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Gene, ISSN 0378-1119, 05/2016, Volume 582, Issue 1, pp. 23 - 32
Cowden syndrome | Odontogenic keratocystic tumors | Gardner syndrome | Peutz–Jeghers syndrome | Gorlin syndrome | Multiple endocrine neoplasia | Lynch/Muir–Torre syndrome | Ameloblastoma | Familial Adenomatous Polyposis (FAP) | Fordyce granules | Lynch/Muir-Torre syndrome | Peutz-Jeghers syndrome | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Peutz-Jeghers Syndrome - pathology | Humans | Peutz-Jeghers Syndrome - therapy | Muir-Torre Syndrome - therapy | Muir-Torre Syndrome - pathology | Multiple Endocrine Neoplasia - genetics | Germ-Line Mutation - genetics | Molecular Targeted Therapy | Adenomatous Polyposis Coli - pathology | Adenomatous Polyposis Coli - complications | Adenomatous Polyposis Coli - therapy | Adenomatous Polyposis Coli - genetics | Mouth Mucosa - pathology | Gardner Syndrome - pathology | Genes, Tumor Suppressor | Gardner Syndrome - therapy | Gardner Syndrome - complications | Peutz-Jeghers Syndrome - complications | Peutz-Jeghers Syndrome - genetics | Multiple Endocrine Neoplasia - complications | Mouth Mucosa - metabolism | Muir-Torre Syndrome - genetics | Phenotype | Muir-Torre Syndrome - complications | Gardner Syndrome - genetics | Multiple Endocrine Neoplasia - therapy | Heterozygote | Multiple Endocrine Neoplasia - pathology | Genetic aspects | Gene mutations | Cancer | Index Medicus
Journal Article
The American journal of surgical pathology, ISSN 0147-5185, 09/2014, Volume 38, Issue 9, pp. 1173 - 1181
ovarian cancer | mismatch repair | Lynch syndrome | Pathology | Life Sciences & Biomedicine | Surgery | Science & Technology | Colorectal Neoplasms, Hereditary Nonpolyposis - classification | Immunohistochemistry | Predictive Value of Tests | Microsatellite Instability | Carcinoma, Endometrioid - classification | Genetic Testing | Early Detection of Cancer - methods | Colorectal Neoplasms, Hereditary Nonpolyposis - pathology | Humans | Middle Aged | Ovarian Neoplasms - pathology | Ovarian Neoplasms - genetics | Ovarian Neoplasms - classification | Carcinoma, Endometrioid - chemistry | Neoplasm Grading | DNA Mutational Analysis | DNA Mismatch Repair | Germ-Line Mutation | Adult | Female | Registries | Carcinoma, Endometrioid - genetics | Genetic Predisposition to Disease | Ovarian Neoplasms - chemistry | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Heredity | BRCA1 Protein - genetics | Canada | Phenotype | Lymphocytes, Tumor-Infiltrating - pathology | Biopsy | Pedigree | Aged | Colorectal Neoplasms, Hereditary Nonpolyposis - chemistry | BRCA2 Protein - genetics | Carcinoma, Endometrioid - pathology | Index Medicus
Journal Article
World journal of gastroenterology : WJG, ISSN 1007-9327, 2015, Volume 21, Issue 31, pp. 9253 - 9261
cancer;Lynch | Hereditary | non-polyposis | colorectal | Hereditary non-polyposis colorectal cancer | Familial colorectal cancer | Lynch-like syndrome | Constitutional mismatch repair deficiency syndrome | Hereditary colorectal cancer | Microsatellite instability | DNA mismatch repair | Familial colorectal cancer type X | Lynch syndrome | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Predictive Value of Tests | Diagnosis, Differential | Genetic Predisposition to Disease | Microsatellite Instability | Colorectal Neoplasms - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Humans | Brain Neoplasms - genetics | Heredity | Phenotype | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | DNA Mutational Analysis | Pedigree | DNA Mismatch Repair | Biomarkers, Tumor - genetics | Neoplastic Syndromes, Hereditary - genetics | Mutation | Index Medicus | Topic Highlight
Journal Article
American journal of obstetrics and gynecology, ISSN 0002-9378, 2017, Volume 217, Issue 5, pp. 512 - 521
Obstetrics and Gynecology | BRCA | risk reduction | screening | ovarian cancer | high risk | endometrial cancer | hereditary cancer | cervical cancer | Lynch syndrome | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Genetic Testing | DNA Polymerase III - genetics | Hereditary Breast and Ovarian Cancer Syndrome - diagnosis | Humans | Li-Fraumeni Syndrome - diagnosis | DNA Mismatch Repair - genetics | Tumor Suppressor Protein p53 - genetics | Genital Neoplasms, Female - diagnosis | Li-Fraumeni Syndrome - genetics | Epithelial Cell Adhesion Molecule - genetics | Genes, BRCA2 | Female | RNA Helicases - genetics | Lynch Syndrome II - genetics | Neoplastic Syndromes, Hereditary - genetics | Genes, BRCA1 | Genital Neoplasms, Female - genetics | Hereditary Breast and Ovarian Cancer Syndrome - genetics | PTEN Phosphohydrolase - genetics | Genetic Predisposition to Disease | Hamartoma Syndrome, Multiple - genetics | Fanconi Anemia Complementation Group Proteins - genetics | Protein-Serine-Threonine Kinases - genetics | Neoplastic Syndromes, Hereditary - diagnosis | MutS Homolog 2 Protein - genetics | DNA-Binding Proteins - genetics | Peutz-Jeghers Syndrome - genetics | Hamartoma Syndrome, Multiple - diagnosis | MutL Protein Homolog 1 - genetics | Peutz-Jeghers Syndrome - diagnosis | Lynch Syndrome II - diagnosis | Mismatch Repair Endonuclease PMS2 - genetics | Gene mutations | Endometrial cancer | Diagnosis | Cervical cancer | Genetic screening | Cancer | Ovarian cancer | Index Medicus | Abridged Index Medicus
Journal Article
The Journal of pathology, ISSN 0022-3417, 04/2020, Volume 250, Issue 5, pp. 518 - 531
colorectal cancer | gene database | immunotherapy | endometrial cancer | apoptosis | DNA mismatch repair | Lynch syndrome | gene variant interpretation | immunoediting | Pathology | Oncology | Life Sciences & Biomedicine | Science & Technology | Colon cancer | Endometrial cancer | Oncology, Experimental | Immunotherapy | Development and progression | Research | Cancer | MLH1 protein | Prophylaxis | MSH2 protein | DNA repair | MSH6 protein | Databases | Immune checkpoint | Mismatch repair | Endometrium | Apoptosis | Tumors | Immune system | Index Medicus
Journal Article
Familial cancer, ISSN 1389-9600, 7/2016, Volume 15, Issue 3, pp. 385 - 393
Human Genetics | Biomedicine | Epimutation | Cancer Research | Tumor spectrum | Mutation | Epidemiology | Biomedicine general | DNA mismatch repair | Lynch syndrome | Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease | Microsatellite Instability | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Genomics | Humans | DNA Repair Enzymes - genetics | MutS Homolog 2 Protein - genetics | DNA Mismatch Repair - genetics | DNA-Binding Proteins - genetics | DNA Methylation | Phenotype | MutL Protein Homolog 1 - genetics | Germ-Line Mutation | Mismatch Repair Endonuclease PMS2 - genetics | Proteins | Gene mutations | Colorectal cancer | Index Medicus | Original
Journal Article
Familial cancer, ISSN 1389-9600, 6/2013, Volume 12, Issue 2, pp. 229 - 240