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Nathalie Scamuffa

Showing results (11-20 of 15) with videos related to

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Plos One|July 14, 2010
Zebrafish ProVEGF-C expression, proteolytic processing and inhibitory effect of unprocessed ProVEGF-C during fin regenerationAbdel-Majid Khatib, Rachid Lahlil, Nathalie Scamuffa, et al.
Nature|December 6, 2002
Numerous potentially functional but non-genic conserved sequences on human chromosome 21Emmanouil T Dermitzakis, Alexandre Reymond, Robert Lyle, et al.
Nature|December 6, 2002
Human chromosome 21 gene expression atlas in the mouseAlexandre Reymond, Valeria Marigo, Murat B Yaylaoglu, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2002
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesiaLucia Bartoloni, Jean-Louis Blouin, Yanzhen Pan, et al.
Human Molecular Genetics|October 24, 2002
The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitroMichel Guipponi, Grégoire Vuagniaux, Marie Wattenhofer, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Plos One|July 14, 2010
Zebrafish ProVEGF-C expression, proteolytic processing and inhibitory effect of unprocessed ProVEGF-C during fin regenerationAbdel-Majid Khatib, Rachid Lahlil, Nathalie Scamuffa, et al.
Nature|December 6, 2002
Numerous potentially functional but non-genic conserved sequences on human chromosome 21Emmanouil T Dermitzakis, Alexandre Reymond, Robert Lyle, et al.
Nature|December 6, 2002
Human chromosome 21 gene expression atlas in the mouseAlexandre Reymond, Valeria Marigo, Murat B Yaylaoglu, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2002
Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesiaLucia Bartoloni, Jean-Louis Blouin, Yanzhen Pan, et al.
Human Molecular Genetics|October 24, 2002
The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitroMichel Guipponi, Grégoire Vuagniaux, Marie Wattenhofer, et al.
Pageof 2