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Christopher A Walsh

Showing results (191-200 of 337) with videos related to

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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 <i>PRNP</i> 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.
Clinical Chemistry|September 29, 2007
Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalanceYiping Shen, Mira Irons, David T Miller, 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.
Elife|August 23, 2015
Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplicationAndrew Kodani, Timothy W Yu, Jeffrey R Johnson, 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.
Pageof 34

Showing results (191-200 of 337) with videos related to

Sort By:
Pageof 34
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 <i>PRNP</i> 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.
Clinical Chemistry|September 29, 2007
Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalanceYiping Shen, Mira Irons, David T Miller, 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.
Elife|August 23, 2015
Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplicationAndrew Kodani, Timothy W Yu, Jeffrey R Johnson, 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.
Pageof 34