Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Naheed W Khan"'
Autor:
Pooja Biswas, Adda L Villanueva, Angel Soto-Hermida, Jacque L Duncan, Hiroko Matsui, Shyamanga Borooah, Berzhan Kurmanov, Gabriele Richard, Shahid Y Khan, Kari Branham, Bonnie Huang, John Suk, Benjamin Bakall, Jeffrey L Goldberg, Luis Gabriel, Naheed W Khan, Pongali B Raghavendra, Jason Zhou, Sindhu Devalaraja, Andrew Huynh, Akhila Alapati, Qais Zawaydeh, Richard G Weleber, John R Heckenlively, J Fielding Hejtmancik, Sheikh Riazuddin, Paul A Sieving, S Amer Riazuddin, Kelly A Frazer, Radha Ayyagari
Publikováno v:
PLoS Genetics, Vol 17, Iss 10, p e1009848 (2021)
Patients with inherited retinal dystrophies (IRDs) were recruited from two understudied populations: Mexico and Pakistan as well as a third well-studied population of European Americans to define the genetic architecture of IRD by performing whole-ge
Externí odkaz:
https://doaj.org/article/100510e296874924a61b4222d50d1e2c
Autor:
Debra A Thompson, Naheed W Khan, Mohammad I Othman, Bo Chang, Lin Jia, Garrett Grahek, Zhijian Wu, Suja Hiriyanna, Jacob Nellissery, Tiansen Li, Hemant Khanna, Peter Colosi, Anand Swaroop, John R Heckenlively
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e35865 (2012)
Animal models of human disease are an invaluable component of studies aimed at understanding disease pathogenesis and therapeutic possibilities. Mutations in the gene encoding retinitis pigmentosa GTPase regulator (RPGR) are the most common cause of
Externí odkaz:
https://doaj.org/article/cc73b1534a6e4e539148044cac915bde
Autor:
Sunil K Parapuram, Radu I Cojocaru, Jessica R Chang, Ritu Khanna, Matthew Brooks, Mohammad Othman, Sepideh Zareparsi, Naheed W Khan, Norimoto Gotoh, Tiziana Cogliati, Anand Swaroop
Publikováno v:
PLoS ONE, Vol 5, Iss 11, p e13885 (2010)
Advanced age contributes to clinical manifestations of many retinopathies and represents a major risk factor for age-related macular degeneration, a leading cause of visual impairment and blindness in the elderly. Rod photoreceptors are especially vu
Externí odkaz:
https://doaj.org/article/525a0e36e0944b94baaef16cb3f559c2
Publikováno v:
International Journal of Retina and Vitreous, Vol 5, Iss 1, Pp 1-6 (2019)
Abstract Background Stargardt disease (STGD) and age-related macular degeneration (AMD) share clinical and pathophysiological features. In AMD, macular hyperpigmentary changes are associated to a worse prognosis. The purpose of this study was to char
Externí odkaz:
https://doaj.org/article/e3d5a1d8c47c41b2b01476f26d2baf72
Autor:
Kecia L. Feathers, Lin Jia, Naheed W. Khan, Alexander J. Smith, Jian-Xing Ma, Robin R. Ali, Debra A. Thompson
Publikováno v:
Human Gene Therapy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1246754c79a829a7f249c80ede73be3b
https://doi.org/10.1089/hum.2022.240
https://doi.org/10.1089/hum.2022.240
Publikováno v:
Ophthalmic Genetics. 43:462-469
Self-determination theory (SDT) of human motivation was used to examine associations between different forms of motivation in Argus II retinal prosthesis users and their engagement and satisfaction with the Argus device.Nine subjects were administere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09b627a860db63a499544322535ca0b7
https://doi.org/10.1080/13816810.2022.2050765
https://doi.org/10.1080/13816810.2022.2050765
Autor:
Pooja Biswas, Anne Marie Berry, Qais Zawaydeh, Dirk-Uwe G. Bartsch, Pongali B. Raghavendra, J. Fielding Hejtmancik, Naheed W. Khan, S. Amer Riazuddin, Radha Ayyagari
Publikováno v:
Genes; Volume 13; Issue 8; Pages: 1461
Genes, vol 13, iss 8
Genes, vol 13, iss 8
We previously identified a homozygous G178R mutation in human ASRGL1 (hASRGL1) through whole-exome analysis responsible for early onset retinal degeneration (RD) in patients with cone–rod dystrophy. The mutant G178R ASRGL1 expressed in Cos-7 cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f79d195e52b8ab7038ca322ef33136b1
Autor:
John Suk, S. Amer Riazuddin, Kelly A. Frazer, Kari Branham, Pooja Biswas, Sindhu Devalaraja, Jeffrey L. Goldberg, Qais Zawaydeh, Benjamin Bakall, Pongali B. Raghavendra, J. Fielding Hejtmancik, Angel Soto-Hermida, Bonnie Huang, Paul A. Sieving, Sheikh Riazuddin, Richard G. Weleber, Berzhan Kurmanov, Jason Zhou, Gabriele Richard, Jacque L. Duncan, Shahid Y. Khan, Adda Villanueva, Akhila Alapati, Shyamanga Borooah, Radha Ayyagari, Hiroko Matsui, Luis Alexandre Rassi Gabriel, Andrew Huynh, Naheed W. Khan, John R. Heckenlively
Publikováno v:
PLoS genetics, vol 17, iss 10
PLoS Genetics, Vol 17, Iss 10, p e1009848 (2021)
PLoS Genetics
PLoS Genetics, Vol 17, Iss 10, p e1009848 (2021)
PLoS Genetics
Patients with inherited retinal dystrophies (IRDs) were recruited from two understudied populations: Mexico and Pakistan as well as a third well-studied population of European Americans to define the genetic architecture of IRD by performing whole-ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76a8c5b8da8ed5400dee9737837f1c5b
https://escholarship.org/uc/item/8tq9x6bw
https://escholarship.org/uc/item/8tq9x6bw
Publikováno v:
International Journal of Retina and Vitreous, Vol 5, Iss 1, Pp 1-6 (2019)
International Journal of Retina and Vitreous
International Journal of Retina and Vitreous
Background Stargardt disease (STGD) and age-related macular degeneration (AMD) share clinical and pathophysiological features. In AMD, macular hyperpigmentary changes are associated to a worse prognosis. The purpose of this study was to characterize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05374fa25c66f854474101c28b06bc53
http://link.springer.com/article/10.1186/s40942-019-0160-4
http://link.springer.com/article/10.1186/s40942-019-0160-4
Publikováno v:
Ophthalmic Genet
BACKGROUND: Several novel treatments of inherited retinal degenerations have undergone phase I/IIa clinical trials with limited sample size, yet investigators must still determine if toxicity or an efficacy signal occurred or if the change was due to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38758f24b462b92a87873097f0729439
https://pubmed.ncbi.nlm.nih.gov/33729062
https://pubmed.ncbi.nlm.nih.gov/33729062