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Michael A Walter

Showing results (31-40 of 56) with videos related to

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Human Molecular Genetics|January 20, 2009
Glaucoma-associated WDR36 variants encode functional defects in a yeast model systemTim K Footz, Jill L Johnson, Stéphane Dubois, et al.
Investigative Ophthalmology & Visual Science|August 5, 2008
Human p32 is a novel FOXC1-interacting protein that regulates FOXC1 transcriptional activity in ocular cellsLijia Huang, Jonathan Chi, Fred B Berry, et al.
Molecular Vision|August 25, 2012
Yeast two-hybrid analysis of a human trabecular meshwork cDNA library identified EFEMP2 as a novel PITX2 interacting proteinMoulinath Acharya, Michael W Sharp, Farideh Mirzayans, et al.
Human Molecular Genetics|September 27, 2006
FGF19 is a target for FOXC1 regulation in ciliary body-derived cellsYahya Tamimi, Jonathan M Skarie, Tim Footz, et al.
Molecules (Basel, Switzerland)|July 2, 2021
Functional Domains and Evolutionary History of the PMEL and GPNMB Family ProteinsPaul W Chrystal, Tim Footz, Elizabeth D Hodges, et al.
Acta Ophthalmologica|March 25, 2016
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndromeMorteza Seifi, Tim Footz, Sherry A M Taylor, et al.
Investigative Ophthalmology & Visual Science|March 13, 2009
Severe molecular defects of a novel FOXC1 W152G mutation result in aniridiaYoko A Ito, Tim K Footz, Fred B Berry, et al.
Human Molecular Genetics|May 23, 2002
Protein localization in the human eye and genetic screen of opticinJames S Friedman, Mathieu Faucher, Paul Hiscott, et al.
BMC Medical Genetics|June 29, 2004
Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairmentDouglas B Gould, Mohamad S Jaafar, Mark K Addison, et al.
Investigative Ophthalmology & Visual Science|August 30, 2011
PITX2 is involved in stress response in cultured human trabecular meshwork cells through regulation of SLC13A3M Hermina Strungaru, Tim Footz, Yi Liu, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|January 20, 2009
Glaucoma-associated WDR36 variants encode functional defects in a yeast model systemTim K Footz, Jill L Johnson, Stéphane Dubois, et al.
Investigative Ophthalmology & Visual Science|August 5, 2008
Human p32 is a novel FOXC1-interacting protein that regulates FOXC1 transcriptional activity in ocular cellsLijia Huang, Jonathan Chi, Fred B Berry, et al.
Molecular Vision|August 25, 2012
Yeast two-hybrid analysis of a human trabecular meshwork cDNA library identified EFEMP2 as a novel PITX2 interacting proteinMoulinath Acharya, Michael W Sharp, Farideh Mirzayans, et al.
Human Molecular Genetics|September 27, 2006
FGF19 is a target for FOXC1 regulation in ciliary body-derived cellsYahya Tamimi, Jonathan M Skarie, Tim Footz, et al.
Molecules (Basel, Switzerland)|July 2, 2021
Functional Domains and Evolutionary History of the PMEL and GPNMB Family ProteinsPaul W Chrystal, Tim Footz, Elizabeth D Hodges, et al.
Acta Ophthalmologica|March 25, 2016
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndromeMorteza Seifi, Tim Footz, Sherry A M Taylor, et al.
Investigative Ophthalmology & Visual Science|March 13, 2009
Severe molecular defects of a novel FOXC1 W152G mutation result in aniridiaYoko A Ito, Tim K Footz, Fred B Berry, et al.
Human Molecular Genetics|May 23, 2002
Protein localization in the human eye and genetic screen of opticinJames S Friedman, Mathieu Faucher, Paul Hiscott, et al.
BMC Medical Genetics|June 29, 2004
Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairmentDouglas B Gould, Mohamad S Jaafar, Mark K Addison, et al.
Investigative Ophthalmology & Visual Science|August 30, 2011
PITX2 is involved in stress response in cultured human trabecular meshwork cells through regulation of SLC13A3M Hermina Strungaru, Tim Footz, Yi Liu, et al.
Pageof 6