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 em 2008

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 em 2011

FOXC1 Transcriptional Regulatory Activity Is Impaired by PBX1 in a Filamin A-Mediated Manner

Por Berry, Fred B., O'Neill, Megan A., Coca-Prados, Miguel, Walter, Michael A.
Publicado em 2005

Human PRKC Apoptosis WT1 Regulator Is a Novel PITX2-interacting Protein That Regulates PITX2 Transcriptional Activity in Ocular Cells

Por Acharya, Moulinath, Lingenfelter, David J., Huang, LiJia, Gage, Philip J., Walter, Michael A.
Publicado em 2009

Analyses of the Effects That Disease-Causing Missense Mutations Have on the Structure and Function of the Winged-Helix Protein FOXC1

Por Saleem, Ramsey A., Banerjee-Basu, Sharmila, Berry, Fred B., Baxevanis, Andreas D., Walter, Michael A.
Publicado em 2001

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 em 2012

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 em 2004

PITX2 Is Involved in Stress Response in Cultured Human Trabecular Meshwork Cells through Regulation of SLC13A3

Por Strungaru, M. Hermina, Footz, Tim, Liu, Yi, Berry, Fred B., Belleau, Pascal, Semina, Elena V., Raymond, Vincent, Walter, Michael A.
Publicado em 2011

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 no Oncotarget (2016)

A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variation

Por Chanda, Bhaskar, Asai-Coakwell, Mika, Ye, Ming, Mungall, Andrew J., Barrow, Margaret, Dobyns, William B., Behesti, Hourinaz, Sowden, Jane C., Carter, Nigel P., Walter, Michael A., Lehmann, Ordan J.
Publicado em 2008

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 em 2012

Foxa1 deletion in luminal epithelium causes prostatic hyperplasia and alteration of differentiated phenotype

Por DeGraff, David J., Grabowska, Magdalena M., Case, Tom, Yu, Xiuping, Herrick, Mary K., Hayward, William, Strand, Douglas W., Cates, Justin M., Hayward, Simon W., Gao, Nan, Walter, Michael A., Buttyan, Ralph, Yi, Yajun, Kaestner, Klaus H., Matusik, Robert J.
Publicado no Lab Invest (2014)