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Hannah Vanyai

Showing results (1-10 of 9) with videos related to

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Journal of Cell Science|November 9, 2018
Enigma proteins regulate YAP mechanotransductionAhmed Elbediwy, Hannah Vanyai, Maria-Del-Carmen Diaz-de-la-Loza, et al.
Neurobiology of Disease|September 5, 2024
Slc35a2 mosaic knockout impacts cortical development, dendritic arborisation, and neuronal firingJames Spyrou, Khaing Phyu Aung, Hannah Vanyai, et al.
Elife|September 21, 2018
YAP drives cutaneous squamous cell carcinoma formation and progressionZoé Vincent-Mistiaen, Ahmed Elbediwy, Hannah Vanyai, et al.
Human Molecular Genetics|February 4, 2017
Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathwayShimon Edvardson, Guoling Tian, Hayley Cullen, et al.
EMBO Reports|April 30, 2025
Transcriptomic changes including p53 dysregulation prime DNMT3A mutant cells for transformationErin M Lawrence, Amali Cooray, Andrew J Kueh, et al.
Molecular Genetics & Genomic Medicine|January 8, 2019
Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetranceKaren J Woodward, Julie Stampalia, Hannah Vanyai, et al.
Elife|December 3, 2014
TNFR1-dependent cell death drives inflammation in Sharpin-deficient miceJames A Rickard, Holly Anderton, Nima Etemadi, et al.
The Biochemical Journal|June 22, 2022
PKN2 deficiency leads both to prenatal 'congenital' cardiomyopathy and defective angiotensin II stress responsesJacqueline J T Marshall, Joshua J Cull, Hajed O Alharbi, et al.
Nature Communications|September 25, 2023
SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in diseaseAndres Tapia Del Fierro, Bianca den Hamer, Natalia Benetti, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Journal of Cell Science|November 9, 2018
Enigma proteins regulate YAP mechanotransductionAhmed Elbediwy, Hannah Vanyai, Maria-Del-Carmen Diaz-de-la-Loza, et al.
Neurobiology of Disease|September 5, 2024
Slc35a2 mosaic knockout impacts cortical development, dendritic arborisation, and neuronal firingJames Spyrou, Khaing Phyu Aung, Hannah Vanyai, et al.
Elife|September 21, 2018
YAP drives cutaneous squamous cell carcinoma formation and progressionZoé Vincent-Mistiaen, Ahmed Elbediwy, Hannah Vanyai, et al.
Human Molecular Genetics|February 4, 2017
Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathwayShimon Edvardson, Guoling Tian, Hayley Cullen, et al.
EMBO Reports|April 30, 2025
Transcriptomic changes including p53 dysregulation prime DNMT3A mutant cells for transformationErin M Lawrence, Amali Cooray, Andrew J Kueh, et al.
Molecular Genetics & Genomic Medicine|January 8, 2019
Atypical nested 22q11.2 duplications between LCR22B and LCR22D are associated with neurodevelopmental phenotypes including autism spectrum disorder with incomplete penetranceKaren J Woodward, Julie Stampalia, Hannah Vanyai, et al.
Elife|December 3, 2014
TNFR1-dependent cell death drives inflammation in Sharpin-deficient miceJames A Rickard, Holly Anderton, Nima Etemadi, et al.
The Biochemical Journal|June 22, 2022
PKN2 deficiency leads both to prenatal 'congenital' cardiomyopathy and defective angiotensin II stress responsesJacqueline J T Marshall, Joshua J Cull, Hajed O Alharbi, et al.
Nature Communications|September 25, 2023
SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in diseaseAndres Tapia Del Fierro, Bianca den Hamer, Natalia Benetti, et al.
Pageof 1