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CANADIAN MEDICAL ASSOCIATION JOURNAL, ISSN 0820-3946, 03/2016, Volume 188, Issue 5, pp. E95 - E95
  Muir-Torre syndrome is an autosomal dominant cancer syndrome expressed clinically as cutaneous tumours (sebaceous neoplasms or multiple keratoacanthomas) and... 
MEDICINE, GENERAL & INTERNAL | Sebaceous Gland Neoplasms - pathology | Humans | Middle Aged | Adenoma - pathology | Muir-Torre Syndrome - pathology | Female | Facial Neoplasms - pathology | Muir-Torre syndrome | Diagnosis | Research | Genetic testing | Biopsy | Genes | Cancer | Index Medicus | Abridged Index Medicus | Practice
Journal Article
Annales de Dermatologie et de Venereologie, ISSN 0151-9638, 08/2017, Volume 144, Issue 8-9, pp. 525 - 529
Introduction Lynch syndrome (LS) is a syndrome that carries a genetic predisposition to certain cancers associating, either in a single individual or in a... 
Muir-Torre syndrome | Turcot syndrome | Sebaceous gland neoplasms | DNA mismatch repair genes | Microsatellite instability
Journal Article
AMERICAN JOURNAL OF GASTROENTEROLOGY, ISSN 0002-9270, 08/2014, Volume 109, Issue 8, pp. 1159 - 1179
The Multi-Society Task Force, in collaboration with invited experts, developed guidelines to assist health care providers with the appropriate provision of... 
COST-EFFECTIVENESS ANALYSIS | NONPOLYPOSIS COLON-CANCER | MUIR-TORRE-SYNDROME | TESTING STRATEGIES | TUMOR MICROSATELLITE INSTABILITY | MISMATCH-REPAIR GENES | GERMLINE MUTATIONS | REVISED BETHESDA GUIDELINES | GASTROENTEROLOGY & HEPATOLOGY | MSH2 MUTATION CARRIERS | ENDOMETRIAL CANCER
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 2015, Volume 74, Issue 3, pp. 437 - 451
Nonmelanoma skin cancers (NMSCs) represent the most common malignancies worldwide, with reported incidence rising each year. Both cutaneous squamous cell... 
Dermatology | Rothmund–Thomson syndrome | Bloom syndrome | dyskeratosis congenita | Gorlin syndrome | genetic testing | nonmelanoma skin cancer | Muir–Torre syndrome | oculocutaneous albinism | Werner syndrome
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 4/2000, Volume 97, Issue 9, pp. 4742 - 4747
To investigate the role of the Fhit gene in carcinogen induction of neoplasia, we have inactivated one Fhit allele in mouse embryonic stem cells and produced... 
Biological Sciences | Carcinogens | Forestomach | Exons | DNA | Alleles | Genetic loci | Papilloma | Mice | Tumors | Cancer | Carcinogen-induced tumorigenesis | N-nitrosomethyibenzylamine | Esophageal | Gastric cancer | Fhit knockout mice | Tumor suppressor gene | NONPOLYPOSIS COLORECTAL-CANCER | MULTIDISCIPLINARY SCIENCES | CELL-PROLIFERATION | TUMOR-CELLS | ESOPHAGEAL | N-nitrosomethylbenzylamine | carcinogen-induced tumorigenesis | LUNG-CANCER | ZINC-DEFICIENCY | GENE | CARCINOMAS | esophageal/gastric cancer | EXPRESSION | tumor suppressor gene | Adenoma - genetics | Humans | Male | Stomach Neoplasms - pathology | Restriction Mapping | Female | Neoplasm Proteins - genetics | Stomach Neoplasms - genetics | Papilloma - genetics | Neoplasms, Multiple Primary - genetics | Mice, Inbred C57BL | Sebaceous Gland Neoplasms - genetics | Mice, Inbred Strains | Neoplasms, Multiple Primary - pathology | Neoplasms, Multiple Primary - chemically induced | Syndrome | Mice, Knockout | Proteins - genetics | Animals | Proteins - metabolism | Acid Anhydride Hydrolases | Dimethylnitrosamine - analogs & derivatives | Stomach Neoplasms - chemically induced | Neoplasm Proteins - deficiency | Care and treatment | Proteins | Rodents | Genes | Muir-Torre syndrome | nitrosomethylbenzylamine | Fhit gene | Fhit protein | Index Medicus | esophageal | gastric cancer
Journal Article
British Journal of Dermatology, ISSN 0007-0963, 08/2018, Volume 179, Issue 2, pp. 522 - 523
Journal Article
Japanese Journal of Gastroenterological Surgery, ISSN 0386-9768, 2016, Volume 49, Issue 4, pp. 342 - 349
Journal Article
Clinical and Experimental Dermatology, ISSN 0307-6938, 07/2019, Volume 44, Issue 5, pp. 506 - 511
Sebaceous neoplasms (SN) may appear sporadically in the general population but may also be part of the Muir-Torre variant of Lynch syndrome (MT-LS). There are... 
DIAGNOSIS | NEOPLASMS | MUIR-TORRE-SYNDROME | FREQUENCY | DERMATOLOGY | Medicine, Experimental | Medical research | Gene mutations | Analysis | Tumors | Carcinoma
Journal Article
International Journal of Gynecological Pathology, ISSN 0277-1691, 12/2018, p. 1
Muir-Torre syndrome is a rare subtype of Lynch syndrome characterized by coincidence of skin neoplasm and visceral malignancies. Here, we report a case of this... 
Muir-Torre syndrome | Multidisciplinary teamwork | MSH2 | Lynch syndrome
Journal Article
Molecular and clinical oncology, ISSN 2049-9450, 02/2018, Volume 8, Issue 2, p. 306
Muir-Torre Syndrome (MTS) is a rare hereditary autosomal dominant cancer syndrome and is linked to hereditary non-polyposis colorectal carcinoma (Lynch... 
Journal Article
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