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Philip Stanier

Showing results (21-30 of 69) with videos related to

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Applied and Environmental Microbiology|May 20, 2018
Enrichment of Clinically Relevant Organisms in Spontaneous Preterm-Delivered Placentas and Reagent Contamination across All Clinical Groups in a Large Pregnancy Cohort in the United KingdomLydia J Leon, Ronan Doyle, Ernest Diez-Benavente, et al.
Scientific Reports|May 28, 2017
Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effectsLucas Alvizi, Xiayi Ke, Luciano Abreu Brito, et al.
American Journal of Human Genetics|October 13, 2006
Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathiesHaiyan Zhou, Martin Brockington, Heinz Jungbluth, et al.
Reproductive Biomedicine Online|September 16, 2015
Investigation of the Annexin A5 M2 haplotype in 500 white European couples who have experienced recurrent spontaneous abortionCharalambos Demetriou, Sayeda Abu-Amero, Shawnelle White, et al.
Disease Models & Mechanisms|November 29, 2021
Vangl2-environment interaction causes severe neural tube defects, without abnormal neuroepithelial convergent extensionOleksandr Nychyk, Gabriel L Galea, Matteo Molè, 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.
Plos One|November 3, 2010
Evaluation of allelic expression of imprinted genes in adult human bloodJennifer M Frost, Dave Monk, Taita Stojilkovic-Mikic, et al.
Placenta|October 5, 2016
A new biological and clinical resource for research into pregnancy complications: The Baby Bio BankLydia J Leon, Nita Solanky, Susanne E Stalman, et al.
Disease Models & Mechanisms|September 30, 2018
Overexpression of <i>Fgfr2c</i> causes craniofacial bone hypoplasia and ameliorates craniosynostosis in the Crouzon mouseKevin K L Lee, Emma Peskett, Charlotte M Quinn, 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.
Pageof 7

Showing results (21-30 of 69) with videos related to

Sort By:
Pageof 7
Applied and Environmental Microbiology|May 20, 2018
Enrichment of Clinically Relevant Organisms in Spontaneous Preterm-Delivered Placentas and Reagent Contamination across All Clinical Groups in a Large Pregnancy Cohort in the United KingdomLydia J Leon, Ronan Doyle, Ernest Diez-Benavente, et al.
Scientific Reports|May 28, 2017
Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effectsLucas Alvizi, Xiayi Ke, Luciano Abreu Brito, et al.
American Journal of Human Genetics|October 13, 2006
Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathiesHaiyan Zhou, Martin Brockington, Heinz Jungbluth, et al.
Reproductive Biomedicine Online|September 16, 2015
Investigation of the Annexin A5 M2 haplotype in 500 white European couples who have experienced recurrent spontaneous abortionCharalambos Demetriou, Sayeda Abu-Amero, Shawnelle White, et al.
Disease Models & Mechanisms|November 29, 2021
Vangl2-environment interaction causes severe neural tube defects, without abnormal neuroepithelial convergent extensionOleksandr Nychyk, Gabriel L Galea, Matteo Molè, 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.
Plos One|November 3, 2010
Evaluation of allelic expression of imprinted genes in adult human bloodJennifer M Frost, Dave Monk, Taita Stojilkovic-Mikic, et al.
Placenta|October 5, 2016
A new biological and clinical resource for research into pregnancy complications: The Baby Bio BankLydia J Leon, Nita Solanky, Susanne E Stalman, et al.
Disease Models & Mechanisms|September 30, 2018
Overexpression of <i>Fgfr2c</i> causes craniofacial bone hypoplasia and ameliorates craniosynostosis in the Crouzon mouseKevin K L Lee, Emma Peskett, Charlotte M Quinn, 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.
Pageof 7