Výsledky vyhledávání - Maaike P.G. Vreeswijk
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Analysis of repair of cyclobutane pyrimidine dimers and pyrimidine 6-4 pyrimidone photoproducts in transcriptionally active and inactive genes in Chinese hamster cells. Autor Maaike P.G. Vreeswijk, Anneke van Hoffen, Birgit Westland, Harry Vrieling, A.A. van Zeeland, L.H. Mullenders
Vydáno 1994Artigo -
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Intronic variants in<i>BRCA1</i>and<i>BRCA2</i>that affect RNA splicing can be reliably selected by splice-site prediction programs Autor Maaike P.G. Vreeswijk, Jaco Kraan, Heleen M. van der Klift, Geraldine R. Vink, Cees J. Cornelisse, Juul Wijnen, Egbert Bakker, Christi J. van Asperen, Peter Devilee
Vydáno 2008Artigo -
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Functional Assays for Analysis of Variants of Uncertain Significance in<i>BRCA2</i> Autor Lucia Guidugli, Aura Carreira, Sandrine M. Caputo, Åsa Ehlén, Alvaro Galli, Álvaro N.A. Monteiro, Susan L. Neuhausen, Thomas van Overeem Hansen, Fergus J. Couch, Maaike P.G. Vreeswijk
Vydáno 2013Revisão -
5
Tumor slice culture system to assess drug response of primary breast cancer Autor Kishan A.T. Naipal, Nicole S. Verkaik, Humberto Sánchez, Carolien H. M. van Deurzen, Michael A. den Bakker, Jan H.J. Hoeijmakers, Roland Kanaar, Maaike P.G. Vreeswijk, Agnes Jager, Dik C. van Gent
Vydáno 2016Artigo -
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Variants of uncertain clinical significance in hereditary breast and ovarian cancer genes: best practices in functional analysis for clinical annotation Autor Álvaro N.A. Monteiro, Peter Bouwman, Arne Nedergaard Kousholt, Diana Eccles, Gaël A. Millot, Jean‐Yves Masson, Marjanka K. Schmidt, Shyam K. Sharan, Ralph Scully, Lisa Wiesmüller, Fergus J. Couch, Maaike P.G. Vreeswijk
Vydáno 2020Revisão -
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The effects of short-term fasting on tolerance to (neo) adjuvant chemotherapy in HER2-negative breast cancer patients: a randomized pilot study Autor Stefanie de Groot, Maaike P.G. Vreeswijk, Marij J.P. Welters, Gido Gravesteijn, J.J.W.A. Boei, Anouk Jochems, Daniel Houtsma, Hein Putter, Jacobus JM van der Hoeven, J.W.R. Nortier, Hanno Pijl, Judith R. Kroep
Vydáno 2015Artigo -
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Functional analysis of genetic variants in the high-risk breast cancer susceptibility gene PALB2 Autor Rick A.C.M. Boonen, Amélie Rodrigue, Chantal Stoepker, Wouter W. Wiegant, Bas Vroling, Milan Sharma, Magdalena B. Rother, Nandi Celosse, Maaike P.G. Vreeswijk, Fergus J. Couch, Jacques Simard, Peter Devilee, Jean‐Yves Masson, Haico van Attikum
Vydáno 2019Artigo -
9
Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-<i>BRCA1/2</i>breast cancer families Autor Inge M. M. Lakeman, Florentine Hilbers, Mar Rodríguez‐Girondo, Andrew Lee, Maaike P.G. Vreeswijk, Antoinette Hollestelle, Caroline Seynaeve, Hanne Meijers‐Heijboer, Jan C. Oosterwijk, Nicoline Hoogerbrugge, Edith Oláh, Hans F. A. Vasen, Christi J. van Asperen, Peter Devilee
Vydáno 2019Artigo -
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The RECAP Test Rapidly and Reliably Identifies Homologous Recombination-Deficient Ovarian Carcinomas Autor Lise M. van Wijk, Sylvia Vermeulen, Matty Meijers, Manuela F. van Diest, Natalja T. ter Haar, Marthe M. de Jonge, Nienke Solleveld‐Westerink, Tom van Wezel, Dik C. van Gent, Judith R. Kroep, Tjalling Bosse, Katja N. Gaarenstroom, Harry Vrieling, Maaike P.G. Vreeswijk
Vydáno 2020Artigo -
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Functional Analysis Identifies Damaging<i>CHEK2</i>Missense Variants Associated with Increased Cancer Risk Autor Rick A.C.M. Boonen, Wouter W. Wiegant, Nandi Celosse, Bas Vroling, Stephan Heijl, Zsofia Kote‐Jarai, Martina Mijušković, Simona Cristea, Nienke Solleveld‐Westerink, Tom van Wezel, Niko Beerenwinkel, Rosalind A. Eeles, Peter Devilee, Maaike P.G. Vreeswijk, Giancarlo Marra, Haico van Attikum
Vydáno 2021Artigo -
12
Clinical correlates of low-risk variants in FGFR2, TNRC9, MAP3K1, LSP1 and 8q24 in a Dutch cohort of incident breast cancer cases Autor Petra E.A. Huijts, Maaike P.G. Vreeswijk, Karin Kroeze‐Jansema, Catharina E. Jacobi, Caroline Seynaeve, Elly MM Krol-Warmerdam, Pauline M. Wijers‐Koster, Jannet Blom, Karen A. Pooley, Jan G.M. Klijn, Rob A.�E.�M. Tollenaar, Peter Devilee, Christi J. van Asperen
Vydáno 2007Artigo -
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A guide for functional analysis of<i>BRCA1</i>variants of uncertain significance Autor Gaël A. Millot, Marcelo A. Carvalho, Sandrine M. Caputo, Maaike P.G. Vreeswijk, Melissa A. Brown, Michelle Webb, Étienne Rouleau, Susan L. Neuhausen, Thomas van Overeem Hansen, Alvaro Galli, Rita D. Brandão, Marinus J. Blok, Aneliya Velkova, Fergus J. Couch, Álvaro N.A. Monteiro
Vydáno 2012Revisão -
14
Germline <i>BRCA</i>-Associated Endometrial Carcinoma Is a Distinct Clinicopathologic Entity Autor Marthe M. de Jonge, Lauren L. Ritterhouse, Cor D. de Kroon, Maaike P.G. Vreeswijk, Jeremy P. Segal, Rutika Puranik, Harry Hollema, Matti A. Rookus, Christi J. van Asperen, Flora E. van Leeuwen, Vincent T.H.B.M. Smit, Brooke E. Howitt, Tjalling Bosse
Vydáno 2019Artigo -
15
Functional <i>Ex Vivo</i> Assay to Select Homologous Recombination–Deficient Breast Tumors for PARP Inhibitor Treatment Autor Kishan A.T. Naipal, Nicole S. Verkaik, Najim Ameziane, Carolien H. M. van Deurzen, Petra ter Brugge, Matty Meijers, Anieta M. Sieuwerts, John W.M. Martens, Mark J. O’Connor, Harry Vrieling, Jan H.J. Hoeijmakers, Jos Jonkers, Roland Kanaar, Johan P. de Winter, Maaike P.G. Vreeswijk, Agnes Jager, Dik C. van Gent
Vydáno 2014Artigo -
16
Frequent Homologous Recombination Deficiency in High-grade Endometrial Carcinomas Autor Marthe M. de Jonge, Aurélie Auguste, Lise M. van Wijk, Philip C. Schouten, Matty Meijers, Natalja T. ter Haar, Vincent T.H.B.M. Smit, Remi A. Nout, Mark A. Glaire, David N. Church, Harry Vrieling, Bastien Job, Yannick Boursin, Cor D. de Kroon, Étienne Rouleau, Alexandra Léary, Maaike P.G. Vreeswijk, Tjalling Bosse
Vydáno 2018Artigo -
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Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease Autor Neil V. Morgan, Mark R. Morris, Hakan Cangül, Diane Gleeson, Anna Straatman-Iwanowska, Nicholas P. Davies, Stephen Keenan, Shanaz Pasha, Fatimah Rahman, Dean Gentle, Maaike P.G. Vreeswijk, Peter Devilee, Margaret A. Knowles, Serdar Ceylaner, Richard C. Trembath, Carlos Dalence, Erol Kısmet, Vedat Köseoğlu, Hans‐Christoph Rossbach, Paul Gissen, David Tannahill, Eamonn R. Maher
Vydáno 2010Artigo -
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Towards controlled terminology for reporting germline cancer susceptibility variants: an ENIGMA report Autor Amanda B. Spurdle, Stephanie Greville‐Heygate, Antonis C. Antoniou, Melissa A. Brown, Leslie Burke, Miguel de la Hoya, Susan M. Domchek, Thilo Dörk, Helen V. Firth, Álvaro N.A. Monteiro, Arjen R. Mensenkamp, Michael T. Parsons, Paolo Radice, Mark E. Robson, Marc Tischkowitz, Emma Tudini, Clare Turnbull, Maaike P.G. Vreeswijk, Logan C. Walker, Sean V. Tavtigian, Diana Eccles
Vydáno 2019Artigo -
19
A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example Autor Leila Mohammadi, Maaike P.G. Vreeswijk, Rogier A. Oldenburg, Ans van den Ouweland, Jan C. Oosterwijk, Annemarie H. van der Hout, Nicoline Hoogerbrugge, Marjolijn J. L. Ligtenberg, Margreet G.E.M. Ausems, Rob B. van der Luijt, Charlotte J. Dommering, Gilles Thomas, Senno Verhoef, Frans B.L. Hogervorst, Theo A. van Os, E. Gómez, Marinus J. Blok, Juul Wijnen, Quinta Helmer, Peter Devilee, Christi J. van Asperen, Hans C. van Houwelingen
Vydáno 2009Artigo -
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BRCA1 Circos: a visualisation resource for functional analysis of missense variants Autor Ankita Jhuraney, Aneliya Velkova, Randall C. Johnson, Bailey Kessing, Renato S. Carvalho, Phillip J Whiley, Amanda B. Spurdle, Maaike P.G. Vreeswijk, Sandrine M. Caputo, Gaël A. Millot, Ana Vega, Nicolas Coquelle, Alvaro Galli, Diana Eccles, Marinus J. Blok, Tuya Pal, Rob B. van der Luijt, Marta Santamariña Pena, Susan L. Neuhausen, Talia Donenberg, Eva Macháčková, Simon Thomas, Maxime Vallée, Fergus J. Couch, Sean V. Tavtigian, J. N. Mark Glover, Marcelo A. Carvalho, Lawrence C. Brody, Shyam K. Sharan, Álvaro N.A. Monteiro
Vydáno 2015Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Cancer
Medicine
Breast cancer
Internal medicine
Oncology
Mutation
Cancer research
Computational biology
Genotype
Bioinformatics
Ovarian cancer
Single-nucleotide polymorphism
Germline mutation
Gynecology
Molecular biology
Allele
Germline
Missense mutation
Phenotype
Chemotherapy
Computer science
DNA repair
Homologous recombination
Odds ratio
Pathology
SNP
Surgical oncology