K. Kozlowski

Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome.

M. Walter, Y. Buys, E. Héon, 2001, Human molecular genetics.

Free radical adducts induce alterations in DNA cytosine methylation.

S. Weitzman, P. Turk, K. Kozlowski, 1994, Proceedings of the National Academy of Sciences of the United States of America.

CLIC5A, a component of the ezrin-podocalyxin complex in glomeruli, is a determinant of podocyte integrity.

B. Ballermann, Marya Obeidat, M. Berryman, 2010, American journal of physiology. Renal physiology.

Variation in residual PITX2 activity underlies the phenotypic spectrum of anterior segment developmental disorders.

M. Walter, K. Kozlowski, 2000, Human molecular genetics.

The protein phosphatase-1 targeting subunit TIMAP regulates LAMR1 phosphorylation.

B. Ballermann, Kwanghee Kim, Hyeon-sook Suh, 2005, Biochemical and biophysical research communications.

Analysis of mutations of the PITX2 transcription factor found in patients with Axenfeld-Rieger syndrome.

M. Walter, K. Kozlowski, F. Idrees, 2009, Investigative ophthalmology & visual science.

Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformations.

M. Walter, E. Héon, M. B. Shields, 2004, Investigative ophthalmology & visual science.

Molecular genetics of Axenfeld-Rieger malformations.

M. Walter, M. Lines, K. Kozlowski, 2002, Human molecular genetics.

Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome.

M. Walter, E. Semina, W. Pearce, 1998, Human molecular genetics.

Phosphorylation of TIMAP by Glycogen Synthase Kinase-3β Activates Its Associated Protein Phosphatase 1*

B. Ballermann, Charles Holmes, Laiji Li, 2007, Journal of Biological Chemistry.