Terms: = Gastric cancer AND MSH6, GTBP, P52701, 2956, ENSG00000116062, HSAP, HNPCC5 AND Diagnosis
41 results:
1. Germline pathogenic variants in patients with early-onset neuroendocrine neoplasms.
Riechelmann RP; Donadio MDS; Jesus VHF; de Carvalho NA; Santiago KM; Barros MJ; Lopes L; Oliveira Dos Santos G; Nirvana Formiga M; Carraro DM; Torrezan GT
Endocr Relat Cancer; 2023 Jun; 30(6):. PubMed ID: 36947458
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2. [Microsatellite instability in gastric cancer is a predictor of a favorable prognosis].
Danilova NV; Chayka AV; Khomyakov VM; Oleynikova NA; Andreeva YY; Malkov PG
Arkh Patol; 2022; 84(6):5-15. PubMed ID: 36469712
[TBL] [Abstract] [Full Text] [Related]
3. Association of Pathogenic Variants in Hereditary cancer Genes With Multiple Diseases.
Zeng C; Bastarache LA; Tao R; Venner E; Hebbring S; Andujar JD; Bland ST; Crosslin DR; Pratap S; Cooley A; Pacheco JA; Christensen KD; Perez E; Zawatsky CLB; Witkowski L; Zouk H; Weng C; Leppig KA; Sleiman PMA; Hakonarson H; Williams MS; Luo Y; Jarvik GP; Green RC; Chung WK; Gharavi AG; Lennon NJ; Rehm HL; Gibbs RA; Peterson JF; Roden DM; Wiesner GL; Denny JC
JAMA Oncol; 2022 Jun; 8(6):835-844. PubMed ID: 35446370
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4. Early age of onset and broad cancer spectrum persist in msh6- and PMS2-associated Lynch syndrome.
Liu YL; Cadoo KA; Maio A; Patel Z; Kemel Y; Salo-Mullen E; Catchings A; Ranganathan M; Kane S; Soslow R; Ceyhan-Birsoy O; Mandelker D; Carlo MI; Walsh MF; Shia J; Markowitz AJ; Offit K; Stadler ZK; Latham A
Genet Med; 2022 Jun; 24(6):1187-1195. PubMed ID: 35346574
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5. Double heterozygotes of BRCA1/BRCA2 and mismatch repair gene pathogenic variants: case series and clinical implications.
Laish I; Friedman E; Levi-Reznick G; Kedar I; Katz L; Levi Z; Halpern N; Parnasa S; Abu-Shatya A; Half E; Goldberg Y
Breast Cancer Res Treat; 2021 Aug; 188(3):685-694. PubMed ID: 34086170
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6. Comprehensive analysis of germline mutations in northern Brazil: a panel of 16 genes for hereditary cancer-predisposing syndrome investigation.
Vidal AF; Ferraz RS; El-Husny A; Silva CS; Vinasco-Sandoval T; Magalhães L; Raiol-Moraes M; Barra WF; Pereira CLBL; de Assumpção PP; de Brito LM; Vialle RA; Santos S; Ribeiro-Dos-Santos Â; Ribeiro-Dos-Santos AM
BMC Cancer; 2021 Apr; 21(1):363. PubMed ID: 33827469
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7. Lynch syndrome-associated repeated stroke with MLH1 frame-shift mutation.
Zhang M; Yang H; Chen Z; Fan Y; Hu X; Liu W
Neurol Sci; 2021 Apr; 42(4):1631-1635. PubMed ID: 33433757
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8. A case of Turcot's syndrome type 1 with loss of immunoexpression of msh6 in colon cancer and liver metastasis due to secondary somatic mutation in coding mononucleotide (C)8 tract: a case report.
Akabane S; Hinoi T; Akagi K; Yamamoto H; Sada H; Shimizu Y; Shimizu W; Sudo T; Onoe T; Ishiyama K; Suzuki T; Tazawa H; Hadano N; Misumi T; Kojima M; Kubota H; Taniyama D; Kuraoka K; Tashiro H
BMC Med Genet; 2020 Jul; 21(1):141. PubMed ID: 32611331
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9. cancer-risk by family history and mismatch-repair mutation in Lynch syndrome.
Marques-de-Sá I; Castro R; Pita I; Dinis-Ribeiro M; Brandão C
Scand J Gastroenterol; 2020 Jun; 55(6):701-705. PubMed ID: 32448028
[No Abstract] [Full Text] [Related]
10. [Current recommendations for surveillance, risk reduction and therapy in Lynch syndrome patients].
Hüneburg R; Aretz S; Büttner R; Daum S; Engel C; Fechner G; Habermann JK; Heling D; Hoffmann K; Holinski-Feder E; Kloor M; von Knebel-Döberitz M; Loeffler M; Möslein G; Perne C; Redler S; Rieß O; Schmiegel W; Seufferlein T; Siebers-Renelt U; Steinke-Lange V; Tecklenburg J; Vangala D; Vilz T; Weitz J; Wiedenmann B; Strassburg CP; Nattermann J
Z Gastroenterol; 2019 Nov; 57(11):1309-1320. PubMed ID: 31739377
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11. Importance of gastric cancer for the diagnosis and surveillance of Japanese Lynch syndrome patients.
Ikenoue T; Arai M; Ishioka C; Iwama T; Kaneko S; Matsubara N; Moriya Y; Nomizu T; Sugano K; Tamura K; Tomita N; Yoshida T; Sugihara K; Naruse H; Yamaguchi K; Nojima M; Nakamura Y; Furukawa Y;
J Hum Genet; 2019 Dec; 64(12):1187-1194. PubMed ID: 31588121
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12. An Update on Inherited Colon cancer and Gastrointestinal Polyposis.
Plevová P
Klin Onkol; 2019; 32(Supplementum2):97-108. PubMed ID: 31409085
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13. Molecular characterization of gastric-type endocervical adenocarcinoma using next-generation sequencing.
Garg S; Nagaria TS; Clarke B; Freedman O; Khan Z; Schwock J; Bernardini MQ; Oza AM; Han K; Smith AC; Stockley TL; Rouzbahman M
Mod Pathol; 2019 Dec; 32(12):1823-1833. PubMed ID: 31308508
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14. Malignant phyllodes tumor in Lynch syndrome: a case report.
Kazmi S; Wagner S; Heintzelman R; Corbman M
J Med Case Rep; 2019 Jul; 13(1):216. PubMed ID: 31307558
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15. Microsatellite instability in mismatch repair and tumor suppressor genes and their expression profiling provide important targets for the development of biomarkers in gastric cancer.
Verma R; Agarwal AK; Sakhuja P; Sharma PC
Gene; 2019 Aug; 710():48-58. PubMed ID: 31145962
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16. Targeted cancer Next-Generation Sequencing as a Primary Screening Tool for Microsatellite Instability and Lynch Syndrome in Upper Gastrointestinal Tract cancers.
Christakis AG; Papke DJ; Nowak JA; Yurgelun MB; Agoston AT; Lindeman NI; MacConaill LE; Sholl LM; Dong F
Cancer Epidemiol Biomarkers Prev; 2019 Jul; 28(7):1246-1251. PubMed ID: 31028081
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17. A frameshift mutation in exon 19 of MLH1 in a Chinese Lynch syndrome family: a pedigree study.
Sui QQ; Jiang W; Wu XD; Ling YH; Pan ZZ; Ding PR
J Zhejiang Univ Sci B; 2019 Jan.; 20(1):105-108. PubMed ID: 30614234
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18. Massively parallel sequencing analysis of mucinous ovarian carcinomas: genomic profiling and differential diagnoses.
Mueller JJ; Schlappe BA; Kumar R; Olvera N; Dao F; Abu-Rustum N; Aghajanian C; DeLair D; Hussein YR; Soslow RA; Levine DA; Weigelt B
Gynecol Oncol; 2018 Jul; 150(1):127-135. PubMed ID: 29793804
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19. Lynch syndrome-associated endometrial carcinoma with MLH1 germline mutation and MLH1 promoter hypermethylation: a case report and literature review.
Yokoyama T; Takehara K; Sugimoto N; Kaneko K; Fujimoto E; Okazawa-Sakai M; Okame S; Shiroyama Y; Yokoyama T; Teramoto N; Ohsumi S; Saito S; Imai K; Sugano K
BMC Cancer; 2018 May; 18(1):576. PubMed ID: 29783979
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20. Tumor development in Japanese patients with Lynch syndrome.
Saita C; Yamaguchi T; Horiguchi SI; Yamada R; Takao M; Iijima T; Wakaume R; Aruga T; Tabata T; Koizumi K
PLoS One; 2018; 13(4):e0195572. PubMed ID: 29672549
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