نتائج البحث

1

Adenoma and colorectal cancer risks in Lynch syndrome, Lynch‐like syndrome and familial colorectal cancer type X

المصدر: International Journal of Cancer. 150:56-66

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::871995e375f9a6cd7de71d0924c92752Test
https://doi.org/10.1002/ijc.33790Test

2

Value of upper gastrointestinal endoscopy for gastric cancer surveillance in patients with Lynch syndrome

المصدر: International Journal of Cancer. 148:106-114

مصطلحات موضوعية: Adult, Male, Cancer Research, medicine.medical_specialty, Disease, Gastroenterology, 03 medical and health sciences, 0302 clinical medicine, Stomach Neoplasms, Germany, Internal medicine, Gastroscopy, medicine, Humans, Genetic Predisposition to Disease, ddc:610, Prospective Studies, Family history, Intestinal Cancer, Early Detection of Cancer, Aged, Neoplasm Staging, medicine.diagnostic_test, business.industry, Age Factors, Cancer, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Lynch syndrome, Early Gastric Cancer, Endoscopy, MutS Homolog 2 Protein, Oncology, Evaluation Studies as Topic, Gastric Mucosa, 030220 oncology & carcinogenesis, Mutation, Practice Guidelines as Topic, Patient Compliance, MutL Protein Homolog 1, business, Cohort study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72d4e94c977f36a987dce05df7758415Test
https://doi.org/10.1002/ijc.33294Test

3

Promoter methylation and expression of MGMT and the DNA mismatch repair genes MLH1, MSH2, MSH6 and PMS2 in paired primary and recurrent glioblastomas

المؤلفون: Bettina Hentschel, Manfred Westphal, Sabina Eigenbrod, Friedrich W. Kreth, Michael Sabel, Niklas Thon, Gabriele Schackert, Michael Weller, Markus Löffler, Jörg C. Tonn, Torsten Pietsch, Guido Reifenberger, Jörg Felsberg

المساهمون: University of Zurich

المصدر: International Journal of Cancer. 129:659-670

مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Methyltransferase, 610 Medicine & health, Antineoplastic Agents, Biology, MLH1, DNA Mismatch Repair, Disease-Free Survival, O(6)-Methylguanine-DNA Methyltransferase, Temozolomide, PMS2, medicine, Humans, 1306 Cancer Research, Promoter Regions, Genetic, neoplasms, Adaptor Proteins, Signal Transducing, Aged, Mismatch Repair Endonuclease PMS2, Adenosine Triphosphatases, Brain Neoplasms, Nuclear Proteins, Methylation, Middle Aged, digestive system diseases, 10040 Clinic for Neurology, DNA-Binding Proteins, Dacarbazine, MSH6, DNA Repair Enzymes, MutS Homolog 2 Protein, Oncology, MSH2, Cancer research, 2730 Oncology, Female, DNA mismatch repair, Neoplasm Recurrence, Local, Glioblastoma, MutL Protein Homolog 1, medicine.drug

وصف الملف: Promoter_PDF_Revision.pdf - application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5ae7a6b0b77653f1f4e1c86da3a5c35Test
https://doi.org/10.1002/ijc.26083Test

4

IGF1 is a modifier of disease risk in hereditary non‐polyposis colorectal cancer

المؤلفون: Rodney J. Scott, Janina Suchy, Stuart G. Reeves, Kim Colyvas, Cliff Meldrum, Jan Lubinski, Dominique Rich, Grzegorz Kurzawski

المصدر: International Journal of Cancer. 123:1339-1343

مصطلحات موضوعية: Adult, Male, Oncology, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, medicine.medical_specialty, Kaplan-Meier Estimate, Gene mutation, MLH1, Polymerase Chain Reaction, Sex Factors, Germline mutation, Risk Factors, Internal medicine, Humans, Medicine, Genetic Predisposition to Disease, Age of Onset, Insulin-Like Growth Factor I, Promoter Regions, Genetic, Survival analysis, Adaptor Proteins, Signal Transducing, Genetics, Polymorphism, Genetic, business.industry, Proportional hazards model, Nuclear Proteins, Cancer, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, MutS Homolog 2 Protein, MSH2, Mutation, Female, Age of onset, MutL Protein Homolog 1, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffde17534fa577f7341b6812e4918bdcTest
https://doi.org/10.1002/ijc.23668Test

5

Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer

المصدر: International Journal of Cancer. 118:115-122

مصطلحات موضوعية: Adult, Male, Oncology, Cancer Research, medicine.medical_specialty, Pathology, Amsterdam criteria, Time Factors, DNA Repair, Base Pair Mismatch, Colorectal cancer, Guidelines as Topic, MLH1, Logistic regression, Sensitivity and Specificity, Diagnosis, Differential, Germline mutation, stomatognathic system, Predictive Value of Tests, Internal medicine, medicine, Humans, Genetic Testing, Germ-Line Mutation, Adaptor Proteins, Signal Transducing, business.industry, Nuclear Proteins, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Immunohistochemistry, MutS Homolog 2 Protein, MSH2, Female, DNA mismatch repair, Carrier Proteins, MutL Protein Homolog 1, business, DNA Damage, Microsatellite Repeats

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f68df81f4f48c76f6e537acc4138dbddTest
https://doi.org/10.1002/ijc.21313Test

6

Microsatellite instability in thorotrast-induced human intrahepatic cholangiocarcinoma

المؤلفون: Hirohito Momoi, Yuichi Ishikawa, Manabu Fukumoto, Duo Liu, Li Li

المصدر: International Journal of Cancer. 102:366-371

مصطلحات موضوعية: Adult, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Pathology, medicine.medical_specialty, Neoplasms, Radiation-Induced, DNA Repair, Base Pair Mismatch, Loss of Heterozygosity, Biology, Frameshift mutation, Cholangiocarcinoma, Loss of heterozygosity, chemistry.chemical_compound, Proto-Oncogene Proteins, medicine, Humans, Gene Silencing, Promoter Regions, Genetic, neoplasms, Thorotrast, Carcinogen, Adaptor Proteins, Signal Transducing, Nuclear Proteins, nutritional and metabolic diseases, Microsatellite instability, Methylation, DNA Methylation, Middle Aged, medicine.disease, digestive system diseases, Neoplasm Proteins, DNA-Binding Proteins, Bile Ducts, Intrahepatic, MutS Homolog 2 Protein, Bile Duct Neoplasms, Oncology, chemistry, Cancer cell, DNA methylation, Carcinogens, Thorium Dioxide, Carrier Proteins, MutL Protein Homolog 1, Microsatellite Repeats

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::837569c737e9f1a6fd575442db01dbffTest
https://doi.org/10.1002/ijc.10726Test

7

Prevalence of germline mutations ofMLH1 andMSH2 in hereditary nonpolyposis colorectal cancer families from Spain

المؤلفون: Javier Godino, Iciar Garcia Carbonero, Trinidad Caldés, Charis Eng, Manuel Benito, Eduardo Díaz-Rubio, Miguel de la Hoya, Pedro Pérez Segura

المصدر: International Journal of Cancer. 98:774-779

مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Amsterdam criteria, DNA Mutational Analysis, Biology, MLH1, medicine.disease_cause, Polymerase Chain Reaction, Germline mutation, Proto-Oncogene Proteins, medicine, PMS2, Humans, Age of Onset, neoplasms, Germ-Line Mutation, Adaptor Proteins, Signal Transducing, Genetic testing, Genetics, Mutation, medicine.diagnostic_test, Nuclear Proteins, nutritional and metabolic diseases, DNA, Neoplasm, Middle Aged, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, Neoplasm Proteins, Pedigree, DNA-Binding Proteins, MSH6, MutS Homolog 2 Protein, Oncology, Spain, MSH2, Female, Carrier Proteins, MutL Protein Homolog 1, Microsatellite Repeats

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::195c714f76fe1894d0825d025a99b098Test
https://doi.org/10.1002/ijc.10240Test

8

Association between genetic polymorphisms in DNA mismatch repair-related genes with risk and prognosis of head and neck squamous cell carcinoma

المؤلفون: Guilherme Augusto Silva, Nogueira, Gustavo Jacob, Lourenço, Camila Borges Martins, Oliveira, Fernando Augusto Lima, Marson, Leisa, Lopes-Aguiar, Ericka Francislaine Dias, Costa, Tathiane Regine Penna, Lima, Vitor Teixeira, Liutti, Frederico, Leal, Vivian Castro Antunes, Santos, José Augusto, Rinck-Junior, Carmen Silvia Passos, Lima

المصدر: International journal of cancer. 137(4)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::ecd19925cf2df5fac4561a79427e28f2Test
https://pubmed.ncbi.nlm.nih.gov/25598504Test

9

Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer

المؤلفون: Richard Fishel, Steffen Pistorius, H. K. Schackert, Jens Plaschke, Hans Detlev Saeger, Henning Dralle, Tina Bocker, Christian Kruppa, René Tischler, Josef Rüschoff

المصدر: International Journal of Cancer. 85:606-613

مصطلحات موضوعية: Adult, Male, Cancer Research, Genotype, Base Pair Mismatch, Colorectal cancer, Mutation, Missense, Biology, medicine.disease_cause, Germline, Germline mutation, Breast cancer, Proto-Oncogene Proteins, Carcinoma, medicine, Humans, Intestinal Mucosa, Frameshift Mutation, Germ-Line Mutation, Adaptor Proteins, Signal Transducing, Aged, DNA Primers, Sequence Deletion, Genetics, Mutation, Nuclear Proteins, Microsatellite instability, Exons, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Immunohistochemistry, Introns, Neoplasm Proteins, DNA-Binding Proteins, MutS Homolog 2 Protein, Amino Acid Substitution, Oncology, Female, DNA mismatch repair, Carrier Proteins, Colorectal Neoplasms, MutL Protein Homolog 1, Microsatellite Repeats

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0849f7d96005aae98135b6fdf00b053Test
https://doi.org/10.1002Test/(sici)1097-0215(20000301)85:5<606::aid-ijc2>3.0.co;2-b

10

hMLH1, hMSH2 andhMSH6 mutations in hereditary non-polyposis colorectal cancer families from Southern Sweden

المؤلفون: Maria Planck, Eva Fernebro, Mef Nilbert, Peter Mangell, Eva Wenngren, Ulf Kristoffersson, Anjila Koul, Håkan Olsson, Åke Borg

المصدر: Lund University

مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, DNA Repair, Base Pair Mismatch, DNA Mutational Analysis, Nonsense mutation, Biology, Gene mutation, medicine.disease_cause, Frameshift mutation, Germline mutation, Proto-Oncogene Proteins, medicine, Humans, Genetic Testing, Family history, Frameshift Mutation, Germ-Line Mutation, Adaptor Proteins, Signal Transducing, Sweden, Genetics, Mutation, Endometrial cancer, Nuclear Proteins, Cancer, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, Neoplasm Proteins, DNA-Binding Proteins, MutS Homolog 2 Protein, Oncology, Female, Carrier Proteins, MutL Protein Homolog 1

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0131dc6c8c79a9b871225a4512a15083Test
https://doi.org/10.1002Test/(sici)1097-0215(19991008)83:2<197::aid-ijc9>3.0.co;2-x

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