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Journal Abstract Search

176 related items for PubMed ID: 24845513

  • 1. The rare intracellular RET mutation p.S891A in a Chinese Han family with familial medullary thyroid carcinoma.
    Qi XP, Zhang RX, Cao JL, Chen ZG, Jin HY, Yang RR.
    J Biosci; 2014 Jun; 39(3):505-12. PubMed ID: 24845513
    [Abstract] [Full Text] [Related]

  • 2. RET mutation p.S891A in a Chinese family with familial medullary thyroid carcinoma and associated cutaneous amyloidosis binding OSMR variant p.G513D.
    Qi XP, Zhao JQ, Chen ZG, Cao JL, Du J, Liu NF, Li F, Sheng M, Fu E, Guo J, Jia H, Zhang YM, Ma JM.
    Oncotarget; 2015 Oct 20; 6(32):33993-4003. PubMed ID: 26356818
    [Abstract] [Full Text] [Related]

  • 3. Prophylactic thyroidectomy for MEN 2-related medullary thyroid carcinoma based on predictive testing for RET proto-oncogene mutation and basal serum calcitonin in China.
    Qi XP, Zhao JQ, Du ZF, Yang RR, Ma JM, Fei J, Cheng J, Han JS, Jin HY, Chen ZG, Wang JQ, Yang YP, Ying RB, Chen XL, Liu WT, Zhao Y, Jiang HL, Zhang XN.
    Eur J Surg Oncol; 2013 Sep 20; 39(9):1007-12. PubMed ID: 23849459
    [Abstract] [Full Text] [Related]

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  • 5. RET germline mutations identified by exome sequencing in a Chinese multiple endocrine neoplasia type 2A/familial medullary thyroid carcinoma family.
    Qi XP, Ma JM, Du ZF, Ying RB, Fei J, Jin HY, Han JS, Wang JQ, Chen XL, Chen CY, Liu WT, Lu JJ, Zhang JG, Zhang XN.
    PLoS One; 2011 Sep 20; 6(5):e20353. PubMed ID: 21655256
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  • 7. A rare RET mutation in an Indian pedigree with familial medullary thyroid carcinoma.
    Vijayan R, Nair V, Menon U, Kumar H.
    Indian J Cancer; 2021 Sep 20; 58(1):98-100. PubMed ID: 33402557
    [Abstract] [Full Text] [Related]

  • 8. Characterization of V804M-mutated RET proto-oncogene associated with familial medullary thyroid cancer, report of the largest Turkish family.
    Basaran MN, Tuna MM, Karakılıç E, Doğan BA, İmga NN, Berker D, Güler S.
    J Endocrinol Invest; 2015 May 20; 38(5):541-6. PubMed ID: 25501606
    [Abstract] [Full Text] [Related]

  • 9. [Clinical diagnosis and treatment of familial medullary thyroid carcinoma caused by a p.C618Y RET proto-oncogene mutation in a Chinese pedigree].
    Zhao JQ, Guo L, Qi XP, Chen ZG, Wang KJ, Lou JL, Yu XH, Cheng J, Jin HY, Li XL, Ying RB, Zhang XN.
    Zhonghua Yi Xue Za Zhi; 2013 Feb 05; 93(6):440-4. PubMed ID: 23660264
    [Abstract] [Full Text] [Related]

  • 10. 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 Feb 05; 84(3):152-160. PubMed ID: 27798940
    [Abstract] [Full Text] [Related]

  • 11. Clinical utility of genetic diagnosis for sporadic and hereditary medullary thyroid carcinoma.
    Elisei R, Bottici V, Cappagli V, Ramone T, Tacito A, Ciampi R, Romei C.
    Ann Endocrinol (Paris); 2019 Jun 05; 80(3):187-190. PubMed ID: 31053251
    [Abstract] [Full Text] [Related]

  • 12. Modifying impact of RET gene haplotypes on medullary thyroid carcinoma clinical course.
    Kaczmarek-Ryś M, Ziemnicka K, Pławski A, Budny B, Michalak M, Hryhorowicz S, Hoppe-Gołębiewska J, Boruń P, Gołąb M, Czetwertyńska M, Sromek M, Szalata M, Ruchała M, Słomski R.
    Endocr Relat Cancer; 2018 Apr 05; 25(4):421-436. PubMed ID: 29386230
    [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 05; 23(12):909-920. PubMed ID: 27807060
    [Abstract] [Full Text] [Related]

  • 14. Current understanding and management of medullary thyroid cancer.
    Roy M, Chen H, Sippel RS.
    Oncologist; 2013 Dec 05; 18(10):1093-100. PubMed ID: 24037980
    [Abstract] [Full Text] [Related]

  • 15. A Nationwide Study of Multiple Endocrine Neoplasia Type 2A in Norway: Predictive and Prognostic Factors for the Clinical Course of Medullary Thyroid Carcinoma.
    Opsahl EM, Brauckhoff M, Schlichting E, Helset K, Svartberg J, Brauckhoff K, Mæhle L, Engebretsen LF, Sigstad E, Grøholt KK, Akslen LA, Jørgensen LH, Varhaug JE, Bjøro T.
    Thyroid; 2016 Sep 05; 26(9):1225-38. PubMed ID: 27400880
    [Abstract] [Full Text] [Related]

  • 16. Distribution of RET Mutations and Evaluation of Treatment Approaches in Hereditary Medullary Thyroid Carcinoma in Turkey.
    Aydoğan Bİ, Yüksel B, Tuna MM, Navdar Başaran M, Akkurt Kocaeli A, Ertörer ME, Aydın K, Güldiken S, Şimşek Y, Cihan Karaca Z, Yılmaz M, Aktürk M, Anaforoğlu İ, Kebapçı N, Duran C, Taşlıpınar A, Kulaksızoğlu M, Gürsoy A, Dağdelen S, Erdoğan MF.
    J Clin Res Pediatr Endocrinol; 2016 Mar 05; 8(1):13-20. PubMed ID: 26758973
    [Abstract] [Full Text] [Related]

  • 17. 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 Mar 05; 752(1):36-44. PubMed ID: 23059849
    [Abstract] [Full Text] [Related]

  • 18. Penetrance of inherited medullary thyroid carcinoma and genotype-phenotype correlation in a large multiple endocrine neoplasia type 2A family with C634Y RET mutation.
    González-Yebra B, Medrano ME, Mantilla A, Palma V, Colin C, Hernández DM, Tapia J, Dawson B, Salcedo M.
    Endocr Pathol; 2003 Mar 05; 14(1):71-80. PubMed ID: 12746565
    [Abstract] [Full Text] [Related]

  • 19. Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma.
    Frilling A, Dralle H, Eng C, Raue F, Broelsch CE.
    Surgery; 1995 Dec 05; 118(6):1099-103; discussion 1103-4. PubMed ID: 7491529
    [Abstract] [Full Text] [Related]

  • 20. 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]

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