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Michael A Walter

Showing results (21-30 of 56) with videos related to

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Investigative Ophthalmology & Visual Science|November 26, 2003
Opticin binds retinal growth hormone in the embryonic vitreousEsmond J Sanders, Michael A Walter, Eve Parker, et al.
Molecular and Cellular Biology|February 3, 2005
FOXC1 transcriptional regulatory activity is impaired by PBX1 in a filamin A-mediated mannerFred B Berry, Megan A O'Neill, Miguel Coca-Prados, et al.
American Journal of Medical Genetics. Part A|May 9, 2007
Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld-Rieger anomaly, hydrocephaly, hearing loss): a 25-year follow upR Brian Lowry, Douglas B Gould, Michael A Walter, et al.
Human Molecular Genetics|February 2, 2011
A complex regulatory network of transcription factors critical for ocular development and diseaseMoulinath Acharya, Lijia Huang, Valerie C Fleisch, et al.
Plos One|June 3, 2017
FOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25Alexandra Rasnitsyn, Lance Doucette, Morteza Seifi, et al.
The Journal of Biological Chemistry|October 6, 2009
Human PRKC apoptosis WT1 regulator is a novel PITX2-interacting protein that regulates PITX2 transcriptional activity in ocular cellsMoulinath Acharya, David J Lingenfelter, Lijia Huang, et al.
Human Molecular Genetics|August 6, 2005
The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasisFred B Berry, Yahya Tamimi, Michelle V Carle, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Analyses of a novel L130F missense mutation in FOXC1Yoko A Ito, Tim K Footz, Tara C Murphy, et al.
Investigative Ophthalmology & Visual Science|July 28, 2004
The wing 2 region of the FOXC1 forkhead domain is necessary for normal DNA-binding and transactivation functionsTara C Murphy, Ramsey A Saleem, Tim Footz, et al.
Human Molecular Genetics|September 25, 2003
Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1Ramsey A Saleem, Sharmila Banerjee-Basu, Fred B Berry, et al.
Pageof 6

Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
Investigative Ophthalmology & Visual Science|November 26, 2003
Opticin binds retinal growth hormone in the embryonic vitreousEsmond J Sanders, Michael A Walter, Eve Parker, et al.
Molecular and Cellular Biology|February 3, 2005
FOXC1 transcriptional regulatory activity is impaired by PBX1 in a filamin A-mediated mannerFred B Berry, Megan A O'Neill, Miguel Coca-Prados, et al.
American Journal of Medical Genetics. Part A|May 9, 2007
Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld-Rieger anomaly, hydrocephaly, hearing loss): a 25-year follow upR Brian Lowry, Douglas B Gould, Michael A Walter, et al.
Human Molecular Genetics|February 2, 2011
A complex regulatory network of transcription factors critical for ocular development and diseaseMoulinath Acharya, Lijia Huang, Valerie C Fleisch, et al.
Plos One|June 3, 2017
FOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25Alexandra Rasnitsyn, Lance Doucette, Morteza Seifi, et al.
The Journal of Biological Chemistry|October 6, 2009
Human PRKC apoptosis WT1 regulator is a novel PITX2-interacting protein that regulates PITX2 transcriptional activity in ocular cellsMoulinath Acharya, David J Lingenfelter, Lijia Huang, et al.
Human Molecular Genetics|August 6, 2005
The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasisFred B Berry, Yahya Tamimi, Michelle V Carle, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Analyses of a novel L130F missense mutation in FOXC1Yoko A Ito, Tim K Footz, Tara C Murphy, et al.
Investigative Ophthalmology & Visual Science|July 28, 2004
The wing 2 region of the FOXC1 forkhead domain is necessary for normal DNA-binding and transactivation functionsTara C Murphy, Ramsey A Saleem, Tim Footz, et al.
Human Molecular Genetics|September 25, 2003
Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1Ramsey A Saleem, Sharmila Banerjee-Basu, Fred B Berry, et al.
Pageof 6