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Brain & Development|May 29, 2004
Etiological heterogeneity of familial periventricular heterotopia and hydrocephalusVolney L Sheen, Lina Basel-Vanagaite, Jean R Goodman, et al.
Neuron|April 20, 2010
The apical complex couples cell fate and cell survival to cerebral cortical developmentSeonhee Kim, Maria K Lehtinen, Alessandro Sessa, et al.
BMC Research Notes|December 15, 2011
Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2Claudia Di Blasi, Emanuela Bellafiore, Mustafa Am Salih, et al.
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.
Rapid Communications in Mass Spectrometry : RCM|June 14, 2026
Toward Metabolomics Analyses With Combined Capillary Vibrating Sharp-Edge Spray Ionization and Atmospheric Pressure Chemical IonizationMadison Pursell, Adefolake Ojanuga, Chandrima Banerjee, 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.
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