Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithms

por Seifi, Morteza, Walter, Michael A.
Publicado 2018

Molecular Genetics of Pigment Dispersion Syndrome and Pigmentary Glaucoma: New Insights into Mechanisms

por Lahola-Chomiak, Adrian A., Walter, Michael A.
Publicado 2018

Identification and analysis of evolutionary selection pressures acting at the molecular level in five forkhead subfamilies

por Fetterman, Christina D, Rannala, Bruce, Walter, Michael A
Publicado 2008

FOXC1, the new player in the cancer sandbox

por Elian, Fahed A., Yan, Elizabeth, Walter, Michael A.
Publicado 2017

Co-variation of STI1 and WDR36/UTP21 alters cell proliferation in a glaucoma model

por Footz, Tim, Dubois, Stéphane, Sarfarazi, Mansoor, Raymond, Vincent, Walter, Michael A.
Publicado 2011

FOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25

por Rasnitsyn, Alexandra, Doucette, Lance, Seifi, Morteza, Footz, Tim, Raymond, Vincent, Walter, Michael A.
Publicado 2017

Yeast two-hybrid analysis of a human trabecular meshwork cDNA library identified EFEMP2 as a novel PITX2 interacting protein

por Acharya, Moulinath, Sharp, Michael W., Mirzayans, Farideh, Footz, Tim, Huang, LiJia, Birdi, Chanchal, Walter, Michael A.
Publicado 2012

Functional Domains and Evolutionary History of the PMEL and GPNMB Family Proteins

por Chrystal, Paul W., Footz, Tim, Hodges, Elizabeth D., Jensen, Justin A., Walter, Michael A., Allison, W. Ted
Publicado 2021

Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: Relevance to ocular dysgenesis and hearing impairment

por Gould, Douglas B, Jaafar, Mohamad S, Addison, Mark K, Munier, Francis, Ritch, Robert, MacDonald, Ian M, Walter, Michael A
Publicado 2004

FOXC2 disease-mutations identified in lymphedema-distichiasis patients cause both loss and gain of protein function

por Tavian, Daniela, Missaglia, Sara, Maltese, Paolo E., Michelini, Sandro, Fiorentino, Alessandro, Ricci, Maurizio, Serrani, Roberta, Walter, Michael A., Bertelli, Matteo
Publicado 2016

FOXQ1 is Differentially Expressed Across Breast Cancer Subtypes with Low Expression Associated with Poor Overall Survival

por Elian, Fahed A, Are, Ubah, Ghosh, Sunita, Nuin, Paulo, Footz, Tim, McMullen, Todd P W, Brindley, David N, Walter, Michael A
Publicado 2021

Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary Glaucoma

por Hodges, Elizabeth D., Chrystal, Paul W., Footz, Tim, Doucette, Lance P., Noel, Nicole C. L., Li, Zixuan, Walter, Michael A., Allison, W. Ted
Publicado 2023

Absence of NR2E1 mutations in patients with aniridia

por Corso-Díaz, Ximena, Borrie, Adrienne E., Bonaguro, Russell, Schuetz, Johanna M., Rosenberg, Thomas, Jensen, Hanne, Brooks, Brian P., MacDonald, Ian M., Pasutto, Francesca, Walter, Michael A., Grønskov, Karen, Brooks-Wilson, Angela, Simpson, Elizabeth M.
Publicado 2012