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Jozef Gecz

Showing results (21-30 of 244) with videos related to

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American Journal of Medical Genetics. Part A|July 17, 2009
A novel de novo 27 bp duplication of the ARX gene, resulting from postzygotic mosaicism and leading to three severely affected males in two generationsOrit Reish, Tod Fullston, Miriam Regev, et al.
Current Opinion in Genetics & Development|July 12, 2025
Transcription-Export complex in neurodevelopmental disordersRudrarup Bhattacharjee, Shreya Agarwala, Danielle Mazurkiewicz, et al.
Human Molecular Genetics|November 1, 2016
Embryonic forebrain transcriptome of mice with polyalanine expansion mutations in the ARX homeobox geneTessa Mattiske, Kristie Lee, Jozef Gecz, et al.
Epilepsia|March 25, 2010
Genetics of the epilepsies: genetic twists in the channels and other talesIngrid E Scheffer, Yue-Hua Zhang, Jozef Gecz, et al.
Biological Psychiatry|June 6, 2022
The DUB Club: Deubiquitinating Enzymes and Neurodevelopmental DisordersLachlan A Jolly, Raman Kumar, Peter Penzes, et al.
Seminars in Fetal & Neonatal Medicine|November 10, 2024
Cerebral palsy as a childhood-onset neurological disorder caused by both genetic and environmental factorsNandini G Sandran, Nadia Badawi, Jozef Gecz, et al.
Journal of Human Genetics|June 22, 2018
Robust imaging and gene delivery to study human lymphoblastoid cell linesLachlan A Jolly, Ying Sun, Renée Carroll, et al.
Human Molecular Genetics|July 4, 2013
The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowthLachlan A Jolly, Claire C Homan, Reuben Jacob, et al.
Human Molecular Genetics|April 9, 2013
Loss of FMR2 further emphasizes the link between deregulation of immediate early response genes FOS and JUN and intellectual disabilityMireille Melko, Lam S Nguyen, Marie Shaw, et al.
Developmental Medicine and Child Neurology|January 3, 2017
The genetic basis of cerebral palsyMichael C Fahey, Alastair H Maclennan, Doris Kretzschmar, et al.
Pageof 25

Showing results (21-30 of 244) with videos related to

Sort By:
Pageof 25
American Journal of Medical Genetics. Part A|July 17, 2009
A novel de novo 27 bp duplication of the ARX gene, resulting from postzygotic mosaicism and leading to three severely affected males in two generationsOrit Reish, Tod Fullston, Miriam Regev, et al.
Current Opinion in Genetics & Development|July 12, 2025
Transcription-Export complex in neurodevelopmental disordersRudrarup Bhattacharjee, Shreya Agarwala, Danielle Mazurkiewicz, et al.
Human Molecular Genetics|November 1, 2016
Embryonic forebrain transcriptome of mice with polyalanine expansion mutations in the ARX homeobox geneTessa Mattiske, Kristie Lee, Jozef Gecz, et al.
Epilepsia|March 25, 2010
Genetics of the epilepsies: genetic twists in the channels and other talesIngrid E Scheffer, Yue-Hua Zhang, Jozef Gecz, et al.
Biological Psychiatry|June 6, 2022
The DUB Club: Deubiquitinating Enzymes and Neurodevelopmental DisordersLachlan A Jolly, Raman Kumar, Peter Penzes, et al.
Seminars in Fetal & Neonatal Medicine|November 10, 2024
Cerebral palsy as a childhood-onset neurological disorder caused by both genetic and environmental factorsNandini G Sandran, Nadia Badawi, Jozef Gecz, et al.
Journal of Human Genetics|June 22, 2018
Robust imaging and gene delivery to study human lymphoblastoid cell linesLachlan A Jolly, Ying Sun, Renée Carroll, et al.
Human Molecular Genetics|July 4, 2013
The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowthLachlan A Jolly, Claire C Homan, Reuben Jacob, et al.
Human Molecular Genetics|April 9, 2013
Loss of FMR2 further emphasizes the link between deregulation of immediate early response genes FOS and JUN and intellectual disabilityMireille Melko, Lam S Nguyen, Marie Shaw, et al.
Developmental Medicine and Child Neurology|January 3, 2017
The genetic basis of cerebral palsyMichael C Fahey, Alastair H Maclennan, Doris Kretzschmar, et al.
Pageof 25