Hasil Pencarian - Jason Comander

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  1. 1
    Efficient In Silico Identification of a Common Insertion in the MAK Gene which Causes Retinitis Pigmentosa.

    Efficient In Silico Identification of a Common Insertion in the MAK Gene which Causes Retinitis Pigmentosa. oleh Kinga M Bujakowska, Joseph White, Emily Place, Mark Consugar, Jason Comander

    Diterbitkan 2015-01-01
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  2. 2
    Predictive value of genetic testing for inherited retinal diseases in patients with suspected atypical autoimmune retinopathy

    Predictive value of genetic testing for inherited retinal diseases in patients with suspected atypical autoimmune retinopathy oleh Lynn K. Stanwyck, Emily M. Place, Jason Comander, Rachel M. Huckfeldt, Lucia Sobrin

    Diterbitkan 2019-09-01
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  3. 3
    P259: The impact of no-cost testing programs for inherited retinal degeneration on post-testing follow-up genetic services

    P259: The impact of no-cost testing programs for inherited retinal degeneration on post-testing follow-up genetic services oleh Kaitlin O'Connell, John Borchert, Jason Comander, Rachel Huckfeldt, Eric Pierce, Emily Place

    Diterbitkan 2023-01-01
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  4. 4
    Tauroursodeoxycholic acid (TUDCA) protects photoreceptors from cell death after experimental retinal detachment.

    Tauroursodeoxycholic acid (TUDCA) protects photoreceptors from cell death after experimental retinal detachment. oleh Dimosthenis Mantopoulos, Yusuke Murakami, Jason Comander, Aristomenis Thanos, Miin Roh, Joan W Miller, Demetrios G Vavvas

    Diterbitkan 2011-01-01
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  5. 5
    Natural history of retinitis pigmentosa based on genotype, vitamin A/E supplementation, and an electroretinogram biomarker

    Natural history of retinitis pigmentosa based on genotype, vitamin A/E supplementation, and an electroretinogram biomarker oleh Jason Comander, Carol Weigel DiFranco, Kit Sanderson, Emily Place, Matthew Maher, Erin Zampaglione, Yan Zhao, Rachel M. Huckfeldt, Kinga M. Bujakowska, Eric Pierce

    Diterbitkan 2023-08-01
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  6. 6
    NOD2 genetic variants and sarcoidosis-associated uveitis

    NOD2 genetic variants and sarcoidosis-associated uveitis oleh Samaneh Davoudi, Daniel Navarro-Gomez, Lishuang Shen, Cindy Ung, Aiai Ren, Lynn Sullivan, Mindy Kwong, Maria Janessian, Jason Comander, Xiaowu Gai, Ann-Marie Lobo, George N. Papaliodis, Lucia Sobrin

    Diterbitkan 2016-10-01
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  7. 7
    Structure-based network analysis predicts pathogenic variants in human proteins associated with inherited retinal disease

    Structure-based network analysis predicts pathogenic variants in human proteins associated with inherited retinal disease oleh Blake M. Hauser, Yuyang Luo, Anusha Nathan, Ahmad Al-Moujahed, Demetrios G. Vavvas, Jason Comander, Eric A. Pierce, Emily M. Place, Kinga M. Bujakowska, Gaurav D. Gaiha, Elizabeth J. Rossin

    Diterbitkan 2024-05-01
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  8. 8
    P408: Perspectives of rare disease experts on sequencing newborns for treatable genetic conditions*

    P408: Perspectives of rare disease experts on sequencing newborns for treatable genetic conditions* oleh Nidhi Shah, Nina Gold, Sophia Adelson, Shardae Williams, Sarah Bick, Jessica Gold, Alanna Strong, Rebecca Ganetzky, Amy Roberts, Melissa Walker, Alexander Holtz, Vijay Sankaran, Ottavia Delmonte, Weizhen Tan, Ingrid Holm, Jay Thiagarajah, Junne Kamihara, Jason Comander, Emily Place, Janey Wiggs, Robert Green

    Diterbitkan 2023-01-01
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