檢索結果 - Michael A. Walter

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  1. 1
    SOX Genes: Architects of Development

    SOX Genes: Architects of Development 由 Heather Prior, Michael A. Walter

    出版 1996
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    Artigo
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  2. 2
    Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithms

    Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithms 由 Morteza Seifi, Michael A. Walter

    出版 2018
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  3. 3
    FOXC1, the new player in the cancer sandbox

    FOXC1, the new player in the cancer sandbox 由 Fahed Elian, Elizabeth Yan, Michael A. Walter

    出版 2017
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    Revisão
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  4. 4
    FOXC1 Transcriptional Regulation Is Mediated by N- and C-terminal Activation Domains and Contains a Phosphorylated Transcriptional Inhibitory Domain

    FOXC1 Transcriptional Regulation Is Mediated by N- and C-terminal Activation Domains and Contains a Phosphorylated Transcriptional Inhibitory Domain 由 Fred B. Berry, Ramsey A. Saleem, Michael A. Walter

    出版 2002
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  5. 5
    Complete physical map of the human immunoglobulin heavy chain constant region gene complex.

    Complete physical map of the human immunoglobulin heavy chain constant region gene complex. 由 Marten H. Hofker, Michael A. Walter, D W Cox

    出版 1989
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  6. 6
    Susceptibility to multiple sclerosis is associated with the proximal immunoglobulin heavy chain variable region.

    Susceptibility to multiple sclerosis is associated with the proximal immunoglobulin heavy chain variable region. 由 Michael A. Walter, William T. Gibson, George C. Ebers, D W Cox

    出版 1991
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  7. 7
    The physical organization of the human immunoglobulin heavy chain gene complex.

    The physical organization of the human immunoglobulin heavy chain gene complex. 由 Michael A. Walter, Urvashi Surti, Marten H. Hofker, D W Cox

    出版 1990
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  8. 8
    A complex regulatory network of transcription factors critical for ocular development and disease

    A complex regulatory network of transcription factors critical for ocular development and disease 由 Moulinath Acharya, Lijia Huang, Valerie C. Fleisch, W. Ted Allison, Michael A. Walter

    出版 2011
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  9. 9
    Analyses of the Effects That Disease-Causing Missense Mutations Have on the Structure and Function of the Winged-Helix Protein FOXC1

    Analyses of the Effects That Disease-Causing Missense Mutations Have on the Structure and Function of the Winged-Helix Protein FOXC1 由 Ramsey A. Saleem, Sharmila Banerjee‐Basu, Fred B. Berry, Andreas D. Baxevanis, Michael A. Walter

    出版 2001
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  10. 10
    The Forkhead/Winged Helix Gene Mf1 Is Disrupted in the Pleiotropic Mouse Mutation congenital hydrocephalus

    The Forkhead/Winged Helix Gene Mf1 Is Disrupted in the Pleiotropic Mouse Mutation congenital hydrocephalus 由 Tsutomu Kume, Ke-Yu Deng, Virginia P. Winfrey, Douglas B. Gould, Michael A. Walter, Brigid L.M. Hogan

    出版 1998
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  11. 11
    Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25

    Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25 由 Farideh Mirzayans, Douglas B. Gould, Elise Héon, Gail Billingsley, Jason C. Cheung, Alan J. Mears, Michael A. Walter

    出版 2000
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  12. 12
    Circular transcripts of the testis-determining gene Sry in adult mouse testis

    Circular transcripts of the testis-determining gene Sry in adult mouse testis 由 Blanche Capel, Amanda Swain, Silvia K. Nicolis, Adam Hacker, Michael A. Walter, Peter Koopman, P.N. Goodfellow, Robin Lovell‐Badge

    出版 1993
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  13. 13
    FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A

    FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A 由 Fred B. Berry, Jonathan M. Skarie, Farideh Mirzayans, Yannick Fortin, Thomas J. Hudson, Vincent Raymond, Brian A. Link, Michael A. Walter

    出版 2007
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  14. 14
    Roles for the Winged Helix Transcription Factors MF1 and MFH1 in Cardiovascular Development Revealed by Nonallelic Noncomplementation of Null Alleles

    Roles for the Winged Helix Transcription Factors MF1 and MFH1 in Cardiovascular Development Revealed by Nonallelic Noncomplementation of Null Alleles 由 Glenn E. Winnier, Tsutomu Kume, Ke‐Yu Deng, Rhonda Rogers, Justin Bundy, C. Douglas Raines, Michael A. Walter, Brigid L.M. Hogan, Simon J. Conway

    出版 1999
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  15. 15
    Physical linkage of a human immunoglobulin heavy chain variable region gene segment to diversity and joining region elements.

    Physical linkage of a human immunoglobulin heavy chain variable region gene segment to diversity and joining region elements. 由 Harry W. Schroeder, Michael A. Walter, Marten H. Hofker, Allen Ebens, Ko Willems van Dijk, Li‐Jen Liao, D W Cox, E C Milner, Roger M. Perlmutter

    出版 1988
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  16. 16
    Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly

    Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly 由 Andrea L. Vincent, Gail Billingsley, Megan Priston, Donna Williams-Lyn, Joanne Sutherland, Thomas Gläser, Edward R. Oliver, Michael A. Walter, Godfrey Heathcote, Alex V. Levin, Elise Héon

    出版 2001
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    Carta
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  17. 17
    FOXC1 Is a Potential Prognostic Biomarker with Functional Significance in Basal-like Breast Cancer

    FOXC1 Is a Potential Prognostic Biomarker with Functional Significance in Basal-like Breast Cancer 由 Partha Ray, Jinhua Wang, Ying Qu, Myung‐Shin Sim, Jaime Shamonki, Sanjay P. Bagaria, Xing Ye, Bingya Liu, David Elashoff, Dave S.�B. Hoon, Michael A. Walter, John W.M. Martens, Andrea L. Richardson, Armando E. Giuliano, Xiaojiang Cui

    出版 2010
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  18. 18
    FOXA1 deletion in luminal epithelium causes prostatic hyperplasia and alteration of differentiated phenotype

    FOXA1 deletion in luminal epithelium causes prostatic hyperplasia and alteration of differentiated phenotype 由 David J. DeGraff, Magdalena M. Grabowska, Tom Case, Xiuping Yu, Mary K. Herrick, William J. Hayward, Douglas W. Strand, Justin Cates, Simon W. Hayward, Nan Gao, Michael A. Walter, Ralph Buttyan, Yajun Yi, Klaus H. Kaestner, Robert J. Matusik

    出版 2014
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  19. 19
    Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly

    Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly 由 Alan J. Mears, Tim Jordan, Farideh Mirzayans, Stéphane Dubois, Tsutomu Kume, Michael Parlee, Robert Ritch, Ben F. Koop, Wen-Lin Kuo, Colin C. Collins, Jody Marshall, Douglas B. Gould, W G Pearce, Peter Carlsson, Sven Enerbäck, Jean Morissette, Shomi S. Bhattacharya, Brigid L.M. Hogan, Vincent Raymond, Michael A. Walter

    出版 1998
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  20. 20
    Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma

    Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma 由 Adrian Lahola-Chomiak, Tim Footz, Kim Nguyen-Phuoc, Gavin J. Neil, Bao Jian Fan, Keri F. Allen, David S. Greenfield, Richard Parrish, Kevin Linkroum, Louis R. Pasquale, Ralf M. Leonhardt, Robert Ritch, Shari Javadiyan, Jamie E. Craig, W. Ted Allison, Ordan J. Lehmann, Michael A. Walter, Janey L. Wiggs

    出版 2018
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