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Journal of Cellular Physiology|March 26, 2014
N-cadherin/wnt interaction controls bone marrow mesenchymal cell fate and bone mass during agingEric Haÿ, François-Xavier Dieudonné, Zuzana Saidak, et al.
The Biochemical Journal|March 15, 1985
Characterization and metabolic regulation of a liver-specific 5.4-kilobase mRNA whose synthesis is transcriptionally induced by carbohydrates and repressed by glucagon and cyclic AMPA L Pichard, A Munnich, M C Meienhofer, et al.
Nature|August 20, 1992
Point mutation of an FGF receptor abolishes phosphatidylinositol turnover and Ca2+ flux but not mitogenesisK G Peters, J Marie, E Wilson, et al.
The Journal of Clinical Investigation|July 4, 2003
Enhancing DNA vaccine potency by coadministration of DNA encoding antiapoptotic proteinsTae Woo Kim, Chien-Fu Hung, Morris Ling, et al.
The Journal of Biological Chemistry|June 11, 2015
Increased NF-κB Activity and Decreased Wnt/β-Catenin Signaling Mediate Reduced Osteoblast Differentiation and Function in ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) MiceCarole Le Henaff, Rafik Mansouri, Dominique Modrowski, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 22, 2009
Priming integrin alpha5 promotes human mesenchymal stromal cell osteoblast differentiation and osteogenesisZahia Hamidouche, Olivia Fromigué, Jochen Ringe, et al.
Diabetes & Metabolism|December 22, 2005
Impact of high- and low-intensity targeted exercise training on the type of substrate utilization in obese boys submitted to a hypocaloric dietF Brandou, A M Savy-Pacaux, J Marie, et al.
Bone|February 14, 2012
Different sympathetic pathways control the metabolism of distinct bone envelopesCaroline Bataille, Cédric Mauprivez, Eric Haÿ, et al.
Gene|April 2, 2013
ErbB3 silencing reduces osteosarcoma cell proliferation and tumor growth in vivoNicolas Jullien, François-Xavier Dieudonné, Nadia Habel, et al.
American Journal of Medical Genetics|April 1, 1983
Panostotic fibrous dysplasia: a congenital disorder of bone with unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemiaD E Cole, F C Fraser, F H Glorieux, et al.
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