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The Journal of Investigative Dermatology|April 7, 2023
Gene Expression Signatures in Inflammatory and Sclerotic Morphea Skin and Sera Distinguish Morphea from Systemic SclerosisHenry W Chen, Jane L Zhu, Viktor Martyanov, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosisB A Hosler, G A Nicholson, P C Sapp, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
Subclonal IDH1/2 Mutations as a Targetable Vulnerability in Vascular TumorsDong-Min Yu, Eunice Lee, Gabriel J Starrett, et al.
Journal of Cutaneous Pathology|March 22, 2019
Muir-Torre syndrome appropriate use criteria: Effect of patient age on appropriate use scores, Claudia I Vidal, Angela Sutton, et al.
Journal of Clinical Immunology|December 20, 2019
A Germline Mutation in the C2 Domain of PLCγ2 Associated with Gain-of-Function Expands the Phenotype for PLCG2-Related DiseasesTaylor Novice, Amina Kariminia, Kate L Del Bel, et al.
Nature Genetics|October 5, 2001
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2S Hadano, C K Hand, H Osuga, et al.
Physical Review Letters|September 28, 2010
Ultraintense x-ray induced ionization, dissociation, and frustrated absorption in molecular nitrogenM Hoener, L Fang, O Kornilov, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|July 9, 2008
50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosisWendy J Broom, Matthew Greenway, Ghazaleh Sadri-Vakili, et al.
The Journal of Investigative Dermatology|January 28, 2023
CXCL9 Links Skin Inflammation and Fibrosis through CXCR3-Dependent Upregulation of Col1a1 in FibroblastsJillian M Richmond, Dhrumil Patel, Tomoya Watanabe, et al.
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