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Cheryl Shoubridge

Showing results (1-10 of 51) with videos related to

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Advances in Experimental Medicine and Biology|April 6, 2013
Polyalanine tract disorders and neurocognitive phenotypesCheryl Shoubridge, Jozef Gecz
Trends in Genetics : TIG|June 27, 2009
The genetic landscape of intellectual disability arising from chromosome XJozef Gécz, Cheryl Shoubridge, Mark Corbett
Human Mutation|May 28, 2010
ARX spectrum disorders: making inroads into the molecular pathologyCheryl Shoubridge, Tod Fullston, Jozef Gécz
Methods in Molecular Biology (Clifton, N.J.)|May 31, 2013
PCR amplification and sequence analysis of GC-rich sequences: Aristaless-related homeobox exampleMay H Tan, Jozef Gécz, Cheryl Shoubridge
Human Mutation|October 18, 2018
IQSEC2 mutation update and review of the female-specific phenotype spectrum including intellectual disability and epilepsyCheryl Shoubridge, Robert J Harvey, Tracy Dudding-Byth
European Journal of Medical Genetics|August 22, 2021
A novel ARX loss of function variant in female monozygotic twins is associated with choreaJonathan Rodgers, Sophie Calvert, Cheryl Shoubridge, et al.
Human Molecular Genetics|December 24, 2011
ARX homeodomain mutations abolish DNA binding and lead to a loss of transcriptional repressionCheryl Shoubridge, May Huey Tan, Grace Seiboth, et al.
Small Gtpases|June 21, 2011
Subtle functional defects in the Arf-specific guanine nucleotide exchange factor IQSEC2 cause non-syndromic X-linked intellectual disabilityCheryl Shoubridge, Randall S Walikonis, Jozef Gécz, et al.
Methods in Molecular Biology (Clifton, N.J.)|May 31, 2013
Challenges of "sticky" co-immunoprecipitation: polyalanine tract protein-protein interactionsT R Mattiske, May H Tan, Jozef Gécz, 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.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
Advances in Experimental Medicine and Biology|April 6, 2013
Polyalanine tract disorders and neurocognitive phenotypesCheryl Shoubridge, Jozef Gecz
Trends in Genetics : TIG|June 27, 2009
The genetic landscape of intellectual disability arising from chromosome XJozef Gécz, Cheryl Shoubridge, Mark Corbett
Human Mutation|May 28, 2010
ARX spectrum disorders: making inroads into the molecular pathologyCheryl Shoubridge, Tod Fullston, Jozef Gécz
Methods in Molecular Biology (Clifton, N.J.)|May 31, 2013
PCR amplification and sequence analysis of GC-rich sequences: Aristaless-related homeobox exampleMay H Tan, Jozef Gécz, Cheryl Shoubridge
Human Mutation|October 18, 2018
IQSEC2 mutation update and review of the female-specific phenotype spectrum including intellectual disability and epilepsyCheryl Shoubridge, Robert J Harvey, Tracy Dudding-Byth
European Journal of Medical Genetics|August 22, 2021
A novel ARX loss of function variant in female monozygotic twins is associated with choreaJonathan Rodgers, Sophie Calvert, Cheryl Shoubridge, et al.
Human Molecular Genetics|December 24, 2011
ARX homeodomain mutations abolish DNA binding and lead to a loss of transcriptional repressionCheryl Shoubridge, May Huey Tan, Grace Seiboth, et al.
Small Gtpases|June 21, 2011
Subtle functional defects in the Arf-specific guanine nucleotide exchange factor IQSEC2 cause non-syndromic X-linked intellectual disabilityCheryl Shoubridge, Randall S Walikonis, Jozef Gécz, et al.
Methods in Molecular Biology (Clifton, N.J.)|May 31, 2013
Challenges of "sticky" co-immunoprecipitation: polyalanine tract protein-protein interactionsT R Mattiske, May H Tan, Jozef Gécz, 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.
Pageof 6