Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Renske A. Kuiper"'
Publikováno v:
Cancers, Vol 5, Iss 2, Pp 462-490 (2013)
Recent advances in high-throughput sequencing technology have identified the transcription of a much larger portion of the genome than previously anticipated. Especially in the context of cancer it has become clear that aberrant transcription of both
Externí odkaz:
https://doaj.org/article/b2294eff7d9145d3a881482a0bde5e99
Autor:
M. Elisa Vink-Börger, Ian Tomlinson, Janet R. Vos, Barbara Rivera, Dagmara Dymerska, Na Li, Sanne W. ten Broeke, Isabel Spier, Hildegunn Høberg-Vetti, Gabriel Capellá, Clara Ruiz-Ponte, Erik A. M. Jansen, Mark Clendenning, Renske A. Kuiper, Laura Valle, Stefan Aretz, Rolf H. Sijmons, Tom van Wezel, Claire Palles, Judith E. Grolleman, William D. Foulkes, Ian G. Campbell, Julian Adlard, Sue Kenwrick, Olivera Spasic-Boskovic, Frederik J. Hes, Eveline J. Kamping, Robert Hüneburg, Noel F C C de Miranda, Wenche Sjursen, Ad Geurts van Kessel, Richarda M. de Voer, Isabell Popp, Jan Lubinski, Fadwa A. Elsayed, Detlev Schindler, Marija Staninova, Hans K. Schackert, Robbert D.A. Weren, Aleksandar Dimovski, Nicoline Hoogerbrugge, Kevin Sweet, Helen Lindsay, Alois Lang, Roland P. Kuiper, Kornelia Neveling, David Cockburn, Maartje Nielsen, Daniel D. Buchanan, Hans Morreau, Marjolijn J. L. Ligtenberg, Marjolijn C.J. Jongmans, Paul A. James
Publikováno v:
SSRN Electronic Journal.
Biallelic germline mutations affecting NTHL1 predispose to adenomatous polyposis and colorectal cancer, but the complete phenotype is unknown, which hampers patient recognition. We describe 29 individuals from 17 families, of which 26 developed one (
Autor:
Roland P. Kuiper, Kevin Sweet, Robbert D.A. Weren, Robert Hüneburg, Alois Lang, Jan Lubinski, Hildegunn Høberg-Vetti, Janet R. Vos, Erik A. M. Jansen, Marija Staninova, Barbara Rivera, Stefan Aretz, M. Elisa Vink-Börger, Claire Palles, Noel F C C de Miranda, Daniel D. Buchanan, Wenche Sjursen, William D. Foulkes, Kornelia Neveling, Clara Ruiz-Ponte, Ad Geurts van Kessel, Sue Kenwrick, Renske A. Kuiper, Laura Valle, Aleksandar Dimovski, Judith E. Grolleman, Paul A. James, Isabel Spier, David Cockburn, Maartje Nielsen, Hans Morreau, Hans K. Schackert, Nicoline Hoogerbrugge, Tom van Wezel, Helen Lindsay, Ian G. Campbell, Isabell Popp, Dagmara Dymerska, Na Li, Rolf H. Sijmons, Frederik J. Hes, Marjolijn J. L. Ligtenberg, Marjolijn C.J. Jongmans, Detlev Schindler, Ian Tomlinson, Eveline J. Kamping, Mark Clendenning, Olivera Spasic-Boskovic, Richarda M. de Voer, Sanne W. ten Broeke, Julian Adlard, Gabriel Capellá, Fadwa A. Elsayed
Publikováno v:
Cancer Cell, 35, 256
Cancer Cell, 35, 2, pp. 256
Cancer Cell, 35(2), 256-+. CELL PRESS
Cancer cell, 35(2), 256-266.e5. CELL PRESS
Cancer Cell, 35(2), 256. Cell Press
Cancer Cell, 35, 2, pp. 256
Cancer Cell, 35(2), 256-+. CELL PRESS
Cancer cell, 35(2), 256-266.e5. CELL PRESS
Cancer Cell, 35(2), 256. Cell Press
Biallelic germline mutations affecting NTHL1 predispose carriers to adenomatous polyposis and colorectal cancer, but the complete phenotype is unknown. We describe 29 individuals carrying biallelic germline NTHL1 mutations from 17 families, of which
Publikováno v:
Cancers
Cancers, 5, 462-490
Cancers, Vol 5, Iss 2, Pp 462-490 (2013)
Cancers, 5, 2, pp. 462-490
Cancers, 5, 462-490
Cancers, Vol 5, Iss 2, Pp 462-490 (2013)
Cancers, 5, 2, pp. 462-490
Contains fulltext : 117195.pdf (Publisher’s version ) (Open Access) Recent advances in high-throughput sequencing technology have identified the transcription of a much larger portion of the genome than previously anticipated. Especially in the con
Autor:
S van Reijmersdal, Eric F.P.M. Schoenmakers, Martinus F. Niermeijer, Rolph Pfundt, Renske A. Kuiper, Lambertus A. Kiemeney, Katja K.H. Aben, Mark P. Schoenberg, Fred Witjes
Publikováno v:
ResearcherID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fcb20592e9bfbb56387575f8268ce44
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000238132900441&KeyUID=WOS:000238132900441
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000238132900441&KeyUID=WOS:000238132900441
Autor:
Jiangyan Yu, Renske A. Kuiper, Esmé Waanders, Roland P. Kuiper, Peter M. Hoogerbrugge, Edwin Sonneveld, Frank N. van Leeuwen, Simon V. van Reijmersdal, Zeljko Antic
Publikováno v:
ResearcherID
Relapse represents the most common cause of therapy failure in B-cell precursor ALL acute lymphoblastic leukemia (BCP-ALL), and is caused by selective outgrowth of therapy-resistant leukemic cells. Two-third of BCP-ALL relapses present after treatmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7e9a602326c8123a87ae1a0c1e1260c
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000394452306146&KeyUID=WOS:000394452306146
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000394452306146&KeyUID=WOS:000394452306146