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Michael A Walter

Showing results (11-20 of 56) with videos related to

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BMC Evolutionary Biology|September 26, 2008
Identification and analysis of evolutionary selection pressures acting at the molecular level in five forkhead subfamiliesChristina D Fetterman, Bruce Rannala, Michael A Walter
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 1, 2020
Introduction to the special issue on Ophthalmic Genetics: Vision in 2020Robert B Hufnagel, Michael A Walter, Gavin Arno
The Journal of Biological Chemistry|January 10, 2002
FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domainFred B Berry, Ramsey A Saleem, Michael A Walter
Survey of Ophthalmology|April 25, 2015
The interactions of genes, age, and environment in glaucoma pathogenesisLance P Doucette, Alexandra Rasnitsyn, Morteza Seifi, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 8, 2020
Ocular genetics in the genomics ageMichael A Walter, Tayebeh Rezaie, Robert B Hufnagel, et al.
Investigative Ophthalmology & Visual Science|October 27, 2004
Identification of target genes regulated by FOXC1 using nickel agarose-based chromatin enrichmentYahya Tamimi, Matthew Lines, Miguel Coca-Prados, et al.
Investigative Ophthalmology & Visual Science|February 17, 2009
Analysis of mutations of the PITX2 transcription factor found in patients with Axenfeld-Rieger syndromeTim Footz, Faisal Idrees, Moulinath Acharya, et al.
Molecular Vision|August 19, 2011
Co-variation of STI1 and WDR36/UTP21 alters cell proliferation in a glaucoma modelTim Footz, Stéphane Dubois, Mansoor Sarfarazi, et al.
Human Mutation|November 3, 2016
Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses of FOXC1 Mutations in Patients with Axenfeld-Rieger SyndromeMorteza Seifi, Tim Footz, Sherry A M Taylor, et al.
Investigative Ophthalmology & Visual Science|October 28, 2003
Identification and analysis of a novel mutation in the FOXC1 forkhead domainRamsey A Saleem, Tara C Murphy, Jeffery M Liebmann, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
BMC Evolutionary Biology|September 26, 2008
Identification and analysis of evolutionary selection pressures acting at the molecular level in five forkhead subfamiliesChristina D Fetterman, Bruce Rannala, Michael A Walter
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 1, 2020
Introduction to the special issue on Ophthalmic Genetics: Vision in 2020Robert B Hufnagel, Michael A Walter, Gavin Arno
The Journal of Biological Chemistry|January 10, 2002
FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domainFred B Berry, Ramsey A Saleem, Michael A Walter
Survey of Ophthalmology|April 25, 2015
The interactions of genes, age, and environment in glaucoma pathogenesisLance P Doucette, Alexandra Rasnitsyn, Morteza Seifi, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 8, 2020
Ocular genetics in the genomics ageMichael A Walter, Tayebeh Rezaie, Robert B Hufnagel, et al.
Investigative Ophthalmology & Visual Science|October 27, 2004
Identification of target genes regulated by FOXC1 using nickel agarose-based chromatin enrichmentYahya Tamimi, Matthew Lines, Miguel Coca-Prados, et al.
Investigative Ophthalmology & Visual Science|February 17, 2009
Analysis of mutations of the PITX2 transcription factor found in patients with Axenfeld-Rieger syndromeTim Footz, Faisal Idrees, Moulinath Acharya, et al.
Molecular Vision|August 19, 2011
Co-variation of STI1 and WDR36/UTP21 alters cell proliferation in a glaucoma modelTim Footz, Stéphane Dubois, Mansoor Sarfarazi, et al.
Human Mutation|November 3, 2016
Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses of FOXC1 Mutations in Patients with Axenfeld-Rieger SyndromeMorteza Seifi, Tim Footz, Sherry A M Taylor, et al.
Investigative Ophthalmology & Visual Science|October 28, 2003
Identification and analysis of a novel mutation in the FOXC1 forkhead domainRamsey A Saleem, Tara C Murphy, Jeffery M Liebmann, et al.
Pageof 6