Zobrazeno 1 - 10
of 56
pro vyhledávání: '"H. Booler"'
Publikováno v:
PLoS ONE, Vol 11, Iss 7, p e0159853 (2016)
LARGE is a glycosyltransferase involved in glycosylation of α-dystroglycan (α-DG). Absence of this protein in the LARGEmyd mouse results in α-DG hypoglycosylation, and is associated with central nervous system abnormalities and progressive muscula
Externí odkaz:
https://doaj.org/article/2a6741c27e6e42bf8406c9bf88c45bb6
Autor:
D. Chan, G. J. Won, A. T. Read, C. R. Ethier, E. Thackaberry, S. R. Crowell, H. Booler, V. Bantseev, J. M. Sivak
Publikováno v:
Journal of the Royal Society Interface
Intravitreal (ITV) drug delivery is a new cornerstone for retinal therapeutics. Yet, predicting the disposition of formulations in the human eye remains a major translational hurdle. A prominent, but poorly understood, issue in pre-clinical ITV toxic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0e6c195f6874f613c5685c62d554dfe
http://europepmc.org/articles/PMC8790337
http://europepmc.org/articles/PMC8790337
Akademický článek
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Akademický článek
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Akademický článek
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Publikováno v:
Brain Pathology. 26:465-478
The secondary dystroglycanopathies are characterized by the hypoglycosylation of alpha dystroglycan, and are associated with mutations in at least 18 genes that act on the glycosylation of this cell surface receptor rather than the Dag1 gene itself.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83db7e213b8630dbbc538763be4f7056
https://doi.org/10.1111/bpa.12306
https://doi.org/10.1111/bpa.12306
Publikováno v:
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
Aims The secondary dystroglycanopathies represent a heterogeneous group of congenital muscular dystrophies characterized by the defective glycosylation of alpha dystroglycan. These disorders are associated with mutations in at least 17 genes, includi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16ab97d784991969b12ccaca628d8bab
https://researchonline.rvc.ac.uk/id/eprint/10851/1/10851.pdf
https://researchonline.rvc.ac.uk/id/eprint/10851/1/10851.pdf
Publikováno v:
Veterinary Ophthalmology. 14:195-199
Objectives To describe the bacterial and fungal flora of the normal conjunctiva of horses in the UK; to determine the effect of horse age, sex, geographic location, and housing on this flora; and to determine the most appropriate antimicrobial drug(s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8e6d368ba93f7f7354b27b653e52508
https://doi.org/10.1111/j.1463-5224.2010.00867.x
https://doi.org/10.1111/j.1463-5224.2010.00867.x
Autor:
Dominic J. Wells, H. Booler, R L Terry, Callum Parr, M.R. Ackroyd, M. Fernandez-Fuente, J. Kim, Manoli Kavishwar, E. Lacey, K E Wells, C. Whitmore, Attia Ashraf, Francesco Muntoni, Susan C. Brown
Publikováno v:
Human molecular genetics. 23(7)
Mutations in fukutin-related protein (FKRP) underlie a group of muscular dystrophies associated with the hypoglycosylation of α-dystroglycan (α-DG), a proportion of which show central nervous system involvement. Our original FKRP knock-down mouse (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fb1d45834892130b9187ffd12480cbe
https://pubmed.ncbi.nlm.nih.gov/24234655
https://pubmed.ncbi.nlm.nih.gov/24234655
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 7, p e0159853 (2016)
PLoS One
PLoS ONE, Vol 11, Iss 7, p e0159853 (2016)
PLoS One
LARGE is a glycosyltransferase involved in glycosylation of α-dystroglycan (α-DG). Absence of this protein in the LARGEmyd mouse results in α-DG hypoglycosylation, and is associated with central nervous system abnormalities and progressive muscula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5483505feeadb7b7473a5eee43ad0f3
https://doi.org/10.1371/journal.pone.0159853
https://doi.org/10.1371/journal.pone.0159853