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Michael A Walter

Showing results (41-50 of 56) with videos related to

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Oncotarget|June 9, 2016
FOXC2 disease-mutations identified in lymphedema-distichiasis patients cause both loss and gain of protein functionDaniela Tavian, Sara Missaglia, Paolo E Maltese, et al.
Human Molecular Genetics|February 2, 2006
Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesisFred B Berry, Matthew A Lines, J Martin Oas, et al.
Human Molecular Genetics|November 13, 2007
FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1AFred B Berry, Jonathan M Skarie, Farideh Mirzayans, et al.
Breast Cancer (Dove Medical Press)|March 10, 2021
<i>FOXQ1</i> is Differentially Expressed Across Breast Cancer Subtypes with Low Expression Associated with Poor Overall SurvivalFahed A Elian, Ubah Are, Sunita Ghosh, et al.
International Journal of Molecular Sciences|October 14, 2023
Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary GlaucomaElizabeth D Hodges, Paul W Chrystal, Tim Footz, et al.
Human Mutation|June 29, 2004
Chromosomal anomalies on 6p25 in iris hypoplasia and Axenfeld-Rieger syndrome patients defined on a purpose-built genomic microarrayRosemary Ekong, Steve Jeremiah, David Judah, et al.
Investigative Ophthalmology & Visual Science|February 27, 2004
Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformationsMatthew A Lines, Kathy Kozlowski, Stephen C Kulak, et al.
Human Molecular Genetics|September 16, 2017
Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucomaMeredith E Protas, Eric Weh, Tim Footz, et al.
Human Molecular Genetics|August 13, 2008
A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variationBhaskar Chanda, Mika Asai-Coakwell, Ming Ye, et al.
Molecular Vision|December 6, 2012
Absence of NR2E1 mutations in patients with aniridiaXimena Corso-Díaz, Adrienne E Borrie, Russell Bonaguro, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Oncotarget|June 9, 2016
FOXC2 disease-mutations identified in lymphedema-distichiasis patients cause both loss and gain of protein functionDaniela Tavian, Sara Missaglia, Paolo E Maltese, et al.
Human Molecular Genetics|February 2, 2006
Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesisFred B Berry, Matthew A Lines, J Martin Oas, et al.
Human Molecular Genetics|November 13, 2007
FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1AFred B Berry, Jonathan M Skarie, Farideh Mirzayans, et al.
Breast Cancer (Dove Medical Press)|March 10, 2021
<i>FOXQ1</i> is Differentially Expressed Across Breast Cancer Subtypes with Low Expression Associated with Poor Overall SurvivalFahed A Elian, Ubah Are, Sunita Ghosh, et al.
International Journal of Molecular Sciences|October 14, 2023
Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary GlaucomaElizabeth D Hodges, Paul W Chrystal, Tim Footz, et al.
Human Mutation|June 29, 2004
Chromosomal anomalies on 6p25 in iris hypoplasia and Axenfeld-Rieger syndrome patients defined on a purpose-built genomic microarrayRosemary Ekong, Steve Jeremiah, David Judah, et al.
Investigative Ophthalmology & Visual Science|February 27, 2004
Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformationsMatthew A Lines, Kathy Kozlowski, Stephen C Kulak, et al.
Human Molecular Genetics|September 16, 2017
Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucomaMeredith E Protas, Eric Weh, Tim Footz, et al.
Human Molecular Genetics|August 13, 2008
A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variationBhaskar Chanda, Mika Asai-Coakwell, Ming Ye, et al.
Molecular Vision|December 6, 2012
Absence of NR2E1 mutations in patients with aniridiaXimena Corso-Díaz, Adrienne E Borrie, Russell Bonaguro, et al.
Pageof 6