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Andrew J Copp

Showing results (101-110 of 153) with videos related to

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The Journal of Clinical Investigation|December 4, 2019
Impaired folate 1-carbon metabolism causes formate-preventable hydrocephalus in glycine decarboxylase-deficient miceChloe Santos, Yun Jin Pai, M Raasib Mahmood, et al.
Stem Cell Reports|November 25, 2021
Rescuing human fetal tissue research in the United States: A call for additional regulatory reformKatherine E MacDuffie, Insoo Hyun, Michaela M Krogen, et al.
Molecular Genetics and Metabolism|May 18, 2024
AAV-mediated expression of mouse or human GLDC normalises metabolic biomarkers in a GLDC-deficient mouse model of Non-Ketotic HyperglycinemiaKit-Yi Leung, Chloe Santos, Sandra C P De Castro, et al.
Human Molecular Genetics|December 25, 2002
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouseJennifer N Murdoch, Deborah J Henderson, Kit Doudney, et al.
Disease Models & Mechanisms|March 18, 2026
Chiari II brain malformation is secondary to open spina bifidaMaryam Clark, Timothy J Edwards, Dawn Savery, et al.
Human Molecular Genetics|August 30, 2008
Gene-environment interactions in the causation of neural tube defects: folate deficiency increases susceptibility conferred by loss of Pax3 functionKatie A Burren, Dawn Savery, Valentina Massa, et al.
Developmental Biology|February 6, 2018
Neural tube closure depends on expression of Grainyhead-like 3 in multiple tissuesSandra C P De Castro, Caroline S Hirst, Dawn Savery, et al.
Disease Models & Mechanisms|March 29, 2018
Vangl2 disruption alters the biomechanics of late spinal neurulation leading to spina bifida in mouse embryosGabriel L Galea, Oleksandr Nychyk, Matteo A Mole, et al.
Development (Cambridge, England)|June 14, 2013
Syndecan 4 interacts genetically with Vangl2 to regulate neural tube closure and planar cell polarityNoelia Escobedo, Osvaldo Contreras, Rosana Muñoz, et al.
Development (Cambridge, England)|September 27, 2023
Caudal Fgfr1 disruption produces localised spinal mis-patterning and a terminal myelocystocele-like phenotype in miceEirini Maniou, Faduma Farah, Abigail R Marshall, et al.
Pageof 16

Showing results (101-110 of 153) with videos related to

Sort By:
Pageof 16
The Journal of Clinical Investigation|December 4, 2019
Impaired folate 1-carbon metabolism causes formate-preventable hydrocephalus in glycine decarboxylase-deficient miceChloe Santos, Yun Jin Pai, M Raasib Mahmood, et al.
Stem Cell Reports|November 25, 2021
Rescuing human fetal tissue research in the United States: A call for additional regulatory reformKatherine E MacDuffie, Insoo Hyun, Michaela M Krogen, et al.
Molecular Genetics and Metabolism|May 18, 2024
AAV-mediated expression of mouse or human GLDC normalises metabolic biomarkers in a GLDC-deficient mouse model of Non-Ketotic HyperglycinemiaKit-Yi Leung, Chloe Santos, Sandra C P De Castro, et al.
Human Molecular Genetics|December 25, 2002
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouseJennifer N Murdoch, Deborah J Henderson, Kit Doudney, et al.
Disease Models & Mechanisms|March 18, 2026
Chiari II brain malformation is secondary to open spina bifidaMaryam Clark, Timothy J Edwards, Dawn Savery, et al.
Human Molecular Genetics|August 30, 2008
Gene-environment interactions in the causation of neural tube defects: folate deficiency increases susceptibility conferred by loss of Pax3 functionKatie A Burren, Dawn Savery, Valentina Massa, et al.
Developmental Biology|February 6, 2018
Neural tube closure depends on expression of Grainyhead-like 3 in multiple tissuesSandra C P De Castro, Caroline S Hirst, Dawn Savery, et al.
Disease Models & Mechanisms|March 29, 2018
Vangl2 disruption alters the biomechanics of late spinal neurulation leading to spina bifida in mouse embryosGabriel L Galea, Oleksandr Nychyk, Matteo A Mole, et al.
Development (Cambridge, England)|June 14, 2013
Syndecan 4 interacts genetically with Vangl2 to regulate neural tube closure and planar cell polarityNoelia Escobedo, Osvaldo Contreras, Rosana Muñoz, et al.
Development (Cambridge, England)|September 27, 2023
Caudal Fgfr1 disruption produces localised spinal mis-patterning and a terminal myelocystocele-like phenotype in miceEirini Maniou, Faduma Farah, Abigail R Marshall, et al.
Pageof 16