Zobrazeno 1 - 10
of 204
pro vyhledávání: '"C J Lintott"'
Autor:
Pardeep Kaurah, Magali Svrcek, Toshikazu Ushijima, James Whitworth, Yasmin Nouri, Kirsty L. Harris, Emily Schulpen, Jeremy L. Davis, Lynn DeGregorio, Hidetaka Yamada, Richard H. Hardwick, Tanis D Godwin, Julie Arnold, Carla Oliveira, Jolanda M. van Dieren, Helen L. Fisher, Bostjan Humar, Katharine Nichole Holm, Han Kwang Yang, Parry Guilford, Joana Figueiredo, Fátima Carneiro, Sonia S. Kupfer, Daniel G. Coit, Paul F. Mansfield, Andrew Latchford, Ana Sofia Ribeiro, Rebecca C. Fitzgerald, Anthony E. Reeve, Nicola Bougen-Zhukov, Patrick R. Benusiglio, Enrique Norero, Kimberley Gamet, Erin Gardner, Andrew A. Sporle, Patrícia Carneiro, Joao Sanches, Johanna L. D'Addario, Marc Tischkowitz, Maybelle McLeod, Tom Brew, Elizabeth C. Monroe, Alex Boussioutas, Rachel S. van der Post, Nicoline Hoogerbrugge, Mark D. Muller, Simone Busija, Haruhiko Sugimura, Irene Gullo, Tanya M. Bisseling, Karyn Paringatai, Liying Zhang, Joana Paredes, Raquel Seruca, David G. Huntsman, Karen E Chelcun Schreiber, James M. Ford, Jeremy Rossaak, Vanessa Blair, Amanda Charlton, Susan Parry, Takeshi Nakajima, Massimiliano di Pietro, C. J. Lintott, Adrian Claydon, Annemieke Cats
Publikováno v:
Lancet Oncology, 21, 8, pp. e386-e397
Lancet Oncol
Lancet Oncology, 21, e386-e397
Lancet Oncol
Lancet Oncology, 21, e386-e397
Contains fulltext : 225261.pdf (Publisher’s version ) (Closed access) Hereditary diffuse gastric cancer (HDGC) is an autosomal dominant cancer syndrome that is characterised by a high prevalence of diffuse gastric cancer and lobular breast cancer.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e170c9ddf442b6b43660788219059b7b
https://hdl.handle.net/2066/225261
https://hdl.handle.net/2066/225261
Autor:
N L Eisner, C Johnston, S Toonen, A J Frost, S Janssens, C J Lintott, S Aigrain, H Sana, M Abdul-Masih, K Z Arellano-Córdova, P G Beck, E Bordier, E Cannon, A Escorza, M Fabry, L Hermansson, S B Howell, G Miller, S Sheyte, S Alhassan, E M L Baeten, F Barnet, S J Bean, M Bernau, D M Bundy, M Z Di Fraia, F M Emralino, B L Goodwin, P Hermes, T Hoffman, M Huten, R Janíček, S Lee, M T Mazzucato, D J Rogers, M P Rout, J Sejpka, C Tanner, I A Terentev, D Urvoy
Publikováno v:
Monthly Notices of the Royal Astronomical Society, 511, 4, pp. 4710-4723
Monthly Notices of the Royal Astronomical Society, 511, 4710-4723
Monthly Notices of the Royal Astronomical Society, 511(4), 4710-4723. Oxford University Press
Monthly Notices of the Royal Astronomical Society, 511, 4710-4723
Monthly Notices of the Royal Astronomical Society, 511(4), 4710-4723. Oxford University Press
We report the discovery and analysis of a massive, compact, hierarchical triple system (TIC 470710327) initially identified by citizen scientists in data obtained by NASA's Transiting Exoplanet Survey Satellite (TESS). Spectroscopic follow-up observa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad3569668e908fbbf8233ad6cab511a3
http://arxiv.org/abs/2202.06964
http://arxiv.org/abs/2202.06964
Publikováno v:
Alzheimer Disease & Associated Disorders. 35:350-352
We report a case of familial dementia having some clinical features characteristic of dementia with Lewy bodies, in which a novel mutation Ala275Ser within the presenilin-1 (PSEN1) gene was identified. We review the association of PSEN1 mutation with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e6eeea5eddb3bf45b6d0b26de928561
https://doi.org/10.1097/wad.0000000000000444
https://doi.org/10.1097/wad.0000000000000444
Autor:
R J Smethurst, B D Simmons, C J Lintott, J Shanahan, A L Coil, W C Keel, E Glikman, E C Moran, K L Masters, M Urry, K Willett
Publikováno v:
Monthly Notices of the Royal Astronomical Society. 506:3419-3420
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f92a34832aebff74c83ff544514addf4
https://doi.org/10.1093/mnras/stab2006
https://doi.org/10.1093/mnras/stab2006
Autor:
Donald R. Love, Jonathan R. Skinner, Klaus Lehnert, Russell G. Snell, Alex L. Binfield, Peter P. Jones, Jessie C. Jacobsen, Kathryn E. Waddell‐Smith, Martin A. Kennedy, C. J. Lintott, Kate Gibson, Ian Crozier, R. J McKinlay Gardner
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Isolated cardiac arrhythmia due to a variant in CACNA1C is of recent knowledge. Most reports have been of singleton cases or of quite small families, and estimates of penetrance and expressivity have been difficult to obtain. We here descr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d010afc92cd1244a67db94b3859bf7a
https://doi.org/10.1002/mgg3.476
https://doi.org/10.1002/mgg3.476
Publikováno v:
Diabetes Research and Clinical Practice. 43:179-185
Individuals with type 2 diabetes mellitus (n = 105; age 36-71 years) on diet therapy alone, and with quite good glycaemic control (mean HbA1c approximately 7.0%) were randomized to receive acarbose (100 mg three times daily) or placebo for 16 weeks,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccb29b626616635097d963c4a230f4dc
https://doi.org/10.1016/s0168-8227(99)00009-1
https://doi.org/10.1016/s0168-8227(99)00009-1
Publikováno v:
The American Journal of Cardiology. 76:97A-101A
Renal insufficiency is frequently associated with both quantitative and qualitative abnormalities in lipid and hemorheologic profiles. Although this may lead to increased risk of cardiovascular disease, a number of studies have also shown dyslipidemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::132e01b5c534a3bacaf4b4be11d8a956
https://doi.org/10.1016/s0002-9149(05)80027-x
https://doi.org/10.1016/s0002-9149(05)80027-x
Autor:
C. J. Lintott, Leonora Theart, E. Langenhoven, Odell Loubser, Maritha J. Kotze, Russell S. Scott, Armand V. Peeters
Publikováno v:
Journal of Medical Genetics. 32:379-382
DNA from 14 unrelated New Zealand familial hypercholesterolaemia (FH) heterozygotes, originating from the United Kingdom, was screened for mutations in exon 4 of the low density lipoprotein receptor (LDLR) gene. One patient was heterozygous for mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0fc0b67296c10600a7adc622938714b
https://doi.org/10.1136/jmg.32.5.379
https://doi.org/10.1136/jmg.32.5.379
Publikováno v:
Australian and New Zealand Journal of Medicine. 23:162-167
The aim of this study was to determine the lipid, lipoprotein and apolipoprotein distribution in an ambulant elderly New Zealand population, and to consider the association between these and other variables (including body mass index, diabetes mellit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efa5b4bf83bbc7334cb38a5a432fbff0
https://doi.org/10.1111/j.1445-5994.1993.tb01811.x
https://doi.org/10.1111/j.1445-5994.1993.tb01811.x
Publikováno v:
Diabetes Research and Clinical Practice. 16:131-136
The prevalence of diabetes mellitus (both known and previously undiagnosed) was studied in a population sample, predominantly Caucasoid and resident in the community with an age/sex distribution representative of the New Zealand population aged 65 +
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e11f2ed09c66e11d98ded9a186c8d6a5
https://doi.org/10.1016/0168-8227(92)90084-5
https://doi.org/10.1016/0168-8227(92)90084-5