Claire Farrington‐Rock

Ciliary Abnormalities Due to Defects in the Retrograde Transport Protein DYNC2H1 in Short-Rib Polydactyly Syndrome

Amy E. Merrill, Barry Merriman, Claire Farrington‐Rock et al. · The American Journal of Human Genetics · 2009 · 167 citations · Full text

Genetic Disorder, Short-rib Polydactyly Syndrome, Genetics +6

A molecular and clinical study of Larsen syndrome caused by mutations in <i>FLNB</i>

Louise S. Bicknell, Claire Farrington‐Rock, Yousef Shafeghati et al. · Journal of Medical Genetics · 2006 · 125 citations · Full text

Mutations in two regions of<i>FLNB</i>result in atelosteogenesis I and III

Claire Farrington‐Rock, Marc H. Firestein, Louise S. Bicknell et al. · Human Mutation · 2006 · 72 citations

Sclerostin, Exon 28, Genetics +18

Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome

Claire Farrington‐Rock, Veneta T. Kirilova, Lisa Dillard‐Telm et al. · Human Molecular Genetics · 2007 · 64 citations · Full text

Mice Phenocopies, Sclerostin, Genetics +17

Bisindolylmaleimide I Suppresses Fibroblast Growth Factor-mediated Activation of Erk MAP Kinase in Chondrocytes by Preventing Shp2 Association with the Frs2 and Gab1 Adaptor Proteins

Pavel Krejčı́, Bernard Masri, Lisa Salazar et al. · Journal of Biological Chemistry · 2006 · 36 citations · Full text