Hasil Pencarian - J Fielding Hejtmancik

Perbaiki Hasil
  1. 1
    Germ-line and somatic EPHA2 coding variants in lens aging and cataract.

    Germ-line and somatic EPHA2 coding variants in lens aging and cataract. oleh Thomas M Bennett, Oussama M'Hamdi, J Fielding Hejtmancik, Alan Shiels

    Diterbitkan 2017-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    Molecular Genetic Analysis of Ukrainian Families with Congenital Cataracts

    Molecular Genetic Analysis of Ukrainian Families with Congenital Cataracts oleh Xiaodong Jiao, Mariia Viswanathan, Nadiia Fedorivna Bobrova, Tatiana Viktorivna Romanova, J. Fielding Hejtmancik

    Diterbitkan 2022-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Changes in DNA methylation hallmark alterations in chromatin accessibility and gene expression for eye lens differentiation

    Changes in DNA methylation hallmark alterations in chromatin accessibility and gene expression for eye lens differentiation oleh Joshua Disatham, Lisa Brennan, Xiaodong Jiao, Zhiwei Ma, J. Fielding Hejtmancik, Marc Kantorow

    Diterbitkan 2022-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    Human γS-Crystallin Mutation F10_Y11delinsLN in the First Greek Key Pair Destabilizes and Impairs Tight Packing Causing Cortical Lamellar Cataract

    Human γS-Crystallin Mutation F10_Y11delinsLN in the First Greek Key Pair Destabilizes and Impairs Tight Packing Causing Cortical Lamellar Cataract oleh Venkata Pulla Rao Vendra, Christian Ostrowski, Marzena A. Dyba, Sergey G. Tarasov, J. Fielding Hejtmancik

    Diterbitkan 2023-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    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. oleh Dan Cao, Xiaodong Jiao, Xing Liu, Anselm Hennis, M Cristina Leske, Barbara Nemesure, J Fielding Hejtmancik

    Diterbitkan 2012-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    A novel MIP gene mutation analysis in a Chinese family affected with congenital progressive punctate cataract.

    A novel MIP gene mutation analysis in a Chinese family affected with congenital progressive punctate cataract. oleh Xuchen Ding, Nan Zhou, Hui Lin, Jianjun Chen, Chunyuan Zhao, Guangkai Zhou, J Fielding Hejtmancik, Yanhua Qi

    Diterbitkan 2014-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  7. 7
    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). oleh Ciana Deveau, Xiaodong Jiao, Sachihiro C Suzuki, Asha Krishnakumar, Takeshi Yoshimatsu, J Fielding Hejtmancik, Ralph F Nelson

    Diterbitkan 2020-06-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  8. 8
    Autophagy Requirements for Eye Lens Differentiation and Transparency

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

    Diterbitkan 2023-02-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  9. 9
    Functional validation of hydrophobic adaptation to physiological temperature in the small heat shock protein αA-crystallin.

    Functional validation of hydrophobic adaptation to physiological temperature in the small heat shock protein αA-crystallin. oleh Mason Posner, Andor J Kiss, Jackie Skiba, Amy Drossman, Monika B Dolinska, J Fielding Hejtmancik, Yuri V Sergeev

    Diterbitkan 2012-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  10. 10
    A Bietti Crystalline Dystrophy Mouse Model Shows Increased Sensitivity to Light-Induced Injury

    A Bietti Crystalline Dystrophy Mouse Model Shows Increased Sensitivity to Light-Induced Injury oleh Zhiwei Ma, Xiaodong Jiao, Martin-Paul Agbaga, Robert E. Anderson, Haohua Qian, Qian Li, Lijin Dong, J. Fielding Hejtmancik

    Diterbitkan 2022-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  11. 11
    Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family.

    Autosomal recessive congenital cataracts linked to HSF4 in a consanguineous Pakistani family. oleh Xiaodong Jiao, Shahid Y Khan, Haiba Kaul, Tariq Butt, Muhammad Asif Naeem, Sheikh Riazuddin, J Fielding Hejtmancik, S Amer Riazuddin

    Diterbitkan 2019-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  12. 12
    Detection of variants in 15 genes in 87 unrelated Chinese patients with Leber congenital amaurosis.

    Detection of variants in 15 genes in 87 unrelated Chinese patients with Leber congenital amaurosis. oleh Lin Li, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, Xiangming Guo, Xiaodong Jiao, Qingjiong Zhang, J Fielding Hejtmancik

    Diterbitkan 2011-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  13. 13
    Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia

    Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia oleh Yi Jiang, Xueshan Xiao, Wenmin Sun, Yingwei Wang, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, J. Fielding Hejtmancik, Qingjiong Zhang

    Diterbitkan 2024-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  14. 14
    SARS-CoV-2 ORF3A interacts with the Clic-like chloride channel-1 (CLCC1) and triggers an unfolded protein response

    SARS-CoV-2 ORF3A interacts with the Clic-like chloride channel-1 (CLCC1) and triggers an unfolded protein response oleh Hannah N. Gruner, Yaohuan Zhang, Kaavian Shariati, Nicholas Yiv, Zicheng Hu, Yuhao Wang, J. Fielding Hejtmancik, Michael T. McManus, Kevin Tharp, Gregory Ku

    Diterbitkan 2023-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  15. 15
    A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts

    A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts oleh Bushra Irum, Firoz Kabir, Nadav Shoshany, Shahid Y. Khan, Bushra Rauf, Muhammad Asif Naeem, Tanveer A. Qaiser, Sheikh Riazuddin, J. Fielding Hejtmancik, S. Amer Riazuddin

    Diterbitkan 2022-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  16. 16
    Retinal Development and Pathophysiology in Kcnj13 Knockout Mice

    Retinal Development and Pathophysiology in Kcnj13 Knockout Mice oleh Xiaodong Jiao, Zhiwei Ma, Jingqi Lei, Pinghu Liu, Xiaoyu Cai, Pawan K. Shahi, Chi-Chao Chan, Robert Fariss, Bikash R. Pattnaik, Lijin Dong, J. Fielding Hejtmancik

    Diterbitkan 2022-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  17. 17
    A Common Ancestral Mutation in CRYBB3 Identified in Multiple Consanguineous Families with Congenital Cataracts.

    A Common Ancestral Mutation in CRYBB3 Identified in Multiple Consanguineous Families with Congenital Cataracts. oleh Xiaodong Jiao, Firoz Kabir, Bushra Irum, Arif O Khan, Qiwei Wang, David Li, Asma A Khan, Tayyab Husnain, Javed Akram, Sheikh Riazuddin, J Fielding Hejtmancik, S Amer Riazuddin

    Diterbitkan 2016-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  18. 18
    MITF protects against oxidative damage-induced retinal degeneration by regulating the NRF2 pathway in the retinal pigment epithelium

    MITF protects against oxidative damage-induced retinal degeneration by regulating the NRF2 pathway in the retinal pigment epithelium oleh Shuxian Han, Jianjun Chen, Jiajia Hua, Xiaojuan Hu, Shuhui Jian, Guoxiao Zheng, Jing Wang, Huirong Li, Jinglei Yang, J. Fielding Hejtmancik, Jia Qu, Xiaoyin Ma, Ling Hou

    Diterbitkan 2020-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  19. 19
    Correction: Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts.

    Correction: Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts. oleh Xiaodong Jiao, Shahid Y Khan, Bushra Irum, Arif O Khan, Qiwei Wang, Firoz Kabir, Asma A Khan, Tayyab Husnain, Javed Akram, Sheikh Riazuddin, J Fielding Hejtmancik, S Amer Riazuddin

    Diterbitkan 2017-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  20. 20
    Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts.

    Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts. oleh Xiaodong Jiao, Shahid Y Khan, Bushra Irum, Arif O Khan, Qiwei Wang, Firoz Kabir, Asma A Khan, Tayyab Husnain, Javed Akram, Sheikh Riazuddin, J Fielding Hejtmancik, S Amer Riazuddin

    Diterbitkan 2015-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: