Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Paul G. Horan"'
Autor:
Michael J. Moore, David McCarty, Mark S. Spence, Gillian Murphy, Tracy Jardine, Paul G. Horan, Paul G. McGlinchey, Christopher Patterson, Pascal P. McKeown, Muhammad S. Kamaruddin
Publikováno v:
European Journal of Cardiovascular Prevention & Rehabilitation. 14:521-525
Background Cardiovascular disease (CVD) occurs more frequently in individuals with a family history of premature CVD. Within families the demographics of CVD are poorly described. Design We examined the risk estimation based on the Systematic Coronar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0d995a49f3bc83e62fa31bda9689cdb
https://doi.org/10.1097/hjr.0b013e328011c493
https://doi.org/10.1097/hjr.0b013e328011c493
Autor:
Damian Fogarty, Christine Belton, Adrian R. Allen, Alun Evans, Mark S. Spence, Paul G. Horan, Paul G. McGlinchey, Pascal P. McKeown, Christopher Patterson
Publikováno v:
The American Journal of Cardiology. 96:52-55
Dysfunction of lipid-metabolizing proteins is implicated in the pathogenesis of coronary artery disease. Single nucleotide polymorphisms in genes that encode sterol regulatory binding protein-1a, adenosine triphosphate binding cassette-A1, hepatic li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14a54184c1a7d016a19d9c9c6fc9d20e
https://doi.org/10.1016/j.amjcard.2005.02.043
https://doi.org/10.1016/j.amjcard.2005.02.043
Autor:
Declan Carey, Paul G Horan, Mary Drake, Robert J. G. Cuthbert, Simon D. Johnston, R. Neil Patterson
Publikováno v:
European Journal of Gastroenterology & Hepatology. 15:205-207
A 78-year-old man presented with a 5-day history of epistaxis and spontaneous bruising, and a 2-day history of acute dysphagia. Barium swallow, computerized tomography scan of the chest and upper gastrointestinal endoscopy were suggestive of an upper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a01d64d362947e45bc207df382f07396
https://doi.org/10.1097/00042737-200302000-00018
https://doi.org/10.1097/00042737-200302000-00018
Autor:
Aisling M O'Halloran, Paul G. Horan, Ronan Curtin, Pascal P. McKeown, Andrew O. Maree, Christopher Patterson, Alice Stanton, Denis C. Shields
Publikováno v:
O'Halloran, A M, Patterson, C, Horan, P, Maree, A, Curtin, R, Stanton, A, McKeown, P & Shields, D C 2009, ' Genetic polymorphisms in platelet-related proteins and coronary artery disease: investigation of candidate genes, including N-acetylgalactosaminyltransferase 4 (GALNT4) and sulphotransferase 1A1/2 (SULT1A1/2) ' Journal of Thrombosis and Thrombolysis, vol 27, no. 2, pp. 175-184 . DOI: 10.1007/s11239-008-0196-z
Background Both platelet function and heart disease show strong genetic components, many of which remain to be elucidated. Materials and methods The roles of candidate polymorphisms in ten platelet-associated genes were compared between 1,237 Acute C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62760372790a4dc0f1e9ae60e69bcb50
Autor:
Anne E. Hughes, Weihua Meng, Muhammad S. Kamaruddin, Christopher Patterson, Paul G. Horan, Pascal P. McKeown, Frank Kee, Christine Belton
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 8, Iss 1, p 62 (2007)
BMC Medical Genetics, Vol 8, Iss 1, p 62 (2007)
Background The complement factor H (CFH) gene has been recently confirmed to play an essential role in the development of age-related macular degeneration (AMD). There are conflicting reports of its role in coronary heart disease. This study was desi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65bafe0b363af6fae39f7fe84847b181
https://pubmed.ncbi.nlm.nih.gov/17877809
https://pubmed.ncbi.nlm.nih.gov/17877809
Publikováno v:
SPIE Proceedings.
Optimum structures for an InGaAs MQW pin diode modulator operating at low voltage (< equals 5V) are explored where the criterion is maximum reflectivity change.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::098bbb7a7884cbc64aab6bbf93003cb7
https://doi.org/10.1117/12.308972
https://doi.org/10.1117/12.308972
Publikováno v:
European Heart Journal. 27:1137-1138
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98f0b34a3ae41dee47cf4517b30386c9
https://doi.org/10.1093/eurheartj/ehi702
https://doi.org/10.1093/eurheartj/ehi702
Autor:
Michelle Spence, Paul G. Horan, Adrian R. Allen, Pascal P. McKeown, Paul G. McGlinchey, Christopher Patterson
Publikováno v:
Heart. 92:395-396
Coronary artery disease (CAD) and myocardial infarction (MI) are polygenic disorders caused by a complex interaction between environmental and genetic factors. A family history of MI is also an independent risk factor for MI.1 Several methods have be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0abf2ba1ccaf4e5d49a65dcac631c031
https://doi.org/10.1136/hrt.2004.055665
https://doi.org/10.1136/hrt.2004.055665
Autor:
Christine Belton, Christopher Patterson, Anne E. Hughes, Paul G. Horan, Pascal P. McKeown, Adrian R. Allen, Paul G. McGlinchey, Tracy Jardine, Mark S. Spence
Publikováno v:
BMC Medical Genetics
Horan, P G, Allen, A R, Hughes, A, Patterson, C, Spence, M, McGlinchey, P G, Belton, C, Jardine, T C L & McKeown, P 2006, ' Lack of MEF2A Δ7aa mutation in Irish families with early onset ischaemic heart disease, a family based study ' BMC Medical Genetics, vol 7, 65, pp. 65 . DOI: 10.1186/1471-2350-7-65
BMC Medical Genetics, Vol 7, Iss 1, p 65 (2006)
Horan, P G, Allen, A R, Hughes, A, Patterson, C, Spence, M, McGlinchey, P G, Belton, C, Jardine, T C L & McKeown, P 2006, ' Lack of MEF2A Δ7aa mutation in Irish families with early onset ischaemic heart disease, a family based study ' BMC Medical Genetics, vol 7, 65, pp. 65 . DOI: 10.1186/1471-2350-7-65
BMC Medical Genetics, Vol 7, Iss 1, p 65 (2006)
Background Ischaemic heart disease (IHD) is a complex disease due to the combination of environmental and genetic factors. Mutations in the MEF2A gene have recently been reported in patients with IHD. In particular, a 21 base pair deletion (Δ7aa) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8164b0a4a1e7fe3aa422113013e920a0
http://europepmc.org/articles/PMC1552052
http://europepmc.org/articles/PMC1552052