Results 221 to 230 of about 4,207 (232)
Some of the next articles are maybe not open access.

A novel CCM1/KRIT1 heterozygous deletion mutation (c.1919delT) in a Chinese family with familial cerebral cavernous malformation

Clinical neurology and neurosurgery (Dutch-Flemish ed. Print), 2018
Chenlong Yang   +5 more
semanticscholar   +1 more source

Loss of p53 Sensitizes Mice with a Mutation in Ccm1 (KRIT1) to Development of Cerebral Vascular Malformations

American Journal of Pathology, 2004
Sudha Srinivasan, Douglas A Marchuk
exaly  

High-throughput sequencing of the entire genomic regions of CCM1/KRIT1, CCM2 and CCM3/PDCD10 to search for pathogenic deep-intronic splice mutations in cerebral cavernous malformations.

European Journal of Medical Genetics, 2017
M. Rath   +7 more
semanticscholar   +1 more source

CCM111 prevents hepatic fibrosis via cooperative inhibition of TGF-β, Wnt and STAT3 signaling pathways

Journal of Food and Drug Analysis, 2019
Yi-Shiou Chiou   +2 more
exaly  

Exome capture sequencing identifies a novel CCM1 mutation in a Chinese family with multiple cerebral cavernous malformations

International Journal of Neuroscience, 2016
Chengyuan Mao   +12 more
semanticscholar   +1 more source

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