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The Journal of Clinical Investigation|August 30, 2005
Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2Petra Seemann, Raphaela Schwappacher, Klaus W Kjaer, et al.Nature Communications|January 7, 2026
The dorsal aortic compartment is a developmental source of brown adipose tissue in miceSophie Heider, Cornelius Fischer, Ali Kerim Secener, et al.Immunity|May 9, 2023
A local subset of mesenchymal cells expressing the transcription factor Osr1 orchestrates lymph node initiationPedro Vallecillo-García, Mickael Orgeur, Glenda Comai, et al.Nature Communications|February 15, 2024
Neurofibromin 1 controls metabolic balance and Notch-dependent quiescence of murine juvenile myogenic progenitorsXiaoyan Wei, Angelos Rigopoulos, Matthias Lienhard, et al.The Journal of Biological Chemistry|May 27, 2006
Expression of type XXIII collagen mRNA and proteinManuel Koch, Guido Veit, Sigmar Stricker, et al.Plos Genetics|June 21, 2013
Deregulation of the protocadherin gene FAT1 alters muscle shapes: implications for the pathogenesis of facioscapulohumeral dystrophyNathalie Caruso, Balàzs Herberth, Marc Bartoli, et al.Nature Genetics|October 1, 2013
BMP signaling controls muscle massRoberta Sartori, Elija Schirwis, Bert Blaauw, et al.Human Mutation|January 24, 2015
Identification of variants in the 4q35 gene FAT1 in patients with a facioscapulohumeral dystrophy-like phenotypeFrancesca Puppo, Eugenie Dionnet, Marie-Cécile Gaillard, et al.Stem Cell Reports|September 17, 2019
Lgr5 and Col22a1 Mark Progenitor Cells in the Lineage toward Juvenile Articular ChondrocytesChen Feng, Wilson Cheuk Wing Chan, Yan Lam, et al.Life Science Alliance|February 8, 2024
ADAM19 cleaves the PTH receptor and associates with brachydactyly type EAtakan Aydin, Christoph Klenk, Katarina Nemec, et al.Pageof 10