메뉴 건너뛰기




Volumn 11, Issue 1, 2016, Pages

HABP2 G534E variant in papillary thyroid carcinoma

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER SUSCEPTIBILITY; CARCINOGENESIS; CONTROLLED STUDY; FEMALE; GENE; GENE EXPRESSION; GENE FREQUENCY; GENE FUNCTION; GENE SEGREGATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HABP2 GENE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; SINGLE NUCLEOTIDE POLYMORPHISM; SINGLE NUCLEOTIDE VARIANT; THYROID CARCINOMA; ANTIBODY SPECIFICITY; CARCINOMA; CASE CONTROL STUDY; ENZYMOLOGY; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; HAPLOTYPE; LIVER; METABOLISM; MISSENSE MUTATION; PEDIGREE; THYROID TUMOR;

EID: 84954341906     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0146315     Document Type: Article
Times cited : (31)

References (14)
  • 1
    • 0034927358 scopus 로고    scopus 로고
    • The genetic epidemiology of cancer: Interpreting family and twin studies and their implications for molecular genetic approaches
    • 11440958
    • Risch N. The genetic epidemiology of cancer: Interpreting family and twin studies and their implications for molecular genetic approaches. Cancer Epidemiol Biomarkers Prev. 2001; 10:733-741. PMID: 11440958
    • (2001) Cancer Epidemiol Biomarkers Prev. , vol.10 , pp. 733-741
    • Risch, N.1
  • 2
    • 0037052644 scopus 로고    scopus 로고
    • Environmental and heritable causes of cancer among 9.6 million individuals in the Swedish family-cancer database
    • 11979442
    • Czene K, Lichtenstein P, Hemminki K. Environmental and heritable causes of cancer among 9.6 million individuals in the Swedish family-cancer database. Int J Cancer. 2002; 99: 260-266. PMID: 11979442
    • (2002) Int J Cancer , vol.99 , pp. 260-266
    • Czene, K.1    Lichtenstein, P.2    Hemminki, K.3
  • 4
    • 84859165567 scopus 로고    scopus 로고
    • Significant evidence for a heritable contribution to cancer predisposition: A review of cancer familiality by site
    • 22471249
    • Albright F, Teerlink C, Werner T, Cannon-Albright L. Significant evidence for a heritable contribution to cancer predisposition: a review of cancer familiality by site. BMC Cancer. 2012; 12: 138-144. doi: 10.1186/1471-2407-12-138 PMID: 22471249
    • (2012) BMC Cancer , vol.12 , pp. 138-144
    • Albright, F.1    Teerlink, C.2    Werner, T.3    Cannon-Albright, L.4
  • 5
    • 84886436211 scopus 로고    scopus 로고
    • Risk of thyroid cancer in relatives of patients with medullary thyroid carcinoma by age at diagnosis
    • 23928562
    • Fallah M, Sundquist K, Hemminki K. Risk of thyroid cancer in relatives of patients with medullary thyroid carcinoma by age at diagnosis. Endocr Relat Cancer. 2013; 20: 717-724. doi: 10.1530/ERC-13-0021 PMID: 23928562
    • (2013) Endocr Relat Cancer , vol.20 , pp. 717-724
    • Fallah, M.1    Sundquist, K.2    Hemminki, K.3
  • 6
    • 77954617010 scopus 로고    scopus 로고
    • Genetic predisposition to familial nonmedullary thyroid cancer: An update of molecular findings and state-of-The-art studies
    • Bonora E, Tallini G, Romeo G. Genetic predisposition to familial nonmedullary thyroid cancer: An update of molecular findings and state-of-the-art studies. J Oncol. 2010; 385: 206.
    • (2010) J Oncol. , vol.385 , pp. 206
    • Bonora, E.1    Tallini, G.2    Romeo, G.3
  • 7
    • 84877788249 scopus 로고    scopus 로고
    • Ultra-rare mutation in long-range enhancer predisposes to thyroid carcinoma with high penetrance
    • 23690926
    • He H, Li W, Wu D, Nagy R, Liyanarachchi S, Akagi K, et al. Ultra-rare mutation in long-range enhancer predisposes to thyroid carcinoma with high penetrance. PLoS One. 2013; 8: e61920. doi: 10.1371/journal.pone.0061920 PMID: 23690926
    • (2013) PLoS One , vol.8 , pp. e61920
    • He, H.1    Li, W.2    Wu, D.3    Nagy, R.4    Liyanarachchi, S.5    Akagi, K.6
  • 9
    • 58349088314 scopus 로고    scopus 로고
    • A susceptibility locus for papillary thyroid carcinoma on chromosome 8q24
    • 19147577
    • He H, Nagy R, Liyanarachchi S, Jiao H, Li W, Suster S, Kere J, de la Chapelle A. A susceptibility locus for papillary thyroid carcinoma on chromosome 8q24. Cancer Res. 2009; 69: 625-631. doi: 10.1158/0008-5472.CAN-08-1071 PMID: 19147577
    • (2009) Cancer Res. , vol.69 , pp. 625-631
    • He, H.1    Nagy, R.2    Liyanarachchi, S.3    Jiao, H.4    Li, W.5    Suster, S.6    Kere, J.7    De La-Chapelle, A.8
  • 10
    • 85018220225 scopus 로고    scopus 로고
    • A germline mutation in SRRM2, a splicing factor gene, is implicated in papillary thyroid carcinoma predisposition
    • 26135620
    • Tomsic J, He H, Akagi K, Liyanarachchi S, Pan Q, Bertani B, et al. A germline mutation in SRRM2, a splicing factor gene, is implicated in papillary thyroid carcinoma predisposition. Sci Rep. 2015; 5: 10566. doi: 10.1038/srep10566 PMID: 26135620
    • (2015) Sci Rep. , vol.5 , pp. 10566
    • Tomsic, J.1    He, H.2    Akagi, K.3    Liyanarachchi, S.4    Pan, Q.5    Bertani, B.6
  • 11
    • 84890372228 scopus 로고    scopus 로고
    • Cumulative risk impact of five genetic variants associated with papillary thyroid carcinoma
    • 23659773
    • Liyanarachchi S, Wojcicka A, Li W, Czertwertynska M, Stachlewska E, Nagy R, et al. Cumulative risk impact of five genetic variants associated with papillary thyroid carcinoma. Thyroid. 2013; 23: 1532-1540. doi: 10.1089/thy.2013.0102 PMID: 23659773
    • (2013) Thyroid , vol.23 , pp. 1532-1540
    • Liyanarachchi, S.1    Wojcicka, A.2    Li, W.3    Czertwertynska, M.4    Stachlewska, E.5    Nagy, R.6
  • 12
    • 84938346586 scopus 로고    scopus 로고
    • Germline HABP2 mutation causing familial nonmedullary thyroid cancer
    • 26222560
    • Gara SK, Jia L, Merino MJ, Agarwal SK, Zhang L, Cam M, et al. Germline HABP2 Mutation Causing Familial Nonmedullary Thyroid Cancer. N Engl J Med. 2015; 373: 448-455. doi: 10.1056/NEJMoa1502449 PMID: 26222560
    • (2015) N Engl J Med. , vol.373 , pp. 448-455
    • Gara, S.K.1    Jia, L.2    Merino, M.J.3    Agarwal, S.K.4    Zhang, L.5    Cam, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.