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D E Greene

Showing results (71-80 of 145) with videos related to

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Physiological Research|July 24, 2018
Genetically determined folate deficiency is associated with abnormal hepatic folate profiles in the spontaneously hypertensive ratM Pravenec, K Y Leung, V Zídek, et al.
Nature Communications|February 20, 2021
Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in miceGabriel L Galea, Eirini Maniou, Timothy J Edwards, et al.
Journal of Cell Science|June 12, 2019
Rho kinase-dependent apical constriction counteracts M-phase apical expansion to enable mouse neural tube closureMax B Butler, Nina E Short, Eirini Maniou, et al.
Disease Models & Mechanisms|August 17, 2014
Genetic interactions between planar cell polarity genes cause diverse neural tube defects in miceJennifer N Murdoch, Christine Damrau, Anju Paudyal, et al.
Human Mutation|November 19, 2011
Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisisAlexis Robinson, Sarah Escuin, Kit Doudney, et al.
Human Molecular Genetics|August 28, 2007
Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse modelPeter Gustavsson, Nicholas D E Greene, Dina Lad, et al.
Nature Communications|May 29, 2021
Author Correction: Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in miceGabriel L Galea, Eirini Maniou, Timothy J Edwards, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 4, 2021
Hindbrain neuropore tissue geometry determines asymmetric cell-mediated closure dynamics in mouse embryosEirini Maniou, Michael F Staddon, Abigail R Marshall, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 1, 2010
Neural tube defects induced by folate deficiency in mutant curly tail (Grhl3) embryos are associated with alteration in folate one-carbon metabolism but are unlikely to result from diminished methylationSandra C P De Castro, Kit-Yi Leung, Dawn Savery, et al.
Scientific Reports|February 22, 2018
Spina bifida-predisposing heterozygous mutations in Planar Cell Polarity genes and Zic2 reduce bone mass in young miceIsabel R Orriss, Stuart Lanham, Dawn Savery, et al.
Pageof 15

Showing results (71-80 of 145) with videos related to

Sort By:
Pageof 15
Physiological Research|July 24, 2018
Genetically determined folate deficiency is associated with abnormal hepatic folate profiles in the spontaneously hypertensive ratM Pravenec, K Y Leung, V Zídek, et al.
Nature Communications|February 20, 2021
Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in miceGabriel L Galea, Eirini Maniou, Timothy J Edwards, et al.
Journal of Cell Science|June 12, 2019
Rho kinase-dependent apical constriction counteracts M-phase apical expansion to enable mouse neural tube closureMax B Butler, Nina E Short, Eirini Maniou, et al.
Disease Models & Mechanisms|August 17, 2014
Genetic interactions between planar cell polarity genes cause diverse neural tube defects in miceJennifer N Murdoch, Christine Damrau, Anju Paudyal, et al.
Human Mutation|November 19, 2011
Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisisAlexis Robinson, Sarah Escuin, Kit Doudney, et al.
Human Molecular Genetics|August 28, 2007
Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse modelPeter Gustavsson, Nicholas D E Greene, Dina Lad, et al.
Nature Communications|May 29, 2021
Author Correction: Cell non-autonomy amplifies disruption of neurulation by mosaic Vangl2 deletion in miceGabriel L Galea, Eirini Maniou, Timothy J Edwards, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 4, 2021
Hindbrain neuropore tissue geometry determines asymmetric cell-mediated closure dynamics in mouse embryosEirini Maniou, Michael F Staddon, Abigail R Marshall, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 1, 2010
Neural tube defects induced by folate deficiency in mutant curly tail (Grhl3) embryos are associated with alteration in folate one-carbon metabolism but are unlikely to result from diminished methylationSandra C P De Castro, Kit-Yi Leung, Dawn Savery, et al.
Scientific Reports|February 22, 2018
Spina bifida-predisposing heterozygous mutations in Planar Cell Polarity genes and Zic2 reduce bone mass in young miceIsabel R Orriss, Stuart Lanham, Dawn Savery, et al.
Pageof 15