Zobrazeno 1 - 10
of 25
pro vyhledávání: '"To Ha Loi"'
Autor:
Hani Jieun Kim, Michelle O’Hara-Wright, Daniel Kim, To Ha Loi, Benjamin Y. Lim, Robyn V. Jamieson, Anai Gonzalez-Cordero, Pengyi Yang
Publikováno v:
Stem Cell Reports, Vol 18, Iss 1, Pp 175-189 (2023)
Summary: Characterizing cell identity in complex tissues such as the human retina is essential for studying its development and disease. While retinal organoids derived from pluripotent stem cells have been widely used to model development and diseas
Externí odkaz:
https://doaj.org/article/ee3beb06dd65444dba96d1a761b4dc4b
Autor:
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
Publikováno v:
Stem Cells International, Vol 2021 (2021)
Human induced pluripotent stem cells (hiPSCs) generated from patients and the derivative retinal cells enable the investigation of pathological and novel variants in relevant cell populations. Biallelic pathogenic variants in RPE65 cause early-onset
Externí odkaz:
https://doaj.org/article/efc0b3e3faab4cc08d30e555d2e914e1
Autor:
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
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 7, p 3905 (2022)
The inherited retinal dystrophies (IRDs) are a clinically and genetically complex group of disorders primarily affecting the rod and cone photoreceptors or other retinal neuronal layers, with emerging therapies heralding the need for accurate molecul
Externí odkaz:
https://doaj.org/article/0cebdd4d5ce8417199fe976e77ef071a
Akademický článek
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Akademický článek
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Autor:
Timothy J. Molloy, Ernst J. Wolvetang, Melinda L. Tursky, David D.F. Ma, Helen Tao, Suad Alateeq, To Ha Loi, Crisbel M. Artuz
Publikováno v:
Stem Cell Reports
Summary Induced pluripotent stem cells (iPSCs) are an invaluable resource for the study of human disease. However, there are no standardized methods for differentiation into hematopoietic cells, and there is a lack of robust, direct comparisons of di
Autor:
Fidelle, Chahine Karam, To Ha, Loi, Alan, Ma, Benjamin M, Nash, John R, Grigg, Darshan, Parekh, Lisa G, Riley, Elizabeth, Farnsworth, Bruce, Bennetts, Anai, Gonzalez-Cordero, Robyn V, Jamieson
Publikováno v:
Journal of personalized medicine. 12(3)
The
Publikováno v:
Essentials in Ophthalmology ISBN: 9789811591839
Phosphodiesterase 6B (PDE6B) is one of the most commonly mutated genes to cause autosomal recessive retinitis pigmentosa (RP), also known as rod-cone dystrophy. The PDE6B protein plays a crucial role in the phototransduction cascade. With the emergin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::414fdf30e6ecc732a174a2ad5ed33cb7
https://doi.org/10.1007/978-981-15-9184-6_15
https://doi.org/10.1007/978-981-15-9184-6_15
Autor:
To Ha Loi, Diana Jelovic, Bruce Bennetts, Mark Gorbatov, Edward H. Hughes, Philip J Polkinghorne, Christopher J. G. Watson, Robyn V. Jamieson, Benjamin M. Nash, John R. Grigg, Alec Lin Hou, Andrea L Vincent
Publikováno v:
Eur J Hum Genet
The COL9A3 gene encodes one of the three alpha chains of Type IX collagen, with heterozygous variants reported to cause multiple epiphyseal dysplasia, and suggested as contributory in some cases of sensorineural hearing loss. Patients with homozygous
Autor:
Melinda Tursky, Suad Alateeq, Crisbel Artuz, To Ha Loi, David Ma, Tim Molloy, Helen Tao, Ernst Wolvetang
Publikováno v:
Experimental Hematology. 100:S107