Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Noelle C. Orton"'
Autor:
Renata Rehak, Clinton J. Doering, John E. McRory, Yves Sauve, R. Tobias, Silvina C. Mema, Stephan Bonfield, N. T. Bech-Hansen, Nidhi Lodha, Noelle C. Orton, William K. Stell
Publikováno v:
Retinal Degenerative Diseases ISBN: 9781441913982
Background: Mutations in CACNA1F, which encodes the Cav1.4 subunit of a voltage-gated L-type calcium channel, cause X-linked incomplete congenital stationary night blindness (CSNB2), a condition of defective retinal neurotransmission which results in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c19480d3c8d6cb28494b1c1faa3b73c3
https://doi.org/10.1007/978-1-4419-1399-9_63
https://doi.org/10.1007/978-1-4419-1399-9_63
Autor:
Edna F. Einsiedel, Thushaanthini Thavaratnam, Laura K. Bennett, Noelle C. Orton, Rose Geransar, Shainur Premji
Publikováno v:
Stem cell reviews and reports. 5(2)
Studies of public views on stem cell research have traditionally focused on human embryonic stem cells. With more recent scientific research on developing other stem cell sources, a series of focus group studies was undertaken with Canadian adults to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a04731407cd0dd1e3c2f78ece79b98b
https://pubmed.ncbi.nlm.nih.gov/19521801
https://pubmed.ncbi.nlm.nih.gov/19521801
Publikováno v:
American journal of medical genetics. Part A. (8)
The Dutch-German Mennonites are a religious isolate with foundational roots in the 16th century. A tradition of endogamy, large families, detailed genealogical records, and a unique disease history all contribute to making this a valuable population
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deb7efc9faa44c727bd29231133bce8e
https://pubmed.ncbi.nlm.nih.gov/18348259
https://pubmed.ncbi.nlm.nih.gov/18348259
Autor:
N. Torben Bech-Hansen, Derrick E. Rancourt, Noelle C. Orton, Steven Barnes, Fiona C. Mansergh, Melanie R. Lalonde, John P. Vessey, William K. Stell, François Tremblay
Publikováno v:
Human molecular genetics. 14(20)
Retinal neural transmission represents a key function of the eye. Identifying the molecular components of this vital process is helped by studies of selected human genetic eye disorders. For example, mutations in the calcium channel subunit gene CACN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56f06f69eb978044f58adf09955111b5
https://pubmed.ncbi.nlm.nih.gov/16155113
https://pubmed.ncbi.nlm.nih.gov/16155113