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1دورية أكاديمية
المؤلفون: Moller, P, Seppala, TT, Ahadova, A, Crosbie, EJ, Holinski-Feder, E, Scott, R, Haupt, S, Moslein, G, Winship, I, Bajwa-ten Broeke, SW, Kohut, KE, Ryan, N, Bauerfeind, P, Thomas, LE, Evans, DG, Aretz, S, Sijmons, RH, Half, E, Heinimann, K, Horisberger, K, Monahan, K, Engel, C, Cavestro, GM, Fruscio, R, Abu-Freha, N, Zohar, L, Laghi, L, Bertario, L, Bonanni, B, Tibiletti, MG, Lino-Silva, LS, Vaccaro, C, Della Valle, A, Rossi, BM, da Silva, LA, Nascimento, ILD, Rossi, NT, Debniak, T, Mecklin, JP, Bernstein, I, Lindblom, A, Sunde, L, Nakken, S, Heuveline, V, Burn, J, Hovig, E, Kloor, M, Sampson, JR, Dominguez-Valentin, M
المصدر: Hereditary cancer in clinical practice. 21(1):19
مصطلحات موضوعية: Medicin och hälsovetenskap
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2دورية أكاديميةDelineating genotype and parent-of-origin effect on the phenotype in MSH6-associated Lynch syndrome.
المؤلفون: van der Werf-'t Lam AS; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., Rodriguez-Girondo M; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands., Villasmil M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., Tops CM; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., van Hest L; Department of Clinical Genetics, Amsterdam UMC, location Vrije Universiteit Amsterdam and location University of Amsterdam, Amsterdam, The Netherlands., Gille HJP; Department of Clinical Genetics, Amsterdam UMC, location Vrije Universiteit Amsterdam and location University of Amsterdam, Amsterdam, The Netherlands., Duijkers FAM; Department of Human Genetics, Amsterdam University Medical Center, location Amsterdam Medical Center, Amsterdam, The Netherlands., Wagner A; Department of Clinical Genetics, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands., Eikenboom E; Department of Clinical Genetics, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.; Department of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands., Letteboer TGW; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands., de Jong MM; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Bajwa-Ten Broeke SW; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Bleeker F; Department of Clinical Genetics, Netherlands Cancer Institute, Amsterdam, The Netherlands., Gomez Garcia EB; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands., Dominguez-Valentin M; Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway., Møller P; Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway., Suerink M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., Nielsen M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
المصدر: Genes, chromosomes & cancer [Genes Chromosomes Cancer] 2024 May; Vol. 63 (5), pp. e23237.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9007329 Publication Model: Print Cited Medium: Internet ISSN: 1098-2264 (Electronic) Linking ISSN: 10452257 NLM ISO Abbreviation: Genes Chromosomes Cancer Subsets: MEDLINE
مواضيع طبية MeSH: Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics , DNA-Binding Proteins*/genetics , Phenotype* , Genotype*, Humans ; Female ; Male ; Middle Aged ; Adult ; Germ-Line Mutation ; Aged ; Genetic Predisposition to Disease ; Endometrial Neoplasms/genetics ; Endometrial Neoplasms/pathology
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3دورية أكاديمية
المؤلفون: Helderman NC; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands., Andini KD; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., van Leerdam ME; Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, the Netherlands; Department of Gastrointestinal Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands., van Hest LP; Department of Human Genetics, Amsterdam University Medical Center, Vrije Universiteit Amsterdam and University of Amsterdam, Amsterdam, the Netherlands., Hoekman DR; Department of Human Genetics, Amsterdam University Medical Center, Vrije Universiteit Amsterdam and University of Amsterdam, Amsterdam, the Netherlands., Ahadova A; Department of Applied Tumor Biology, Heidelberg University Hospital, Clinical Cooperation Unit Applied Tumor Biology, German Cancer Research Centre, Heidelberg, Germany., Bajwa-Ten Broeke SW; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., Bosse T; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands., van der Logt EMJ; Department of Molecular Diagnostics, Pathology Friesland, Leeuwarden, the Netherlands., Imhann F; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands., Kloor M; Department of Applied Tumor Biology, Heidelberg University Hospital, Clinical Cooperation Unit Applied Tumor Biology, German Cancer Research Centre, Heidelberg, Germany., Langers AMJ; Department of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, the Netherlands., Smit VTHBM; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands., Terlouw D; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands., van Wezel T; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands., Morreau H; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands., Nielsen M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands. Electronic address: m.nielsen@lumc.nl.
المصدر: The Journal of molecular diagnostics : JMD [J Mol Diagn] 2024 Feb; Vol. 26 (2), pp. 106-114. Date of Electronic Publication: 2023 Dec 05.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 100893612 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1943-7811 (Electronic) Linking ISSN: 15251578 NLM ISO Abbreviation: J Mol Diagn Subsets: MEDLINE
مواضيع طبية MeSH: Colorectal Neoplasms, Hereditary Nonpolyposis*/diagnosis , Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics , Endometrial Neoplasms*/diagnosis , Endometrial Neoplasms*/genetics , Endometrial Neoplasms*/pathology, Female ; Humans ; Middle Aged ; Aged ; MutL Protein Homolog 1/genetics ; MutL Protein Homolog 1/metabolism ; Genetic Testing ; Promoter Regions, Genetic ; DNA Mismatch Repair/genetics ; Mismatch Repair Endonuclease PMS2/genetics ; Mismatch Repair Endonuclease PMS2/metabolism ; Germ-Line Mutation
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4دورية أكاديمية
المؤلفون: van der Werf-'t Lam AS; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., Terlouw D; Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands., Tops CM; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., van Kan MS; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., van Hest LP; Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands., Gille HJP; Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands., Duijkers FAM; Department of Clinical Genetics, Amsterdam Medical Center, Amsterdam, The Netherlands., Wagner A; Department of Clinical Genetics, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands., Eikenboom EL; Department of Clinical Genetics, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands; Department of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands., Letteboer TGW; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands., de Jong MM; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Bajwa-Ten Broeke SW; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Bleeker FE; Department of Clinical Genetics, Netherlands Cancer Institute, Amsterdam, The Netherlands., Gomez Garcia EB; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands., de Wind N; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., van Wezel JT; Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands., Morreau H; Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands., Suerink M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands., Nielsen M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands. Electronic address: m.nielsen@lumc.nl.
المصدر: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc [Mod Pathol] 2023 Sep; Vol. 36 (9), pp. 100240. Date of Electronic Publication: 2023 Jun 10.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Elsevier Inc Country of Publication: United States NLM ID: 8806605 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0285 (Electronic) Linking ISSN: 08933952 NLM ISO Abbreviation: Mod Pathol Subsets: MEDLINE
مواضيع طبية MeSH: Colorectal Neoplasms, Hereditary Nonpolyposis*/diagnosis , Colorectal Neoplasms, Hereditary Nonpolyposis*/genetics , Colorectal Neoplasms, Hereditary Nonpolyposis*/pathology , Colonic Neoplasms*/genetics , Endometrial Neoplasms*/genetics , Colorectal Neoplasms*/pathology, Female ; Humans ; Microsatellite Repeats ; Microsatellite Instability ; DNA Mismatch Repair/genetics ; DNA-Binding Proteins/genetics
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5دورية أكاديمية
المؤلفون: Andini KD; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Nielsen M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, Netherlands., Suerink M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, Netherlands., Helderman NC; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Koornstra JJ; Department of Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Ahadova A; Department of Applied Tumour Biology, Institute of Pathology, Heidelberg University Hospital, and Clinical Cooperation Unit Applied Tumor Biology, German Cancer Research Center, Heidelberg, Germany., Kloor M; Department of Applied Tumour Biology, Institute of Pathology, Heidelberg University Hospital, and Clinical Cooperation Unit Applied Tumor Biology, German Cancer Research Center, Heidelberg, Germany., Mourits MJE; Department of Gynaecology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Kok K; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Sijmons RH; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands., Bajwa-Ten Broeke SW; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
المصدر: Frontiers in oncology [Front Oncol] 2023 Feb 21; Vol. 13, pp. 1127329. Date of Electronic Publication: 2023 Feb 21 (Print Publication: 2023).
نوع المنشور: Journal Article; Review
بيانات الدورية: Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101568867 Publication Model: eCollection Cited Medium: Print ISSN: 2234-943X (Print) Linking ISSN: 2234943X NLM ISO Abbreviation: Front Oncol Subsets: PubMed not MEDLINE
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6دورية أكاديمية
المؤلفون: Bajwa-Ten Broeke SW; Department of Genetics, University Medical Center Groningen, Groningen, the Netherlands; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands. Electronic address: s.w.ten.broeke@umcg.nl., Ballhausen A; Department of Applied Tumor Biology, Institute of Pathology, University Hospital Heidelberg, Cooperation Unit Applied Tumor Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany; Department of Hematology, Oncology and Tumor Immunology, Charité-Universitätsmedizin Berlin, Berlin, Germany; Molecular Medicine Partnership Unit (MMPU), University Hospital Heidelberg, Heidelberg, Germany., Ahadova A; Department of Applied Tumor Biology, Institute of Pathology, University Hospital Heidelberg, Cooperation Unit Applied Tumor Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany; Molecular Medicine Partnership Unit (MMPU), University Hospital Heidelberg, Heidelberg, Germany., Suerink M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands., Bohaumilitzky L; Department of Applied Tumor Biology, Institute of Pathology, University Hospital Heidelberg, Cooperation Unit Applied Tumor Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany; Molecular Medicine Partnership Unit (MMPU), University Hospital Heidelberg, Heidelberg, Germany., Seidler F; Department of Applied Tumor Biology, Institute of Pathology, University Hospital Heidelberg, Cooperation Unit Applied Tumor Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany; Molecular Medicine Partnership Unit (MMPU), University Hospital Heidelberg, Heidelberg, Germany., Morreau H; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands., van Wezel T; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands., Krzykalla J; Division of Biostatistics, German Cancer Research Center (DKFZ), Heidelberg, Germany., Benner A; Division of Biostatistics, German Cancer Research Center (DKFZ), Heidelberg, Germany., de Miranda NF; Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands., von Knebel Doeberitz M; Department of Applied Tumor Biology, Institute of Pathology, University Hospital Heidelberg, Cooperation Unit Applied Tumor Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany; Molecular Medicine Partnership Unit (MMPU), University Hospital Heidelberg, Heidelberg, Germany., Nielsen M; Department of Clinical Genetics, Leiden University Medical Center, Leiden, the Netherlands., Kloor M; Department of Applied Tumor Biology, Institute of Pathology, University Hospital Heidelberg, Cooperation Unit Applied Tumor Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany; Molecular Medicine Partnership Unit (MMPU), University Hospital Heidelberg, Heidelberg, Germany.
المصدر: Experimental and molecular pathology [Exp Mol Pathol] 2021 Oct; Vol. 122, pp. 104668. Date of Electronic Publication: 2021 Jul 22.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 0370711 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-0945 (Electronic) Linking ISSN: 00144800 NLM ISO Abbreviation: Exp Mol Pathol Subsets: MEDLINE
مواضيع طبية MeSH: Colorectal Neoplasms/*genetics , Colorectal Neoplasms, Hereditary Nonpolyposis/*genetics , DNA Mismatch Repair/*genetics , Mismatch Repair Endonuclease PMS2/*genetics, Aged ; Colorectal Neoplasms/complications ; Colorectal Neoplasms/pathology ; Colorectal Neoplasms, Hereditary Nonpolyposis/complications ; Colorectal Neoplasms, Hereditary Nonpolyposis/pathology ; DNA-Binding Proteins/genetics ; Female ; Germ-Line Mutation/genetics ; Humans ; Male ; Microsatellite Instability ; Microsatellite Repeats/genetics ; Middle Aged ; MutL Protein Homolog 1/genetics ; MutS Homolog 2 Protein/genetics
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7دورية أكاديمية
المؤلفون: Helderman NC; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, the Netherlands., Bajwa-Ten Broeke SW; Department of Clinical Genetics, UMC Groningen, the Netherlands., Morreau H; Department of Pathology, Leiden University Medical Centre, Leiden, the Netherlands., Suerink M; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, the Netherlands., Terlouw D; Department of Pathology, Leiden University Medical Centre, Leiden, the Netherlands., van der Werf-' T Lam AS; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, the Netherlands., van Wezel T; Department of Pathology, Leiden University Medical Centre, Leiden, the Netherlands., Nielsen M; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, the Netherlands. Electronic address: m.nielsen@lumc.nl.
المصدر: Critical reviews in oncology/hematology [Crit Rev Oncol Hematol] 2021 Jul; Vol. 163, pp. 103338. Date of Electronic Publication: 2021 May 25.
نوع المنشور: Journal Article; Review
بيانات الدورية: Publisher: Elsevier Scientific Publishers Country of Publication: Netherlands NLM ID: 8916049 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0461 (Electronic) Linking ISSN: 10408428 NLM ISO Abbreviation: Crit Rev Oncol Hematol Subsets: MEDLINE