Zobrazeno 1 - 10
of 23
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.
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
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
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
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,
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
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
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
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 +