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American Journal of Gastroenterology, ISSN 0002-9270, 02/2015, Volume 110, Issue 2, pp. 223 - 262
Journal Article
Gene, ISSN 0378-1119, 05/2016, Volume 582, Issue 1, pp. 23 - 32
Numerous familial tumor syndromes are associated with distinctive oral mucosal findings, which may make possible an early diagnosis as an efficacious marker... 
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 | LYNCH-SYNDROME | NONPOLYPOSIS COLORECTAL-CANCER | PEUTZ-JEGHERS-SYNDROME | COWDEN-DISEASE | Peutz-jeghers syndrome | GARDNERS-SYNDROME | MUIR-TORRE-SYNDROME | BASAL-CELL CARCINOMA | GENETICS & HEREDITY | MUCOCUTANEOUS PIGMENTATION | FAMILIAL ADENOMATOUS POLYPOSIS | 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
Journal Article
Gut, ISSN 0017-5749, 07/2010, Volume 59, Issue 7, pp. 975 - 986
Journal Article
Clinical Gastroenterology and Hepatology, ISSN 1542-3565, 2006, Volume 4, Issue 4, pp. 408 - 415
Journal Article
Annual Review of Biochemistry, ISSN 0066-4154, 2006, Volume 75, Issue 1, pp. 137 - 163
This review focuses on remarkable recent findings concerning the mechanism by which the LKB1 protein kinase that is mutated in Peutz-Jeghers cancer syndrome... 
Cell growth | mTOR | Tuberous sclerosis | AMPK | Polarity | Tumor suppressor | Peutz-Jeghers syndrome | Cancer | MOLECULAR CHARACTERIZATION | ACTIVATED PROTEIN-KINASE | SERINE-THREONINE KINASE | PEUTZ-JEGHERS-SYNDROME | CYTOPLASMIC LOCALIZATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | cell growth | tumor suppressor | tuberous sclerosis | TUBEROUS SCLEROSIS COMPLEX | SALT-INDUCIBLE KINASE | C-ELEGANS EMBRYOS | cancer | CANCER SYNDROME | polarity | LKB1 TUMOR-SUPPRESSOR | Cell Polarity | Humans | Peutz-Jeghers Syndrome - therapy | Protein-Serine-Threonine Kinases - classification | Adaptor Proteins, Vesicular Transport - genetics | Molecular Sequence Data | Multienzyme Complexes - metabolism | Phylogeny | Adaptor Proteins, Vesicular Transport - metabolism | AMP-Activated Protein Kinases | Isoenzymes - classification | Isoenzymes - metabolism | Genes, Tumor Suppressor | Protein-Serine-Threonine Kinases - metabolism | Amino Acid Sequence | Multienzyme Complexes - classification | Isoenzymes - genetics | Protein-Serine-Threonine Kinases - genetics | Multienzyme Complexes - genetics | Peutz-Jeghers Syndrome - genetics | Sequence Alignment | Animals | Peutz-Jeghers Syndrome - metabolism | Signal Transduction - physiology | Protein Processing, Post-Translational | Enzyme Activation | Mutation | Care and treatment | Physiological aspects | Genetic aspects | Research | Protein kinases
Journal Article
Breast Cancer Research and Treatment, ISSN 0167-6806, 12/2016, Volume 160, Issue 3, pp. 393 - 410
Genetic evaluation is increasingly becoming an integral part of the management of women with newly diagnosed breast and ovarian cancer (OC), and of individuals... 
BRCA | Breast and ovarian cancer | Medicine & Public Health | Surveillance | Multiple-gene panel testing | Oncology | Cancer genetic counseling | Genetic counselors | LYNCH-SYNDROME | PEUTZ-JEGHERS-SYNDROME | REVISED BETHESDA GUIDELINES | CLINICAL CHARACTERISTICS | HEREDITARY COLORECTAL-CANCER | ONCOLOGY | INCREASED RISK | SOCIETY TASK-FORCE | ATM GENE | DIFFUSE GASTRIC-CANCER | BRCA2 MUTATION | Breast Neoplasms, Male - genetics | Hereditary Breast and Ovarian Cancer Syndrome - diagnosis | Humans | Male | Biomarkers, Tumor | Genetic Testing - methods | Breast Neoplasms - therapy | Ovarian Neoplasms - genetics | Hereditary Breast and Ovarian Cancer Syndrome - therapy | Genes, BRCA2 | Germ-Line Mutation | Female | Genes, BRCA1 | Stomach Neoplasms - genetics | Breast Neoplasms, Male - diagnosis | Hereditary Breast and Ovarian Cancer Syndrome - genetics | Genetic Predisposition to Disease | Stomach Neoplasms - diagnosis | Ovarian Neoplasms - prevention & control | Fanconi Anemia Complementation Group N Protein - genetics | Ovarian Neoplasms - diagnosis | Stomach Neoplasms - therapy | Penetrance | Breast Neoplasms - prevention & control | Breast Neoplasms - genetics | Breast Neoplasms, Male - therapy | Stomach Neoplasms - prevention & control | Ovarian Neoplasms - therapy | Breast Neoplasms - diagnosis | Disease Management | Mutation | Medical research | Care and treatment | Breast cancer | Disease susceptibility | Patients | Genetic screening | Ovarian cancer | Cancer patients | Risk assessment | Medicine, Experimental | Genetic aspects | Tumor proteins | Cancer
Journal Article
Surgery Today, ISSN 0941-1291, 10/2016, Volume 46, Issue 10, pp. 1115 - 1122
Journal Article