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The Journal of Clinical Endocrinology and Metabolism|December 25, 2019
Functional Analysis of the SIM1 Variant p.G715V in 2 Patients With ObesityPatrick R Blackburn, Adrienne E Sullivan, Alexis G Gerassimou, et al.
Human Molecular Genetics|July 13, 2016
Identification of genetic modifiers of age-at-onset for familial Parkinson's diseaseErin M Hill-Burns, Owen A Ross, William T Wissemann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 4, 2009
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's diseaseKenya Nishioka, Mounir Kefi, Barbara Jasinska-Myga, et al.
Brain Communications|January 11, 2021
Variants in PPP2R2B and IGF2BP3 are associated with higher tau depositionVijay K Ramanan, Xuewei Wang, Scott A Przybelski, et al.
Plos One|October 3, 2013
NOTCH3 variants and risk of ischemic strokeOwen A Ross, Alexandra I Soto-Ortolaza, Michael G Heckman, et al.
Molecular Neurodegeneration Advances|June 22, 2026
miRNA family miR-29 inhibits PINK1-PRKN signaling via ATG9ABriana N Markham, Chloe Ramnarine, Songeun Kim, et al.
Acta Neuropathologica Communications|December 8, 2020
MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical featuresRebecca R Valentino, Shunsuke Koga, Ronald L Walton, et al.
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