Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Monique Goossens"'
Autor:
Sabine Venderbosch, Shannon van Lent-van Vliet, Anton F J de Haan, Marjolijn J Ligtenberg, Monique Goossens, Cornelis J A Punt, Miriam Koopman, Iris D Nagtegaal
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0124538 (2015)
PurposeTo determine the frequency and prognostic value of elevated microsatellite alterations at selected tetranucleotide repeats (EMAST) in metastatic colorectal cancer (mCRC) patients in relation to microsatellite instability (MSI) status and MSH3
Externí odkaz:
https://doaj.org/article/73113240e7d94246b0ef74adc0fbc31f
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study
Autor:
Tsun Leung Chan, Eugène T P Verwiel, Irma Kluijt, Diana Eccles, Rolf H. Sijmons, Egbert J.W. Redeker, Rachel S. van der Post, Encarna B. Gomez Garcia, Reinhard Büttner, Cora M. Aalfs, Roland P. Kuiper, Johan J.P. Gille, Bernadette P M van Nesselrooij, Frans B. L. Hogervorst, Marjolijn J L Ligtenberg, Tracy Graham, Julie O. Culver, Edith Olah, Monique Goossens, Carli M. J. Tops, Elke Holinski-Feder, David J. Bunyan, Marielle E. van Gijn, Frederik J. Hes, Suet Yi Leung, Pierre O. Chappuis, Monika Morak, Edward M Leter, Nils Rahner, Lea Velsher, János Papp, Renee C. Niessen, J. Han van Krieken, Lambertus A. Kiemeney, Ad Geurts van Kessel, Charlotte W. Ockeloen, Nicoline Hoogerbrugge, Marlies Kempers, Iris D. Nagtegaal, Verena Steinke, Hans K. Schackert, Matthias Kloor, Melanie R. Palomares, Sapna Syngal, Pierre Hutter, Elena M. Stoffel
Publikováno v:
Kempers, M J E, Kuiper, R P, Ockeloen, C W, Chappuis, P O, Hutter, P, Rahner, N, Schackert, H K, Steinke, V, Holinski-Feder, E, Morak, M, Kloor, M, Buttner, R, Verwiel, E T P, van Krieken, J H, Nagtegaal, I D, Goossens, M, van der Post, R S, Niessen, R C, Sijmons, RH, Kluijt, I, Hogervorst, F B L, Leter, E M, Gille, J J P, Aalfs, C M, Redeker, E J W, Hes, F J, Tops, C M J, van Nesselrooij, B P M, van Gijn, M E, Garcia, E B G, Eccles, D M, Bunyan, D J, Syngal, S, Stoffel, E M, Culver, J O, Palomares, M R, Graham, T, Velsher, L, Papp, J, Olah, E, Chan, T L, Leung, S Y, van Kessel, A G, Kiemeney, L A L M, Hoogerbrugge, N & Ligtenberg, M J L 2011, ' Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study ', Lancet Oncology, vol. 12, no. 1, pp. 49-55 . https://doi.org/10.1016/S1470-2045(10)70265-5
The Lancet Oncology, 49-55
STARTPAGE=49;ENDPAGE=55;TITLE=The Lancet Oncology
Lancet Oncology, 12, 1, pp. 49-55
Lancet oncology, 12(1), 49-55. Elsevier Science
Lancet Oncology, 12, 49-55
lancet oncology, 12(1), 49-55. Lancet Publishing Group
Lancet Oncology, 12(1), 49-55. ELSEVIER SCIENCE INC
Lancet Oncology, 12(1), 49-55. Lancet Publishing Group
The Lancet Oncology, 49-55
STARTPAGE=49;ENDPAGE=55;TITLE=The Lancet Oncology
Lancet Oncology, 12, 1, pp. 49-55
Lancet oncology, 12(1), 49-55. Elsevier Science
Lancet Oncology, 12, 49-55
lancet oncology, 12(1), 49-55. Lancet Publishing Group
Lancet Oncology, 12(1), 49-55. ELSEVIER SCIENCE INC
Lancet Oncology, 12(1), 49-55. Lancet Publishing Group
Summary Background Lynch syndrome is caused by germline mutations in MSH2, MLH1, MSH6 , and PMS2 mismatch-repair genes and leads to a high risk of colorectal and endometrial cancer. We previously showed that constitutional 3′ end deletions of EPCAM
Autor:
M Voorendt, Jhjm van Krieken, Tsun Leung Chan, Sy Leung, Monique Goossens, Nicoline Hoogerbrugge, Danielle Bodmer, Roland P. Kuiper, A. Geurts van Kessel, M.J.L. Ligtenberg, H.G. Brunner, Konnie M. Hebeda, Eveline Hoenselaar, Sjb Hendriks-Cornelissen
Publikováno v:
Familial Cancer. 9:713-748
Autor:
Kyu Pil Lee, Monique Goossens, Catalin N. Topala, Kirsten Y. Renkema, Joost G. J. Hoenderop, René J. M. Bindels, Pascal Houillier
Publikováno v:
Nephrology, Dialysis, Transplantation, 24, 1919-24
Nephrology, Dialysis, Transplantation, 24, 6, pp. 1919-24
Nephrology, Dialysis, Transplantation, 24, 6, pp. 1919-24
Contains fulltext : 81402.pdf (Publisher’s version ) (Open Access) BACKGROUND: Kidney stone formation is a major socioeconomic problem in humans, involving pain, recurrent treatment and renal insufficiency. As most renal precipitates contain calciu
Autor:
Cornelis J. A. Punt, Anton F.J. de Haan, Marjolijn J. L. Ligtenberg, Iris D. Nagtegaal, Shannon van Vliet, Miriam Koopman, Sabine Venderbosch, Monique Goossens
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0124538 (2015)
PLoS One, 10, 4
PLoS One, 10
PLoS ONE, 10(4). Public Library of Science
PLoS ONE
PLoS One, 10, 4
PLoS One, 10
PLoS ONE, 10(4). Public Library of Science
PLoS ONE
Contains fulltext : 155092.PDF (Publisher’s version ) (Open Access) PURPOSE: To determine the frequency and prognostic value of elevated microsatellite alterations at selected tetranucleotide repeats (EMAST) in metastatic colorectal cancer (mCRC) p
Autor:
Sandra J B Cornelissen, Monique Goossens, Hicham Ouchene, Marjolijn J. L. Ligtenberg, Ingrid P. Vogelaar, Michael Kwint, Nicoline Hoogerbrugge, Iris D. Nagtegaal, Arjen R. Mensenkamp, Wendy A.G. van Zelst–Stams
Publikováno v:
Gastroenterology, 146, 3, pp. 643-646 e8
Gastroenterology, 146, 643-646 e8
Gastroenterology, 146, 643-646 e8
Contains fulltext : 136846pub.pdf (Publisher’s version ) (Closed access) Lynch syndrome is caused by germline mutations in the mismatch repair (MMR) genes. Tumors are characterized by microsatellite instability (MSI). However, a considerable number
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc59e96d9d3b7033e6fae02ede4d5836
https://hdl.handle.net/2066/136846
https://hdl.handle.net/2066/136846
Autor:
Ramprasath Venkatachalam, Aline Haufe, Tracy Graham, Marielle E. van Gijn, Frans B. L. Hogervorst, Beate Betz, Hans K. Schackert, Lisenka E.L.M. Vissers, Matthias Kloor, Carli M. J. Tops, Iris D. Nagtegaal, Tsun Leung Chan, Verena Steinke, Julie O. Culver, J. Han van Krieken, Eveline J. Kamping, Elke Holinski-Feder, Nicoline Hoogerbrugge, Eveline Hoenselaar, Ans M.W. van den Ouweland, Renee C. Niessen, Nils Rahner, Monique Goossens, Danielle Bodmer, Monika Morak, Johan J.P. Gille, Marjolijn J L Ligtenberg, David J. Bunyan, Roland P. Kuiper, Ad Geurts van Kessel, Susanne Stemmler, Philip Kahl, Sapna Syngal, Pierre Hutter, B. Redeker
Publikováno v:
Kuiper, R P, Vissers, L E L M, Venkatachalam, R, Bodmer, D, Hoenselaar, E, Goossens, M, Haufe, A, Kamping, E, Niessen, R C, Hogervorst, F B L, Gille, J J P, Redeker, B, Tops, C M J, van Gijn, M E, van den Ouweland, A M W, Rahner, N, Steinke, V, Kahl, P, Holinski-Feder, E, Morak, M, Kloor, M, Stemmler, S, Betz, B, Hutter, P, Bunyan, D J, Syngal, S, Culver, J O, Graham, T, Chan, T L, Nagtegaal, I D, van Krieken, J H J M, Schackert, H K, Hoogerbrugge, N, van Kessel, A G & Ligtenberg, M J L 2011, ' Recurrence and Variability of Germline EPCAM Deletions in Lynch Syndrome ', Human Mutation, vol. 32, no. 4, pp. 407-414 . https://doi.org/10.1002/humu.21446
Human Mutation, 32(4), 407-414. Wiley
Human Mutation
Human Mutation, Wiley, 2011, 32 (4), pp.407. ⟨10.1002/humu.21446⟩
Human Mutation, 32, 407-14
Human Mutation, 32(4), 407-414. Wiley-Liss Inc.
Human Mutation, 32, 4, pp. 407-14
Human Mutation, 32(4), 407-414
Human mutation, 32(4), 407-414. Wiley-Liss Inc.
Human Mutation, 32(4), 407-414. Wiley
Human Mutation
Human Mutation, Wiley, 2011, 32 (4), pp.407. ⟨10.1002/humu.21446⟩
Human Mutation, 32, 407-14
Human Mutation, 32(4), 407-414. Wiley-Liss Inc.
Human Mutation, 32, 4, pp. 407-14
Human Mutation, 32(4), 407-414
Human mutation, 32(4), 407-414. Wiley-Liss Inc.
Contains fulltext : 96266.pdf (Publisher’s version ) (Closed access) Recently, we identified 3' end deletions in the EPCAM gene as a novel cause of Lynch syndrome. These truncating EPCAM deletions cause allele-specific epigenetic silencing of the n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acd9f0a3462e34cfe5b79e413b8e9225
https://research.vumc.nl/en/publications/3046c84c-09af-4327-8073-c1bd009a1583
https://research.vumc.nl/en/publications/3046c84c-09af-4327-8073-c1bd009a1583
Autor:
Mike Churchman, Monique Goossens, Ramprasath Venkatachalam, Erica van der Looij, Ian Tomlinson, Eveline Hoenselaar, Luis G. Carvajal-Carmona, Roland P. Kuiper, Lilian Vreede, Marjolijn J. L. Ligtenberg, Hans K. Schackert, Heike Görgens, Nicoline Hoogerbrugge, Ad Geurts van Kessel, Diederik R.H. de Bruijn, Eveline J. Kamping, Marc Manuel Hahn
Publikováno v:
Gastroenterology, 139, 2221-4
Gastroenterology, 139, 6, pp. 2221-4
Gastroenterology, 139, 6, pp. 2221-4
Contains fulltext : 88484.pdf (Publisher’s version ) (Closed access) 01 december 2010
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec07f6e43b8d16db190cad5f26ce8ea2
https://doi.org/10.1053/j.gastro.2010.08.063
https://doi.org/10.1053/j.gastro.2010.08.063
Autor:
Wai Yin Tsui, Tsun Leung Chan, Marsha Voorendt, Nicoline Hoogerbrugge, Suet Yi Leung, Monique Goossens, Sandra J B Hendriks-Cornelissen, Chi Kwan Kong, Han G. Brunner, Danielle Bodmer, Ad Geurts van Kessel, Tracy Y H Lee, Konnie M. Hebeda, J. Han van Krieken, Eveline Hoenselaar, Roland P. Kuiper, Siu Tsan Yuen, Marjolijn J L Ligtenberg
Publikováno v:
Nature Genetics, 41, 1, pp. 112-7
Nature Genetics, 41, 112-7
Nature Genetics, 41, 112-7
Contains fulltext : 80569.pdf (Publisher’s version ) (Closed access) Lynch syndrome patients are susceptible to colorectal and endometrial cancers owing to inactivating germline mutations in mismatch repair genes, including MSH2 (ref. 1). Here we d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe1ae8e1fefde699cf294b6995933c78
https://doi.org/10.1038/ng.283
https://doi.org/10.1038/ng.283
Autor:
Carolien M. Kets, Han G. Brunner, Marjolijn J L Ligtenberg, Joannes H.J.M. Van Krieken, Nicoline Hoogerbrugge, Monique Goossens
Publikováno v:
European Journal of Human Genetics, 17, 2, pp. 159-64
European Journal of Human Genetics, 17, 159-64
European Journal of Human Genetics, 17, 159-64
Contains fulltext : 81706.pdf (Publisher’s version ) (Closed access) Mono-allelic germline mutations in mismatch repair (MMR) genes lead to Lynch syndrome, an autosomal dominant syndrome with an increased risk of predominantly colorectal and endome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0b741397c6a5cad7e3f897e35d5110a
https://hdl.handle.net/2066/81706
https://hdl.handle.net/2066/81706