Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mireille J. De Wit"'
Autor:
Koen Kas, Alain Calender, Sophie Giraud, Catherine M. Phelan, Jo W.M. Höppener, Anna A.J. Pannett, George Carle, Janine Salandre, Wim J.M. Van de Ven, Shideh Khodaei, Patrick Gaudray, Catharina Larsson, Gilbert M. Lenoir, Bin Tean Teh, Günther Weber, Chang X. Zhang, Soili Kytölä, Ko De Witte, Virginie Wautot, Simon A. Forbes, Abby L. Grant, J. H. Duncan Bassett, Danielle Quincey, Cornelis J.M. Lips, Irma Lemmens, Nathalie Buisson, Sean M. Grimmond, Rajesh V. Thakker, Jozef Merregaert, Fabienne Parente, Mireille J. De Wit, Anouk Courseaux, Filip Farnebo
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant familial cancer syndrome characterized by parathyroid, pancreatic, and anterior pituitary tumors. The MEN1 locus has been previously localized to chromosome 11q13, and a 2-Mb gene-ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76ac6b18b0e8603f946f8dc541770824
https://ora.ox.ac.uk/objects/uuid:47db75a7-1bbe-4aac-8436-a5be6f957158
https://ora.ox.ac.uk/objects/uuid:47db75a7-1bbe-4aac-8436-a5be6f957158
Autor:
Remigio W. Rouse, Guido N. J. Tytgat, G. Johan A. Offerhaus, J. Jan B. van Lanschot, Carel J. M. van Noesel, Bastiaan P. van Rees, Mireille J. de Wit
Publikováno v:
Gastroenterology, 122(3), 784-788. W.B. Saunders Ltd
We describe an uncommon case of adenosquamous carcinoma arising in a Barrett esophagus in a 72-year-old white man who occasionally used alcohol, and was a nonsmoker for 34 years. Polymerase chain reaction–based microsatellite analysis was performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9a06c18b29964c69457487a6f88ba4c
https://doi.org/10.1053/gast.2002.31903
https://doi.org/10.1053/gast.2002.31903
Autor:
Cornelis J.M. Lips, Joke Jansen, Bin Tean Teh, Fung Ki Wong, Rob B. van der Luijt, Carola J. Haven, Janine Roijers, Catharina Larsson, Jo W.M. Höppener, Christi J. van Asperen, Hans Morreau, Mireille J. De Wit, Eveline W. C. M. van Dam, Carla Rosenberg
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 85:1449-1454
Familial primary hyperparathyroidism is the main feature of 2 familial endocrine neoplasia syndromes: multiple endocrine neoplasia type 1 (MEN 1) and hyperparathyroidism-jaw tumor syndrome (HPT-JT). The latter is a recently described syndrome that ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5c3d016c78a4198816e6285641bc0ad
https://doi.org/10.1210/jcem.85.4.6518
https://doi.org/10.1210/jcem.85.4.6518
Autor:
Patrick Gaudray, Fabienne Parente, Sophie Giraud, Gilbert M. Lenoir, Bin Tean Teh, Chang X. Zhang, Cornelis J.M. Lips, Jo W.M. Höppener, Catharina Larsson, Soili Kytölä, Alain Calender, Shideh Khodaei, Filip Farnebo, Virginie Wautot, Catherine M. Phelan, Abby L. Grant, J. H. Duncan Bassett, Anna A.J. Pannett, Mireille J. De Wit, Nicholas K. Hayward, Koen Kas, Michel Pugeat, Günther Weber, Rajesh V. Thakker, Wim J.M. Van de Ven, Nathalie Buisson, Simon A. Forbes, Danielle Quincey, Janine Salandre, Ko De Witte, Irma Lemmens
Publikováno v:
Human Molecular Genetics. 6:1177-1183
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by tumours of the parathyroids, pancreas and anterior pituitary that represents one of the familial cancer syndromes. The MEN1 locus has been previously locali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::546cd1b44c0f593b260204388e9a3768
https://doi.org/10.1093/hmg/6.7.1177
https://doi.org/10.1093/hmg/6.7.1177
Autor:
Laura A, Smit, Febe, van Maldegem, Anton W, Langerak, C Ellen, van der Schoot, Mireille J, de Wit, Silvia, Bea, Elias, Campo, Richard J, Bende, Carel J M, van Noesel
Publikováno v:
Haematologica. 91(7)
Activation-induced cytidine deaminase is essential for somatic hypermutation and class switch recombination of the immunoglobulin genes in B cells. It has been proposed that aberrant targeting of the somatic hypermutation machinery is instrumental in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad4062c699b8f8f4dc475890a09c0942
https://pubmed.ncbi.nlm.nih.gov/16818267
https://pubmed.ncbi.nlm.nih.gov/16818267
Publikováno v:
British journal of haematology, 118(4). Wiley-Blackwell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22a6250909cabf0938533cb7e715b2ff
https://pubmed.ncbi.nlm.nih.gov/12199769
https://pubmed.ncbi.nlm.nih.gov/12199769
Autor:
Mireille J. de Wit, Rudy M. Landsvater, Richard J. Sinke, A. Geurts van Kessel, Cornelis J. M. Lips, J. W. M. Höppener
Publikováno v:
HUMAN GENETICS, 99(1), 133-7. SPRINGER
Multiple endocrine neoplasia type 1 (MEN 1) is inherited as an autosomal dominant disorder, characterized by hyperplasia and neoplasia in several endocrine organs. The MEN 1 gene, which is most probably a tumor suppressor gene, has been localized to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00543fa2946b1679fbbd1373c87821ee
https://pubmed.ncbi.nlm.nih.gov/9003511
https://pubmed.ncbi.nlm.nih.gov/9003511
Autor:
Cornelis Lips, Rudy M. Landsvater, Jo Hoppener, Rolf A. Geerdink, Geert Blijham, Joke M. Jansen-Schillhorn van Veen, Adriaan van Gils, Mireille J. de Wit, Richard A. Zewald, Marianne Berends, Frits A. Beemer, Joanneke Brouwers-Smalbraak, Rumo Jansen, Hans Kristian Ploos van Amstel, Theo van Vroonhoven, Thea M. Vroom
Publikováno v:
The New England journal of medicine. 331(13)
Multiple endocrine neoplasia type 2A (MEN-2A) is characterized by medullary thyroid carcinoma in combination with pheochromocytoma and sometimes parathyroid adenoma. Missense mutations in the RET proto-oncogene are associated with MEN-2A. Their detec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fd586ecf381ba2a7e1a4466a189545d
https://pubmed.ncbi.nlm.nih.gov/7915823
https://pubmed.ncbi.nlm.nih.gov/7915823