Canlyniadau Chwilio - Eric Weh

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Mireinio'r Canlyniadau
  1. 1
    Hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress

    Hexokinase 2 is dispensable for photoreceptor development but is required for survival during aging and outer retinal stress gan Eric Weh, Zuzanna Lutrzykowska, Andrew D. Smith, Heather Hager, Mercy Pawar, Thomas J. Wubben, Cagri G. Besirli

    Cyhoeddwyd 2020
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  2. 2
    Whole exome sequence analysis of Peters anomaly

    Whole exome sequence analysis of Peters anomaly gan Eric Weh, Linda M. Reis, Hannah C. Happ, Alex V. Levin, Patricia G. Wheeler, Karen L. David, Erin Carney, Brad Angle, Natalie Hauser, Elena V. Semina

    Cyhoeddwyd 2014
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  3. 3
    Race- and Sex-Related Differences in Retinal Thickness and Foveal Pit Morphology

    Race- and Sex-Related Differences in Retinal Thickness and Foveal Pit Morphology gan Melissa Wagner-Schuman, Adam M. Dubis, Rick N. Nordgren, Yuming Lei, Daniel W. Odell, Hellen Chiao, Eric Weh, William Fischer, Yusufu N. Sulai, Alfredo Dubra, Joseph Carroll

    Cyhoeddwyd 2010
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  4. 4
    Small molecule activation of metabolic enzyme pyruvate kinase muscle isozyme 2, PKM2, circumvents photoreceptor apoptosis

    Small molecule activation of metabolic enzyme pyruvate kinase muscle isozyme 2, PKM2, circumvents photoreceptor apoptosis gan Thomas J. Wubben, Mercy Pawar, Eric Weh, Andrew D. Smith, Peter Sajjakulnukit, Li Zhang, Lipeng Dai, Heather Hager, Manjunath P. Pai, Costas A. Lyssiotis, Cagri G. Besirli

    Cyhoeddwyd 2020
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  5. 5
    Novel <i><scp>B3GALTL</scp></i> mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes

    Novel <i><scp>B3GALTL</scp></i> mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes gan Eric Weh, Linda M. Reis, Rebecca C. Tyler, David Bick, William J. Rhead, Stephanie E Wallace, Tracy L. McGregor, Shelley K. Dills, Mei Chao, J.C. Murray, Elena V. Semina

    Cyhoeddwyd 2013
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:

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