메뉴 건너뛰기




Volumn 86, Issue 8, 2001, Pages 3746-3753

Familial medullary thyroid carcinoma with noncysteine RET mutations: Phenotype-genotype relationship in a large series of patients

Author keywords

[No Author keywords available]

Indexed keywords

CALCITONIN; GENE PRODUCT; PROTEIN RET; UNCLASSIFIED DRUG;

EID: 17944370976     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jcem.86.8.7767     Document Type: Article
Times cited : (133)

References (44)
  • 2
    • 4644256817 scopus 로고    scopus 로고
    • The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2: International RET Mutation Consortium analysis
    • (1996) JAMA , vol.276 , pp. 1575-1579
    • Eng, C.1    Clayton, D.2    Schuffenecker, I.3
  • 13
    • 0033045514 scopus 로고    scopus 로고
    • Two germline missense mutations at codons 804 and 806 of the RET protooncogene in the same allele in a patient with multiple endocrine neoplasia type 2B without codon 918 mutation
    • (1999) Jpn J Cancer Res , vol.90 , pp. 1-5
    • Miyauchi, A.1    Futami, H.2    Yokozawa, T.3
  • 14
    • 0030981891 scopus 로고    scopus 로고
    • A duplication of 12 bp in the critical cysteine rich domain of the RET proto-oncogene results in a distinct phenotype of multiple endocrine neoplasia type 2A
    • (1997) Hum Mol Genet , vol.6 , pp. 587-590
    • Hoppner, W.1    Ritter, M.M.2
  • 15
    • 0031984908 scopus 로고    scopus 로고
    • A duplication of 9 base pairs in the critical cysteine rich domain of the RET proto-oncogene causes multiple endocrine neoplasia type 2A
    • (1998) Hum Mut , vol.1 , pp. 128-130
    • Hoppner, W.1    Dralle, H.2    Brabant, G.3
  • 19
  • 20
    • 0028838075 scopus 로고
    • A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC
    • (1995) Oncogene , vol.20 , pp. 509-513
    • Eng, C.1    Smith, D.P.2    Mulligan, M.L.3
  • 24
    • 0031984945 scopus 로고    scopus 로고
    • A GTG to ATG novel point mutation at codon 804 in exon 14 of the RET proto-oncogene in two families affected by familial medullary thyroid carcinoma
    • (1998) Hum Mut , vol.1
    • Fattoruso, O.1    Quadro, L.2    Libroia, A.3
  • 36
    • 0028850673 scopus 로고
    • Early treatment of hereditary medullary thyroid carcinoma after attribution of multiple endocrine neoplasia type 2 gene carrier status by screening for ret gene mutations
    • (1995) Surgery , vol.118 , pp. 1031-1035
    • Pacini, F.1    Romei, C.2    Miccoli, P.3
  • 37
    • 0004311769 scopus 로고    scopus 로고
    • Deleted in proof
  • 38
    • 0033166442 scopus 로고    scopus 로고
    • Biological and biochemical properties of RET with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma
    • (1999) Oncogene , vol.18 , pp. 3919-3922
    • Iwashita, T.1    Kato, M.2    Murakami, H.3
  • 39


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.