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Neuron
|
April 20, 2010
The apical complex couples cell fate and cell survival to cerebral cortical development
Seonhee 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 LAMA2
Claudia 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 disease
Gannon 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 genotoxicity
Sangita Choudhury, August Yue Huang, Junho Kim, et al.
Neuron
|
March 9, 2011
The cerebrospinal fluid provides a proliferative niche for neural progenitor cells
Maria 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 imbalance
Yiping 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 history
Michael 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 duplication
Andrew 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 Deficits
Adam 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 disorders
Rebecca E Andersen, Ibrahim F Alkuraya, Abna Ajeesh, et al.
Page
of 34
Search research articles
Search
Showing results (191-200 of 337) with videos related to
Sort By:
Page
of 34
Neuron
|
April 20, 2010
The apical complex couples cell fate and cell survival to cerebral cortical development
Seonhee 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 LAMA2
Claudia 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 disease
Gannon 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 genotoxicity
Sangita Choudhury, August Yue Huang, Junho Kim, et al.
Neuron
|
March 9, 2011
The cerebrospinal fluid provides a proliferative niche for neural progenitor cells
Maria 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 imbalance
Yiping 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 history
Michael 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 duplication
Andrew 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 Deficits
Adam 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 disorders
Rebecca E Andersen, Ibrahim F Alkuraya, Abna Ajeesh, et al.
Page
of 34