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Journal Abstract Search

205 related items for PubMed ID: 27798940

  • 1. Rare RET Variant p.D707E in a Chinese Pedigree with Hereditary Medullary Thyroid Carcinoma.
    Zhang L, Li X, Li Q, Ge S, Chen M, Huang S, Chen B, Li P, Teng B, Xu J, Zhao S, Qi F, Zhang Y.
    Pathobiology; 2017; 84(3):152-160. PubMed ID: 27798940
    [Abstract] [Full Text] [Related]

  • 2. Screening of RET gene mutations in Chinese patients with medullary thyroid carcinoma and their relatives.
    Wang J, Zhang B, Liu W, Zhang Y, Di X, Yang Y, Yan D.
    Fam Cancer; 2016 Jan; 15(1):99-104. PubMed ID: 26254625
    [Abstract] [Full Text] [Related]

  • 3. Chinese siblings with hereditary medullary thyroid carcinoma caused by RET mutation: implications for RET oncogene detection.
    Huang Q, Hu A, Zhang M.
    BMC Endocr Disord; 2020 May 14; 20(1):64. PubMed ID: 32408902
    [Abstract] [Full Text] [Related]

  • 4. Genotype-specific progression of hereditary medullary thyroid cancer.
    Machens A, Lorenz K, Weber F, Dralle H.
    Hum Mutat; 2018 Jun 14; 39(6):860-869. PubMed ID: 29656518
    [Abstract] [Full Text] [Related]

  • 5. Medullary thyroid carcinoma (MTC) and RET proto-oncogene: mutation spectrum in the familial cases and a meta-analysis of studies on the sporadic form.
    Figlioli G, Landi S, Romei C, Elisei R, Gemignani F.
    Mutat Res; 2013 Jun 14; 752(1):36-44. PubMed ID: 23059849
    [Abstract] [Full Text] [Related]

  • 6. Germline RET mutation carriers in Japanese patients with apparently sporadic medullary thyroid carcinoma: A single institution experience.
    Kihara M, Miyauchi A, Yoshioka K, Oda H, Nakayama A, Sasai H, Yabuta T, Masuoka H, Higashiyama T, Fukushima M, Ito Y, Kobayashi K, Miya A.
    Auris Nasus Larynx; 2016 Oct 14; 43(5):551-5. PubMed ID: 26837867
    [Abstract] [Full Text] [Related]

  • 7. Multiple endocrine neoplasia type 2A in two families with the familial medullary thyroid carcinoma associated G533C mutation of the RET proto-oncogene.
    Peppa M, Boutati E, Kamakari S, Pikounis V, Peros G, Panayiotides IG, Economopoulos T, Raptis SA, Hadjidakis D.
    Eur J Endocrinol; 2008 Dec 14; 159(6):767-71. PubMed ID: 18805915
    [Abstract] [Full Text] [Related]

  • 8. Nationwide French Study of RET Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as Modifiers.
    Lebeault M, Pinson S, Guillaud-Bataille M, Gimenez-Roqueplo AP, Carrie A, Barbu V, Pigny P, Bezieau S, Rey JM, Delvincourt C, Giraud S, Veyrat-Durebex C, Saulnier P, Bouzamondo N, Chabbert M, Blin J, Mohamed A, Romanet P, Borson-Chazot F, Rohmer V, Barlier A, Mirebeau-Prunier D.
    Thyroid; 2017 Dec 14; 27(12):1511-1522. PubMed ID: 28946813
    [Abstract] [Full Text] [Related]

  • 9. RET codon 618 mutations in Saudi families with multiple endocrine neoplasia Type 2A and familial medullary thyroid carcinoma.
    Qari F.
    Ann Saudi Med; 2013 Dec 14; 33(2):155-8. PubMed ID: 23563004
    [Abstract] [Full Text] [Related]

  • 10. Case report: a p.C618S RET proto-oncogene germline mutation in a large Chinese pedigree with familial medullary thyroid carcinoma.
    Qi XP, Ying RB, Ma JM, Liu WT, Du ZF, Fei J, Yang CP, Song QZ, Jin HY, Chen ZG, Han JS, Wang JQ, Chen XL, Zhao Y, Lu JJ, Zhang XN.
    Fam Cancer; 2012 Mar 14; 11(1):131-6. PubMed ID: 22068382
    [Abstract] [Full Text] [Related]

  • 11. The relationship of cytomorphology of medullary thyroid carcinomas between family members with the same RET proto-oncogene mutation.
    Chang JS, Chang CF, Yang WS, Chang TC.
    Acta Cytol; 2011 Mar 14; 55(6):556-62. PubMed ID: 22156466
    [Abstract] [Full Text] [Related]

  • 12. A rare missense variant in RET exon 8 in a Portuguese family with atypical multiple endocrine neoplasia type 2A.
    Martins AF, Martins JM, do Vale S, Dias T, Silveira C, da Silva IR, Carmo-Fonseca M.
    Hormones (Athens); 2016 Jul 14; 15(3):435-440. PubMed ID: 27838608
    [Abstract] [Full Text] [Related]

  • 13. M918V RET mutation causes familial medullary thyroid carcinoma: study of 8 affected kindreds.
    Martins-Costa MC, Cunha LL, Lindsey SC, Camacho CP, Dotto RP, Furuzawa GK, Sousa MS, Kasamatsu TS, Kunii IS, Martins MM, Machado AL, Martins JR, Dias-da-Silva MR, Maciel RM.
    Endocr Relat Cancer; 2016 Dec 14; 23(12):909-920. PubMed ID: 27807060
    [Abstract] [Full Text] [Related]

  • 14. High prevalence of exon 8 G533C mutation in apparently sporadic medullary thyroid carcinoma in Greece.
    Sarika HL, Papathoma A, Garofalaki M, Vasileiou V, Vlassopoulou B, Anastasiou E, Alevizaki M.
    Clin Endocrinol (Oxf); 2012 Dec 14; 77(6):857-62. PubMed ID: 22676047
    [Abstract] [Full Text] [Related]

  • 15. RET oncogene mutations in medullary thyroid carcinoma in Mexican families.
    González B, Salcedo M, Medrano ME, Mantilla A, Quiñónez G, Benítez-Bribiesca L, Rodríguez-Cuevas S, Cabrera L, de León B, Altamirano N, Tapia J, Dawson B.
    Arch Med Res; 2003 Dec 14; 34(1):41-9. PubMed ID: 12604374
    [Abstract] [Full Text] [Related]

  • 16. A novel germline variant in RET gene resulting in an additional cysteine in a family with familial medullary thyroid carcinoma.
    Oriola J, Sanchez A, Paniello B, de la Bellacasa JP, Biarnés J.
    Fam Cancer; 2021 Jul 14; 20(3):253-256. PubMed ID: 33084974
    [Abstract] [Full Text] [Related]

  • 17. Mutational analysis of the RET proto-oncogene in 71 Japanese patients with medullary thyroid carcinoma.
    Shirahama S, Ogura K, Takami H, Ito K, Tohsen T, Miyauchi A, Nakamura Y.
    J Hum Genet; 1998 Jul 14; 43(2):101-6. PubMed ID: 9621513
    [Abstract] [Full Text] [Related]

  • 18. The modifier role of RET-G691S polymorphism in hereditary medullary thyroid carcinoma: functional characterization and expression/penetrance studies.
    Colombo C, Minna E, Rizzetti MG, Romeo P, Lecis D, Persani L, Mondellini P, Pierotti MA, Greco A, Fugazzola L, Borrello MG.
    Orphanet J Rare Dis; 2015 Mar 01; 10():25. PubMed ID: 25887804
    [Abstract] [Full Text] [Related]

  • 19. Exon 5 of the RET proto-oncogene: a newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg.
    Dvorakova S, Vaclavikova E, Duskova J, Vlcek P, Ryska A, Bendlova B.
    J Endocrinol Invest; 2005 Nov 01; 28(10):905-9. PubMed ID: 16419493
    [Abstract] [Full Text] [Related]

  • 20. Occurrence of the Cys611Tyr mutation and a novel Arg886Trp substitution in the RET proto-oncogene in multiple endocrine neoplasia type 2 families and sporadic medullary thyroid carcinoma cases originating from the central region of Portugal.
    Prazeres HJ, Rodrigues F, Figueiredo P, Naidenov P, Soares P, Bugalho MJ, Lacerda M, Campos B, Martins TC.
    Clin Endocrinol (Oxf); 2006 Jun 01; 64(6):659-66. PubMed ID: 16712668
    [Abstract] [Full Text] [Related]

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