نتائج البحث - "W. Dinjens"

1

Evaluation of a nationwide Dutch guideline to detect Lynch syndrome in patients with endometrial cancer

المساهمون: Obstetrics & Gynecology, Clinical Genetics, Pathology

المصدر: Gynecologic Oncology, 160(3), 771-776. Academic Press

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::720844fcc6ca13ec30fe22eba65d1abcTest
http://www.scopus.com/inward/record.url?scp=85098892154&partnerID=8YFLogxKTest

2

Highly accurate DNA-based detection and treatment results of MET exon 14 skipping mutations in lung cancer

المؤلفون: Thüsen J.H. von der, Melinda A. Pruis, A-M.C. Dingemans, Willemina R. R. Geurts-Giele, Isabelle C. Meijssen, W. Dinjens, Marthe S. Paats, Hendrikus J. Dubbink, Martijn P. Lolkema, Joachim G.J.V. Aerts

المساهمون: Medical Oncology, Pulmonary Medicine, Pathology, RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy, Pulmonologie, MUMC+: MA Med Staf Spec Longziekten (9)

المصدر: Lung Cancer, 140, 46-54. Elsevier Ireland Ltd

مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Cancer Research, Lung Neoplasms, medicine.medical_treatment, sarcomatoid carcinoma, amplification, medicine.disease_cause, Targeted therapy, Exon, 0302 clinical medicine, Non-small cell lung cancer, Carcinoma, Non-Small-Cell Lung, diagnostics, CRIZOTINIB, met exon 14 skipping, Aged, 80 and over, Mutation, High-Throughput Nucleotide Sequencing, DNA, Neoplasm, Exons, Middle Aged, Proto-Oncogene Proteins c-met, Amplicon, Prognosis, MET Exon 14 Skipping Mutation, Survival Rate, 030220 oncology & carcinogenesis, Female, medicine.drug, Pulmonary and Respiratory Medicine, medicine.medical_specialty, Resistance against cMET inhibition, INHIBITION, Adenocarcinoma of Lung, PATIENT, DNA sequencing, target, resistance, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Internal medicine, Next generation sequencing, met inhibitor, Biomarkers, Tumor, medicine, Humans, Lung cancer, Protein Kinase Inhibitors, Aged, Retrospective Studies, Crizotinib, Diagnostic Tests, Routine, business.industry, driver mutation, medicine.disease, 030104 developmental biology, business, Follow-Up Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::057efac93cf37bf55ac4d294f4b0aedfTest
https://doi.org/10.1016/j.lungcan.2019.11.010Test

3

Abstract P1-06-06: Direct ex vivo observation of homologous recombination defect reversal after DNA damaging chemotherapy in metastatic breast cancer patients

المؤلفون: W. Dinjens, Titia G. Meijer, Nicole S. Verkaik, D C van Gent, C.H.M. van Deurzen, TD Den Toom, Agnes Jager, H.J. Dubbink, Roland Kanaar

المصدر: Cancer Research. 79:P1-06

مصطلحات موضوعية: Cisplatin, Cancer Research, business.industry, PALB2, RAD51, Cancer, medicine.disease, Metastatic breast cancer, Breast cancer, Oncology, Cancer research, Medicine, Multiplex ligation-dependent probe amplification, business, CHEK2, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::d85843c27e4e4e97b67731d632f84294Test
https://doi.org/10.1158/1538-7445.sabcs18-p1-06-06Test

4

Progression of ductal carcinoma in situ to invasive breast cancer: comparative genomic sequencing

المؤلفون: C.H.M. van Deurzen, R. van Marion, J. M. Martens, W. Dinjens, Niels M.G. Krol, W F J van IJcken, Rutger W W Brouwer, Shusma C. Doebar

المساهمون: Pathology, Cell biology, Medical Oncology

المصدر: Virchows Archiv
Virchows Archiv. An International Journal of Pathology, 474(2), 247-251. Springer-Verlag

مصطلحات موضوعية: 0301 basic medicine, In situ, Oncology, Adult, medicine.medical_specialty, Concordance, Genomics, Breast Neoplasms, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, SDG 3 - Good Health and Well-being, Internal medicine, medicine, Biomarkers, Tumor, Humans, Neoplasm Invasiveness, Breast, skin and connective tissue diseases, Molecular Biology, neoplasms, Exome sequencing, Massive parallel sequencing, Progression, business.industry, Genomic sequencing, Brief Report, Carcinoma, Ductal, Breast, Ductal carcinoma in situ, Cell Biology, General Medicine, Sequence Analysis, DNA, Ductal carcinoma, Middle Aged, medicine.disease, Prognosis, body regions, 030104 developmental biology, Carcinoma, Intraductal, Noninfiltrating, 030220 oncology & carcinogenesis, Disease Progression, Female, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9dedefb598fea08fd306b2c11e32caaTest
https://pure.eur.nl/en/publications/854f26ba-41f6-47e6-b799-4d646932d25cTest

5

P89 Implementation of a nationwide guideline to detect of women at risk for Lynch syndrome in endometrial cancer should be improved

المؤلفون: A.S. Tjalsma, W. Dinjens, H. C. van Doorn, Anja Wagner, Patricia C. Ewing-Graham

المصدر: Poster exhibition Day 1.

مصطلحات موضوعية: medicine.medical_specialty, Hysterectomy, medicine.diagnostic_test, Obstetrics, business.industry, Endometrial cancer, Genetic counseling, medicine.medical_treatment, Guideline, medicine.disease, Lynch syndrome, MSH6, Germline mutation, medicine, business, Endometrial biopsy

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::93f12b4ff8c93ae8c6e564b5e0b8610aTest
https://doi.org/10.1136/ijgc-2019-esgo.151Test

6

Germline variant in MSX1 identified in a Dutch family with clustering of Barrett's esophagus and esophageal adenocarcinoma

المؤلفون: A. de Klein, Katharina Biermann, Anja Wagner, W. Dinjens, R. van Marion, B. P. L. Wijnhoven, A. M. J. van Nistelrooij, J. J. B. van Lanschot, M C W Spaander, W F J van IJcken

المساهمون: Pathology, Surgery, Clinical Genetics, Gastroenterology & Hepatology

المصدر: Familial Cancer, 17(3), 435-440. Springer Netherlands
Familial Cancer

مصطلحات موضوعية: Exome sequencing, Male, 0301 basic medicine, Proband, Cancer Research, Genetic testing, Esophageal Neoplasms, Adenocarcinoma, Biology, Familial clustering, Germline, Barrett Esophagus, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Genetics, medicine, Barrett’s esophagus, Cluster Analysis, Humans, Genetic Predisposition to Disease, Esophagus, Germ-Line Mutation, Genetics (clinical), MSX1 Transcription Factor, Cancer, Middle Aged, medicine.disease, digestive system diseases, Pedigree, 030104 developmental biology, medicine.anatomical_structure, Oncology, 030220 oncology & carcinogenesis, Barrett's esophagus, Original Article, Female, Esophageal adenocarcinoma, SNP array

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abf2a50eb3097e40e27c6189481dd498Test
https://hdl.handle.net/1765/102877Test

7

95P Optimizing selection of experimental treatment for patients with advanced cancer using whole genome sequencing

المؤلفون: Martijn P. Lolkema, Floris H. Groenendijk, S. Badloe, Paul Roepman, Stefan Sleijfer, J. Von Der Thüsen, Melinda A. Pruis, Debbie Robbrecht, W. Dinjens, A. van Puffelen

المصدر: Annals of Oncology. 32:S397

مصطلحات موضوعية: Whole genome sequencing, Oncology, business.industry, Medicine, Hematology, Computational biology, business, Advanced cancer, Selection (genetic algorithm)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::0319ddfe6f7aa9773ade6ba5ac9580f9Test
https://doi.org/10.1016/j.annonc.2021.08.375Test

8

دورية أكاديمية

EGFR and KRAS quality assurance schemes in pathology: generating normative data for molecular predictive marker analysis in targeted therapy

المؤلفون: E. Thunnissen, J.V.M.G. Bovée, H. Bruinsma, A.J.C. van den Brule, W. Dinjens, D.A.M. Heideman, E. Meulemans, P. Nederlof, C. van Noesel, C.F.M. Prinsen, K. Scheidel, P.M. van de Ven, R. de Weger, E. Schuuring, M. Ligtenberg

المصدر: Journal of clinical pathology (00219746) vol.64 (2011) nr.10 p.884-892

العلاقة: http://hdl.handle.net/11245/1.365347Test

الإتاحة: http://hdl.handle.net/11245/1.365347Test

View record in BASE

9

25P Breast cancers with heterogeneous HER2 amplification show a diverse distribution of ‘driver’ and ‘passenger’ somatic mutations and copy number variations

المؤلفون: Hein F.B.M. Sleddens, Peggy N. Atmodimedjo, W. Dinjens, Marie Colombe Agahozo, Esther H. Lips, C.H.M. van Deurzen, M.R. Van Bockstal, R. van Marion, Lindy L. Visser, Jelle Wesseling

المصدر: Annals of Oncology. 31:S25

مصطلحات موضوعية: Genetics, Oncology, Distribution (number theory), Somatic cell, business.industry, HER2 Amplification, Medicine, Hematology, Copy-number variation, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::dd6bbd92305a8f0349599ffc6f18009eTest
https://doi.org/10.1016/j.annonc.2020.03.161Test

10

Granular dot-like staining with MLH1 immunohistochemistry is a clone-dependent artefact

المؤلفون: O. Stam, W. Dinjens, Patricia C. Ewing-Graham, Michail Doukas, M.R. Van Bockstal, Shatavisha Dasgupta, Floris H. Groenendijk, Hendrikus J. Dubbink, K.E. Biermann, M.L.F. van Velthuysen

المساهمون: UCL - (SLuc) Service d'anatomie pathologique, UCL - SSS/IREC/SLUC - Pôle St.-Luc, Pathology

المصدر: Pathology, research and practice, Vol. 216, no. 1, p. 152581 [1-5] (2020)
Pathology Research and Practice, 216. Urban und Fischer Verlag GmbH und Co. KG

مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Pathology, medicine.medical_specialty, DNA mismatch repair, Clone (cell biology), Biology, MLH1, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Biomarkers, Tumor, Carcinoma, medicine, PMS2, Humans, Genetic Predisposition to Disease, Promoter Regions, Genetic, neoplasms, nutritional and metabolic diseases, Microsatellite instability, Dot-like staining, Cell Biology, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Immunohistochemistry, digestive system diseases, Endometrial Neoplasms, MSH6, 030104 developmental biology, MSH2, 030220 oncology & carcinogenesis, Female, MutL Protein Homolog 1

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d332ac0b1cea63745fb373be7b7a830Test
https://doi.org/10.1016/j.prp.2019.152581Test

تنقيح النتائج