Sökresultat - J. Fielding Hejtmancik

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  1. 1
    INVITED EDITORIAL The Genetics of Cataract: Our Vision Becomes Clearer

    INVITED EDITORIAL The Genetics of Cataract: Our Vision Becomes Clearer av J. Fielding Hejtmancik

    Publicerad 1998
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  2. 2
    Congenital cataracts and their molecular genetics

    Congenital cataracts and their molecular genetics av J. Fielding Hejtmancik

    Publicerad 2007
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  3. 3
    Genetics of human cataract

    Genetics of human cataract av Alan Shiels, J. Fielding Hejtmancik

    Publicerad 2013
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  4. 4
    Molecular Genetics of Cataract

    Molecular Genetics of Cataract av Alan Shiels, J. Fielding Hejtmancik

    Publicerad 2015
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  5. 5
    Molecular genetics of age-related cataract

    Molecular genetics of age-related cataract av J. Fielding Hejtmancik, Marc Kantorow

    Publicerad 2004
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  6. 6
    Mutations and mechanisms in congenital and age-related cataracts

    Mutations and mechanisms in congenital and age-related cataracts av Alan Shiels, J. Fielding Hejtmancik

    Publicerad 2016
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  7. 7
    Biology of Inherited Cataracts and Opportunities for Treatment

    Biology of Inherited Cataracts and Opportunities for Treatment av Alan Shiels, J. Fielding Hejtmancik

    Publicerad 2019
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  8. 8
    Inherited cataracts: Genetic mechanisms and pathways new and old

    Inherited cataracts: Genetic mechanisms and pathways new and old av Alan Shiels, J. Fielding Hejtmancik

    Publicerad 2021
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  9. 9
    Overview of the Lens

    Overview of the Lens av J. Fielding Hejtmancik, Alan Shiels

    Publicerad 2015
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  10. 10
    Autosomal recessive juvenile onset cataract associated with mutation in BFSP1

    Autosomal recessive juvenile onset cataract associated with mutation in BFSP1 av Ramya Devi Ramachandran, Vijayalakshmi Perumalsamy, J. Fielding Hejtmancik

    Publicerad 2007
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    Artigo
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  11. 11
    Autosomal Recessive Familial Exudative Vitreoretinopathy Is Associated with Mutations in LRP5

    Autosomal Recessive Familial Exudative Vitreoretinopathy Is Associated with Mutations in LRP5 av Xiaodong Jiao, V. Ventruto, Michael T. Trese, Barkur S. Shastry, J. Fielding Hejtmancik

    Publicerad 2004
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    Artigo
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  12. 12
    Thionein can serve as a reducing agent for the methionine sulfoxide reductases

    Thionein can serve as a reducing agent for the methionine sulfoxide reductases av Daphna Sagher, David Brunell, J. Fielding Hejtmancik, Marc Kantorow, Nathan Brot, Herbert Weissbach

    Publicerad 2006
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    Artigo
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  13. 13
    Lens Biology and Biochemistry

    Lens Biology and Biochemistry av J. Fielding Hejtmancik, Sheikh Riazuddin, Rebecca McGreal, Wei Liu, Aleš Cvekl, Alan Shiels

    Publicerad 2015
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  14. 14
    The c.119-123dup5bp mutation in human γC-crystallin destabilizes the protein and activates the unfolded protein response to cause highly variable cataracts

    The c.119-123dup5bp mutation in human γC-crystallin destabilizes the protein and activates the unfolded protein response to cause highly variable cataracts av Mohd Hussain Shah, Venkata Pulla Rao Vendra, Christian Ostrowski, Zhiwei Ma, J. Fielding Hejtmancik

    Publicerad 2025
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    Artigo
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  15. 15
    Association analysis of nine candidate gene polymorphisms in Indian patients with type 2 diabetic retinopathy

    Association analysis of nine candidate gene polymorphisms in Indian patients with type 2 diabetic retinopathy av Suganthalakshmi Balasubbu, Periasamy Sundaresan, Anand Rajendran, Kim Ramasamy, Gowthaman Govindarajan, Perumalsamy Namperumalsamy, J. Fielding Hejtmancik

    Publicerad 2010
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    Artigo
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  16. 16
    CDKN2B Polymorphism Is Associated with Primary Open-Angle Glaucoma (POAG) in the Afro-Caribbean Population of Barbados, West Indies

    CDKN2B Polymorphism Is Associated with Primary Open-Angle Glaucoma (POAG) in the Afro-Caribbean Population of Barbados, West Indies av Dan Cao, Xiaodong Jiao, Xing Liu, Anselm Hennis, M. Cristina Leske, Barbara Nemesure, J. Fielding Hejtmancik

    Publicerad 2012
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    Artigo
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  17. 17
    Clinical and genetic features in Italian Bietti crystalline dystrophy patients

    Clinical and genetic features in Italian Bietti crystalline dystrophy patients av Settimio Rossi, Francesco Testa, Anren Li, Fulya Yaylacıoğlu Tuncay, Carlo Gesualdo, J. Fielding Hejtmancik, Francesca Simonelli

    Publicerad 2012
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    Artigo
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  18. 18
    Thyroid hormone receptor beta mutations alter photoreceptor development and function in Danio rerio (zebrafish)

    Thyroid hormone receptor beta mutations alter photoreceptor development and function in Danio rerio (zebrafish) av Ciana Deveau, Xiaodong Jiao, Sachihiro C. Suzuki, Asha Krishnakumar, Takeshi Yoshimatsu, J. Fielding Hejtmancik, Ralph Nelson

    Publicerad 2020
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  19. 19
    Autophagy Requirements for Eye Lens Differentiation and Transparency

    Autophagy Requirements for Eye Lens Differentiation and Transparency av Lisa Brennan, M. Joseph Costello, J. Fielding Hejtmancik, A. Sue Menko, Sheikh Riazuddin, Alan Shiels, Marc Kantorow

    Publicerad 2023
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  20. 20
    Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11

    Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11 av X. Jiao, Abeda Sultana, Prashant Garg, Ramamurthy Balasubramanya, Geeta K. Vemuganti, Nibaran Gangopadhyay, J. Fielding Hejtmancik, Chitra Kannabiran

    Publicerad 2006
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    Carta
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