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Clinical Cancer Research, ISSN 1078-0432, 06/2017, Volume 23, Issue 11, pp. e32 - e37
Replication proofreading is crucial to avoid mutation accumulation in dividing cells. In humans, proofreading and replication repair is maintained by the... 
HEREDITARY | ONCOLOGY | MICROSATELLITE INSTABILITY | GERMLINE MUTATIONS | EARLY-ONSET | FOLLOW-UP | LYNCH SYNDROME | EUROPEAN CONSORTIUM CARE | CANCER | POLE | CHILDREN | Microsatellite Instability | Neoplastic Syndromes, Hereditary - pathology | Colorectal Neoplasms - genetics | Humans | Brain Neoplasms - pathology | Germ-Line Mutation - genetics | MutL Protein Homolog 1 - deficiency | Colorectal Neoplasms - diagnosis | DNA-Binding Proteins - deficiency | Neoplastic Syndromes, Hereditary - epidemiology | MutS Homolog 2 Protein - deficiency | Neoplastic Syndromes, Hereditary - genetics | Child | Mismatch Repair Endonuclease PMS2 - deficiency | Colorectal Neoplasms - epidemiology | Early Detection of Cancer | Brain Neoplasms - diagnosis | Brain Neoplasms - genetics | Neoplastic Syndromes, Hereditary - diagnosis | MutS Homolog 2 Protein - genetics | DNA-Binding Proteins - genetics | MutL Protein Homolog 1 - genetics | Colorectal Neoplasms - pathology | Mismatch Repair Endonuclease PMS2 - genetics | Brain Neoplasms - epidemiology | Yeast | MLH1 protein | Therapeutic applications | Genes | Organs | MSH2 protein | Disorders | Health risks | MSH6 protein | Exonuclease | Surveillance | Proofreading | Mismatch repair | Replication | Diagnostic systems | Mutation | Children | Genetic recombination | Repair | DNA-directed DNA polymerase | Deoxyribonucleic acid--DNA | Cancer
Journal Article
Gynecologic Oncology, ISSN 0090-8258, 2013, Volume 130, Issue 1, pp. 121 - 126
Abstract Objectives Lynch syndrome (LS) is a hereditary condition that increases the risk for endometrial and other cancers. Recognizing women at risk for LS... 
Hematology, Oncology and Palliative Medicine | Obstetrics and Gynecology | Immunohistochemistry | Genetic counseling | Microsatellite instability | Genetic testing | Endometrial cancer | Lynch syndrome | WOMEN | ONCOLOGY | NONPOLYPOSIS COLORECTAL-CANCER | CARCINOMA | OBSTETRICS & GYNECOLOGY | MutL Protein Homolog 1 | MutS Homolog 2 Protein - biosynthesis | Early Detection of Cancer - methods | Colorectal Neoplasms, Hereditary Nonpolyposis - pathology | Humans | Middle Aged | DNA Repair Enzymes - genetics | Genetic Counseling | DNA-Binding Proteins - deficiency | Endometrial Neoplasms - genetics | Nuclear Proteins - biosynthesis | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | Adenosine Triphosphatases - biosynthesis | MutS Homolog 2 Protein - deficiency | Nuclear Proteins - deficiency | Female | Mismatch Repair Endonuclease PMS2 | Nuclear Proteins - genetics | DNA Repair Enzymes - deficiency | Microsatellite Repeats | Adenosine Triphosphatases - deficiency | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | MutS Homolog 2 Protein - genetics | Academic Medical Centers | DNA-Binding Proteins - genetics | Endometrial Neoplasms - diagnosis | Adaptor Proteins, Signal Transducing - deficiency | DNA Repair Enzymes - biosynthesis | Adaptor Proteins, Signal Transducing - genetics | Endometrial Neoplasms - pathology | Adaptor Proteins, Signal Transducing - biosynthesis | Adenosine Triphosphatases - genetics | DNA-Binding Proteins - biosynthesis | Diagnosis | Medical centers | Cancer
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 11/2014, Volume 38, Issue 11, pp. 1501 - 1509
Lynch syndrome (LS) is an autosomal dominant inherited disorder caused by germline mutations in DNA mismatch repair (MMR) genes. Mutation carriers are at... 
Microsatellite instability | Endometrial adenocarcinoma | Lynch syndrome | Mismatch-repair deficiency | SURGERY | mismatch-repair deficiency | microsatellite instability | NONPOLYPOSIS COLORECTAL-CANCER | REPAIR PROTEIN IMMUNOHISTOCHEMISTRY | RISK | GENE MUTATION | endometrial adenocarcinoma | PATHOLOGY | CLINICAL-CRITERIA | ACADEMIC-MEDICAL-CENTER | TUMOR MORPHOLOGY | GERMLINE MUTATIONS | GYNECOLOGIC CANCERS | Immunohistochemistry | MutL Protein Homolog 1 | Predictive Value of Tests | Microsatellite Instability | Biomarkers, Tumor - deficiency | Colorectal Neoplasms, Hereditary Nonpolyposis - pathology | Humans | Middle Aged | DNA Mismatch Repair - genetics | Mass Screening - methods | DNA-Binding Proteins - deficiency | Neoplasm Grading | Endometrial Neoplasms - genetics | DNA Mutational Analysis | MutS Homolog 2 Protein - deficiency | Nuclear Proteins - deficiency | Aged, 80 and over | Adult | Female | Mismatch Repair Endonuclease PMS2 | DNA Repair Enzymes - deficiency | Adenosine Triphosphatases - deficiency | Endometrial Neoplasms - chemistry | Risk Assessment | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Risk Factors | California | Biopsy | Adaptor Proteins, Signal Transducing - deficiency | Endometrial Neoplasms - pathology | Aged | Biomarkers, Tumor - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - chemistry
Journal Article
Gynecologic Oncology, ISSN 0090-8258, 2013, Volume 131, Issue 2, pp. 309 - 314
Abstract Objective To assess the prevalence of MMR deficiency (dMMR) in contemporary reclassified high-grade endometrial carcinomas and correlate dMMR with... 
Hematology, Oncology and Palliative Medicine | Obstetrics and Gynecology | High grade endometrioid carcinoma | Mismatch repair deficiency | Microsatellite instability | Outcome | ADENOCARCINOMA | PTEN | LYNCH SYNDROME | ADJUVANT THERAPY | OBSTETRICS & GYNECOLOGY | COLON-CANCER | DNA MISMATCH REPAIR | ONCOLOGY | COLORECTAL-CANCER | CLINICAL-TRIALS | MUTATIONS | MutL Protein Homolog 1 | MutS Homolog 2 Protein - biosynthesis | Tissue Array Analysis | Humans | Middle Aged | Cystadenocarcinoma, Serous - metabolism | DNA Repair Enzymes - genetics | Endometrial Neoplasms - metabolism | Cystadenocarcinoma, Serous - genetics | DNA-Binding Proteins - deficiency | Carcinoma, Endometrioid - metabolism | Neoplasm Grading | Endometrial Neoplasms - genetics | Nuclear Proteins - biosynthesis | Adenosine Triphosphatases - biosynthesis | DNA Mismatch Repair | MutS Homolog 2 Protein - deficiency | Nuclear Proteins - deficiency | Aged, 80 and over | Adult | Female | Mismatch Repair Endonuclease PMS2 | Nuclear Proteins - genetics | DNA Repair Enzymes - deficiency | Adenosine Triphosphatases - deficiency | Carcinoma, Endometrioid - genetics | Adenocarcinoma, Clear Cell - metabolism | MutS Homolog 2 Protein - genetics | DNA-Binding Proteins - genetics | Adaptor Proteins, Signal Transducing - deficiency | DNA Repair Enzymes - biosynthesis | Adaptor Proteins, Signal Transducing - genetics | Adaptor Proteins, Signal Transducing - biosynthesis | Adenosine Triphosphatases - genetics | Aged | Adenocarcinoma, Clear Cell - genetics | DNA-Binding Proteins - biosynthesis | Cancer
Journal Article
PLOS GENETICS, ISSN 1553-7390, 05/2009, Volume 5, Issue 5, p. e1000482
Journal Article
Journal Article
by Felton and Gilchrist and Andrew
Clinical Genetics, ISSN 0009-9163, 06/2007, Volume 71, Issue 6, pp. 483 - 498
Felton KEA, Gilchrist DM, Andrew SE. Constitutive deficiency in DNA mismatch repair.Clin Genet 2007: 71: 483-498. © Blackwell Munksgaard, 2007 Mutations in the... 
neurofibromatosis type 1 | microsatellite instability | hereditary non-polyposis colorectal cancer | DNA mismatch repair | Lynch syndrome | hereditary non‐polyposis colorectal cancer | Neurofibromatosis type 1 | Microsatellite instability | Hereditary non-polyposis colorectal cancer | HEMATOLOGICAL MALIGNANCY | NONPOLYPOSIS COLORECTAL-CANCER | COLON-CANCER | TURCOT-SYNDROME | GENETICS & HEREDITY | GERMLINE MUTATIONS | EARLY-ONSET | MSH6 MUTATIONS | HETEROZYGOUS MUTATIONS | NEUROFIBROMATOSIS TYPE-1 | Colorectal Neoplasms, Hereditary Nonpolyposis - classification | Adenosine Triphosphatases - deficiency | MutL Protein Homolog 1 | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - pathology | Humans | DNA Repair Enzymes - genetics | MutS Homolog 2 Protein - genetics | DNA-Binding Proteins - genetics | DNA-Binding Proteins - deficiency | Adaptor Proteins, Signal Transducing - deficiency | DNA Mismatch Repair | MutS Homolog 2 Protein - deficiency | Nuclear Proteins - deficiency | Adaptor Proteins, Signal Transducing - genetics | Adenosine Triphosphatases - genetics | Mismatch Repair Endonuclease PMS2 | Mutation | Nuclear Proteins - genetics | DNA Repair Enzymes - deficiency | Proteins | Genotype & phenotype | Colorectal cancer | Genetics | Heredity | DNA repair
Journal Article
International Journal of Cancer, ISSN 0020-7136, 10/2017, Volume 141, Issue 7, pp. 1365 - 1380
Journal Article
14.