Daniel F Schorderet
Plos One
|
June 20, 2014
A dimerized HMX1 inhibits EPHA6/epha4b in mouse and zebrafish retinas
Fabienne Marcelli, Gaëlle Boisset, Daniel F Schorderet
Gene Expression Patterns : GEP
|
June 19, 2008
Characterization of pip5k3 fleck corneal dystrophy-linked gene in zebrafish
Gaëlle Boisset, Bożena K Polok, Daniel F Schorderet
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
October 3, 2006
Biological characterization of gene response in Rpe65-/- mouse model of Leber's congenital amaurosis during progression of the disease
Sandra Cottet, Lydia Michaut, Gaëlle Boisset, et al.
American Journal of Human Genetics
|
January 4, 2011
Mutations in the SPARC-related modular calcium-binding protein 1 gene, SMOC1, cause waardenburg anophthalmia syndrome
Hana Abouzeid, Gaëlle Boisset, Tatiana Favez, et al.
American Journal of Human Genetics
|
April 22, 2008
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome
Daniel F Schorderet, Olivia Nichini, Gaëlle Boisset, et al.
Cardiovascular Research
|
February 10, 2016
Comparative transcriptome profiling of the injured zebrafish and mouse hearts identifies miRNA-dependent repair pathways
Stefania Crippa, Mohamed Nemir, Samir Ounzain, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Experimental Eye Research
|
October 17, 2012
Zebrafish hmx1 promotes retinogenesis
Gaëlle Boisset, Daniel F Schorderet
Plos One
|
June 20, 2014
A dimerized HMX1 inhibits EPHA6/epha4b in mouse and zebrafish retinas
Fabienne Marcelli, Gaëlle Boisset, Daniel F Schorderet
Gene Expression Patterns : GEP
|
June 19, 2008
Characterization of pip5k3 fleck corneal dystrophy-linked gene in zebrafish
Gaëlle Boisset, Bożena K Polok, Daniel F Schorderet
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
October 3, 2006
Biological characterization of gene response in Rpe65-/- mouse model of Leber's congenital amaurosis during progression of the disease
Sandra Cottet, Lydia Michaut, Gaëlle Boisset, et al.
American Journal of Human Genetics
|
January 4, 2011
Mutations in the SPARC-related modular calcium-binding protein 1 gene, SMOC1, cause waardenburg anophthalmia syndrome
Hana Abouzeid, Gaëlle Boisset, Tatiana Favez, et al.
American Journal of Human Genetics
|
April 22, 2008
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome
Daniel F Schorderet, Olivia Nichini, Gaëlle Boisset, et al.
Cardiovascular Research
|
February 10, 2016
Comparative transcriptome profiling of the injured zebrafish and mouse hearts identifies miRNA-dependent repair pathways
Stefania Crippa, Mohamed Nemir, Samir Ounzain, et al.
Page
of 1