Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Anne Goverde"'
Autor:
Linda Gaillard, Anne Goverde, Quincy C. C. van den Bosch, Fernanda S. Jehee, Erwin Brosens, Danielle Veenma, Frank Magielsen, Annelies de Klein, Irene M. J. Mathijssen, Marieke F. van Dooren
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Congenital diaphragmatic hernia (CDH) is a life-threatening birth defect that presents as either an isolated diaphragm defect or as part of a complex disorder with a wide array of anomalies (complex CDH). Some patients with complex CDH display distin
Externí odkaz:
https://doaj.org/article/0e39453c73344b71ac8d697ccb435594
Autor:
Hellen Houlleberghs, Anne Goverde, Jarnick Lusseveld, Marleen Dekker, Marco J Bruno, Fred H Menko, Arjen R Mensenkamp, Manon C W Spaander, Anja Wagner, Robert M W Hofstra, Hein Te Riele
Publikováno v:
PLoS Genetics, Vol 13, Iss 5, p e1006765 (2017)
Lynch syndrome (LS) is a hereditary cancer predisposition caused by inactivating mutations in DNA mismatch repair (MMR) genes. Mutations in the MSH6 DNA MMR gene account for approximately 18% of LS cases. Many LS-associated sequence variants are nons
Externí odkaz:
https://doaj.org/article/53dbc2752fd7400fb3a74d5fa6f8649b
Autor:
Ellemieke L. Viskil, Erik Jan Dubbink, Michael Doukas, Ellis L. Eikenboom, Manon C.W. Spaander, Anne Goverde, Ans M.W. van den Ouweland, Winand N.M. Dinjens, Robert M.W. Hofstra, Marco J. Bruno, Anja Wagner
Publikováno v:
Clinical Gastroenterology and Hepatology, 18(5), 1112-1120. W.B. Saunders
Background & Aims Patients with Lynch syndrome are offered the same colorectal cancer (CRC) surveillance programs (colonoscopy every 2 years), regardless of the pathogenic DNA mismatch repair gene variant the patient carries. We aimed to assess the y
Autor:
Erwin Brosens, Frank J. Magielsen, Anne Goverde, Linda Gaillard, Annelies de Klein, Fernanda Sarquis Jehee, Quincy C. C. van den Bosch, Danielle Veenma, Marieke F. van Dooren, Irene M.J. Mathijssen
Publikováno v:
Frontiers in Pediatrics
Frontiers in Pediatrics, Vol 9 (2021)
Frontiers in Pediatrics, Vol 9 (2021)
Congenital diaphragmatic hernia (CDH) is a life-threatening birth defect that presents as either an isolated diaphragm defect or as part of a complex disorder with a wide array of anomalies (complex CDH). Some patients with complex CDH display distin
Autor:
Marcel van der Weiden, Hendrikus J. Dubbink, Anne Goverde, Winand N.M. Dinjens, Manon C.W. Spaander, Robert M.W. Hofstra, Michael Doukas, Anja Wagner, Marco J. Bruno
Publikováno v:
Gastroenterology, 155(5), 1410-1415. W.B. Saunders
Background & aims It is important to identify individuals with Lynch syndrome because surveillance programs can reduce their morbidity and mortality from colorectal cancer (CRC). We assessed the diagnostic yield of immunohistochemistry to detect Lync
Autor:
Anja Wagner, Emma J Crosbie, Annika Auranen, Marta Puzzono, Marco J. Bruno, Andrew Latchford, Giulia Martina Cavestro, Monique E. van Leerdam, Ingrid Winship, Anne Goverde, Stefan Aretz, Gabriela Möslein, Anne Marie Jelsig, Anna Lepistö, Veronica Zuber
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 10, Iss 473, p 473 (2021)
Journal of Clinical Medicine, 10(3):473, 1-18. Multidisciplinary Digital Publishing Institute (MDPI)
Journal of Clinical Medicine, 10(3). MDPI
Journal of Clinical Medicine, Vol 10, Iss 473, p 473 (2021)
Journal of Clinical Medicine, 10(3):473, 1-18. Multidisciplinary Digital Publishing Institute (MDPI)
Journal of Clinical Medicine, 10(3). MDPI
The scientific data to guide the management of Peutz–Jeghers syndrome (PJS) are sparse. The available evidence has been reviewed and discussed by diverse medical specialists in the field of PJS to update the previous guideline from 2010 and formula
Autor:
Benjamin D. Solomon, Cynthia Forster Gibson, Kezhi Yan, Juliann M. Savatt, Bert Callewaert, Justine Rousseau, Hannah Verdin, Bryce A. Mendelsohn, Roy Eyal, Kendra Engleman, Gary A. Bellus, Katherine Agre, Lorraine Potocki, Andrea M. Lewis, Keren Machol, Brendan C. Lanpher, Alan F. Riley, Rebecca J. Hale, Anne Goverde, Isabelle Thiffault, Natacha Esber, Xiang-Jiao Yang, Elfride De Baere, Philippe M. Campeau, Megan T. Cho, Hillary M. Porter, Kirsty McWalter, Laura A Cross, Monisa D. Wagner, Dihong Zhou, Meagan K. Hainlen, Maxime Cadieux-Dion
Publikováno v:
Science Advances
SCIENCE ADVANCES
Science advances, 6(4):eaax0021. American Association for the Advancement of Science
SCIENCE ADVANCES
Science advances, 6(4):eaax0021. American Association for the Advancement of Science
Two lysine acyltransferases govern histone H3 propionylation at lysine 23 in normal and pathological conditions.
Lysine acetyltransferase 6A (KAT6A) and its paralog KAT6B form stoichiometric complexes with bromodomain- and PHD finger-containing
Lysine acetyltransferase 6A (KAT6A) and its paralog KAT6B form stoichiometric complexes with bromodomain- and PHD finger-containing
Autor:
Ellis L. Eikenboom, Winand N.M. Dinjens, Helena C. van Doorn, Willemina R. R. Geurts-Giele, Manon C.W. Spaander, Anne Goverde, Carli M. J. Tops, Hendrikus J. Dubbink, Anja Wagner
Publikováno v:
Cancers, 13(3):459, 1-16. Multidisciplinary Digital Publishing Institute (MDPI)
Cancers
Volume 13
Issue 3
Cancers, Vol 13, Iss 459, p 459 (2021)
Cancers, 13(3). MDPI
Cancers
Volume 13
Issue 3
Cancers, Vol 13, Iss 459, p 459 (2021)
Cancers, 13(3). MDPI
Lynch syndrome (LS) is caused by pathogenic germline variants in DNA mismatch repair (MMR) genes, predisposing female carriers for endometrial cancer (EC) and ovarian cancer (OC). Since gynecological LS surveillance guidelines are based on little evi
Autor:
Hendrikus J. Dubbink, Manon C.W. Spaander, Celine H. Leenen, Monique E. van Leerdam, Carli M. J. Tops, Margot G. van Lier, Anja Wagner, Ewout W. Steyerberg, Ernst J. Kuipers, Marco J. Bruno, Anne Goverde, Winand N.M. Dinjens, Ans M.W. van den Ouweland, Esther W. de Bekker-Grob
Publikováno v:
Genetics in Medicine, 18(10), 966-973. Lippincott Williams & Wilkins
Genetics in Medicine, 18(10), 966-973
Genetics in Medicine, 18(10), 966-973
Purpose: To assess the cost-effectiveness of routine Lynch syndrome (LS) screening among colorectal cancer (CRC) patients
Autor:
Anne Goverde, S. W. ten Broeke, W. Dinjens, Robert M.W. Hofstra, M C W Spaander, C. J. Tops, A. M. W. Van Den Ouweland, Marco J. Bruno, Anja Wagner, Hendrikus J. Dubbink, Ewout W. Steyerberg, Daan Nieboer
Publikováno v:
Familial Cancer
Familial Cancer, 17(3), 361-370
Familial Cancer, 17(3), 361-370. Springer Netherlands
Familial Cancer, 17(3), 361-370
Familial Cancer, 17(3), 361-370. Springer Netherlands
Until recently, no prediction models for Lynch syndrome (LS) had been validated for PMS2 mutation carriers. We aimed to evaluate MMRpredict and PREMM5 in a clinical cohort and for PMS2 mutation carriers specifically. In a retrospective, clinic-based
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e34d44202328ef087a658cfcc528cbb
https://hdl.handle.net/1887/76302
https://hdl.handle.net/1887/76302