Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Happerfield Lisa"'
Akademický článek
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Autor:
Casey, Ruth T, McLean, Mary A, Madhu, Basetti, Challis, Benjamin G, Ten Hoopen, Rogier, Roberts, Thomas, Clark, Graeme R, Pitfield, Deborah, Simpson, Helen L, Bulusu, Venkata R, Allinson, Kieren, Happerfield, Lisa, Park, Soo-Mi, Marker, Alison, Giger, Olivier, Maher, Eamonn R, Gallagher, Ferdia A
Purpose Mutations in the mitochondrial enzyme succinate dehydrogenase (SDH) subunit genes are associated with a wide spectrum of tumors, including pheochromocytomas and paragangliomas, GI stromal tumors, renal cell carcinomas, and pituitary adenomas.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b90c12fcc00ff5963ca36395870c4040
https://www.repository.cam.ac.uk/handle/1810/277714
https://www.repository.cam.ac.uk/handle/1810/277714
Autor:
Mitrou Panagiota N, Ball Richard Y, Luben Robert N, Gay Laura J, Kerr Lucy, Happerfield Lisa, Cooke James C, Naguib Adam, McTaggart Alison, Arends Mark J
Publikováno v:
BMC Cancer, Vol 11, Iss 1, p 123 (2011)
Abstract Background The PTEN tumour suppressor gene and PIK3CA proto-oncogene encode proteins which contribute to regulation and propagation of signal transduction through the PI3K/AKT signalling pathway. This study investigates the prevalence of los
Externí odkaz:
https://doaj.org/article/d8352f375bff4dff9fdbc4a6347b5869
Autor:
Lager, Susanne, Sovio, Ulla, Eddershaw, Elizabeth, Linden, Margaretha W., Yazar, Cansu, Cook, Emma, Happerfield, Lisa, Jessop, Flora A., Sebire, Neil J., Charnock‐Jones, D. Stephen, Smith, Gordon C. S.
Publikováno v:
Journal of Physiology; Dec2020, Vol. 598 Issue 23, p5555-5571, 17p
Autor:
van der Weyden, Louise1 lvdw@sanger.ac.uk, Happerfield, Lisa2, Arends, Mark J.2, Adams, David J.1
Publikováno v:
International Journal of Experimental Pathology. Apr2009, Vol. 90 Issue 2, p101-108. 8p. 4 Color Photographs, 1 Chart.
Autor:
Jöhrens, Korinna1, Happerfield, Lisa C.2, Brown, John P.2, Erber, Wendy N.3, Stein, Harald1, Anagnostopoulos, Ioannis1
Publikováno v:
Pathobiology. 2008, Vol. 75 Issue 4, p252-256. 5p.
Akademický článek
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Autor:
Challis, Benjamin G, Kandasamy, Narayanan, Powlson, Andrew S, Koulouri, Olympia, Annamalai, Anand Kumar, Happerfield, Lisa, Marker, Alison J, Arends, Mark J, Nik-Zainal, Serena, Gurnell, Mark
Publikováno v:
Challis, B G, Kandasamy, N, Powlson, A S, Koulouri, O, Annamalai, A K, Happerfield, L, Marker, A, Arends, M, Nik-Zainal, S & Gurnell, M 2016, ' Familial adrenocortical carcinoma in association with Lynch syndrome ', Journal of Clinical Endocrinology & Metabolism . https://doi.org/10.1210/jc.2016-1460#sthash.HPajwAWS.dpuf
CONTEXT: Adrenocortical carcinoma (ACC) is a rare endocrine malignancy with a poor prognosis. Although the majority of childhood ACC arises in the context of inherited cancer susceptibility syndromes, it remains less clear whether a hereditary tumor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6801d4793c3944593fd43df67b1786c1
https://www.pure.ed.ac.uk/ws/files/25180905/Familial_adrenocortical_carcinoma_in_association_with_Lynch_syndrome.pdf
https://www.pure.ed.ac.uk/ws/files/25180905/Familial_adrenocortical_carcinoma_in_association_with_Lynch_syndrome.pdf
Autor:
Whitworth, James, Skytte, Anne-Bine, Sunde, Lone, Lim, Derek H, Arends, Mark, Happerfield, Lisa, Frayling, Ian M, Minkelen, Rick van, Woodward, Emma R, Tischkowitz, Marc D, Maher, Eamonn R
Publikováno v:
Whitworth, J, Skytte, A-B, Sunde, L, Lim, D H, Arends, M, Happerfield, L, Frayling, I M, Minkelen, R V, Woodward, E R, Tischkowitz, M D & Maher, E R 2016, ' Multilocus Inherited Neoplasia Alleles Syndrome (MINAS): Case Series and Literature Review ', JAMA Oncology, vol. 2, no. 3, pp. 373-379 . https://doi.org/10.1001/jamaoncol.2015.4771
Mendelian causes of inherited cancer susceptibility are mostly rare and characterized by variable expression and incomplete penetrance. Phenotypic variability may result from a range of causes including locus heterogeneity, allelic heterogeneity, gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3094::77f41e6b4cb2d5314593eba166c88c14
https://www.pure.ed.ac.uk/ws/files/21732024/Multilocus_Inherited_Neoplasia_Syndrome_MINAS_Case_Reports_and_Literature_Review.pdf
https://www.pure.ed.ac.uk/ws/files/21732024/Multilocus_Inherited_Neoplasia_Syndrome_MINAS_Case_Reports_and_Literature_Review.pdf
Autor:
Whitworth, James, Skytte, Anne-Bine, Sunde, Lone, Lim, Derek H., Arends, Mark J., Happerfield, Lisa, Frayling, Ian, van Minkelen, Rick, Woodward, Emma R., Tischkowitz, Marc D., Maher, Eamonn R.
Mendelian causes of inherited cancer susceptibility are mostly rare and characterized by variable expression and incomplete penetrance. Phenotypic variability may result from a range of causes including locus heterogeneity, allelic heterogeneity, gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::ea5a6656106e0e0ee47710590031ff13
https://orca.cardiff.ac.uk/id/eprint/83818/1/MINAScrv150013.pdf
https://orca.cardiff.ac.uk/id/eprint/83818/1/MINAScrv150013.pdf