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Philip Stanier

Showing results (41-50 of 69) with videos related to

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Human Genetics|October 18, 2002
Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene regionDavid Monk, Louise Bentley, Megan Hitchins, et al.
Human Molecular Genetics|April 18, 2003
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same markPhilippe Arnaud, David Monk, Megan Hitchins, et al.
Brain : a Journal of Neurology|April 18, 2007
Abnormal folate metabolism in foetuses affected by neural tube defectsLouisa P E Dunlevy, Lyn S Chitty, Katie A Burren, et al.
Human Molecular Genetics|October 11, 2002
Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patientsClaire Braybrook, Steven Lisgo, Kit Doudney, et al.
American Journal of Human Genetics|March 27, 2012
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weightMiho Ishida, David Monk, Andrew J Duncan, et al.
Human Molecular Genetics|July 4, 2002
Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32Kazuhiko Nakabayashi, Louise Bentley, Megan P Hitchins, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 5, 2013
Is LMNB1 a susceptibility gene for neural tube defects in humans?Alexis Robinson, Darren Partridge, Ashraf Malhas, et al.
Human Molecular Genetics|September 7, 2018
Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in miceSandra C P De Castro, Peter Gustavsson, Abigail R Marshall, et al.
Human Molecular Genetics|April 11, 2018
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20Dale Bryant, Yang Liu, Sanchari Datta, et al.
The Journal of Investigative Dermatology|May 11, 2012
Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal developmentVeronica A Kinsler, Sayeda Abu-Amero, Peter Budd, et al.
Pageof 7

Showing results (41-50 of 69) with videos related to

Sort By:
Pageof 7
Human Genetics|October 18, 2002
Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene regionDavid Monk, Louise Bentley, Megan Hitchins, et al.
Human Molecular Genetics|April 18, 2003
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same markPhilippe Arnaud, David Monk, Megan Hitchins, et al.
Brain : a Journal of Neurology|April 18, 2007
Abnormal folate metabolism in foetuses affected by neural tube defectsLouisa P E Dunlevy, Lyn S Chitty, Katie A Burren, et al.
Human Molecular Genetics|October 11, 2002
Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patientsClaire Braybrook, Steven Lisgo, Kit Doudney, et al.
American Journal of Human Genetics|March 27, 2012
Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weightMiho Ishida, David Monk, Andrew J Duncan, et al.
Human Molecular Genetics|July 4, 2002
Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32Kazuhiko Nakabayashi, Louise Bentley, Megan P Hitchins, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 5, 2013
Is LMNB1 a susceptibility gene for neural tube defects in humans?Alexis Robinson, Darren Partridge, Ashraf Malhas, et al.
Human Molecular Genetics|September 7, 2018
Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in miceSandra C P De Castro, Peter Gustavsson, Abigail R Marshall, et al.
Human Molecular Genetics|April 11, 2018
SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20Dale Bryant, Yang Liu, Sanchari Datta, et al.
The Journal of Investigative Dermatology|May 11, 2012
Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal developmentVeronica A Kinsler, Sayeda Abu-Amero, Peter Budd, et al.
Pageof 7