Hasil Pencarian - Robyn V. Jamieson

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  1. 1
    Comprehensive characterization of fetal and mature retinal cell identity to assess the fidelity of retinal organoids

    Comprehensive characterization of fetal and mature retinal cell identity to assess the fidelity of retinal organoids oleh Hani Jieun Kim, Michelle O’Hara-Wright, Daniel Kim, To Ha Loi, Benjamin Y. Lim, Robyn V. Jamieson, Anai Gonzalez-Cordero, Pengyi Yang

    Diterbitkan 2023-01-01
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  2. 2
    Evaluation for Retinal Therapy for RPE65 Variation Assessed in hiPSC Retinal Pigment Epithelial Cells

    Evaluation for Retinal Therapy for RPE65 Variation Assessed in hiPSC Retinal Pigment Epithelial Cells oleh Benjamin M. Nash, To Ha Loi, Milan Fernando, Amin Sabri, James Robinson, Anson Cheng, Steven S. Eamegdool, Elizabeth Farnsworth, Bruce Bennetts, John R. Grigg, Seo-Kyung Chung, Anai Gonzalez-Cordero, Robyn V. Jamieson

    Diterbitkan 2021-01-01
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  3. 3
    Patient-Reported Health-Related Quality of Life in Individuals with Inherited Retinal Diseases

    Patient-Reported Health-Related Quality of Life in Individuals with Inherited Retinal Diseases oleh Deborah Schofield, PhD, Joshua Kraindler, MSc, Owen Tan, MComm, Rupendra Shrestha, PhD, Diana Jelovic, BAppSci, Sarah West, MBMSc, Alan Ma, PhD, FRACP, John Grigg, MD, FRANZCO, Robyn V. Jamieson, PhD, FRACP

    Diterbitkan 2022-03-01
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  4. 4
    Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies

    Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies oleh Benjamin M. Nash, Alan Ma, Gladys Ho, Elizabeth Farnsworth, Andre E. Minoche, Mark J. Cowley, Christopher Barnett, Janine M. Smith, To Ha Loi, Karen Wong, Luke St Heaps, Dale Wright, Marcel E. Dinger, Bruce Bennetts, John R. Grigg, Robyn V. Jamieson

    Diterbitkan 2022-03-01
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  5. 5
    AAV capsid bioengineering in primary human retina models

    AAV capsid bioengineering in primary human retina models oleh Adrian Westhaus, Steven S. Eamegdool, Milan Fernando, Paula Fuller-Carter, Alicia A. Brunet, Annie L. Miller, Rabab Rashwan, Maddison Knight, Maciej Daniszewski, Grace E. Lidgerwood, Alice Pébay, Alex Hewitt, Giorgia Santilli, Adrian J. Thrasher, Livia S. Carvalho, Anai Gonzalez-Cordero, Robyn V. Jamieson, Leszek Lisowski

    Diterbitkan 2023-12-01
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  6. 6
    Detection of chromosomal breakpoints in patients with developmental delay and speech disorders.

    Detection of chromosomal breakpoints in patients with developmental delay and speech disorders. oleh Kagistia H Utami, Axel M Hillmer, Irene Aksoy, Elaine G Y Chew, Audrey S M Teo, Zhenshui Zhang, Charlie W H Lee, Pauline J Chen, Chan Chee Seng, Pramila N Ariyaratne, Sigrid L Rouam, Lim Seong Soo, Saira Yousoof, Ivan Prokudin, Gregory Peters, Felicity Collins, Meredith Wilson, Alyson Kakakios, Georges Haddad, Arnaud Menuet, Olivier Perche, Stacey Kiat Hong Tay, Ken W K Sung, Xiaoan Ruan, Yijun Ruan, Edison T Liu, Sylvain Briault, Robyn V Jamieson, Sonia Davila, Valere Cacheux

    Diterbitkan 2014-01-01
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