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Kristin D Kernohan

Showing results (1-10 of 73) with videos related to

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Methodsx|July 8, 2015
Three dimensional dual labelled DNA fluorescent in situ hybridization analysis in fixed tissue sectionsKristin D Kernohan, Nathalie G Bérubé
Nature Reviews. Genetics|January 18, 2024
The expanding diagnostic toolbox for rare genetic diseasesKristin D Kernohan, Kym M Boycott
Epigenomics|November 30, 2011
Genetic and epigenetic dysregulation of imprinted genes in the brainKristin D Kernohan, Nathalie G Bérubé
Human Molecular Genetics|December 3, 2014
ATRX promotes gene expression by facilitating transcriptional elongation through guanine-rich coding regionsMichael A Levy, Kristin D Kernohan, Yan Jiang, et al.
Nucleic Acids Research|July 4, 2014
Analysis of neonatal brain lacking ATRX or MeCP2 reveals changes in nucleosome density, CTCF binding and chromatin loopingKristin D Kernohan, Douglas Vernimmen, Gregory B Gloor, et al.
American Journal of Human Genetics|September 18, 2018
ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide VariantsNajmeh Alirezaie, Kristin D Kernohan, Taila Hartley, et al.
Human Molecular Genetics|July 9, 2015
Receptor tyrosine kinase mutations in developmental syndromes and cancer: two sides of the same coinLaura M McDonell, Kristin D Kernohan, Kym M Boycott, et al.
Journal of Human Genetics|July 4, 2018
Periodic breathing in patients with NALCN mutationsDanielle K Bourque, David A Dyment, Ian MacLusky, et al.
Genes|January 21, 2023
A De Novo Missense Variant in <i>TUBG2</i> in a Child with Global Developmental Delay, Microcephaly, Refractory Epilepsy and Perisylvian PolymicrogyriaSalini Thulasirajah, Xueqi Wang, Erick Sell, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 21, 2014
Dual effect of CTCF loss on neuroprogenitor differentiation and survivalL Ashley Watson, Xu Wang, Adrienne Elbert, et al.
Pageof 8

Showing results (1-10 of 73) with videos related to

Sort By:
Pageof 8
Methodsx|July 8, 2015
Three dimensional dual labelled DNA fluorescent in situ hybridization analysis in fixed tissue sectionsKristin D Kernohan, Nathalie G Bérubé
Nature Reviews. Genetics|January 18, 2024
The expanding diagnostic toolbox for rare genetic diseasesKristin D Kernohan, Kym M Boycott
Epigenomics|November 30, 2011
Genetic and epigenetic dysregulation of imprinted genes in the brainKristin D Kernohan, Nathalie G Bérubé
Human Molecular Genetics|December 3, 2014
ATRX promotes gene expression by facilitating transcriptional elongation through guanine-rich coding regionsMichael A Levy, Kristin D Kernohan, Yan Jiang, et al.
Nucleic Acids Research|July 4, 2014
Analysis of neonatal brain lacking ATRX or MeCP2 reveals changes in nucleosome density, CTCF binding and chromatin loopingKristin D Kernohan, Douglas Vernimmen, Gregory B Gloor, et al.
American Journal of Human Genetics|September 18, 2018
ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide VariantsNajmeh Alirezaie, Kristin D Kernohan, Taila Hartley, et al.
Human Molecular Genetics|July 9, 2015
Receptor tyrosine kinase mutations in developmental syndromes and cancer: two sides of the same coinLaura M McDonell, Kristin D Kernohan, Kym M Boycott, et al.
Journal of Human Genetics|July 4, 2018
Periodic breathing in patients with NALCN mutationsDanielle K Bourque, David A Dyment, Ian MacLusky, et al.
Genes|January 21, 2023
A De Novo Missense Variant in <i>TUBG2</i> in a Child with Global Developmental Delay, Microcephaly, Refractory Epilepsy and Perisylvian PolymicrogyriaSalini Thulasirajah, Xueqi Wang, Erick Sell, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 21, 2014
Dual effect of CTCF loss on neuroprogenitor differentiation and survivalL Ashley Watson, Xu Wang, Adrienne Elbert, et al.
Pageof 8