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Acta Neuropathologica Communications|August 21, 2019
Transcriptome clarifies mechanisms of lesion genesis versus progression in models of Ccm3 cerebral cavernous malformationsJanne Koskimäki, Dongdong Zhang, Yan Li, et al.
Nature|April 28, 2021
PIK3CA and CCM mutations fuel cavernomas through a cancer-like mechanismAileen A Ren, Daniel A Snellings, Yourong S Su, et al.
JAMIA Open|January 11, 2021
The case for open science: rare diseasesYaffa R Rubinstein, Peter N Robinson, William A Gahl, et al.
American Journal of Medical Genetics. Part A|January 27, 2010
Overlapping spectra of SMAD4 mutations in juvenile polyposis (JP) and JP-HHT syndromeCarol Gallione, Arthur S Aylsworth, Jill Beis, et al.
The Journal of Experimental Medicine|July 11, 2020
Cerebral cavernous malformations are driven by ADAMTS5 proteolysis of versicanCourtney C Hong, Alan T Tang, Matthew R Detter, et al.
Science Translational Medicine|November 29, 2019
Distinct cellular roles for PDCD10 define a gut-brain axis in cerebral cavernous malformationAlan T Tang, Katie R Sullivan, Courtney C Hong, et al.
Science (New York, N.Y.)|April 29, 2017
Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism NetworkMichael J McConnell, John V Moran, Alexej Abyzov, et al.
Genome Biology|March 30, 2021
Comprehensive identification of somatic nucleotide variants in human brain tissueYifan Wang, Taejeong Bae, Jeremy Thorpe, et al.
Genome Research|October 4, 2003
Development of human protein reference database as an initial platform for approaching systems biology in humansSuraj Peri, J Daniel Navarro, Ramars Amanchy, et al.
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