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Biorxiv : the Preprint Server for Biology|July 9, 2024
Neuropathologically-directed profiling of PRNP somatic and germline variants in sporadic human prion diseaseGannon A McDonough, Yuchen Cheng, Katherine Morillo, et al.
Nature Aging|September 2, 2022
Somatic mutations in single human cardiomyocytes reveal age-associated DNA damage and widespread oxidative genotoxicitySangita Choudhury, August Yue Huang, Junho Kim, et al.
Neuron|March 9, 2011
The cerebrospinal fluid provides a proliferative niche for neural progenitor cellsMaria K Lehtinen, Mauro W Zappaterra, Xi Chen, et al.
Science (New York, N.Y.)|October 3, 2015
Somatic mutation in single human neurons tracks developmental and transcriptional historyMichael A Lodato, Mollie B Woodworth, Semin Lee, et al.
Cerebral Cortex (New York, N.Y. : 1991)|January 31, 2016
Cc2d1a Loss of Function Disrupts Functional and Morphological Development in Forebrain Neurons Leading to Cognitive and Social DeficitsAdam W Oaks, Marta Zamarbide, Dimira E Tambunan, et al.
Human Genetics|July 26, 2024
Chromosomal structural rearrangements implicate long non-coding RNAs in rare germline disordersRebecca E Andersen, Ibrahim F Alkuraya, Abna Ajeesh, et al.
Medrxiv : the Preprint Server for Health Sciences|July 1, 2024
Rare germline disorders implicate long non-coding RNAs disrupted by chromosomal structural rearrangementsRebecca E Andersen, Ibrahim F Alkuraya, Abna Ajeesh, et al.
Acta Neuropathologica|July 24, 2024
Neuropathologically directed profiling of PRNP somatic and germline variants in sporadic human prion diseaseGannon A McDonough, Yuchen Cheng, Katherine S Morillo, et al.
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