نتائج البحث - "hMSH2 gene"

المصدر: Baglietto, L, Lindor, N M, Dowty, J G, White, D M, Wagner, A, Garcia, E B G, Vriends, A H J T, Cartwright, N R, Barnetson, R A, Farrington, S M, Tenesa, A, Hampel, H, Buchanan, D, Arnold, S, Young, J, Walsh, M D, Jass, J, Macrae, F, Antill, Y, Winship, I M, Giles, G G, Goldblatt, J, Parry, S, Suthers, G, Leggett, B, Butz, M, Aronson, M, Poynter, J N, Baron, J A, Le Marchand, L, Haile, R, Gallinger, S, Hopper, J L, Potter, J, de la Chapelle, A, Vasen, H F, Dunlop, M G & Thibodeau, S N & Jenkins, M A 2010, ' Risks of Lynch Syndrome Cancers for MSH6 Mutation Carriers ', JNCI: Journal of the National Cancer Institute, vol. 102, no. 3, pp. 193-201 . https://doi.org/10.1093/jnci/djp473
Journal of the National Cancer Institute, 102(3), 193-201. Oxford University Press
JNCI: Journal of the National Cancer Institute, 102(3), 193-201

مصطلحات موضوعية: Male, Cancer Research, Gene mutation, medicine.disease_cause, nonpolyposis colorectal-cancer mismatch-repair genes endometrial cancer germline mutations colon-cancer hmsh2 gene family onset ascertainment surveillance, Risk Factors, Neoplasms, Registries, Aged, 80 and over, Genetics, Mutation, Incidence, Medicine (all), Age Factors, Articles, Middle Aged, Lynch syndrome, DNA-Binding Proteins, Europe, Oncology, Female, DNA mismatch repair, Adult, Canada, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, Risk Assessment, Age Distribution, Sex Factors, Germline mutation, medicine, Humans, Sex Distribution, neoplasms, Germ-Line Mutation, Aged, business.industry, Endometrial cancer, Australia, nutritional and metabolic diseases, Cancer, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, United States, digestive system diseases, Endometrial Neoplasms, MSH6, Mutagenesis, Insertional, Cancer research, business, Gene Deletion, New Zealand

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::824937ad810c59a974c056099dae499a
https://doi.org/10.1093/jnci/djp473

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5

Identification and Classification of Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome): Adapting Old Concepts to Recent Advancements. Report from the Italian Association for the Study of Hereditary Colorectal Tumors Consensus Group

المؤلفون: Maurizio Genuardi, Tiziana Venesio, Lucio Bertario, Giovanni Battista Rossi, Guglielmina Nadia Ranzani, Giovanni Lanza, Cristina Oliani, Maurizio Ponz de Leon, Alessandra Viel, Liliana Varesco

المصدر: Diseases of the Colon & Rectum. 50:2126-2134

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64497a0da55a853b798f27617daac57e
https://doi.org/10.1007/s10350-007-9071-9

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6

Prognosis in patients with hepatocellular carcinoma correlates to mutations of p53 and/or hMSH2 genes

المؤلفون: Masatsugu Yano, Kiyohiro Hamatani, Hidetaka Eguchi, Donald G. MacPhee, Kiyohiko Dohi, Keizo Sugino, Toshiyuki Itamoto, Yuko Hirai, Toshimasa Asahara

المصدر: European Journal of Cancer. 43(6):1092-1100

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1aa11fd71cc69e1deca00ad67a1dfc3a
http://ir.lib.hiroshima-u.ac.jp/00020785

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7

Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancer

المؤلفون: Arend Karrenbeld, Mjw Berends, Ying Wu, Rolf H. Sijmons, Jan H. Kleibeuker, de Hermien Walle, M.J.L. Ligtenberg, Charles H.C.M. Buys, van der Aukje Zee, Robert M.W. Hofstra, de Elisabeth G. E. Vries, Harmen Hollema, Renee C. Niessen

المساهمون: Guided Treatment in Optimal Selected Cancer Patients (GUTS), Targeted Gynaecologic Oncology (TARGON), Reproductive Origins of Adult Health and Disease (ROAHD)

المصدر: Gut, 55, 1781-8
Gut, 55(12), 1781-1788. BMJ PUBLISHING GROUP
Gut, 55, 12, pp. 1781-8

مصطلحات موضوعية: Oncology, Male, Pathology, Base Pair Mismatch, MICROSATELLITE INSTABILITY, DNA Mutational Analysis, Gene mutation, DNA Mismatch Repair, Neoplasms, Multiple Primary, GENOMIC DELETIONS, Molecular diagnosis, prognosis and monitoring [UMCN 1.2], Cancer, REVISED BETHESDA GUIDELINES, Gastroenterology, Nuclear Proteins, CLINICAL-CRITERIA, DNA, Neoplasm, GERMLINE MUTATIONS, Middle Aged, CARRIERS, Lynch syndrome, Neoplasm Proteins, DNA-Binding Proteins, MutS Homolog 2 Protein, Growth and differentiation [NCMLS 3], Female, Colorectal Neoplasms, MutL Protein Homolog 1, Adult, medicine.medical_specialty, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Biology, MLH1, LYNCH-SYNDROME, Genomic disorders and inherited multi-system disorders [IGMD 3], Germline mutation, Translational research [ONCOL 3], Predictive Value of Tests, Internal medicine, medicine, HMSH2 GENE, Humans, IMMUNOHISTOCHEMISTRY, neoplasms, Germ-Line Mutation, Adaptor Proteins, Signal Transducing, Aged, Family Health, Hereditary cancer and cancer-related syndromes [ONCOL 1], Microsatellite instability, nutritional and metabolic diseases, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, MSH2, MSH6, Carrier Proteins

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee848a21c011b16acb6994a03e8b6679
https://doi.org/10.1136/gut.2005.090159

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8

Academic Journal

Prognosis in patients with hepatocellular carcinoma correlates to mutations of p53 and/or hMSH2 genes

المؤلفون: Yano, Masatsugu, Hamatani, Kiyohiro, Eguchi, Hidetaka, Hirai, Yuko, MacPhee, Donald G., Sugino, Keizo, Dohi, Kiyohiko, Itamoto, Toshiyuki, Asahara, Toshimasa

مصطلحات موضوعية: p53 gene, hMSH2 gene, Hepatocellular carcinoma, Intrahepatic metastasis, Multicentric occurrence

Time: 490

Relation: AA1075407X; http://dx.doi.org/10.1016/j.ejca.2007.01.032

الاتاحة: http://ir.lib.hiroshima-u.ac.jp/00020785
https://doi.org/10.1016/j.ejca.2007.01.032

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9

Electronic Resource

Identification and classification of hereditary nonpolyposis colorectal cancer (Lynch syndrome): Adapting old concepts to recent advancements. Report from the Italian association for the study of hereditary colorectal tumors consensus group

المؤلفون: de Leon, M, Bertario, L, Genuardi, M, Lanza, G, Oliani, C, Ranzani, G, Rossi, G, Varesco, L, Venesio, T, Viel, A, Genuardi, M (ORCID:0000-0002-7410-8351), Lanza, G (ORCID:0000-0003-2187-6653)

مصطلحات الفهرس: MISMATCH-REPAIR GENES, MICROSATELLITE INSTABILITY, COLON-CANCER, SYNDROME-II, HMSH2 GENE, MUTATIONS, FAMILIES, POPULATION, CARCINOMA, CARRIERS, Settore MED/03 - GENETICA MEDICA, info:eu-repo/semantics/article

URL: https://hdl.handle.net/10807/219845
info:eu-repo/semantics/altIdentifier/wos/WOS:000251641700018
volume:50
issue:12
firstpage:2126
lastpage:2134
numberofpages:9
issueyear:2007
journal:DISEASES OF THE COLON & RECTUM

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10

Electronic Resource

Prognosis in patients with hepatocellular carcinoma correlates to mutations of p53 and/or hMSH2 genes

المؤلفون: Yano, Masatsugu, Hamatani, Kiyohiro, Eguchi, Hidetaka, Hirai, Yuko, MacPhee, Donald G., Sugino, Keizo, Dohi, Kiyohiko, Itamoto, Toshiyuki, Asahara, Toshimasa

مصطلحات الفهرس: p53 gene, hMSH2 gene, Hepatocellular carcinoma, Intrahepatic metastasis, Multicentric occurrence, 490, journal article

URL: http://ir.lib.hiroshima-u.ac.jp/00020785

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