檢索結果 - 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 由 J. Fielding Hejtmancik

    出版 1998
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  2. 2
    Congenital cataracts and their molecular genetics

    Congenital cataracts and their molecular genetics 由 J. Fielding Hejtmancik

    出版 2007
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  3. 3
    Genetics of human cataract

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

    出版 2013
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  4. 4
    Molecular Genetics of Cataract

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

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

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

    出版 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 由 Alan Shiels, J. Fielding Hejtmancik

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

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

    出版 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 由 Alan Shiels, J. Fielding Hejtmancik

    出版 2021
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  9. 9
    Overview of the Lens

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

    出版 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 由 Ramya Devi Ramachandran, Vijayalakshmi Perumalsamy, J. Fielding Hejtmancik

    出版 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 由 Xiaodong Jiao, V. Ventruto, Michael T. Trese, Barkur S. Shastry, J. Fielding Hejtmancik

    出版 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 由 Daphna Sagher, David Brunell, J. Fielding Hejtmancik, Marc Kantorow, Nathan Brot, Herbert Weissbach

    出版 2006
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  13. 13
    Lens Biology and Biochemistry

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

    出版 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 由 Mohd Hussain Shah, Venkata Pulla Rao Vendra, Christian Ostrowski, Zhiwei Ma, J. Fielding Hejtmancik

    出版 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 由 Suganthalakshmi Balasubbu, Periasamy Sundaresan, Anand Rajendran, Kim Ramasamy, Gowthaman Govindarajan, Perumalsamy Namperumalsamy, J. Fielding Hejtmancik

    出版 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 由 Dan Cao, Xiaodong Jiao, Xing Liu, Anselm Hennis, M. Cristina Leske, Barbara Nemesure, J. Fielding Hejtmancik

    出版 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 由 Settimio Rossi, Francesco Testa, Anren Li, Fulya Yaylacıoğlu Tuncay, Carlo Gesualdo, J. Fielding Hejtmancik, Francesca Simonelli

    出版 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) 由 Ciana Deveau, Xiaodong Jiao, Sachihiro C. Suzuki, Asha Krishnakumar, Takeshi Yoshimatsu, J. Fielding Hejtmancik, Ralph Nelson

    出版 2020
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    Artigo
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  19. 19
    Autophagy Requirements for Eye Lens Differentiation and Transparency

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

    出版 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 由 X. Jiao, Abeda Sultana, Prashant Garg, Ramamurthy Balasubramanya, Geeta K. Vemuganti, Nibaran Gangopadhyay, J. Fielding Hejtmancik, Chitra Kannabiran

    出版 2006
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    Carta
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