Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Matthew Carrigan"'
Autor:
Sophia Millington‐Ward, Naomi Chadderton, Laura K. Finnegan, Iris J.M. Post, Matthew Carrigan, Tom Gardiner, Elisa Peixoto, Daniel Maloney, Marian M. Humphries, Alan Stitt, Thierry Léveillard, Pete Humphries, Paul F. Kenna, Arpad Palfi, G. Jane Farrar
Publikováno v:
Clinical and Translational Medicine, Vol 12, Iss 8, Pp n/a-n/a (2022)
Externí odkaz:
https://doaj.org/article/dd509cf8d833486f904bb413d8b73afb
Autor:
Heather A. Stewart, Jennifer L. Wright, Matthew Carrigan, Andrew H. Altieri, David I. Kline, Rafael J. Araújo
Publikováno v:
PLoS ONE, Vol 17, Iss 6 (2022)
Marine ecosystems are structured by coexisting species occurring in adjacent or nested assemblages. Mangroves and corals are typically observed in adjacent assemblages (i.e., mangrove forests and coral reefs) but are increasingly reported in nested m
Externí odkaz:
https://doaj.org/article/a48718c77f224a10838553f4a8bda899
Autor:
Naomi Chadderton, Arpad Palfi, Daniel M. Maloney, Matthew Carrigan, Laura K. Finnegan, Killian S. Hanlon, Ciara Shortall, Mary O’Reilly, Peter Humphries, Lorraine Cassidy, Paul F. Kenna, Sophia Millington-Ward, G. Jane Farrar
Publikováno v:
Pharmaceutics, Vol 15, Iss 2, p 322 (2023)
AAV gene therapy for ocular disease has become a reality with the market authorisation of LuxturnaTM for RPE65-linked inherited retinal degenerations and many AAV gene therapies currently undergoing phase III clinical trials. Many ocular disorders ha
Externí odkaz:
https://doaj.org/article/bd632e8c331249f2b641b632703c689a
Autor:
Kirk Stephenson, Adrian Dockery, Niamh Wynne, Matthew Carrigan, Paul Kenna, G. Jane Farrar, David Keegan
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Background To describe the clinical phenotype and genetic cause underlying the disease pathology in a pedigree (affected n = 9) with X-linked retinoschisis (XLRS1) due to a novel RS1 mutation and to assess suitability for novel therapies usi
Externí odkaz:
https://doaj.org/article/9db300e736f6484298d2014ec8326ebe
Autor:
Ross P Byrne, Rui Martiniano, Lara M Cassidy, Matthew Carrigan, Garrett Hellenthal, Orla Hardiman, Daniel G Bradley, Russell L McLaughlin
Publikováno v:
PLoS Genetics, Vol 14, Iss 1, p e1007152 (2018)
Previous studies of the genetic landscape of Ireland have suggested homogeneity, with population substructure undetectable using single-marker methods. Here we have harnessed the haplotype-based method fineSTRUCTURE in an Irish genome-wide SNP datase
Externí odkaz:
https://doaj.org/article/5db46d63ffd544f1b225be0d78a10be2
Autor:
Matthew Carrigan
Publikováno v:
Journal of Diagnostic Medical Sonography. 38:359-363
The Achilles tendon is the largest and strongest tendon in the body. With increasing age and repetitive use, the Achilles tendon is more prone to injury, ranging from a mild injury to a full thickness tear. Achilles tendon injuries are one of the mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55d0a7351556a75eb7b293a30fde3481
https://doi.org/10.1177/87564793221079779
https://doi.org/10.1177/87564793221079779
Autor:
Sophia Millington-Ward, Naomi Chadderton, Laura K. Finnegan, Iris J. M. Post, Matthew Carrigan, Rachel Nixon, Marian M. Humphries, Pete Humphries, Paul F. Kenna, Arpad Palfi, G. Jane Farrar
Publikováno v:
International Journal of Molecular Sciences
Volume 24
Issue 4
Pages: 3847
Volume 24
Issue 4
Pages: 3847
Age-related macular degeneration (AMD) is the most common cause of blindness in the aged population. However, to date there is no effective treatment for the dry form of the disease, representing 85–90% of cases. AMD is an immensely complex disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::366cae23e0fa92f6d25ab28856e5635c
https://doi.org/10.3390/ijms24043847
https://doi.org/10.3390/ijms24043847
Autor:
Adrian, Dockery, Matthew, Carrigan, Niamh, Wynne, Kirk, Stephenson, David, Keegan, Paul F, Kenna, G Jane, Farrar
Publikováno v:
Advances in experimental medicine and biology. 1185
Here we describe the identification and evaluation of a rare novel autosomal recessive mutation in FLVCR1 which is implicated solely in RP, with no evidence of posterior column ataxia in a number of affected patients. The mutation was detected as par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::07ea875e2b2b287e9354a714c756e9b8
https://pubmed.ncbi.nlm.nih.gov/31884612
https://pubmed.ncbi.nlm.nih.gov/31884612
Autor:
Anna Sophia Kiang, Sophia Millington-Ward, Marian M. Humphries, G. Jane Farrar, Adrian Dockery, Peter Humphries, Naomi Chadderton, Matthew Carrigan, Arpad Palfi, Paul F. Kenna
Publikováno v:
Human Molecular Genetics
While individually classed as rare diseases, hereditary retinal degenerations (IRDs) are the major cause of registered visual handicap in the developed world. Given their hereditary nature, some degree of intergenic heterogeneity was expected, with g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51257325889dadb419c3bef3fb5ec2e5
https://doi.org/10.1093/hmg/ddx185
https://doi.org/10.1093/hmg/ddx185
Autor:
Paul F. Kenna, G. Jane Farrar, Adrian Dockery, David J Keegan, Kirk Stephenson, Niamh Wynne, Matthew Carrigan
Publikováno v:
Retinal Degenerative Diseases ISBN: 9783030273774
Here we describe the identification and evaluation of a rare novel autosomal recessive mutation in FLVCR1 which is implicated solely in RP, with no evidence of posterior column ataxia in a number of affected patients. The mutation was detected as par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82f5489333c5374881537674cdf78c44
https://doi.org/10.1007/978-3-030-27378-1_33
https://doi.org/10.1007/978-3-030-27378-1_33
