Michael A. Wait < Michael A. Walter < Michael A. Weaver

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List of bibliographic references indexed by Michael A. Walter

Number of relevant bibliographic references: 6.

Ident.	Authors (with country if any)	Title
001550 (2016)	Daniela Tavian [Italie] ; Sara Missaglia [Italie] ; Paolo E. Maltese [Italie] ; Sandro Michelini [Italie] ; Alessandro Fiorentino [Italie] ; Maurizio Ricci [Italie] ; Roberta Serrani [Italie] ; Michael A. Walter [Canada] ; Matteo Bertelli [Italie]	FOXC2 disease-mutations identified in lymphedema-distichiasis patients cause both loss and gain of protein function
006A88 (2008)	Christina D. Fetterman [Canada] ; Bruce Rannala [États-Unis] ; Michael A. Walter [Canada]	Identification and analysis of evolutionary selection pressures acting at the molecular level in five forkhead subfamilies
007C60 (2006)	Fred B. Berry ; Matthew A. Lines ; J. Martin Oas [États-Unis] ; Tim Footz ; D. Alan Underhill ; Philip J. Gage [États-Unis] ; Michael A. Walter	Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld–Rieger syndrome and anterior segment dysgenesis
008103 (2005)	Fred B. Berry ; Yahya Tamimi [Canada] ; Michelle V. Carle ; Ordan J. Lehmann [Canada] ; Michael A. Walter [Canada]	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 distichiasis
009007 (2003)	Ramsey A. Saleem ; Sharmila Banerjee-Basu [États-Unis] ; Fred B. Berry [Canada] ; Andreas D. Baxevanis [États-Unis] ; Michael A. Walter [Canada]	Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1
009656 (2002)	Matthew A. Lines [Canada] ; Kathy Kozlowski [Canada] ; Michael A. Walter [Canada]	Molecular genetics of Axenfeld–Rieger malformations

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