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I Scheffer

Showing results (11-20 of 23) with videos related to

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Cell|March 7, 1998
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling proteinJ G Gleeson, K M Allen, J W Fox, et al.
Neurology|May 26, 2004
Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformationB S Chang, X Piao, C Giannini, et al.
Annals of Neurology|February 9, 2000
Genetic and neuroradiological heterogeneity of double cortex syndromeJ G Gleeson, R F Luo, P E Grant, et al.
The Journal of Cell Biology|September 14, 2017
Heterodimeric capping protein is required for stereocilia length and width regulationMatthew R Avenarius, Jocelyn F Krey, Rachel A Dumont, et al.
American Journal of Human Genetics|December 1, 1999
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12L Xiong, M Labuda, D S Li, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 14, 2017
Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAVBence György, Cyrille Sage, Artur A Indzhykulian, et al.
Neurology|September 30, 2010
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutationsL Deprez, S Weckhuysen, P Holmgren, et al.
Gene Therapy|February 3, 2016
Exosome-associated AAV vector as a robust and convenient neuroscience toolE Hudry, C Martin, S Gandhi, et al.
Gene Therapy|November 4, 2016
Exosome-associated AAV vector as a robust and convenient neuroscience toolE Hudry, C Martin, S Gandhi, et al.
Human Molecular Genetics|July 19, 2015
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and lossDragana Vuckovic, Sally Dawson, Deborah I Scheffer, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Cell|March 7, 1998
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling proteinJ G Gleeson, K M Allen, J W Fox, et al.
Neurology|May 26, 2004
Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformationB S Chang, X Piao, C Giannini, et al.
Annals of Neurology|February 9, 2000
Genetic and neuroradiological heterogeneity of double cortex syndromeJ G Gleeson, R F Luo, P E Grant, et al.
The Journal of Cell Biology|September 14, 2017
Heterodimeric capping protein is required for stereocilia length and width regulationMatthew R Avenarius, Jocelyn F Krey, Rachel A Dumont, et al.
American Journal of Human Genetics|December 1, 1999
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12L Xiong, M Labuda, D S Li, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 14, 2017
Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAVBence György, Cyrille Sage, Artur A Indzhykulian, et al.
Neurology|September 30, 2010
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutationsL Deprez, S Weckhuysen, P Holmgren, et al.
Gene Therapy|February 3, 2016
Exosome-associated AAV vector as a robust and convenient neuroscience toolE Hudry, C Martin, S Gandhi, et al.
Gene Therapy|November 4, 2016
Exosome-associated AAV vector as a robust and convenient neuroscience toolE Hudry, C Martin, S Gandhi, et al.
Human Molecular Genetics|July 19, 2015
Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and lossDragana Vuckovic, Sally Dawson, Deborah I Scheffer, et al.
Pageof 3