BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Thyroid cancer AND MSH6, GTBP, P52701, 2956, ENSG00000116062, HSAP, HNPCC5
20 results:

  • 1. [Pan-cancer analysis of ubiquitin-specific protease 7 and its expression changes in the carcinogenesis of scar ulcer].
    Zhang SY; Ruan JJ; Jin DM; Chen N; Xie WG; Ruan QF
    Zhonghua Shao Shang Yu Chuang Mian Xiu Fu Za Zhi; 2023 Jun; 39(6):518-526. PubMed ID: 37805766
    [No Abstract]    [Full Text] [Related]  

  • 2. Clinical Characteristics and Responses to Immune Checkpoint Inhibitors in RET-Aberrant Digestive Tract Tumours.
    Yen CC; Yeh YM; Huang HY; Ting YL; Fu PA; Lin TC; Liu IT; Yen CJ
    Target Oncol; 2023 Jul; 18(4):611-623. PubMed ID: 37347391
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. Cathepsin F genetic mutation is associated with familial papillary thyroid cancer.
    Wang Y; Mei J; Zhang Y; He X; Zheng X; Tan J; Jia Q; Li N; Li D; Wang Y; Meng Z
    Am J Med Sci; 2022 Oct; 364(4):414-424. PubMed ID: 35447134
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. Correlation of mismatch repair deficiency with clinicopathological features and programmed death-ligand 1 expression in thyroid carcinoma.
    Qiao PP; Tian KS; Han LT; Ma B; Shen CK; Zhao RY; Zhang Y; Wei WJ; Chen XP
    Endocrine; 2022 Jun; 76(3):660-670. PubMed ID: 35366156
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. New Perspectives on the Recurrent Monoallelic Germline Mutations of DNA Repair and Checkpoint Genes and Clinical Variability.
    Sahin I; Saat H
    Genet Test Mol Biomarkers; 2022 Jan; 26(1):17-25. PubMed ID: 35089076
    [No Abstract]    [Full Text] [Related]  

  • 6. Co-Occurrence of Familial Non-Medullary thyroid cancer (FNMTC) and Hereditary Non-Polyposis Colorectal cancer (HNPCC) Associated Tumors-A Cohort Study.
    Aswath K; Welch J; Gubbi S; Veeraraghavan P; Avadhanula S; Gara SK; Dikoglu E; Merino M; Raffeld M; Xi L; Kebebew E; Klubo-Gwiezdzinska J
    Front Endocrinol (Lausanne); 2021; 12():653401. PubMed ID: 34326811
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. Somatic Mutation Profiling of Papillary thyroid Carcinomas by Whole-exome Sequencing and Its Relationship with Clinical Characteristics.
    Qi T; Rong X; Feng Q; Sun H; Cao H; Yang Y; Feng H; Zhu L; Wang L; Du Q
    Int J Med Sci; 2021; 18(12):2532-2544. PubMed ID: 34104084
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. Alteration of DNA mismatch repair capacity underlying the co-occurrence of non-small-cell lung cancer and nonmedullary thyroid cancer.
    Fujita S; Masago K
    Sci Rep; 2021 Feb; 11(1):3597. PubMed ID: 33574476
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. msh6/2 and PD-L1 Expressions Are Associated with Tumor Growth and Invasiveness in Silent Pituitary Adenoma Subtypes.
    Uraki S; Ariyasu H; Doi A; Takeshima K; Morita S; Inaba H; Furuta H; Fukuhara N; Inoshita N; Nishioka H; Nakao N; Yamada S; Akamizu T
    Int J Mol Sci; 2020 Apr; 21(8):. PubMed ID: 32325698
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. Comprehensive Immune Profiling of Medullary thyroid cancer.
    Pozdeyev N; Erickson TA; Zhang L; Ellison K; Rivard CJ; Sams S; Hirsch FR; Haugen BR; French JD
    Thyroid; 2020 Sep; 30(9):1263-1279. PubMed ID: 32242507
    [No Abstract]    [Full Text] [Related]  

  • 11. thyroid cancer: The Quest for Genetic Susceptibility Involving DNA Repair Genes.
    Santos LS; Gomes BC; Bastos HN; Gil OM; Azevedo AP; Ferreira TC; Limbert E; Silva SN; Rueff J
    Genes (Basel); 2019 Aug; 10(8):. PubMed ID: 31374908
    [TBL] [Abstract] [Full Text] [Related]  

  • 12. Clinicopathologic Features of Mismatch Repair-Deficient Anaplastic thyroid Carcinomas.
    Wong KS; Lorch JH; Alexander EK; Nehs MA; Nowak JA; Hornick JL; Barletta JA
    Thyroid; 2019 May; 29(5):666-673. PubMed ID: 30869569
    [No Abstract]    [Full Text] [Related]  

  • 13. Germline TP53 and msh6 mutations implicated in sporadic triple-negative breast cancer (TNBC): a preliminary study.
    Yi D; Xu L; Luo J; You X; Huang T; Zi Y; Li X; Wang R; Zhong Z; Tang X; Li A; Shi Y; Rao J; Zhang Y; Sang J
    Hum Genomics; 2019 Jan; 13(1):4. PubMed ID: 30630526
    [TBL] [Abstract] [Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract] [Full Text] [Related]  

  • 15. Risk of colorectal polyps and of malignancies in asymptomatic carriers of mutations in the main DNA mismatch repair genes.
    Ponz de Leon M; Pedroni M; Pezzi A; Sulce B; Roncucci L; Domati F; Rossi G; Reggiani Bonetti L
    Scand J Gastroenterol; 2018 Jan; 53(1):31-37. PubMed ID: 29025352
    [TBL] [Abstract] [Full Text] [Related]  

  • 16. Primary multiple tumor with affection of the thyroid gland, uterus, urinary bladder, mammary gland and other organs.
    Romaniuk А; Lyndin M; Smiyanov V; Sikora V; Rieznik A; Kuzenko Y; Budko H; Moskalenko Y; Karpenko L; Sikora V; Gladchenko O
    Pathol Res Pract; 2017 May; 213(5):574-579. PubMed ID: 28214212
    [TBL] [Abstract] [Full Text] [Related]  

  • 17. Targeted DNA Sequencing Detects Mutations Related to Susceptibility among Familial Non-medullary thyroid cancer.
    Yu Y; Dong L; Li D; Chuai S; Wu Z; Zheng X; Cheng Y; Han L; Yu J; Gao M
    Sci Rep; 2015 Nov; 5():16129. PubMed ID: 26530882
    [TBL] [Abstract] [Full Text] [Related]  

  • 18. Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing.
    Kunstman JW; Juhlin CC; Goh G; Brown TC; Stenman A; Healy JM; Rubinstein JC; Choi M; Kiss N; Nelson-Williams C; Mane S; Rimm DL; Prasad ML; Höög A; Zedenius J; Larsson C; Korah R; Lifton RP; Carling T
    Hum Mol Genet; 2015 Apr; 24(8):2318-29. PubMed ID: 25576899
    [TBL] [Abstract] [Full Text] [Related]  

  • 19. cancer spectrum in DNA mismatch repair gene mutation carriers: results from a hospital based Lynch syndrome registry.
    Pande M; Wei C; Chen J; Amos CI; Lynch PM; Lu KH; Lucio LA; Boyd-Rogers SG; Bannon SA; Mork ME; Frazier ML
    Fam Cancer; 2012 Sep; 11(3):441-7. PubMed ID: 22714864
    [TBL] [Abstract] [Full Text] [Related]  

  • 20. Infrequent frameshift mutations of polynucleotide repeats in multiple primary cancers affecting the esophagus and other organs.
    Iwaya T; Maesawa C; Nishizuka S; Suzuki Y; Sakata K; Sato N; Ikeda K; Koeda K; Ogasawara S; Otsuka K; Kimura Y; Aoki K; Ishida K; Saito K; Tamura G
    Genes Chromosomes Cancer; 1998 Dec; 23(4):317-22. PubMed ID: 9824204
    [TBL] [Abstract] [Full Text] [Related]  


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