Výsledky vyhledávání - "K. De Leeneer"

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miRNA expression profiles in BRCA1-associated breast cancers reveal upregulation of specific miRNAs in tumors lacking a clear second hit in a large proportion of the tumour

Autor: J. Van Dorpe, K De Leeneer, Anne Vral, Kathleen Claes, M.R. Van Bockstal, M. Van Heetvelde

Publikováno v: Annals of Oncology. 30:iii72

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9e6b70f5e03b91be27cb0313f8c429c5
https://doi.org/10.1093/annonc/mdz118

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Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families

Autor: Gert Matthijs, N Hamel, K De Leeneer, Eric Legius, Geneviève Michils, Jocelyne Arseneau, William D. Foulkes, Karin Leunen, Kathleen Claes, Eva Tomiak, Marc Tischkowitz, Patricia N. Tonin, Andrew Y Shuen, Bruce Poppe, Erika Smith, D J Osher

Publikováno v: British Journal of Cancer

BACKGROUND: Recent data show that mutations in RAD51D have an aetiological role in ovarian carcinoma, yet mutations do not appear to be associated with an increased risk for breast cancer. We studied ovarian and breast cancer families having at least

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4722b6c6553e0ea0707ecdd179dc6943
http://europepmc.org/articles/PMC3326673

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BRCA1, BRCA2 and PALB2 mutations and CHEK2 c.1100delC in different South African ethnic groups diagnosed with premenopausal and/or triple negative breast cancer

Autor: Tasha Wainstein, Ans Baeyens, Ilse Coene, Flavia Zita Francies, Anne Vral, Brecht Crombez, Bruce Poppe, A. Cairns, Jacobus Slabbert, K De Leeneer, T. Van Maerken, Kathleen Claes, Amanda Krause, Sarah Nietz, Robyn Kerr, H. Cubasch, Marshall Murdoch

Publikováno v: BMC Cancer

Background Current knowledge of the aetiology of hereditary breast cancer in the four main South African population groups (black, coloured, Indian and white) is limited. Risk assessments in the black, coloured and Indian population groups are challe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ddab0007faf3d18bc75d7b6f845077a
https://doi.org/10.1186/s12885-015-1913-6

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Additional file 1: Table S1. of BRCA1, BRCA2 and PALB2 mutations and CHEK2 c.1100delC in different South African ethnic groups diagnosed with premenopausal and/or triple negative breast cancer

Autor: F. Francies, T. Wainstein, K. De Leeneer, A. Cairns, M. Murdoch, S. Nietz, H. Cubasch, B. Poppe, T. Van Maerken, B. Crombez, I. Coene, R. Kerr, J. Slabbert, A. Vral, A. Krause, A. Baeyens, K. Claes

Overview of grading and staging of breast cancer on diagnosis (DOC 30Â kb)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf2f126e60aa71a4f82d1530bdf395b4

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Additional file 2: Table S2. of BRCA1, BRCA2 and PALB2 mutations and CHEK2 c.1100delC in different South African ethnic groups diagnosed with premenopausal and/or triple negative breast cancer

Overview of sequencing coverage per run (DOC 29Â kb)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d602283acb8d59f785192bb97920618

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Next Generation Sequencing to Determine the Cystic Fibrosis Mutation Spectrum in Palestinian Population

Autor: K De Leeneer, Tamer Essawi, Paul Coucke, Mohammad A. Farraj, Wouter Steyaert, Osama Essawi, K. De Pauw, A De Paepe, Kathleen Claes

Publikováno v: Disease Markers, Vol 2015 (2015)
Disease Markers
DISEASE MARKERS

An extensive molecular analysis of the CF transmembrane regulator (CFTR) gene was performed to establish theCFTRmutation spectrum and frequencies in the Palestinian population, which can be considered as an understudied population. We used a targeted

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63500aa6cad6b548e1c58b579163b66a

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Second hit landscape in BRCA1/2-associated breast cancer

Autor: M. Van Heetvelde, Anne Vral, J. Van Dorpe, K De Leeneer, Kathleen Claes, Bruce Poppe, M. Van Bockstal, Dieter Deforce, Trees Lepez, Kathleen Lambein

Publikováno v: Annals of Oncology. 28:i9

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::52e8893e771abdcc801e5c53d8670ce7
https://doi.org/10.1093/annonc/mdx143

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Novel and known FRMD7 mutations and copy number variation in Belgian patients with X-linked idiopathic infantile nystagmus

Autor: Sophie Walraedt, B.P. Leroy, M Bauwens, Sally Hooghe, K De Leeneer, B. Almoallem, S Al-Obeidan, P Kestelyn, Hannah Verdin, C Van Cauwenbergh, J De Zaeytijd, E. De Baere, Patricia Delbeke

Publikováno v: Acta Ophthalmologica. 92

Purpose Idiopathic Infantile Nystagmus (IIN [MIM# 310700]) is one of the commonest forms of infantile nystagmus characterized by bilateral uncontrollable eye movements that does not manifest until the child starts to fixate objects at the age of thre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a69caf604d36aace2d4b74e749e8ec19
https://doi.org/10.1111/j.1755-3768.2014.t081.x

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