Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marije A Geilenkirchen"'
Autor:
Anne M L Jansen, Marije A Geilenkirchen, Tom van Wezel, Shantie C Jagmohan-Changur, Dina Ruano, Heleen M van der Klift, Brendy E W M van den Akker, Jeroen F J Laros, Michiel van Galen, Anja Wagner, Tom G W Letteboer, Encarna B Gómez-García, Carli M J Tops, Hans F Vasen, Peter Devilee, Frederik J Hes, Hans Morreau, Juul T Wijnen
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0157381 (2016)
BACKGROUND AND AIMS:Lynch Syndrome (LS) is caused by pathogenic germline variants in one of the mismatch repair (MMR) genes. However, up to 60% of MMR-deficient colorectal cancer cases are categorized as suspected Lynch Syndrome (sLS) because no path
Externí odkaz:
https://doaj.org/article/d3a653d49cec4ce4a0f3cab6d6023e4e
Autor:
Claudia M Weller, Joost Haan, Hans Scheffer, Arn M. J. M. van den Maagdenberg, Michèl A.A.P. Willemsen, Boukje de Vries, Gisela M. Terwindt, Michel D. Ferrari, Brian G. R. Neville, Erik-Jan Kamsteeg, John S. Duncan, Wilhelmina G. Leen, Marije A Geilenkirchen
Publikováno v:
Cephalalgia, 35, 1, pp. 10-5
Cephalalgia, 35(1), 10-15
Cephalalgia, 35, 10-5
Cephalalgia, 35(1), 10-15
Cephalalgia, 35, 10-5
Background Hemiplegic migraine (HM) and alternating hemiplegia of childhood (AHC) are rare episodic neurological brain disorders with partial clinical and genetic overlap. Recently, ATP1A3 mutations were shown to account for the majority of AHC patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5fc6345540dfa2fc193d0b798a56bae
https://hdl.handle.net/2066/155256
https://hdl.handle.net/2066/155256
Autor:
Anja Wagner, Heleen M. van der Klift, Brendy E.W.M. van den Akker, Carli M. J. Tops, Encarna B. Gomez-Garcia, Juul T. Wijnen, Dina Ruano, Peter Devilee, Jeroen F. J. Laros, Tom van Wezel, Hans Morreau, Michiel van Galen, Shantie Jagmohan-Changur, Hans F. A. Vasen, Tom G.W. Letteboer, Marije A Geilenkirchen, Anne M.L. Jansen, Frederik J. Hes
Publikováno v:
PLoS One (print), 11(6):e0157381. Public Library of Science
PLoS ONE, 11(6). PUBLIC LIBRARY SCIENCE
PLOS ONE, 11(6):e0157381. Public Library of Science
PLoS ONE, Vol 11, Iss 6, p e0157381 (2016)
PLoS ONE [E], 11(6). Public Library of Science
PLoS ONE
PLoS ONE, 11(6). PUBLIC LIBRARY SCIENCE
PLOS ONE, 11(6):e0157381. Public Library of Science
PLoS ONE, Vol 11, Iss 6, p e0157381 (2016)
PLoS ONE [E], 11(6). Public Library of Science
PLoS ONE
BACKGROUND AND AIMS: Lynch Syndrome (LS) is caused by pathogenic germline variants in one of the mismatch repair (MMR) genes. However, up to 60% of MMR-deficient colorectal cancer cases are categorized as suspected Lynch Syndrome (sLS) because no pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0855c047394f34887630bd5c7c85338
https://pure.eur.nl/en/publications/5987c0f7-9f0c-40c0-bfb5-868f0b5ff07d
https://pure.eur.nl/en/publications/5987c0f7-9f0c-40c0-bfb5-868f0b5ff07d
Autor:
Esther van de Vosse, Marije A Geilenkirchen, Roelof A. de Paus, Jaap T. van Dissel, Sander van Riet
Publikováno v:
Molecular Immunology
Molecular Immunology, 56(4), 380-389
Molecular Immunology, 56(4), 380-389
The receptor for interleukin-12, formed by IL-12Rβ1 and IL-12Rβ2, mediates the type I immune responses of various types of lymphocytes. Polymorphisms in IL12RB2, the gene encoding IL-12Rβ2, were reported to be associated with several immune relate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16ab16dfae31fae91dad1ad09607726d
https://pubmed.ncbi.nlm.nih.gov/23911393
https://pubmed.ncbi.nlm.nih.gov/23911393