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Laetitia Magnol

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

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Open Biology|September 16, 2016
Reduced Notch signalling leads to postnatal skeletal muscle hypertrophy in Pofut1cax/cax miceBilal Al Jaam, Katy Heu, Florian Pennarubia, et al.
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids|July 6, 2017
Myostatin deficiency is associated with lipidomic abnormalities in skeletal musclesNarjes Baati, Christine Feillet-Coudray, Gilles Fouret, et al.
Plos One|November 29, 2007
Proteomic shifts in embryonic stem cells with gene dose modifications suggest the presence of balancer proteins in protein regulatory networksLei Mao, Claus Zabel, Marion Herrmann, et al.
BMC Developmental Biology|July 7, 2007
KIT is required for hepatic function during mouse post-natal developmentLaetitia Magnol, Marie-Clémence Chevallier, Valérie Nalesso, et al.
Human Molecular Genetics|September 29, 2009
A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndromePatricia Lopes Pereira, Laetitia Magnol, Ignasi Sahún, 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.
Open Biology|September 16, 2016
Reduced Notch signalling leads to postnatal skeletal muscle hypertrophy in Pofut1cax/cax miceBilal Al Jaam, Katy Heu, Florian Pennarubia, et al.
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids|July 6, 2017
Myostatin deficiency is associated with lipidomic abnormalities in skeletal musclesNarjes Baati, Christine Feillet-Coudray, Gilles Fouret, et al.
Plos One|November 29, 2007
Proteomic shifts in embryonic stem cells with gene dose modifications suggest the presence of balancer proteins in protein regulatory networksLei Mao, Claus Zabel, Marion Herrmann, et al.
BMC Developmental Biology|July 7, 2007
KIT is required for hepatic function during mouse post-natal developmentLaetitia Magnol, Marie-Clémence Chevallier, Valérie Nalesso, et al.
Human Molecular Genetics|September 29, 2009
A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndromePatricia Lopes Pereira, Laetitia Magnol, Ignasi Sahún, et al.
Pageof 2