المؤلفون: Anita J.W.M. Brouns, Lizza E.L. Hendriks, Iris J. Robbesom-van den Berge, Annemariek J.H.M. Driessen, Guido M.J.M. Roemen, Britt L.J. van Herpen, Zoë Dekkers, Bas Heitzer, Daphne J.G. Leunissen, Laura Moonen, Ragnar Lunde, Marcel Westenend, Marjolein van Driel, Ernst-Jan M. Speel, Anne-Marie C. Dingemans

المصدر: Frontiers in Oncology, Vol 13 (2023)

مصطلحات موضوعية: bone metastases, receptor activator of nuclear factor κb ligand, epidermal growth factor expression, osteoprotegerin, lung adenocarcinoma, epidermal growth factor mutation, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fonc.2023.1145001/full; https://doaj.org/toc/2234-943X

URL الوصول: https://doaj.org/article/a528475313524589b5d2ca5c95872ab2

المؤلفون: Paul Roepman, Danielle Cohen, Stephen P. Finn, Cathal O'Brien, Hein F.B.M. Sleddens, Kim Monkhorst, Karin Weijers, Guido M.J.M. Roemen, Isabelle C. Meijssen, Ernst-Jan M. Speel, Tom van Wezel, Winand N.M. Dinjens, Mirjam C. Boelens, H.J. Dubbink, Willemina R. R. Geurts-Giele, Jan H. von der Thüsen, Kris G. Samsom, Erik Thunnissen, Teodora Radonic

المساهمون: RS: GROW - R2 - Basic and Translational Cancer Biology, Pathologie, Pathology

المصدر: Radonic, T, Geurts-Giele, W R R, Samsom, K G, Roemen, G M J M, von der Thüsen, J H, Thunnissen, E, Meijssen, I C, Sleddens, H F B M, Dinjens, W N M, Boelens, M C, Weijers, K, Speel, E J M, Finn, S P, O'Brien, C, van Wezel, T, Cohen, D, Monkhorst, K, Roepman, P & Dubbink, H J 2021, ' RET Fluorescence In Situ Hybridization Analysis Is a Sensitive but Highly Unspecific Screening Method for RET Fusions in Lung Cancer ', Journal of Thoracic Oncology, vol. 16, no. 5, pp. 798-806 . https://doi.org/10.1016/j.jtho.2021.01.1619
Journal of Thoracic Oncology, 16(5), 798-806. Elsevier Science
Journal of Thoracic Oncology, 16(5), 798-806. International Association for the Study of Lung Cancer

مصطلحات موضوعية: 0301 basic medicine, Pulmonary and Respiratory Medicine, congenital, hereditary, and neonatal diseases and abnormalities, endocrine system, endocrine system diseases, Sequencing data, MULTICENTER, Locus (genetics), ROS1 REARRANGEMENT, 03 medical and health sciences, 0302 clinical medicine, FISH, medicine, ROS1, Screening method, Lung cancer, neoplasms, medicine.diagnostic_test, business.industry, RET Rearrangement, medicine.disease, Molecular biology, 030104 developmental biology, Oncology, ALK, 030220 oncology & carcinogenesis, Fish , RNA NGS, Non-small cell carcinoma, business, RET, Fluorescence in situ hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b1e428c89911a1ba266b62b3867f640
https://doi.org/10.1016/j.jtho.2021.01.1619

المؤلفون: Lisa M. Hillen, Jules L. Derks, M. Van Engeland, D. Leunissen, A-M.C. Dingemans, Alexander Koch, Laura Moonen, E.J.M. Speel, Guido M.J.M. Roemen, Lynnette Fernandez-Cuesta, Aurélie A G Gabriel, L. Lap, Matthieu Foll, Nicolas Alcala, L. Mangiante

المصدر: Journal of Thoracic Oncology. 16:S1196-S1197

مصطلحات موضوعية: Pulmonary and Respiratory Medicine, Orthopedia homeobox, Oncology, business.industry, Cancer research, Medicine, Methylation, business, Differential (mathematics)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::337b5b0aa9877cc46e28c2a971a933c4
https://doi.org/10.1016/j.jtho.2021.08.685

المؤلفون: Kelly A.E. Sinx, Ernst-Jan M. Speel, Virrie van Zutven, Michel van Geel, P.M. Steijlen, Renske Janssen, Guido M.J.M. Roemen, Klara Mosterd

المساهمون: Dermatologie, RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy, MUMC+: MA Dermatologie (9), Promovendi ODB, RS: GROW - R2 - Basic and Translational Cancer Biology, Pathologie, MUMC+: MA AIOS Dermatologie (9), MUMC+: MA Dermatologie (3), MUMC+: DA KG Lab Centraal Lab (9)

المصدر: JAAD Case Reports, 4(5), 408-11. Elsevier Inc.
JAAD Case Reports

مصطلحات موضوعية: 0301 basic medicine, Patched, SHH, sonic hedgehog pathway, Basal Cell Nevus Syndrome, Vismodegib, Case Report, Dermatology, smMIP, single-molecule molecular inversion probes, 03 medical and health sciences, hedgehog pathway, 0302 clinical medicine, Germline mutation, basal cell carcinoma, vismodegib, medicine, Basal cell carcinoma, laBCC, locally advanced BCC, basal cell nevus syndrome, BCC, basal cell carcinoma, business.industry, mBCC, metastatic BCC, medicine.disease, tumor resistance, Hedgehog signaling pathway, 030104 developmental biology, PTCH1, 030220 oncology & carcinogenesis, Cancer research, business, Smoothened, BCNS, basal cell nevus syndrome, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17a9e4ff75fb9b9aa0e5b64c564ad5bd
https://doi.org/10.1016/j.jdcr.2017.11.011

المؤلفون: Henri J. Boersma, P.M. Steijlen, M. van Geel, Guido M.J.M. Roemen, Aimee H.M.M. Arits, M.G.H.C. Reinders, Ernst-Jan M. Speel, Maaike Vreeburg, Aimee D C Paulussen, E.M. Leter, Klara Mosterd

المساهمون: RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy, Promovendi ODB, Dermatologie, MUMC+: MA Dermatologie (9), MUMC+: KIO Innovatie (9), Promovendi PHPC, Health Services Research, MUMC+: DA KG Polikliniek (9), MUMC+: DA KG Lab Centraal Lab (9), Pathologie, RS: GROW - R2 - Basic and Translational Cancer Biology, MUMC+: MA Dermatologie (3), MUMC+: MA AIOS Dermatologie (9)

المصدر: British Journal of Dermatology, 177(1), 249-252. Wiley

مصطلحات موضوعية: 0301 basic medicine, Genetics, Pathology, medicine.medical_specialty, MUTATIONS, Genetic counseling, Germline mosaicism, Dermatology, PTCH1 Gene, 030105 genetics & heredity, Biology, HUMAN HOMOLOG, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, PTCH1, GORLIN-SYNDROME, Mutation (genetic algorithm), medicine, Restriction fragment length polymorphism, Gene, CARCINOMA SYNDROME

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53dd37fb9acee00eefb3b67de0e60370
https://doi.org/10.1111/bjd.15082

المؤلفون: Ernst-Jan M. Speel, Ronald A.M. Damhuis, B. Hermans, Erik Thunnissen, Anne-Marie C. Dingemans, Egbert F. Smit, Michael A. den Bakker, Cecile M. Stallinga, Guido M.J.M. Roemen, Harry J.M. Groen, Robert-Jan van Suylen, Esther C. van den Broek, Jules L. Derks

المصدر: Cancer Research. 79:487-487

مصطلحات موضوعية: clone (Java method), Cancer Research, Pathology, medicine.medical_specialty, business.industry, medicine.medical_treatment, STK11, Cancer, Large cell neuroendocrine carcinoma of the lung, medicine.disease, Targeted therapy, Oncology, medicine, Immunohistochemistry, Notch ligand, business, Immunostaining

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c9979a707fd27fea3856b0162308f295
https://doi.org/10.1158/1538-7445.am2019-487

المؤلفون: Lisa M. Hillen, Constance T. R. M. Stumpel, Jeroen Schoots, Ernst-Jan M. Speel, Anton Tom Tiebosch, Carine J Peutz-Koostra, Guido M.J.M. Roemen, Erik-Jan Kamsteeg

المساهمون: Genetica & Celbiologie, MUMC+: DA Pat Pathologie (9), RS: GROW - R2 - Basic and Translational Cancer Biology, Pathologie, RS: CARIM - R3.06 - The vulnerable plaque: makers and markers, RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Polikliniek (9), Klinische Genetica

المصدر: Fetal and Pediatric Pathology, 35, 112-9
Fetal and Pediatric Pathology, 35, 2, pp. 112-9
Fetal and Pediatric Pathology, 35(2), 112-119. Informa Healthcare

مصطلحات موضوعية: Denys–Drash syndrome, Pathology, medicine.medical_specialty, Genes, Wilms Tumor, Nephrotic Syndrome, Tissue Fixation, Genetic counseling, congenital nephrotic syndrome, 030232 urology & nephrology, Mutation, Missense, Gene mutation, Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12], Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, long-term tissue storage, medicine, Missense mutation, Humans, 030212 general & internal medicine, WT1 Proteins, Congenital nephrotic syndrome, In Situ Hybridization, Fluorescence, Paraffin Embedding, business.industry, Wilms' tumor, General Medicine, medicine.disease, Denys-Drash Syndrome, Frasier syndrome, Wilms tumor 1 suppressor gene, perinatal death, Pediatrics, Perinatology and Child Health, Mutation (genetic algorithm), Female, denys Drash syndrome, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8542515d5a92511e5915f4ce35d0e3f5
http://hdl.handle.net/2066/168099

المؤلفون: Axel zur Hausen, Guido M.J.M. Roemen, Ernst J. M. Speel

المصدر: Lung Cancer

مصطلحات موضوعية: business.industry, Medicine, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9406736500723ad0832461d7f784c574
https://doi.org/10.1183/2312508x.10010014

المؤلفون: Patrick G. Groothuis, Manon van Engeland, Geeske C. Dam de Veen, Johanna M.A. Pijnenborg, Guido M.J.M. Roemen, Jan Willem Voncken, Leonie van de Broek, Jelte de Haan

المصدر: Gynecologic Oncology. 100:397-404

مصطلحات موضوعية: Nonsense mutation, Apoptosis, medicine.disease_cause, Exon, Carcinoma, Humans, Medicine, Missense mutation, neoplasms, Aged, Aged, 80 and over, Mutation, Paraffin Embedding, business.industry, Obstetrics and Gynecology, Proto-Oncogene Proteins c-mdm2, Odds ratio, Middle Aged, medicine.disease, Immunohistochemistry, Endometrial Neoplasms, Oncology, Concomitant, Cancer research, Keratins, Female, Neoplasm Recurrence, Local, Tumor Suppressor Protein p53, business, Carcinoma, Endometrioid

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::288d52657d37bd98503ef7899189c1a1
https://doi.org/10.1016/j.ygyno.2005.09.056

المؤلفون: Matty P. Weijenberg, Marjolein H.F.M. Lentjes, Adriaan P. de Bruïne, Piet A. van den Brandt, Anton F.P.M. de Goeij, Margreet Lüchtenborg, Stefan de Vogel, R. Alexandra Goldbohm, Guido M.J.M. Roemen, Manon van Engeland

المساهمون: Pathologie, Epidemiologie, RS: NUTRIM School of Nutrition and Translational Research in Metabolism, RS: GROW - School for Oncology and Reproduction, TNO Kwaliteit van Leven

المصدر: Journal of Nutrition, 136(12), 3015-3021. Oxford University Press
King's College London
Scopus-Elsevier
Journal of Nutrition, 12, 136, 3015-3021

مصطلحات موضوعية: Questionnaires, Male, Colorectal cancer, Medicine (miscellaneous), colon polyposis, cancer risk, Gene mutation, Gastroenterology, protein MLH1, Cohort Studies, Diet and cancer, Surveys and Questionnaires, gene mutation, Netherlands, vitamin intake, Nutrition and Dietetics, adult, Incidence (epidemiology), article, Nuclear Proteins, DNA, Neoplasm, Middle Aged, Micronutrient, female, rectum cancer, Cohort, Colonic Neoplasms, Female, Colorectal Neoplasms, MutL Protein Homolog 1, Cohort study, medicine.medical_specialty, Genes, APC, Food and Chemical Risk Analysis, colorectal cancer, oncogene K ras, folic acid, Folic Acid, Internal medicine, medicine, Humans, controlled study, human, protein expression, Nutrition, Adaptor Proteins, Signal Transducing, Aged, Proportional Hazards Models, Proportional hazards model, business.industry, Rectal Neoplasms, Patient Selection, medicine.disease, major clinical study, human tissue, Diet, Mutation, incidence, dietary intake, business, Carrier Proteins

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9426c0fd5852e09944a464345ed4f943
https://doi.org/10.1093/jn/136.12.3015