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Sally H Cross

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

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Human Molecular Genetics|May 20, 2004
Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndromeSally H Cross, Joanne E Morgan, Alexandre Pattyn, et al.
Investigative Ophthalmology & Visual Science|July 3, 2019
Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the MouseSally H Cross, Lisa Mckie, Margaret Keighren, et al.
Plos Genetics|April 3, 2020
The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specificationSally H Cross, Lisa Mckie, Toby W Hurd, et al.
Investigative Ophthalmology & Visual Science|March 5, 2015
Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunctionShalini Jadeja, Alun R Barnard, Lisa McKie, et al.
Disease Models & Mechanisms|November 7, 2015
The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cellsAndrew Parker, Sally H Cross, Ian J Jackson, et al.
Human Molecular Genetics|September 15, 2005
Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathyTom Van Agtmael, Ursula Schlötzer-Schrehardt, Lisa McKie, et al.
Human Molecular Genetics|April 4, 2002
Novel ENU-induced eye mutations in the mouse: models for human eye diseaseCaroline Thaung, Katrine West, Brian J Clark, et al.
Human Molecular Genetics|November 29, 2011
A meckelin-filamin A interaction mediates ciliogenesisMatthew Adams, Roslyn J Simms, Zakia Abdelhamed, et al.
Disease Models & Mechanisms|November 28, 2018
Mouse <i>Idh3a</i> mutations cause retinal degeneration and reduced mitochondrial functionAmy S Findlay, Roderick N Carter, Becky Starbuck, et al.
Disease Models & Mechanisms|January 19, 2021
Genetic background modifies vulnerability to glaucoma-related phenotypes in <i>Lmx1b</i> mutant miceNicholas G Tolman, Revathi Balasubramanian, Danilo G Macalinao, et al.
Pageof 3

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

Sort By:
Pageof 3
Human Molecular Genetics|May 20, 2004
Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndromeSally H Cross, Joanne E Morgan, Alexandre Pattyn, et al.
Investigative Ophthalmology & Visual Science|July 3, 2019
Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the MouseSally H Cross, Lisa Mckie, Margaret Keighren, et al.
Plos Genetics|April 3, 2020
The nanophthalmos protein TMEM98 inhibits MYRF self-cleavage and is required for eye size specificationSally H Cross, Lisa Mckie, Toby W Hurd, et al.
Investigative Ophthalmology & Visual Science|March 5, 2015
Mouse slc9a8 mutants exhibit retinal defects due to retinal pigmented epithelium dysfunctionShalini Jadeja, Alun R Barnard, Lisa McKie, et al.
Disease Models & Mechanisms|November 7, 2015
The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cellsAndrew Parker, Sally H Cross, Ian J Jackson, et al.
Human Molecular Genetics|September 15, 2005
Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathyTom Van Agtmael, Ursula Schlötzer-Schrehardt, Lisa McKie, et al.
Human Molecular Genetics|April 4, 2002
Novel ENU-induced eye mutations in the mouse: models for human eye diseaseCaroline Thaung, Katrine West, Brian J Clark, et al.
Human Molecular Genetics|November 29, 2011
A meckelin-filamin A interaction mediates ciliogenesisMatthew Adams, Roslyn J Simms, Zakia Abdelhamed, et al.
Disease Models & Mechanisms|November 28, 2018
Mouse <i>Idh3a</i> mutations cause retinal degeneration and reduced mitochondrial functionAmy S Findlay, Roderick N Carter, Becky Starbuck, et al.
Disease Models & Mechanisms|January 19, 2021
Genetic background modifies vulnerability to glaucoma-related phenotypes in <i>Lmx1b</i> mutant miceNicholas G Tolman, Revathi Balasubramanian, Danilo G Macalinao, et al.
Pageof 3