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Andrew J Copp

Showing results (141-150 of 153) with videos related to

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Magnetic Resonance in Medicine|March 18, 2014
Diffusion microscopic MRI of the mouse embryo: Protocol and practical implementation in the splotch mouse modelFrancesca C Norris, Bernard M Siow, Jon O Cleary, et al.
Developmental Biology|December 12, 2022
Synchronisation of apical constriction and cell cycle progression is a conserved behaviour of pseudostratified neuroepithelia informed by their tissue geometryIoakeim Ampartzidis, Christoforos Efstathiou, Francesco Paonessa, et al.
Ebiomedicine|August 16, 2023
Folate deficiency increases the incidence of dolutegravir-associated foetal defects in a mouse pregnancy modelHaneesha Mohan, Jessica Nguyen, Ben MacKenzie, et al.
Human Molecular Genetics|June 26, 2023
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephaloceleZoe Crane-Smith, Sandra C P De Castro, Evanthia Nikolopoulou, et al.
Current Biology : CB|July 5, 2003
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseJohn A Curtin, Elizabeth Quint, Vicky Tsipouri, et al.
Human Molecular Genetics|January 26, 2011
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouseMadeleine R Brouns, Sandra C P De Castro, Els A Terwindt-Rouwenhorst, et al.
Human Molecular Genetics|December 23, 2006
The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formationHelen R Dawe, Ursula M Smith, Andrew R Cullinane, et al.
AJNR. American Journal of Neuroradiology|February 15, 2024
International Consensus Statement on the Radiological Evaluation of Dysraphic Malformations of the Spine and Spinal CordAnkit Balani, Jai Sidpra, Sniya Sudhakar, et al.
Human Molecular Genetics|April 8, 2006
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migrationSilvia Paracchini, Ankur Thomas, Sandra Castro, et al.
Cell Reports|January 18, 2016
Knockout of the PKN Family of Rho Effector Kinases Reveals a Non-redundant Role for PKN2 in Developmental Mesoderm ExpansionIvan Quétier, Jacqueline J T Marshall, Bradley Spencer-Dene, et al.
Pageof 16

Showing results (141-150 of 153) with videos related to

Sort By:
Pageof 16
Magnetic Resonance in Medicine|March 18, 2014
Diffusion microscopic MRI of the mouse embryo: Protocol and practical implementation in the splotch mouse modelFrancesca C Norris, Bernard M Siow, Jon O Cleary, et al.
Developmental Biology|December 12, 2022
Synchronisation of apical constriction and cell cycle progression is a conserved behaviour of pseudostratified neuroepithelia informed by their tissue geometryIoakeim Ampartzidis, Christoforos Efstathiou, Francesco Paonessa, et al.
Ebiomedicine|August 16, 2023
Folate deficiency increases the incidence of dolutegravir-associated foetal defects in a mouse pregnancy modelHaneesha Mohan, Jessica Nguyen, Ben MacKenzie, et al.
Human Molecular Genetics|June 26, 2023
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephaloceleZoe Crane-Smith, Sandra C P De Castro, Evanthia Nikolopoulou, et al.
Current Biology : CB|July 5, 2003
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseJohn A Curtin, Elizabeth Quint, Vicky Tsipouri, et al.
Human Molecular Genetics|January 26, 2011
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouseMadeleine R Brouns, Sandra C P De Castro, Els A Terwindt-Rouwenhorst, et al.
Human Molecular Genetics|December 23, 2006
The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formationHelen R Dawe, Ursula M Smith, Andrew R Cullinane, et al.
AJNR. American Journal of Neuroradiology|February 15, 2024
International Consensus Statement on the Radiological Evaluation of Dysraphic Malformations of the Spine and Spinal CordAnkit Balani, Jai Sidpra, Sniya Sudhakar, et al.
Human Molecular Genetics|April 8, 2006
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migrationSilvia Paracchini, Ankur Thomas, Sandra Castro, et al.
Cell Reports|January 18, 2016
Knockout of the PKN Family of Rho Effector Kinases Reveals a Non-redundant Role for PKN2 in Developmental Mesoderm ExpansionIvan Quétier, Jacqueline J T Marshall, Bradley Spencer-Dene, et al.
Pageof 16