Catherine Benoist-Lasselin

ADAMTS10 Mutations in Autosomal Recessive Weill-Marchesani Syndrome

Nathalie Dagoneau, Catherine Benoist-Lasselin, Céline Huber et al. · The American Journal of Human Genetics · 2004 · 278 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +4

Evaluation of the Therapeutic Potential of a CNP Analog in a Fgfr3 Mouse Model Recapitulating Achondroplasia

Florence Lorget, Nabil Kaci, Jeff Peng et al. · The American Journal of Human Genetics · 2012 · 199 citations · Full text

Regenerative Medicine, Therapeutic Potential, Cnp Analog +8

Spatio-temporal expression of FGFR 1, 2 and 3 genes during human embryo-fetal ossification

Anne‐Lise Delezoide, Catherine Benoist-Lasselin, Laurence Legeai‐Mallet et al. · Mechanisms of Development · 1998 · 177 citations

Mechanobiology, Developmental Biology, Spatio-temporal Expression +9

Fibroblast Growth Factor Receptor 3 Mutations Promote Apoptosis but Do Not Alter Chondrocyte Proliferation in Thanatophoric Dysplasia

Laurence Legeai‐Mallet, Catherine Benoist-Lasselin, Anne‐Lise Delezoide et al. · Journal of Biological Chemistry · 1998 · 137 citations · Full text

Tyrosine kinase inhibitor NVP-BGJ398 functionally improves FGFR3-related dwarfism in mouse model

Davide Komla‐Ebri, Emilie Dambroise, Ina Krämer et al. · Journal of Clinical Investigation · 2016 · 106 citations · Full text

Fgfr3-related Dwarfism, Excessive Fgfr3 Activation, Developmental Biology +14