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Genome Research|September 3, 2013
Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutationsDaniel M Ibrahim, Peter Hansen, Christian Rödelsperger, et al.American Journal of Human Genetics|December 21, 2010
Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosisEva Klopocki, Silke Lohan, Francesco Brancati, et al.Plos One|January 5, 2011
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysisBernd Timmermann, Martin Kerick, Christina Roehr, et al.Plos Genetics|December 4, 2009
Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGINPetra Seemann, Anja Brehm, Jana König, et al.Clinical Orthopaedics and Related Research|May 8, 2023
Most Fractures Treated Nonoperatively in Individuals With Fibrodysplasia Ossificans Progressiva Heal With a Paucity of Flareups, Heterotopic Ossification, and Loss of MobilityCarter M Lindborg, Mona Al Mukaddam, Genevieve Baujat, et al.Human Mutation|December 17, 2008
Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1Frederick S Kaplan, Meiqi Xu, Petra Seemann, et al.Cardiovascular Research|March 8, 2023
Clinical and prognostic associations of autoantibodies recognizing adrenergic/muscarinic receptors in patients with heart failureGeorge Markousis-Mavrogenis, Waldemar B Minich, Ali A Al-Mubarak, et al.Nature Genetics|August 4, 2009
Mutations in PYCR1 cause cutis laxa with progeroid featuresBruno Reversade, Nathalie Escande-Beillard, Aikaterini Dimopoulou, et al.Pageof 5