Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Carla B. Mellough"'
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 18 (2024)
Externí odkaz:
https://doaj.org/article/6055cfcf8d684f30b057d23a95fd74f5
Autor:
Carla B. Mellough, Joseph Collin, Rachel Queen, Gerrit Hilgen, Birthe Dorgau, Darin Zerti, Majed Felemban, Kathryn White, Evelyne Sernagor, Majlinda Lako
Publikováno v:
Stem Cells Translational Medicine, Vol 8, Iss 7, Pp 694-706 (2019)
Abstract A major goal in the stem cell field is to generate tissues that can be utilized as a universal tool for in vitro models of development and disease, drug development, or as a resource for patients suffering from disease or injury. Great effor
Externí odkaz:
https://doaj.org/article/48026f595dbd4856afad7887514cb82b
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 14 (2020)
Usher syndrome is a genetic disorder causing neurosensory hearing loss and blindness from retinitis pigmentosa (RP). Adaptive techniques such as braille, digital and optical magnifiers, mobility training, cochlear implants, or other assistive listeni
Externí odkaz:
https://doaj.org/article/737e353ad3bf40cbb284d379db4283af
Autor:
Jason Charng, Enid Chelva, Jennifer A. Thompson, Saumya Shekhar Jamuar, John N. De Roach, Carla B. Mellough, Luke Jennings, Danial Roshandel, Choi Mun Chan, Dan Zhang, Fred K. Chen, Samuel McLenachan, Terri L. McLaren, Shang Chih Chen, Tina M. Lamey, Zhiqin Huang
Publikováno v:
Ophthalmic Genetics. 42:266-275
Background: Mutations in the RCC1 and BTB domain-containing protein 1 (RCBTB1) gene have been implicated in a rare form of retinal dystrophy. Herein, we report the clinical features of a 45-year-ol...
Autor:
Carla B Mellough, Majlinda Lako
Publikováno v:
eLife, Vol 5 (2016)
The genes that control the development of specific tissues and organs in human embryos have been identified.
Externí odkaz:
https://doaj.org/article/905576a40f1b42a788a8a2b232bc9889
Autor:
Jennifer A. Thompson, John N. De Roach, Khine Zaw, Samuel McLenachan, Carla B. Mellough, Dan Zhang, Xiao Zhang, Shang Chih Chen, Tina M. Lamey, Yaqin Alziyadat, Terri L. McLaren, Fred K. Chen
Publikováno v:
Stem Cell Research, Vol 51, Iss, Pp 102154-(2021)
The human induced pluripotent stem cell (iPSC) lines LEIi015-A and LEIi015-B were derived from a patient with inherited retinal disease caused by compound heterozygous mutations in the SNRNP200 gene (c.[1792C>T];[3341T>C]). Dermal fibroblasts were tr
Publikováno v:
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience, Vol 14 (2020)
Frontiers in Cellular Neuroscience, Vol 14 (2020)
Usher syndrome is a genetic disorder causing neurosensory hearing loss and blindness from retinitis pigmentosa (RP). Adaptive techniques such as braille, digital and optical magnifiers, mobility training, cochlear implants, or other assistive listeni
Publikováno v:
Clinical & Experimental Ophthalmology
Age-related macular degeneration (AMD) is a progressive degenerative disease that is the leading cause of vision loss in the elderly population. Degeneration/dysregulation of the retinal pigment epithelium (RPE), a supportive monolayer of cells under
Autor:
Livia S, Carvalho, Carla B, Mellough
Publikováno v:
Advances in experimental medicine and biology. 1185
High visual acuity and the ability to identify colours is solely dependent upon healthy cone photoreceptors in the retina. Little is known about cone migration mechanisms during postmitotic retinal maturation which, if it occurs erroneously, can resu
Autor:
Carla B. Mellough, Livia S. Carvalho
Publikováno v:
Retinal Degenerative Diseases ISBN: 9783030273774
High visual acuity and the ability to identify colours is solely dependent upon healthy cone photoreceptors in the retina. Little is known about cone migration mechanisms during postmitotic retinal maturation which, if it occurs erroneously, can resu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d7695204449fb199c9429e839b73207
https://doi.org/10.1007/978-3-030-27378-1_80
https://doi.org/10.1007/978-3-030-27378-1_80