메뉴 건너뛰기




Volumn 24, Issue 5, 2010, Pages 861-883

Genitourinary cancer predisposition syndromes

Author keywords

Cancer; Genetic; Genitourinary; Predisposition

Indexed keywords

ARYLAMINE ACETYLTRANSFERASE; BRCA1 PROTEIN; BRCA2 PROTEIN; GLUTATHIONE TRANSFERASE; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE INHIBITOR;

EID: 77956314658     PISSN: 08898588     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hoc.2010.06.002     Document Type: Review
Times cited : (4)

References (209)
  • 2
    • 0028143018 scopus 로고
    • Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands
    • Goldgar D.E., Easton D.F., Cannon-Albright L.A., et al. Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands. J Natl Cancer Inst 1994, 86:1600-1608.
    • (1994) J Natl Cancer Inst , vol.86 , pp. 1600-1608
    • Goldgar, D.E.1    Easton, D.F.2    Cannon-Albright, L.A.3
  • 3
    • 67649805085 scopus 로고    scopus 로고
    • Molecular biology underlying the clinical heterogeneity of prostate cancer: an update
    • Mackinnon A.C., Yan B.C., Joseph L.J., et al. Molecular biology underlying the clinical heterogeneity of prostate cancer: an update. Arch Pathol Lab Med 2009, 133:1033-1040.
    • (2009) Arch Pathol Lab Med , vol.133 , pp. 1033-1040
    • Mackinnon, A.C.1    Yan, B.C.2    Joseph, L.J.3
  • 4
    • 0034644185 scopus 로고    scopus 로고
    • Environmental and heritable factors in the causation of cancer-analyses of cohorts of twins from Sweden, Denmark, and Finland
    • Lichtenstein P., Holm N.V., Verkasalo P.K., et al. Environmental and heritable factors in the causation of cancer-analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med 2000, 343:78-85.
    • (2000) N Engl J Med , vol.343 , pp. 78-85
    • Lichtenstein, P.1    Holm, N.V.2    Verkasalo, P.K.3
  • 5
    • 1842612064 scopus 로고    scopus 로고
    • The complex genetic epidemiology of prostate cancer
    • Schaid D.J. The complex genetic epidemiology of prostate cancer. Hum Mol Genet 2004, 13(1):R103-R121.
    • (2004) Hum Mol Genet , vol.13 , Issue.1
    • Schaid, D.J.1
  • 6
    • 0028052231 scopus 로고
    • Studies of genetic factors in prostate cancer in a twin population
    • [discussion: 1487-9]
    • Gronberg H., Damber L., Damber J.E. Studies of genetic factors in prostate cancer in a twin population. J Urol 1994, 152:1484-1487. [discussion: 1487-9].
    • (1994) J Urol , vol.152 , pp. 1484-1487
    • Gronberg, H.1    Damber, L.2    Damber, J.E.3
  • 7
    • 0030731852 scopus 로고    scopus 로고
    • Heredity and prostate cancer: a study of World War II veteran twins
    • Page W.F., Braun M.M., Partin A.W., et al. Heredity and prostate cancer: a study of World War II veteran twins. Prostate 1997, 33:240-245.
    • (1997) Prostate , vol.33 , pp. 240-245
    • Page, W.F.1    Braun, M.M.2    Partin, A.W.3
  • 8
    • 0000009909 scopus 로고    scopus 로고
    • Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search
    • Smith J.R., Freije D., Carpten J.D., et al. Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search. Science 1996, 274:1371-1374.
    • (1996) Science , vol.274 , pp. 1371-1374
    • Smith, J.R.1    Freije, D.2    Carpten, J.D.3
  • 9
    • 1842415957 scopus 로고    scopus 로고
    • Early age at diagnosis in families providing evidence of linkage to the hereditary prostate cancer locus (HPC1) on chromosome 1
    • Gronberg H., Xu J., Smith J.R., et al. Early age at diagnosis in families providing evidence of linkage to the hereditary prostate cancer locus (HPC1) on chromosome 1. Cancer Res 1997, 57:4707-4709.
    • (1997) Cancer Res , vol.57 , pp. 4707-4709
    • Gronberg, H.1    Xu, J.2    Smith, J.R.3
  • 10
    • 18544377048 scopus 로고    scopus 로고
    • Germline mutations in the ribonuclease L gene in families showing linkage with HPC1
    • Carpten J., Nupponen N., Isaacs S., et al. Germline mutations in the ribonuclease L gene in families showing linkage with HPC1. Nat Genet 2002, 30:181-184.
    • (2002) Nat Genet , vol.30 , pp. 181-184
    • Carpten, J.1    Nupponen, N.2    Isaacs, S.3
  • 11
    • 0030966230 scopus 로고    scopus 로고
    • Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study
    • Cooney K.A., McCarthy J.D., Lange E., et al. Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study. J Natl Cancer Inst 1997, 89:955-959.
    • (1997) J Natl Cancer Inst , vol.89 , pp. 955-959
    • Cooney, K.A.1    McCarthy, J.D.2    Lange, E.3
  • 12
    • 0031576567 scopus 로고    scopus 로고
    • Re: prostate cancer susceptibility locus on chromosome 1q: a confirmatory study
    • Hsieh C.L., Oakley-Girvan I., Gallagher R.P., et al. Re: prostate cancer susceptibility locus on chromosome 1q: a confirmatory study. J Natl Cancer Inst 1997, 89:1893-1894.
    • (1997) J Natl Cancer Inst , vol.89 , pp. 1893-1894
    • Hsieh, C.L.1    Oakley-Girvan, I.2    Gallagher, R.P.3
  • 13
    • 16944364641 scopus 로고    scopus 로고
    • Linkage analysis of 49 high-risk families does not support a common familial prostate cancer-susceptibility gene at 1q24-25
    • McIndoe R.A., Stanford J.L., Gibbs M., et al. Linkage analysis of 49 high-risk families does not support a common familial prostate cancer-susceptibility gene at 1q24-25. Am J Hum Genet 1997, 61:347-353.
    • (1997) Am J Hum Genet , vol.61 , pp. 347-353
    • McIndoe, R.A.1    Stanford, J.L.2    Gibbs, M.3
  • 14
    • 17344373672 scopus 로고    scopus 로고
    • Linkage analysis of chromosome 1q markers in 136 prostate cancer families. The Cancer Research Campaign/British Prostate Group U.K. Familial Prostate Cancer Study Collaborators
    • Eeles R.A., Durocher F., Edwards S., et al. Linkage analysis of chromosome 1q markers in 136 prostate cancer families. The Cancer Research Campaign/British Prostate Group U.K. Familial Prostate Cancer Study Collaborators. Am J Hum Genet 1998, 62:653-658.
    • (1998) Am J Hum Genet , vol.62 , pp. 653-658
    • Eeles, R.A.1    Durocher, F.2    Edwards, S.3
  • 15
    • 0033758108 scopus 로고    scopus 로고
    • Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer
    • Bergthorsson J.T., Johannesdottir G., Arason A., et al. Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer. Hum Genet 2000, 107:372-375.
    • (2000) Hum Genet , vol.107 , pp. 372-375
    • Bergthorsson, J.T.1    Johannesdottir, G.2    Arason, A.3
  • 16
    • 0035131464 scopus 로고    scopus 로고
    • PCAP is the major known prostate cancer predisposing locus in families from south and west Europe
    • Cancel-Tassin G., Latil A., Valeri A., et al. PCAP is the major known prostate cancer predisposing locus in families from south and west Europe. Eur J Hum Genet 2001, 9:135-142.
    • (2001) Eur J Hum Genet , vol.9 , pp. 135-142
    • Cancel-Tassin, G.1    Latil, A.2    Valeri, A.3
  • 17
    • 0033819782 scopus 로고    scopus 로고
    • Replication linkage study for prostate cancer susceptibility genes
    • Suarez B.K., Lin J., Witte J.S., et al. Replication linkage study for prostate cancer susceptibility genes. Prostate 2000, 45:106-114.
    • (2000) Prostate , vol.45 , pp. 106-114
    • Suarez, B.K.1    Lin, J.2    Witte, J.S.3
  • 18
    • 0033912711 scopus 로고    scopus 로고
    • Linkage analyses at the chromosome 1 loci 1q24-25 (HPC1), 1q42.2-43 (PCAP), and 1p36 (CAPB) in families with hereditary prostate cancer
    • Berry R., Schaid D.J., Smith J.R., et al. Linkage analyses at the chromosome 1 loci 1q24-25 (HPC1), 1q42.2-43 (PCAP), and 1p36 (CAPB) in families with hereditary prostate cancer. Am J Hum Genet 2000, 66:539-546.
    • (2000) Am J Hum Genet , vol.66 , pp. 539-546
    • Berry, R.1    Schaid, D.J.2    Smith, J.R.3
  • 19
    • 12944289481 scopus 로고    scopus 로고
    • Confirmation of the HPCX prostate cancer predisposition locus in large Utah prostate cancer pedigrees
    • Farnham J.M., Camp N.J., Swensen J., et al. Confirmation of the HPCX prostate cancer predisposition locus in large Utah prostate cancer pedigrees. Hum Genet 2005, 116:179-185.
    • (2005) Hum Genet , vol.116 , pp. 179-185
    • Farnham, J.M.1    Camp, N.J.2    Swensen, J.3
  • 20
    • 17344367857 scopus 로고    scopus 로고
    • Evidence for a prostate cancer susceptibility locus on the X chromosome
    • Xu J., Meyers D., Freije D., et al. Evidence for a prostate cancer susceptibility locus on the X chromosome. Nat Genet 1998, 20:175-179.
    • (1998) Nat Genet , vol.20 , pp. 175-179
    • Xu, J.1    Meyers, D.2    Freije, D.3
  • 21
    • 0033911539 scopus 로고    scopus 로고
    • Combined analysis of hereditary prostate cancer linkage to 1q24-25: results from 772 hereditary prostate cancer families from the International Consortium for Prostate Cancer Genetics
    • Xu J. Combined analysis of hereditary prostate cancer linkage to 1q24-25: results from 772 hereditary prostate cancer families from the International Consortium for Prostate Cancer Genetics. Am J Hum Genet 2000, 66:945-957.
    • (2000) Am J Hum Genet , vol.66 , pp. 945-957
    • Xu, J.1
  • 22
    • 17344367365 scopus 로고    scopus 로고
    • Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43
    • Berthon P., Valeri A., Cohen-Akenine A., et al. Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43. Am J Hum Genet 1998, 62:1416-1424.
    • (1998) Am J Hum Genet , vol.62 , pp. 1416-1424
    • Berthon, P.1    Valeri, A.2    Cohen-Akenine, A.3
  • 23
    • 0033358086 scopus 로고    scopus 로고
    • Analysis of chromosome 1q42.2-43 in 152 families with high risk of prostate cancer
    • Gibbs M., Chakrabarti L., Stanford J.L., et al. Analysis of chromosome 1q42.2-43 in 152 families with high risk of prostate cancer. Am J Hum Genet 1999, 64:1087-1095.
    • (1999) Am J Hum Genet , vol.64 , pp. 1087-1095
    • Gibbs, M.1    Chakrabarti, L.2    Stanford, J.L.3
  • 24
    • 0033357994 scopus 로고    scopus 로고
    • Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36
    • Gibbs M., Stanford J.L., McIndoe R.A., et al. Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36. Am J Hum Genet 1999, 64:776-787.
    • (1999) Am J Hum Genet , vol.64 , pp. 776-787
    • Gibbs, M.1    Stanford, J.L.2    McIndoe, R.A.3
  • 25
    • 0033362159 scopus 로고    scopus 로고
    • No evidence of linkage for chromosome 1q42.2-43 in prostate cancer
    • Whittemore A.S., Lin I.G., Oakley-Girvan I., et al. No evidence of linkage for chromosome 1q42.2-43 in prostate cancer. Am J Hum Genet 1999, 65:254-256.
    • (1999) Am J Hum Genet , vol.65 , pp. 254-256
    • Whittemore, A.S.1    Lin, I.G.2    Oakley-Girvan, I.3
  • 26
    • 0345279859 scopus 로고    scopus 로고
    • Age specific risks of familial prostate carcinoma: a basis for screening recommendations in high risk populations
    • Gronberg H., Wiklund F., Damber J.E. Age specific risks of familial prostate carcinoma: a basis for screening recommendations in high risk populations. Cancer 1999, 86:477-483.
    • (1999) Cancer , vol.86 , pp. 477-483
    • Gronberg, H.1    Wiklund, F.2    Damber, J.E.3
  • 27
    • 0037445964 scopus 로고    scopus 로고
    • Empiric risk of prostate carcinoma for relatives of patients with prostate carcinoma: a meta-analysis
    • Zeegers M.P., Jellema A., Ostrer H. Empiric risk of prostate carcinoma for relatives of patients with prostate carcinoma: a meta-analysis. Cancer 2003, 97:1894-1903.
    • (2003) Cancer , vol.97 , pp. 1894-1903
    • Zeegers, M.P.1    Jellema, A.2    Ostrer, H.3
  • 28
    • 0030772173 scopus 로고    scopus 로고
    • Epidemiology of prostate cancer
    • Haas G.P., Sakr W.A. Epidemiology of prostate cancer. CA Cancer J Clin 1997, 47:273-287.
    • (1997) CA Cancer J Clin , vol.47 , pp. 273-287
    • Haas, G.P.1    Sakr, W.A.2
  • 29
    • 0141958604 scopus 로고    scopus 로고
    • Segregation analysis of prostate cancer in France: evidence for autosomal dominant inheritance and residual brother-brother dependence
    • Valeri A., Briollais L., Azzouzi R., et al. Segregation analysis of prostate cancer in France: evidence for autosomal dominant inheritance and residual brother-brother dependence. Ann Hum Genet 2003, 67:125-137.
    • (2003) Ann Hum Genet , vol.67 , pp. 125-137
    • Valeri, A.1    Briollais, L.2    Azzouzi, R.3
  • 30
    • 0031747067 scopus 로고    scopus 로고
    • Evidence for autosomal dominant inheritance of prostate cancer
    • Schaid D.J., McDonnell S.K., Blute M.L., et al. Evidence for autosomal dominant inheritance of prostate cancer. Am J Hum Genet 1998, 62:1425-1438.
    • (1998) Am J Hum Genet , vol.62 , pp. 1425-1438
    • Schaid, D.J.1    McDonnell, S.K.2    Blute, M.L.3
  • 31
    • 0035148123 scopus 로고    scopus 로고
    • Autosomal dominant inheritance of prostate cancer: a confirmatory study
    • Verhage B.A., Baffoe-Bonnie A.B., Baglietto L., et al. Autosomal dominant inheritance of prostate cancer: a confirmatory study. Urology 2001, 57:97-101.
    • (2001) Urology , vol.57 , pp. 97-101
    • Verhage, B.A.1    Baffoe-Bonnie, A.B.2    Baglietto, L.3
  • 34
    • 34347263034 scopus 로고    scopus 로고
    • Genetic etiology of hereditary prostate cancer
    • Langeberg W.J., Isaacs W.B., Stanford J.L. Genetic etiology of hereditary prostate cancer. Front Biosci 2007, 12:4101-4110.
    • (2007) Front Biosci , vol.12 , pp. 4101-4110
    • Langeberg, W.J.1    Isaacs, W.B.2    Stanford, J.L.3
  • 35
    • 35748939671 scopus 로고    scopus 로고
    • Clinicians are poor raters of life-expectancy before radical prostatectomy or definitive radiotherapy for localized prostate cancer
    • Walz J., Gallina A., Perrotte P., et al. Clinicians are poor raters of life-expectancy before radical prostatectomy or definitive radiotherapy for localized prostate cancer. BJU Int 2007, 100:1254-1258.
    • (2007) BJU Int , vol.100 , pp. 1254-1258
    • Walz, J.1    Gallina, A.2    Perrotte, P.3
  • 36
    • 2442440933 scopus 로고    scopus 로고
    • BRCA mutations and risk of prostate cancer in Ashkenazi Jews
    • Kirchhoff T., Kauff N.D., Mitra N., et al. BRCA mutations and risk of prostate cancer in Ashkenazi Jews. Clin Cancer Res 2004, 10:2918-2921.
    • (2004) Clin Cancer Res , vol.10 , pp. 2918-2921
    • Kirchhoff, T.1    Kauff, N.D.2    Mitra, N.3
  • 37
    • 0033358578 scopus 로고    scopus 로고
    • The Jewish Ashkenazi founder mutations in the BRCA1/BRCA2 genes are not found at an increased frequency in Ashkenazi patients with prostate cancer
    • Hubert A., Peretz T., Manor O., et al. The Jewish Ashkenazi founder mutations in the BRCA1/BRCA2 genes are not found at an increased frequency in Ashkenazi patients with prostate cancer. Am J Hum Genet 1999, 65:921-924.
    • (1999) Am J Hum Genet , vol.65 , pp. 921-924
    • Hubert, A.1    Peretz, T.2    Manor, O.3
  • 38
    • 0031711516 scopus 로고    scopus 로고
    • Absence of 185delAG mutation of the BRCA1 gene and 6174delT mutation of the BRCA2 gene in Ashkenazi Jewish men with prostate cancer
    • Lehrer S., Fodor F., Stock R.G., et al. Absence of 185delAG mutation of the BRCA1 gene and 6174delT mutation of the BRCA2 gene in Ashkenazi Jewish men with prostate cancer. Br J Cancer 1998, 78:771-773.
    • (1998) Br J Cancer , vol.78 , pp. 771-773
    • Lehrer, S.1    Fodor, F.2    Stock, R.G.3
  • 39
    • 0032764893 scopus 로고    scopus 로고
    • Common mutations in BRCA1 and BRCA2 do not contribute to early prostate cancer in Jewish men
    • Nastiuk K.L., Mansukhani M., Terry M.B., et al. Common mutations in BRCA1 and BRCA2 do not contribute to early prostate cancer in Jewish men. Prostate 1999, 40:172-177.
    • (1999) Prostate , vol.40 , pp. 172-177
    • Nastiuk, K.L.1    Mansukhani, M.2    Terry, M.B.3
  • 40
    • 0033943282 scopus 로고    scopus 로고
    • The rate of the founder Jewish mutations in BRCA1 and BRCA2 in prostate cancer patients in Israel
    • Vazina A., Baniel J., Yaacobi Y., et al. The rate of the founder Jewish mutations in BRCA1 and BRCA2 in prostate cancer patients in Israel. Br J Cancer 2000, 83:463-466.
    • (2000) Br J Cancer , vol.83 , pp. 463-466
    • Vazina, A.1    Baniel, J.2    Yaacobi, Y.3
  • 41
    • 0142209176 scopus 로고    scopus 로고
    • A twofold increase in BRCA mutation related prostate cancer among Ashkenazi Israelis is not associated with distinctive histopathology
    • Giusti R.M., Rutter J.L., Duray P.H., et al. A twofold increase in BRCA mutation related prostate cancer among Ashkenazi Israelis is not associated with distinctive histopathology. J Med Genet 2003, 40:787-792.
    • (2003) J Med Genet , vol.40 , pp. 787-792
    • Giusti, R.M.1    Rutter, J.L.2    Duray, P.H.3
  • 42
    • 0030910022 scopus 로고    scopus 로고
    • The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews
    • Struewing J.P., Hartge P., Wacholder S., et al. The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews. N Engl J Med 1997, 336:1401-1408.
    • (1997) N Engl J Med , vol.336 , pp. 1401-1408
    • Struewing, J.P.1    Hartge, P.2    Wacholder, S.3
  • 43
    • 0033591850 scopus 로고    scopus 로고
    • Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer
    • Warner E., Foulkes W., Goodwin P., et al. Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer. J Natl Cancer Inst 1999, 91:1241-1247.
    • (1999) J Natl Cancer Inst , vol.91 , pp. 1241-1247
    • Warner, E.1    Foulkes, W.2    Goodwin, P.3
  • 44
    • 34548570038 scopus 로고    scopus 로고
    • Rare germline mutations in the BRCA2 gene are associated with early-onset prostate cancer
    • Agalliu I., Karlins E., Kwon E.M., et al. Rare germline mutations in the BRCA2 gene are associated with early-onset prostate cancer. Br J Cancer 2007, 97:826-831.
    • (2007) Br J Cancer , vol.97 , pp. 826-831
    • Agalliu, I.1    Karlins, E.2    Kwon, E.M.3
  • 46
    • 49649115901 scopus 로고    scopus 로고
    • Loss of heterozygosity at the BRCA2 locus detected by multiplex ligation-dependent probe amplification is common in prostate cancers from men with a germline BRCA2 mutation
    • Willems A.J., Dawson S.J., Samaratunga H., et al. Loss of heterozygosity at the BRCA2 locus detected by multiplex ligation-dependent probe amplification is common in prostate cancers from men with a germline BRCA2 mutation. Clin Cancer Res 2008, 14:2953-2961.
    • (2008) Clin Cancer Res , vol.14 , pp. 2953-2961
    • Willems, A.J.1    Dawson, S.J.2    Samaratunga, H.3
  • 47
    • 0037130887 scopus 로고    scopus 로고
    • Cancer incidence in BRCA1 mutation carriers
    • Thompson D., Easton D.F. Cancer incidence in BRCA1 mutation carriers. J Natl Cancer Inst 2002, 94:1358-1365.
    • (2002) J Natl Cancer Inst , vol.94 , pp. 1358-1365
    • Thompson, D.1    Easton, D.F.2
  • 48
    • 0033523268 scopus 로고    scopus 로고
    • Cancer risks in BRCA2 mutation carriers. The Breast Cancer Linkage Consortium
    • Cancer risks in BRCA2 mutation carriers. The Breast Cancer Linkage Consortium. J Natl Cancer Inst 1999, 91:1310-1316.
    • (1999) J Natl Cancer Inst , vol.91 , pp. 1310-1316
  • 49
    • 34347273049 scopus 로고    scopus 로고
    • Prostate cancer progression and survival in BRCA2 mutation carriers
    • Tryggvadóttir L., Vidarsdóttir L., Thorgeirsson T., et al. Prostate cancer progression and survival in BRCA2 mutation carriers. J Natl Cancer Inst 2007, 99:929-935.
    • (2007) J Natl Cancer Inst , vol.99 , pp. 929-935
    • Tryggvadóttir, L.1    Vidarsdóttir, L.2    Thorgeirsson, T.3
  • 50
    • 77950650763 scopus 로고    scopus 로고
    • Germline BRCA mutations denote a clinicopathologic subset of prostate cancer
    • Gallagher D.J., Gaudet M.M., Pal P., et al. Germline BRCA mutations denote a clinicopathologic subset of prostate cancer. Clin Cancer Res 2010, 16(7):2115-2121.
    • (2010) Clin Cancer Res , vol.16 , Issue.7 , pp. 2115-2121
    • Gallagher, D.J.1    Gaudet, M.M.2    Pal, P.3
  • 51
    • 67650471685 scopus 로고    scopus 로고
    • Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers
    • Fong P.C., Boss D.S., Yap T.A., et al. Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers. N Engl J Med 2009, 361:123-134.
    • (2009) N Engl J Med , vol.361 , pp. 123-134
    • Fong, P.C.1    Boss, D.S.2    Yap, T.A.3
  • 52
    • 0037320555 scopus 로고    scopus 로고
    • Mutations in CHEK2 associated with prostate cancer risk
    • Dong X., Wang L., Taniguchi K., et al. Mutations in CHEK2 associated with prostate cancer risk. Am J Hum Genet 2003, 72:270-280.
    • (2003) Am J Hum Genet , vol.72 , pp. 270-280
    • Dong, X.1    Wang, L.2    Taniguchi, K.3
  • 53
    • 33746943715 scopus 로고    scopus 로고
    • Characterization of CHEK2 mutations in prostate cancer
    • Wu X., Dong X., Liu W., et al. Characterization of CHEK2 mutations in prostate cancer. Hum Mutat 2006, 27:742-747.
    • (2006) Hum Mutat , vol.27 , pp. 742-747
    • Wu, X.1    Dong, X.2    Liu, W.3
  • 54
    • 33751202144 scopus 로고    scopus 로고
    • A large germline deletion in the Chek2 kinase gene is associated with an increased risk of prostate cancer
    • Cybulski C., Wokolorczyk D., Huzarski T., et al. A large germline deletion in the Chek2 kinase gene is associated with an increased risk of prostate cancer. J Med Genet 2006, 43:863-866.
    • (2006) J Med Genet , vol.43 , pp. 863-866
    • Cybulski, C.1    Wokolorczyk, D.2    Huzarski, T.3
  • 55
    • 8844283535 scopus 로고    scopus 로고
    • A novel founder CHEK2 mutation is associated with increased prostate cancer risk
    • Cybulski C., Huzarski T., Gorski B., et al. A novel founder CHEK2 mutation is associated with increased prostate cancer risk. Cancer Res 2004, 64:2677-2679.
    • (2004) Cancer Res , vol.64 , pp. 2677-2679
    • Cybulski, C.1    Huzarski, T.2    Gorski, B.3
  • 56
    • 50949112322 scopus 로고    scopus 로고
    • Identification and characterization of novel SNPs in CHEK2 in Ashkenazi Jewish men with prostate cancer
    • Tischkowitz M.D., Yilmaz A., Chen L.Q., et al. Identification and characterization of novel SNPs in CHEK2 in Ashkenazi Jewish men with prostate cancer. Cancer Lett 2008, 270:173-180.
    • (2008) Cancer Lett , vol.270 , pp. 173-180
    • Tischkowitz, M.D.1    Yilmaz, A.2    Chen, L.Q.3
  • 57
    • 18344385832 scopus 로고    scopus 로고
    • Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer
    • Rokman A., Ikonen T., Seppala E.H., et al. Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer. Am J Hum Genet 2002, 70:1299-1304.
    • (2002) Am J Hum Genet , vol.70 , pp. 1299-1304
    • Rokman, A.1    Ikonen, T.2    Seppala, E.H.3
  • 58
    • 19044373249 scopus 로고    scopus 로고
    • A novel founder mutation in the RNASEL gene, 471delAAAG, is associated with prostate cancer in Ashkenazi Jews
    • Rennert H., Bercovich D., Hubert A., et al. A novel founder mutation in the RNASEL gene, 471delAAAG, is associated with prostate cancer in Ashkenazi Jews. Am J Hum Genet 2002, 71:981-984.
    • (2002) Am J Hum Genet , vol.71 , pp. 981-984
    • Rennert, H.1    Bercovich, D.2    Hubert, A.3
  • 59
    • 1842408358 scopus 로고    scopus 로고
    • Characteristics of prostate cancer in families potentially linked to the hereditary prostate cancer 1 (HPC1) locus
    • Gronberg H., Isaacs S.D., Smith J.R., et al. Characteristics of prostate cancer in families potentially linked to the hereditary prostate cancer 1 (HPC1) locus. JAMA 1997, 278:1251-1255.
    • (1997) JAMA , vol.278 , pp. 1251-1255
    • Gronberg, H.1    Isaacs, S.D.2    Smith, J.R.3
  • 60
    • 19244386016 scopus 로고    scopus 로고
    • Linkage analysis of 150 high-risk prostate cancer families at 1q24-25
    • Goode E.L., Stanford J.L., Chakrabarti L., et al. Linkage analysis of 150 high-risk prostate cancer families at 1q24-25. Genet Epidemiol 2000, 18:251-275.
    • (2000) Genet Epidemiol , vol.18 , pp. 251-275
    • Goode, E.L.1    Stanford, J.L.2    Chakrabarti, L.3
  • 61
    • 39749129053 scopus 로고    scopus 로고
    • Multiple newly identified loci associated with prostate cancer susceptibility
    • Eeles R.A., Kote-Jarai Z., Giles G.G., et al. Multiple newly identified loci associated with prostate cancer susceptibility. Nat Genet 2008, 40:316-321.
    • (2008) Nat Genet , vol.40 , pp. 316-321
    • Eeles, R.A.1    Kote-Jarai, Z.2    Giles, G.G.3
  • 62
    • 39749118602 scopus 로고    scopus 로고
    • Multiple loci identified in a genome-wide association study of prostate cancer
    • Thomas G., Jacobs K.B., Yeager M., et al. Multiple loci identified in a genome-wide association study of prostate cancer. Nat Genet 2008, 40:310-315.
    • (2008) Nat Genet , vol.40 , pp. 310-315
    • Thomas, G.1    Jacobs, K.B.2    Yeager, M.3
  • 63
    • 34247548755 scopus 로고    scopus 로고
    • Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
    • Yeager M., Orr N., Hayes R.B., et al. Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. Nat Genet 2007, 39:645-649.
    • (2007) Nat Genet , vol.39 , pp. 645-649
    • Yeager, M.1    Orr, N.2    Hayes, R.B.3
  • 64
    • 70349540906 scopus 로고    scopus 로고
    • Identification of a new prostate cancer susceptibility locus on chromosome 8q24
    • Yeager M., Chatterjee N., Ciampa J., et al. Identification of a new prostate cancer susceptibility locus on chromosome 8q24. Nat Genet 2009, 41:1055-1057.
    • (2009) Nat Genet , vol.41 , pp. 1055-1057
    • Yeager, M.1    Chatterjee, N.2    Ciampa, J.3
  • 65
    • 70349545839 scopus 로고    scopus 로고
    • Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
    • Eeles R.A., Kote-Jarai Z., Al Olama A.A., et al. Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. Nat Genet 2009, 41:1116-1121.
    • (2009) Nat Genet , vol.41 , pp. 1116-1121
    • Eeles, R.A.1    Kote-Jarai, Z.2    Al Olama, A.A.3
  • 66
    • 34247563453 scopus 로고    scopus 로고
    • Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24
    • Gudmundsson J., Sulem P., Manolescu A., et al. Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. Nat Genet 2007, 39:631-637.
    • (2007) Nat Genet , vol.39 , pp. 631-637
    • Gudmundsson, J.1    Sulem, P.2    Manolescu, A.3
  • 67
    • 39749159112 scopus 로고    scopus 로고
    • Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
    • Gudmundsson J., Sulem P., Rafnar T., et al. Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. Nat Genet 2008, 40:281-283.
    • (2008) Nat Genet , vol.40 , pp. 281-283
    • Gudmundsson, J.1    Sulem, P.2    Rafnar, T.3
  • 68
    • 70349547128 scopus 로고    scopus 로고
    • Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
    • Gudmundsson J., Sulem P., Gudbjartsson D.F., et al. Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. Nat Genet 2009, 41:1122-1126.
    • (2009) Nat Genet , vol.41 , pp. 1122-1126
    • Gudmundsson, J.1    Sulem, P.2    Gudbjartsson, D.F.3
  • 69
    • 33745169697 scopus 로고    scopus 로고
    • A common variant associated with prostate cancer in European and African populations
    • Amundadottir L.T., Sulem P., Gudmundsson J., et al. A common variant associated with prostate cancer in European and African populations. Nat Genet 2006, 38:652-658.
    • (2006) Nat Genet , vol.38 , pp. 652-658
    • Amundadottir, L.T.1    Sulem, P.2    Gudmundsson, J.3
  • 70
    • 33749003979 scopus 로고    scopus 로고
    • Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men
    • Freedman M.L., Haiman C.A., Patterson N., et al. Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men. Proc Natl Acad Sci U S A 2006, 103:14068-14073.
    • (2006) Proc Natl Acad Sci U S A , vol.103 , pp. 14068-14073
    • Freedman, M.L.1    Haiman, C.A.2    Patterson, N.3
  • 71
    • 70349548806 scopus 로고    scopus 로고
    • Multiple loci on 8q24 associated with prostate cancer susceptibility
    • Al Olama A.A., Kote-Jarai Z., Giles G.G., et al. Multiple loci on 8q24 associated with prostate cancer susceptibility. Nat Genet 2009, 41:1058-1060.
    • (2009) Nat Genet , vol.41 , pp. 1058-1060
    • Al Olama, A.A.1    Kote-Jarai, Z.2    Giles, G.G.3
  • 72
    • 52949115663 scopus 로고    scopus 로고
    • Evidence for two independent prostate cancer risk-associated loci in the HNF1B gene at 17q12
    • Sun J., Zheng S.L., Wiklund F., et al. Evidence for two independent prostate cancer risk-associated loci in the HNF1B gene at 17q12. Nat Genet 2008, 40:1153-1155.
    • (2008) Nat Genet , vol.40 , pp. 1153-1155
    • Sun, J.1    Zheng, S.L.2    Wiklund, F.3
  • 73
    • 39149134006 scopus 로고    scopus 로고
    • Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility
    • Sole X., Hernandez P., de Heredia M.L., et al. Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility. BMC Genomics 2008, 9:12.
    • (2008) BMC Genomics , vol.9 , pp. 12
    • Sole, X.1    Hernandez, P.2    de Heredia, M.L.3
  • 74
    • 68149180901 scopus 로고    scopus 로고
    • The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer
    • Pomerantz M.M., Ahmadiyeh N., Jia L., et al. The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer. Nat Genet 2009, 41:882-884.
    • (2009) Nat Genet , vol.41 , pp. 882-884
    • Pomerantz, M.M.1    Ahmadiyeh, N.2    Jia, L.3
  • 75
    • 68149170044 scopus 로고    scopus 로고
    • The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling
    • Tuupanen S., Turunen M., Lehtonen R., et al. The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling. Nat Genet 2009, 41:885-890.
    • (2009) Nat Genet , vol.41 , pp. 885-890
    • Tuupanen, S.1    Turunen, M.2    Lehtonen, R.3
  • 76
    • 10744233070 scopus 로고    scopus 로고
    • NBS1 is a prostate cancer susceptibility gene
    • Cybulski C., Gorski B., Debniak T., et al. NBS1 is a prostate cancer susceptibility gene. Cancer Res 2004, 64:1215-1219.
    • (2004) Cancer Res , vol.64 , pp. 1215-1219
    • Cybulski, C.1    Gorski, B.2    Debniak, T.3
  • 77
    • 43049103453 scopus 로고    scopus 로고
    • Chromosome 8q24 markers: risk of early-onset and familial prostate cancer
    • Beebe-Dimmer J.L., Levin A.M., Ray A.M., et al. Chromosome 8q24 markers: risk of early-onset and familial prostate cancer. Int J Cancer 2008, 122:2876-2879.
    • (2008) Int J Cancer , vol.122 , pp. 2876-2879
    • Beebe-Dimmer, J.L.1    Levin, A.M.2    Ray, A.M.3
  • 78
    • 0033854639 scopus 로고    scopus 로고
    • Molecular mechanisms and pathways in bladder cancer development and progression
    • Jung I., Messing E. Molecular mechanisms and pathways in bladder cancer development and progression. Cancer Control 2000, 7:325-334.
    • (2000) Cancer Control , vol.7 , pp. 325-334
    • Jung, I.1    Messing, E.2
  • 79
    • 33745167997 scopus 로고    scopus 로고
    • Hair dye use is not associated with risk for bladder cancer: evidence from a case-control study in Spain
    • Kogevinas M., Fernandez F., Garcia-Closas M., et al. Hair dye use is not associated with risk for bladder cancer: evidence from a case-control study in Spain. Eur J Cancer 2006, 42:1448-1454.
    • (2006) Eur J Cancer , vol.42 , pp. 1448-1454
    • Kogevinas, M.1    Fernandez, F.2    Garcia-Closas, M.3
  • 80
    • 0026750169 scopus 로고
    • Chlorination, chlorination by-products, and cancer: a meta-analysis
    • Morris R.D., Audet A.M., Angelillo I.F., et al. Chlorination, chlorination by-products, and cancer: a meta-analysis. Am J Public Health 1992, 82:955-963.
    • (1992) Am J Public Health , vol.82 , pp. 955-963
    • Morris, R.D.1    Audet, A.M.2    Angelillo, I.F.3
  • 81
    • 34347269594 scopus 로고    scopus 로고
    • Fifty-year study of lung and bladder cancer mortality in Chile related to arsenic in drinking water
    • Marshall G., Ferreccio C., Yuan Y., et al. Fifty-year study of lung and bladder cancer mortality in Chile related to arsenic in drinking water. J Natl Cancer Inst 2007, 99:920-928.
    • (2007) J Natl Cancer Inst , vol.99 , pp. 920-928
    • Marshall, G.1    Ferreccio, C.2    Yuan, Y.3
  • 82
    • 0031975887 scopus 로고    scopus 로고
    • Drinking water source and chlorination byproducts. I. Risk of bladder cancer
    • Cantor K.P., Lynch C.F., Hildesheim M.E., et al. Drinking water source and chlorination byproducts. I. Risk of bladder cancer. Epidemiology 1998, 9:21-28.
    • (1998) Epidemiology , vol.9 , pp. 21-28
    • Cantor, K.P.1    Lynch, C.F.2    Hildesheim, M.E.3
  • 83
    • 0001532692 scopus 로고
    • The association of smoking with cancer of the urinary bladder in humans
    • Lillienfeld A., Levin M. The association of smoking with cancer of the urinary bladder in humans. Arch Intern Med 1956, 98:129-135.
    • (1956) Arch Intern Med , vol.98 , pp. 129-135
    • Lillienfeld, A.1    Levin, M.2
  • 84
    • 50949129989 scopus 로고    scopus 로고
    • Familial and genetic risk of transitional cell carcinoma of the urinary tract
    • Mueller C.M., Caporaso N., Greene M.H. Familial and genetic risk of transitional cell carcinoma of the urinary tract. Urol Oncol 2008, 26:451-464.
    • (2008) Urol Oncol , vol.26 , pp. 451-464
    • Mueller, C.M.1    Caporaso, N.2    Greene, M.H.3
  • 85
    • 0037051091 scopus 로고    scopus 로고
    • Familial aggregation of urothelial cell carcinoma
    • Aben K.K., Witjes J.A., Schoenberg M.P., et al. Familial aggregation of urothelial cell carcinoma. Int J Cancer 2002, 98:274-278.
    • (2002) Int J Cancer , vol.98 , pp. 274-278
    • Aben, K.K.1    Witjes, J.A.2    Schoenberg, M.P.3
  • 86
    • 36249026453 scopus 로고    scopus 로고
    • Family history of urogenital cancers in patients with bladder, renal cell and prostate cancers
    • Randi G., Pelucchi C., Negri E., et al. Family history of urogenital cancers in patients with bladder, renal cell and prostate cancers. Int J Cancer 2007, 121:2748-2752.
    • (2007) Int J Cancer , vol.121 , pp. 2748-2752
    • Randi, G.1    Pelucchi, C.2    Negri, E.3
  • 87
    • 0018804419 scopus 로고
    • Genetic association with bladder cancer
    • Cartwright R.A. Genetic association with bladder cancer. Br Med J 1979, 2:798.
    • (1979) Br Med J , vol.2 , pp. 798
    • Cartwright, R.A.1
  • 88
    • 0021854935 scopus 로고
    • Familial and environmental interactions in bladder cancer risk
    • Kantor A.F., Hartge P., Hoover R.N., et al. Familial and environmental interactions in bladder cancer risk. Int J Cancer 1985, 35:703-706.
    • (1985) Int J Cancer , vol.35 , pp. 703-706
    • Kantor, A.F.1    Hartge, P.2    Hoover, R.N.3
  • 89
    • 0030897075 scopus 로고    scopus 로고
    • Familial transitional cell carcinoma among the population of Iceland
    • Kiemeney L.A., Moret N.C., Witjes J.A., et al. Familial transitional cell carcinoma among the population of Iceland. J Urol 1997, 157:1649-1651.
    • (1997) J Urol , vol.157 , pp. 1649-1651
    • Kiemeney, L.A.1    Moret, N.C.2    Witjes, J.A.3
  • 90
    • 0025976834 scopus 로고
    • Familial aggregation of bladder cancer stratified by smoking status
    • Kramer A.A., Graham S., Burnett W.S., et al. Familial aggregation of bladder cancer stratified by smoking status. Epidemiology 1991, 2:145-148.
    • (1991) Epidemiology , vol.2 , pp. 145-148
    • Kramer, A.A.1    Graham, S.2    Burnett, W.S.3
  • 91
    • 0026551614 scopus 로고
    • Life style and occupational risk factors for bladder cancer in Germany. A case-control study
    • Kunze E., Chang-Claude J., Frentzel-Beyme R. Life style and occupational risk factors for bladder cancer in Germany. A case-control study. Cancer 1992, 69:1776-1790.
    • (1992) Cancer , vol.69 , pp. 1776-1790
    • Kunze, E.1    Chang-Claude, J.2    Frentzel-Beyme, R.3
  • 92
    • 33747168789 scopus 로고    scopus 로고
    • Bladder cancer risk as modified by family history and smoking
    • Lin J., Spitz M.R., Dinney C.P., et al. Bladder cancer risk as modified by family history and smoking. Cancer 2006, 107:705-711.
    • (2006) Cancer , vol.107 , pp. 705-711
    • Lin, J.1    Spitz, M.R.2    Dinney, C.P.3
  • 95
    • 10744233937 scopus 로고    scopus 로고
    • Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
    • Umar A., Boland C.R., Terdiman J.P., et al. Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 2004, 96:261-268.
    • (2004) J Natl Cancer Inst , vol.96 , pp. 261-268
    • Umar, A.1    Boland, C.R.2    Terdiman, J.P.3
  • 96
    • 0032322195 scopus 로고    scopus 로고
    • Urinary tract cancer and hereditary nonpolyposis colorectal cancer: risks and screening options
    • Sijmons R.H., Kiemeney L.A., Witjes J.A., et al. Urinary tract cancer and hereditary nonpolyposis colorectal cancer: risks and screening options. J Urol 1998, 160:466-470.
    • (1998) J Urol , vol.160 , pp. 466-470
    • Sijmons, R.H.1    Kiemeney, L.A.2    Witjes, J.A.3
  • 97
    • 76549120768 scopus 로고    scopus 로고
    • NCCN clinical practice guidelines in oncology. Colorectal cancer screening
    • Burt R.W., Barthel J.S., Dunn K.B., et al. NCCN clinical practice guidelines in oncology. Colorectal cancer screening. J Natl Compr Canc Netw 2010, 8:8-61.
    • (2010) J Natl Compr Canc Netw , vol.8 , pp. 8-61
    • Burt, R.W.1    Barthel, J.S.2    Dunn, K.B.3
  • 98
    • 0022623369 scopus 로고
    • Second primary neoplasms in patients with retinoblastoma
    • Draper G.J., Sanders B.M., Kingston J.E. Second primary neoplasms in patients with retinoblastoma. Br J Cancer 1986, 53:661-671.
    • (1986) Br J Cancer , vol.53 , pp. 661-671
    • Draper, G.J.1    Sanders, B.M.2    Kingston, J.E.3
  • 99
    • 3843124553 scopus 로고    scopus 로고
    • Nonocular second primary tumors after retinoblastoma: retrospective study of 111 patients treated by electron beam radiotherapy with or without TEM
    • Schlienger P., Campana F., Vilcoq J.R., et al. Nonocular second primary tumors after retinoblastoma: retrospective study of 111 patients treated by electron beam radiotherapy with or without TEM. Am J Clin Oncol 2004, 27:411-419.
    • (2004) Am J Clin Oncol , vol.27 , pp. 411-419
    • Schlienger, P.1    Campana, F.2    Vilcoq, J.R.3
  • 100
    • 1542318327 scopus 로고    scopus 로고
    • Lifetime risks of common cancers among retinoblastoma survivors
    • Fletcher O., Easton D., Anderson K., et al. Lifetime risks of common cancers among retinoblastoma survivors. J Natl Cancer Inst 2004, 96:357-363.
    • (2004) J Natl Cancer Inst , vol.96 , pp. 357-363
    • Fletcher, O.1    Easton, D.2    Anderson, K.3
  • 101
    • 25444467767 scopus 로고    scopus 로고
    • Urothelial tumorigenesis: a tale of divergent pathways
    • Wu X.R. Urothelial tumorigenesis: a tale of divergent pathways. Nat Rev Cancer 2005, 5:713-725.
    • (2005) Nat Rev Cancer , vol.5 , pp. 713-725
    • Wu, X.R.1
  • 103
    • 27144531386 scopus 로고    scopus 로고
    • Germline mutations in HRAS proto-oncogene cause Costello syndrome
    • Aoki Y., Niihori T., Kawame H., et al. Germline mutations in HRAS proto-oncogene cause Costello syndrome. Nat Genet 2005, 37:1038-1040.
    • (2005) Nat Genet , vol.37 , pp. 1038-1040
    • Aoki, Y.1    Niihori, T.2    Kawame, H.3
  • 105
  • 106
    • 0033960051 scopus 로고    scopus 로고
    • Molecular genetics and epidemiology of the NAT1 and NAT2 acetylation polymorphisms
    • Hein D.W., Doll M.A., Fretland A.J., et al. Molecular genetics and epidemiology of the NAT1 and NAT2 acetylation polymorphisms. Cancer Epidemiol Biomarkers Prev 2000, 9:29-42.
    • (2000) Cancer Epidemiol Biomarkers Prev , vol.9 , pp. 29-42
    • Hein, D.W.1    Doll, M.A.2    Fretland, A.J.3
  • 107
    • 23844512858 scopus 로고    scopus 로고
    • NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses
    • Garcia-Closas M., Malats N., Silverman D., et al. NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses. Lancet 2005, 366:649-659.
    • (2005) Lancet , vol.366 , pp. 649-659
    • Garcia-Closas, M.1    Malats, N.2    Silverman, D.3
  • 108
    • 55049112064 scopus 로고    scopus 로고
    • Sequence variant on 8q24 confers susceptibility to urinary bladder cancer
    • Kiemeney L.A., Thorlacius S., Sulem P., et al. Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. Nat Genet 2008, 40:1307-1312.
    • (2008) Nat Genet , vol.40 , pp. 1307-1312
    • Kiemeney, L.A.1    Thorlacius, S.2    Sulem, P.3
  • 109
    • 58549118238 scopus 로고    scopus 로고
    • Prostate cancer genomics: towards a new understanding
    • Witte J.S. Prostate cancer genomics: towards a new understanding. Nat Rev Genet 2009, 10:77-82.
    • (2009) Nat Rev Genet , vol.10 , pp. 77-82
    • Witte, J.S.1
  • 110
    • 69349100058 scopus 로고    scopus 로고
    • Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer
    • Wu X., Ye Y., Kiemeney L.A., et al. Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer. Nat Genet 2009, 41:991-995.
    • (2009) Nat Genet , vol.41 , pp. 991-995
    • Wu, X.1    Ye, Y.2    Kiemeney, L.A.3
  • 111
    • 33846136971 scopus 로고    scopus 로고
    • Familial renal carcinoma: clinical evaluation, clinical subtypes and risk of renal carcinoma development
    • [discussion: 465]
    • Zbar B., Glenn G., Merino M., et al. Familial renal carcinoma: clinical evaluation, clinical subtypes and risk of renal carcinoma development. J Urol 2007, 177:461-465. [discussion: 465].
    • (2007) J Urol , vol.177 , pp. 461-465
    • Zbar, B.1    Glenn, G.2    Merino, M.3
  • 112
    • 0029028652 scopus 로고
    • Characterization of the VHL tumor suppressor gene product: localization, complex formation, and the effect of natural inactivating mutations
    • Duan D.R., Humphrey J.S., Chen D.Y., et al. Characterization of the VHL tumor suppressor gene product: localization, complex formation, and the effect of natural inactivating mutations. Proc Natl Acad Sci U S A 1995, 92:6459-6463.
    • (1995) Proc Natl Acad Sci U S A , vol.92 , pp. 6459-6463
    • Duan, D.R.1    Humphrey, J.S.2    Chen, D.Y.3
  • 113
    • 33846181370 scopus 로고    scopus 로고
    • Sunitinib versus interferon alfa in metastatic renal-cell carcinoma
    • Motzer R.J., Hutson T.E., Tomczak P., et al. Sunitinib versus interferon alfa in metastatic renal-cell carcinoma. N Engl J Med 2007, 356:115-124.
    • (2007) N Engl J Med , vol.356 , pp. 115-124
    • Motzer, R.J.1    Hutson, T.E.2    Tomczak, P.3
  • 114
    • 33748122746 scopus 로고    scopus 로고
    • The history of von Hippel-Lindau disease
    • Molino D., Sepe J., Anastasio P., et al. The history of von Hippel-Lindau disease. J Nephrol 2006, 19(Suppl 10):S119-S123.
    • (2006) J Nephrol , vol.19 , Issue.SUPPL 10
    • Molino, D.1    Sepe, J.2    Anastasio, P.3
  • 115
    • 0003379614 scopus 로고
    • Retinal and central nervous hemangioblastomatosis with visceral changes (von Hippel-Lindau's disease)
    • Davison C., Brock S., Dyke C.G. Retinal and central nervous hemangioblastomatosis with visceral changes (von Hippel-Lindau's disease). Bull Neurol Instit NY 1936, 5:72-93.
    • (1936) Bull Neurol Instit NY , vol.5 , pp. 72-93
    • Davison, C.1    Brock, S.2    Dyke, C.G.3
  • 116
    • 0023865666 scopus 로고
    • Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma
    • Seizinger B.R., Rouleau G.A., Ozelius L.J., et al. Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma. Nature 1988, 332:268-269.
    • (1988) Nature , vol.332 , pp. 268-269
    • Seizinger, B.R.1    Rouleau, G.A.2    Ozelius, L.J.3
  • 117
    • 45549090890 scopus 로고    scopus 로고
    • Genetic basis for kidney cancer: opportunity for disease-specific approaches to therapy
    • Pfaffenroth E.C., Linehan W.M. Genetic basis for kidney cancer: opportunity for disease-specific approaches to therapy. Expert Opin Biol Ther 2008, 8:779-790.
    • (2008) Expert Opin Biol Ther , vol.8 , pp. 779-790
    • Pfaffenroth, E.C.1    Linehan, W.M.2
  • 118
    • 16144365122 scopus 로고    scopus 로고
    • Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan
    • Zbar B., Kishida T., Chen F., et al. Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan. Hum Mutat 1996, 8:348-357.
    • (1996) Hum Mutat , vol.8 , pp. 348-357
    • Zbar, B.1    Kishida, T.2    Chen, F.3
  • 119
    • 0037709883 scopus 로고    scopus 로고
    • Von Hippel-Lindau disease
    • Lonser R.R., Glenn G.M., Walther M., et al. von Hippel-Lindau disease. Lancet 2003, 361:2059-2067.
    • (2003) Lancet , vol.361 , pp. 2059-2067
    • Lonser, R.R.1    Glenn, G.M.2    Walther, M.3
  • 120
    • 33846990552 scopus 로고    scopus 로고
    • Genotype-phenotype correlation in von Hippel-Lindau disease with retinal angiomatosis
    • Wong W.T., Agron E., Coleman H.R., et al. Genotype-phenotype correlation in von Hippel-Lindau disease with retinal angiomatosis. Arch Ophthalmol 2007, 125:239-245.
    • (2007) Arch Ophthalmol , vol.125 , pp. 239-245
    • Wong, W.T.1    Agron, E.2    Coleman, H.R.3
  • 121
    • 17344381429 scopus 로고    scopus 로고
    • Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas
    • Schmidt L., Duh F.M., Chen F., et al. Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas. Nat Genet 1997, 16:68-73.
    • (1997) Nat Genet , vol.16 , pp. 68-73
    • Schmidt, L.1    Duh, F.M.2    Chen, F.3
  • 122
    • 0034869788 scopus 로고    scopus 로고
    • Papillary renal cell carcinoma: analysis of germline mutations in the MET proto-oncogene in a clinic-based population
    • Lindor N.M., Dechet C.B., Greene M.H., et al. Papillary renal cell carcinoma: analysis of germline mutations in the MET proto-oncogene in a clinic-based population. Genet Test 2001, 5:101-106.
    • (2001) Genet Test , vol.5 , pp. 101-106
    • Lindor, N.M.1    Dechet, C.B.2    Greene, M.H.3
  • 123
    • 4544306559 scopus 로고    scopus 로고
    • Early onset hereditary papillary renal carcinoma: germline missense mutations in the tyrosine kinase domain of the met proto-oncogene
    • Schmidt L.S., Nickerson M.L., Angeloni D., et al. Early onset hereditary papillary renal carcinoma: germline missense mutations in the tyrosine kinase domain of the met proto-oncogene. J Urol 2004, 172:1256-1261.
    • (2004) J Urol , vol.172 , pp. 1256-1261
    • Schmidt, L.S.1    Nickerson, M.L.2    Angeloni, D.3
  • 124
    • 33748355130 scopus 로고    scopus 로고
    • Presence of phosphorylated hepatocyte growth factor receptor/c-Met is associated with tumor progression and survival in patients with conventional renal cell carcinoma
    • Miyata Y., Kanetake H., Kanda S. Presence of phosphorylated hepatocyte growth factor receptor/c-Met is associated with tumor progression and survival in patients with conventional renal cell carcinoma. Clin Cancer Res 2006, 12:4876-4881.
    • (2006) Clin Cancer Res , vol.12 , pp. 4876-4881
    • Miyata, Y.1    Kanetake, H.2    Kanda, S.3
  • 126
    • 0032514365 scopus 로고    scopus 로고
    • Duplication and overexpression of the mutant allele of the MET proto-oncogene in multiple hereditary papillary renal cell tumours
    • Fischer J., Palmedo G., von Knobloch R., et al. Duplication and overexpression of the mutant allele of the MET proto-oncogene in multiple hereditary papillary renal cell tumours. Oncogene 1998, 17:733-739.
    • (1998) Oncogene , vol.17 , pp. 733-739
    • Fischer, J.1    Palmedo, G.2    von Knobloch, R.3
  • 127
    • 0032946543 scopus 로고    scopus 로고
    • Duplications of DNA sequences between loci D20S478 and D20S206 at 20q11.2 and between loci D20S902 and D20S480 at 20q13.2 mark new tumor genes in papillary renal cell carcinoma
    • Palmedo G., Fischer J., Kovacs G. Duplications of DNA sequences between loci D20S478 and D20S206 at 20q11.2 and between loci D20S902 and D20S480 at 20q13.2 mark new tumor genes in papillary renal cell carcinoma. Lab Invest 1999, 79:311-316.
    • (1999) Lab Invest , vol.79 , pp. 311-316
    • Palmedo, G.1    Fischer, J.2    Kovacs, G.3
  • 128
    • 0028897350 scopus 로고
    • Hereditary papillary renal cell carcinoma: clinical studies in 10 families
    • Zbar B., Glenn G., Lubensky I., et al. Hereditary papillary renal cell carcinoma: clinical studies in 10 families. J Urol 1995, 153:907-912.
    • (1995) J Urol , vol.153 , pp. 907-912
    • Zbar, B.1    Glenn, G.2    Lubensky, I.3
  • 129
    • 0032522486 scopus 로고    scopus 로고
    • Two North American families with hereditary papillary renal carcinoma and identical novel mutations in the MET proto-oncogene
    • Schmidt L., Junker K., Weirich G., et al. Two North American families with hereditary papillary renal carcinoma and identical novel mutations in the MET proto-oncogene. Cancer Res 1998, 58:1719-1722.
    • (1998) Cancer Res , vol.58 , pp. 1719-1722
    • Schmidt, L.1    Junker, K.2    Weirich, G.3
  • 130
    • 0033983875 scopus 로고    scopus 로고
    • Prevalence of microscopic tumors in normal appearing renal parenchyma of patients with hereditary papillary renal cancer
    • Ornstein D.K., Lubensky I.A., Venzon D., et al. Prevalence of microscopic tumors in normal appearing renal parenchyma of patients with hereditary papillary renal cancer. J Urol 2000, 163:431-433.
    • (2000) J Urol , vol.163 , pp. 431-433
    • Ornstein, D.K.1    Lubensky, I.A.2    Venzon, D.3
  • 131
    • 41449107739 scopus 로고    scopus 로고
    • C-Met inhibitors with novel binding mode show activity against several hereditary papillary renal cell carcinoma-related mutations
    • Bellon S.F., Kaplan-Lefko P., Yang Y., et al. c-Met inhibitors with novel binding mode show activity against several hereditary papillary renal cell carcinoma-related mutations. J Biol Chem 2008, 283:2675-2683.
    • (2008) J Biol Chem , vol.283 , pp. 2675-2683
    • Bellon, S.F.1    Kaplan-Lefko, P.2    Yang, Y.3
  • 132
    • 70849136880 scopus 로고    scopus 로고
    • Birt-Hogg-Dube syndrome: diagnosis and management
    • Menko F.H., van Steensel M.A., Giraud S., et al. Birt-Hogg-Dube syndrome: diagnosis and management. Lancet Oncol 2009, 10:1199-1206.
    • (2009) Lancet Oncol , vol.10 , pp. 1199-1206
    • Menko, F.H.1    van Steensel, M.A.2    Giraud, S.3
  • 133
    • 65949089138 scopus 로고    scopus 로고
    • Hereditary kidney cancer: unique opportunity for disease-based therapy
    • Linehan W.M., Pinto P.A., Bratslavsky G., et al. Hereditary kidney cancer: unique opportunity for disease-based therapy. Cancer 2009, 115:2252-2261.
    • (2009) Cancer , vol.115 , pp. 2252-2261
    • Linehan, W.M.1    Pinto, P.A.2    Bratslavsky, G.3
  • 134
    • 0036122090 scopus 로고    scopus 로고
    • Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dube syndrome
    • Zbar B., Alvord W.G., Glenn G., et al. Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dube syndrome. Cancer Epidemiol Biomarkers Prev 2002, 11:393-400.
    • (2002) Cancer Epidemiol Biomarkers Prev , vol.11 , pp. 393-400
    • Zbar, B.1    Alvord, W.G.2    Glenn, G.3
  • 135
    • 30744457565 scopus 로고    scopus 로고
    • Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer
    • Wei M.H., Toure O., Glenn G.M., et al. Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer. J Med Genet 2006, 43:18-27.
    • (2006) J Med Genet , vol.43 , pp. 18-27
    • Wei, M.H.1    Toure, O.2    Glenn, G.M.3
  • 136
    • 45249103326 scopus 로고    scopus 로고
    • BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dube syndrome: a new series of 50 families and a review of published reports
    • Toro J.R., Wei M.H., Glenn G.M., et al. BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dube syndrome: a new series of 50 families and a review of published reports. J Med Genet 2008, 45:321-331.
    • (2008) J Med Genet , vol.45 , pp. 321-331
    • Toro, J.R.1    Wei, M.H.2    Glenn, G.M.3
  • 137
    • 33947670382 scopus 로고    scopus 로고
    • Identification and characterization of Birt-Hogg-Dube associated renal carcinoma
    • Murakami T., Sano F., Huang Y., et al. Identification and characterization of Birt-Hogg-Dube associated renal carcinoma. J Pathol 2007, 211:524-531.
    • (2007) J Pathol , vol.211 , pp. 524-531
    • Murakami, T.1    Sano, F.2    Huang, Y.3
  • 138
    • 0036783597 scopus 로고    scopus 로고
    • Chromophobe renal cell carcinoma in a patient with the Birt-Hogg-Dube syndrome
    • Durrani O.H., Ng L., Bihrle W. Chromophobe renal cell carcinoma in a patient with the Birt-Hogg-Dube syndrome. J Urol 2002, 168:1484-1485.
    • (2002) J Urol , vol.168 , pp. 1484-1485
    • Durrani, O.H.1    Ng, L.2    Bihrle, W.3
  • 140
    • 66149118251 scopus 로고    scopus 로고
    • Birt-Hogg-Dube syndrome with clear-cell and oncocytic renal tumour and trichoblastoma associated with a novel FLCN mutation
    • Imada K., Dainichi T., Yokomizo A., et al. Birt-Hogg-Dube syndrome with clear-cell and oncocytic renal tumour and trichoblastoma associated with a novel FLCN mutation. Br J Dermatol 2009, 160:1350-1353.
    • (2009) Br J Dermatol , vol.160 , pp. 1350-1353
    • Imada, K.1    Dainichi, T.2    Yokomizo, A.3
  • 142
    • 33749005396 scopus 로고    scopus 로고
    • Cytologic and histologic findings in multiple renal hybrid oncocytic tumors in a patient with Birt-Hogg-Dube syndrome: a case report
    • Adley B.P., Schafernak K.T., Yeldandi A.V., et al. Cytologic and histologic findings in multiple renal hybrid oncocytic tumors in a patient with Birt-Hogg-Dube syndrome: a case report. Acta Cytol 2006, 50:584-588.
    • (2006) Acta Cytol , vol.50 , pp. 584-588
    • Adley, B.P.1    Schafernak, K.T.2    Yeldandi, A.V.3
  • 143
  • 144
    • 33845413247 scopus 로고    scopus 로고
    • Birt-Hogg-Dube syndrome: clinicopathologic findings and genetic alterations
    • Adley B.P., Smith N.D., Nayar R., et al. Birt-Hogg-Dube syndrome: clinicopathologic findings and genetic alterations. Arch Pathol Lab Med 2006, 130:1865-1870.
    • (2006) Arch Pathol Lab Med , vol.130 , pp. 1865-1870
    • Adley, B.P.1    Smith, N.D.2    Nayar, R.3
  • 145
    • 0035939821 scopus 로고    scopus 로고
    • Birt-Hogg-Dube syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2
    • Khoo S.K., Bradley M., Wong F.K., et al. Birt-Hogg-Dube syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2. Oncogene 2001, 20:5239-5242.
    • (2001) Oncogene , vol.20 , pp. 5239-5242
    • Khoo, S.K.1    Bradley, M.2    Wong, F.K.3
  • 146
    • 77949681085 scopus 로고    scopus 로고
    • Renal tumor suppressor function of the Birt-Hogg-Dube syndrome gene product folliculin
    • Hudon V., Sabourin S., Dydensborg A.B., et al. Renal tumor suppressor function of the Birt-Hogg-Dube syndrome gene product folliculin. J Med Genet 2009, 47(3):182-189.
    • (2009) J Med Genet , vol.47 , Issue.3 , pp. 182-189
    • Hudon, V.1    Sabourin, S.2    Dydensborg, A.B.3
  • 147
    • 0034821623 scopus 로고    scopus 로고
    • Birt-Hogg-Dube syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2
    • Schmidt L.S., Warren M.B., Nickerson M.L., et al. Birt-Hogg-Dube syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2. Am J Hum Genet 2001, 69:876-882.
    • (2001) Am J Hum Genet , vol.69 , pp. 876-882
    • Schmidt, L.S.1    Warren, M.B.2    Nickerson, M.L.3
  • 148
    • 3342906998 scopus 로고    scopus 로고
    • Expression of Birt-Hogg-Dube gene mRNA in normal and neoplastic human tissues
    • Warren M.B., Torres-Cabala C.A., Turner M.L., et al. Expression of Birt-Hogg-Dube gene mRNA in normal and neoplastic human tissues. Mod Pathol 2004, 17:998-1011.
    • (2004) Mod Pathol , vol.17 , pp. 998-1011
    • Warren, M.B.1    Torres-Cabala, C.A.2    Turner, M.L.3
  • 149
    • 0000939691 scopus 로고    scopus 로고
    • Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dube syndrome
    • Nickerson M.L., Warren M.B., Toro J.R., et al. Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dube syndrome. Cancer Cell 2002, 2:157-164.
    • (2002) Cancer Cell , vol.2 , pp. 157-164
    • Nickerson, M.L.1    Warren, M.B.2    Toro, J.R.3
  • 150
    • 21044457377 scopus 로고    scopus 로고
    • Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dube syndrome
    • Schmidt L.S., Nickerson M.L., Warren M.B., et al. Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dube syndrome. Am J Hum Genet 2005, 76:1023-1033.
    • (2005) Am J Hum Genet , vol.76 , pp. 1023-1033
    • Schmidt, L.S.1    Nickerson, M.L.2    Warren, M.B.3
  • 151
    • 33750293584 scopus 로고    scopus 로고
    • Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
    • Baba M., Hong S.B., Sharma N., et al. Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling. Proc Natl Acad Sci U S A 2006, 103:15552-15557.
    • (2006) Proc Natl Acad Sci U S A , vol.103 , pp. 15552-15557
    • Baba, M.1    Hong, S.B.2    Sharma, N.3
  • 152
    • 9744276042 scopus 로고    scopus 로고
    • Hereditary leiomyomatosis and renal cell cancer (HLRCC)
    • Kiuru M., Launonen V. Hereditary leiomyomatosis and renal cell cancer (HLRCC). Curr Mol Med 2004, 4:869-875.
    • (2004) Curr Mol Med , vol.4 , pp. 869-875
    • Kiuru, M.1    Launonen, V.2
  • 153
    • 33846816976 scopus 로고    scopus 로고
    • HIF and fumarate hydratase in renal cancer
    • Sudarshan S., Linehan W.M., Neckers L. HIF and fumarate hydratase in renal cancer. Br J Cancer 2007, 96:403-407.
    • (2007) Br J Cancer , vol.96 , pp. 403-407
    • Sudarshan, S.1    Linehan, W.M.2    Neckers, L.3
  • 154
    • 34748836454 scopus 로고    scopus 로고
    • The morphologic spectrum of kidney tumors in hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome
    • Merino M.J., Torres-Cabala C., Pinto P., et al. The morphologic spectrum of kidney tumors in hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome. Am J Surg Pathol 2007, 31:1578-1585.
    • (2007) Am J Surg Pathol , vol.31 , pp. 1578-1585
    • Merino, M.J.1    Torres-Cabala, C.2    Pinto, P.3
  • 155
    • 58049204264 scopus 로고    scopus 로고
    • Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer
    • Stewart L., Glenn G.M., Stratton P., et al. Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer. Arch Dermatol 2008, 144:1584-1592.
    • (2008) Arch Dermatol , vol.144 , pp. 1584-1592
    • Stewart, L.1    Glenn, G.M.2    Stratton, P.3
  • 156
    • 0037713729 scopus 로고    scopus 로고
    • Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America
    • Toro J.R., Nickerson M.L., Wei M.H., et al. Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America. Am J Hum Genet 2003, 73:95-106.
    • (2003) Am J Hum Genet , vol.73 , pp. 95-106
    • Toro, J.R.1    Nickerson, M.L.2    Wei, M.H.3
  • 157
    • 1542469716 scopus 로고    scopus 로고
    • Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors
    • Lehtonen R., Kiuru M., Vanharanta S., et al. Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors. Am J Pathol 2004, 164:17-22.
    • (2004) Am J Pathol , vol.164 , pp. 17-22
    • Lehtonen, R.1    Kiuru, M.2    Vanharanta, S.3
  • 158
    • 0035007528 scopus 로고    scopus 로고
    • Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43
    • Alam N.A., Bevan S., Churchman M., et al. Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43. Am J Hum Genet 2001, 68:1264-1269.
    • (2001) Am J Hum Genet , vol.68 , pp. 1264-1269
    • Alam, N.A.1    Bevan, S.2    Churchman, M.3
  • 159
    • 26944467604 scopus 로고    scopus 로고
    • Missense mutations in fumarate hydratase in multiple cutaneous and uterine leiomyomatosis and renal cell cancer
    • Alam N.A., Olpin S., Rowan A., et al. Missense mutations in fumarate hydratase in multiple cutaneous and uterine leiomyomatosis and renal cell cancer. J Mol Diagn 2005, 7:437-443.
    • (2005) J Mol Diagn , vol.7 , pp. 437-443
    • Alam, N.A.1    Olpin, S.2    Rowan, A.3
  • 160
    • 26444570010 scopus 로고    scopus 로고
    • Accumulation of Krebs cycle intermediates and over-expression of HIF1alpha in tumours which result from germline FH and SDH mutations
    • Pollard P.J., Briere J.J., Alam N.A., et al. Accumulation of Krebs cycle intermediates and over-expression of HIF1alpha in tumours which result from germline FH and SDH mutations. Hum Mol Genet 2005, 14:2231-2239.
    • (2005) Hum Mol Genet , vol.14 , pp. 2231-2239
    • Pollard, P.J.1    Briere, J.J.2    Alam, N.A.3
  • 161
    • 37849000143 scopus 로고    scopus 로고
    • Evidence for a founder effect of the germline fumarate hydratase gene mutation R58P causing hereditary leiomyomatosis and renal cell cancer (HLRCC)
    • Heinritz W., Paasch U., Sticherling M., et al. Evidence for a founder effect of the germline fumarate hydratase gene mutation R58P causing hereditary leiomyomatosis and renal cell cancer (HLRCC). Ann Hum Genet 2008, 72:35-40.
    • (2008) Ann Hum Genet , vol.72 , pp. 35-40
    • Heinritz, W.1    Paasch, U.2    Sticherling, M.3
  • 162
    • 18544365990 scopus 로고    scopus 로고
    • Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer
    • Tomlinson I.P., Alam N.A., Rowan A.J., et al. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer. Nat Genet 2002, 30:406-410.
    • (2002) Nat Genet , vol.30 , pp. 406-410
    • Tomlinson, I.P.1    Alam, N.A.2    Rowan, A.J.3
  • 163
    • 12444259659 scopus 로고    scopus 로고
    • Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency
    • Alam N.A., Rowan A.J., Wortham N.C., et al. Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency. Hum Mol Genet 2003, 12:1241-1252.
    • (2003) Hum Mol Genet , vol.12 , pp. 1241-1252
    • Alam, N.A.1    Rowan, A.J.2    Wortham, N.C.3
  • 164
    • 33749250917 scopus 로고    scopus 로고
    • Aberrant expression of apoptosis proteins and ultrastructural aberrations in uterine leiomyomas from patients with hereditary leiomyomatosis and renal cell carcinoma
    • Wortham N.C., Alam N.A., Barclay E., et al. Aberrant expression of apoptosis proteins and ultrastructural aberrations in uterine leiomyomas from patients with hereditary leiomyomatosis and renal cell carcinoma. Fertil Steril 2006, 86:961-971.
    • (2006) Fertil Steril , vol.86 , pp. 961-971
    • Wortham, N.C.1    Alam, N.A.2    Barclay, E.3
  • 165
    • 11144284227 scopus 로고    scopus 로고
    • Evidence of increased microvessel density and activation of the hypoxia pathway in tumours from the hereditary leiomyomatosis and renal cell cancer syndrome
    • Pollard P., Wortham N., Barclay E., et al. Evidence of increased microvessel density and activation of the hypoxia pathway in tumours from the hereditary leiomyomatosis and renal cell cancer syndrome. J Pathol 2005, 205:41-49.
    • (2005) J Pathol , vol.205 , pp. 41-49
    • Pollard, P.1    Wortham, N.2    Barclay, E.3
  • 166
    • 34147117259 scopus 로고    scopus 로고
    • Conventional renal cancer in a patient with fumarate hydratase mutation
    • Lehtonen H.J., Blanco I., Piulats J.M., et al. Conventional renal cancer in a patient with fumarate hydratase mutation. Hum Pathol 2007, 38:793-796.
    • (2007) Hum Pathol , vol.38 , pp. 793-796
    • Lehtonen, H.J.1    Blanco, I.2    Piulats, J.M.3
  • 167
    • 33749449442 scopus 로고    scopus 로고
    • Genetic basis of cancer of the kidney
    • Sudarshan S., Linehan W.M. Genetic basis of cancer of the kidney. Semin Oncol 2006, 33:544-551.
    • (2006) Semin Oncol , vol.33 , pp. 544-551
    • Sudarshan, S.1    Linehan, W.M.2
  • 168
    • 4644258333 scopus 로고    scopus 로고
    • Radio frequency ablation of small renal tumors: intermediate results
    • Hwang J.J., Walther M.M., Pautler S.E., et al. Radio frequency ablation of small renal tumors: intermediate results. J Urol 2004, 171:1814-1818.
    • (2004) J Urol , vol.171 , pp. 1814-1818
    • Hwang, J.J.1    Walther, M.M.2    Pautler, S.E.3
  • 169
    • 33747832155 scopus 로고    scopus 로고
    • Chronic kidney disease after nephrectomy in patients with renal cortical tumours: a retrospective cohort study
    • Huang W.C., Levey A.S., Serio A.M., et al. Chronic kidney disease after nephrectomy in patients with renal cortical tumours: a retrospective cohort study. Lancet Oncol 2006, 7:735-740.
    • (2006) Lancet Oncol , vol.7 , pp. 735-740
    • Huang, W.C.1    Levey, A.S.2    Serio, A.M.3
  • 170
    • 34547759799 scopus 로고    scopus 로고
    • Radiofrequency-assisted laparoscopic partial nephrectomy: clinical and histologic results
    • Coleman J., Singh A., Pinto P., et al. Radiofrequency-assisted laparoscopic partial nephrectomy: clinical and histologic results. J Endourol 2007, 21:600-605.
    • (2007) J Endourol , vol.21 , pp. 600-605
    • Coleman, J.1    Singh, A.2    Pinto, P.3
  • 171
    • 0037364268 scopus 로고    scopus 로고
    • Surgical management of multi-organ visceral tumors in patients with von Hippel-Lindau disease: a single stage approach
    • Hwang J.J., Uchio E.M., Pavlovich C.P., et al. Surgical management of multi-organ visceral tumors in patients with von Hippel-Lindau disease: a single stage approach. J Urol 2003, 169:895-898.
    • (2003) J Urol , vol.169 , pp. 895-898
    • Hwang, J.J.1    Uchio, E.M.2    Pavlovich, C.P.3
  • 172
    • 77956336099 scopus 로고    scopus 로고
    • Analysis of 3-cm tumor size threshold for intervention in patients with Birt-Hogg-Dubé and hereditary papillary renal cancer [abstract 980]
    • American Urological Association National Conference;
    • Grubb RL, Corbin NS, Choyke P, et al. Analysis of 3-cm tumor size threshold for intervention in patients with Birt-Hogg-Dubé and hereditary papillary renal cancer [abstract 980]. American Urological Association National Conference; 2005.
    • Grubb, R.L.1    Corbin, N.S.2    Choyke, P.3
  • 173
    • 36849078165 scopus 로고    scopus 로고
    • Salvage partial nephrectomy for hereditary renal cancer: feasibility and outcomes
    • Bratslavsky G., Liu J.J., Johnson A.D., et al. Salvage partial nephrectomy for hereditary renal cancer: feasibility and outcomes. J Urol 2008, 179:67-70.
    • (2008) J Urol , vol.179 , pp. 67-70
    • Bratslavsky, G.1    Liu, J.J.2    Johnson, A.D.3
  • 174
    • 0035131313 scopus 로고    scopus 로고
    • Parenchymal sparing surgery in patients with hereditary renal cell carcinoma: 10-year experience
    • Herring J.C., Enquist E.G., Chernoff A., et al. Parenchymal sparing surgery in patients with hereditary renal cell carcinoma: 10-year experience. J Urol 2001, 165:777-781.
    • (2001) J Urol , vol.165 , pp. 777-781
    • Herring, J.C.1    Enquist, E.G.2    Chernoff, A.3
  • 175
    • 65349190528 scopus 로고    scopus 로고
    • Renal carcinoma: minimally invasive surgery of the small renal mass
    • Pinto P.A. Renal carcinoma: minimally invasive surgery of the small renal mass. Urol Oncol 2009, 27:335-336.
    • (2009) Urol Oncol , vol.27 , pp. 335-336
    • Pinto, P.A.1
  • 176
    • 74549206666 scopus 로고    scopus 로고
    • Current status of nephron-sparing robotic partial nephrectomy
    • Hsieh T.C., Jarrett T.W., Pinto P.A. Current status of nephron-sparing robotic partial nephrectomy. Curr Opin Urol 2010, 20:65-69.
    • (2010) Curr Opin Urol , vol.20 , pp. 65-69
    • Hsieh, T.C.1    Jarrett, T.W.2    Pinto, P.A.3
  • 177
    • 33846107990 scopus 로고    scopus 로고
    • Partial nephrectomy achieves local tumor control and prevents chronic kidney disease
    • Russo P. Partial nephrectomy achieves local tumor control and prevents chronic kidney disease. Expert Rev Anticancer Ther 2006, 6:1745-1751.
    • (2006) Expert Rev Anticancer Ther , vol.6 , pp. 1745-1751
    • Russo, P.1
  • 178
    • 0033037128 scopus 로고    scopus 로고
    • Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutation
    • Webster A.R., Maher E.R., Moore A.T. Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutation. Arch Ophthalmol 1999, 117:371-378.
    • (1999) Arch Ophthalmol , vol.117 , pp. 371-378
    • Webster, A.R.1    Maher, E.R.2    Moore, A.T.3
  • 179
    • 51949103244 scopus 로고    scopus 로고
    • Neurologic manifestations of von Hippel-Lindau disease
    • Butman J.A., Linehan W.M., Lonser R.R. Neurologic manifestations of von Hippel-Lindau disease. JAMA 2008, 300:1334-1342.
    • (2008) JAMA , vol.300 , pp. 1334-1342
    • Butman, J.A.1    Linehan, W.M.2    Lonser, R.R.3
  • 180
    • 33747256320 scopus 로고    scopus 로고
    • Long-term natural history of hemangioblastomas in patients with von Hippel-Lindau disease: implications for treatment
    • Ammerman J.M., Lonser R.R., Dambrosia J., et al. Long-term natural history of hemangioblastomas in patients with von Hippel-Lindau disease: implications for treatment. J Neurosurg 2006, 105:248-255.
    • (2006) J Neurosurg , vol.105 , pp. 248-255
    • Ammerman, J.M.1    Lonser, R.R.2    Dambrosia, J.3
  • 181
    • 0036274254 scopus 로고    scopus 로고
    • Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: a role for laparoscopic and cortical-sparing surgery
    • [discussion: 688-9]
    • Baghai M., Thompson G.B., Young W.F., et al. Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: a role for laparoscopic and cortical-sparing surgery. Arch Surg 2002, 137:682-688. [discussion: 688-9].
    • (2002) Arch Surg , vol.137 , pp. 682-688
    • Baghai, M.1    Thompson, G.B.2    Young, W.F.3
  • 182
    • 22344431700 scopus 로고    scopus 로고
    • Partial adrenalectomy: the National Cancer Institute experience
    • Diner E.K., Franks M.E., Behari A., et al. Partial adrenalectomy: the National Cancer Institute experience. Urology 2005, 66:19-23.
    • (2005) Urology , vol.66 , pp. 19-23
    • Diner, E.K.1    Franks, M.E.2    Behari, A.3
  • 183
    • 0035853166 scopus 로고    scopus 로고
    • Inherited susceptibility to uterine leiomyomas and renal cell cancer
    • Launonen V., Vierimaa O., Kiuru M., et al. Inherited susceptibility to uterine leiomyomas and renal cell cancer. Proc Natl Acad Sci U S A 2001, 98:3387-3392.
    • (2001) Proc Natl Acad Sci U S A , vol.98 , pp. 3387-3392
    • Launonen, V.1    Vierimaa, O.2    Kiuru, M.3
  • 184
    • 34047103477 scopus 로고    scopus 로고
    • Hereditary leiomyomatosis and renal cell cancer: an unusual and aggressive form of hereditary renal carcinoma
    • Refae M.A., Wong N., Patenaude F., et al. Hereditary leiomyomatosis and renal cell cancer: an unusual and aggressive form of hereditary renal carcinoma. Nat Clin Pract Oncol 2007, 4:256-261.
    • (2007) Nat Clin Pract Oncol , vol.4 , pp. 256-261
    • Refae, M.A.1    Wong, N.2    Patenaude, F.3
  • 185
    • 34248336258 scopus 로고    scopus 로고
    • Hereditary leiomyomatosis and renal cell cancer: a syndrome associated with an aggressive form of inherited renal cancer
    • [discussion: 2079-80]
    • Grubb R.L., Franks M.E., Toro J., et al. Hereditary leiomyomatosis and renal cell cancer: a syndrome associated with an aggressive form of inherited renal cancer. J Urol 2007, 177:2074-2079. [discussion: 2079-80].
    • (2007) J Urol , vol.177 , pp. 2074-2079
    • Grubb, R.L.1    Franks, M.E.2    Toro, J.3
  • 186
    • 77954978039 scopus 로고    scopus 로고
    • Hereditary leiomyomatosis and renal cell carcinoma: very early diagnosis of renal cancer in a paediatric patient
    • Alrashdi I., Levine S., Paterson J., et al. Hereditary leiomyomatosis and renal cell carcinoma: very early diagnosis of renal cancer in a paediatric patient. Fam Cancer 2009, 9(2):239-243.
    • (2009) Fam Cancer , vol.9 , Issue.2 , pp. 239-243
    • Alrashdi, I.1    Levine, S.2    Paterson, J.3
  • 187
    • 33846998680 scopus 로고    scopus 로고
    • Mechanisms of disease: hereditary leiomyomatosis and renal cell cancer-a distinct form of hereditary kidney cancer
    • Sudarshan S., Pinto P.A., Neckers L., et al. Mechanisms of disease: hereditary leiomyomatosis and renal cell cancer-a distinct form of hereditary kidney cancer. Nat Clin Pract Urol 2007, 4:104-110.
    • (2007) Nat Clin Pract Urol , vol.4 , pp. 104-110
    • Sudarshan, S.1    Pinto, P.A.2    Neckers, L.3
  • 188
    • 61649115441 scopus 로고    scopus 로고
    • The clinical implications of the genetics of renal cell carcinoma
    • Rosner I., Bratslavsky G., Pinto P.A., et al. The clinical implications of the genetics of renal cell carcinoma. Urol Oncol 2009, 27:131-136.
    • (2009) Urol Oncol , vol.27 , pp. 131-136
    • Rosner, I.1    Bratslavsky, G.2    Pinto, P.A.3
  • 189
    • 34247344445 scopus 로고    scopus 로고
    • Biology and genetics of adult male germ cell tumors
    • Houldsworth J., Korkola J.E., Bosl G.J., et al. Biology and genetics of adult male germ cell tumors. J Clin Oncol 2006, 24:5512-5518.
    • (2006) J Clin Oncol , vol.24 , pp. 5512-5518
    • Houldsworth, J.1    Korkola, J.E.2    Bosl, G.J.3
  • 190
    • 41749092093 scopus 로고    scopus 로고
    • Testicular dysgenesis syndrome: mechanistic insights and potential new downstream effects
    • Sharpe R.M., Skakkebaek N.E. Testicular dysgenesis syndrome: mechanistic insights and potential new downstream effects. Fertil Steril 2008, 89:e33-e38.
    • (2008) Fertil Steril , vol.89
    • Sharpe, R.M.1    Skakkebaek, N.E.2
  • 191
    • 28144443108 scopus 로고    scopus 로고
    • The Y deletion gr/gr and susceptibility to testicular germ cell tumor
    • Nathanson K.L., Kanetsky P.A., Hawes R., et al. The Y deletion gr/gr and susceptibility to testicular germ cell tumor. Am J Hum Genet 2005, 77:1034-1043.
    • (2005) Am J Hum Genet , vol.77 , pp. 1034-1043
    • Nathanson, K.L.1    Kanetsky, P.A.2    Hawes, R.3
  • 192
    • 0029920620 scopus 로고    scopus 로고
    • Familial testicular cancer in Norway and southern Sweden
    • Heimdal K., Olsson H., Tretli S., et al. Familial testicular cancer in Norway and southern Sweden. Br J Cancer 1996, 73:964-969.
    • (1996) Br J Cancer , vol.73 , pp. 964-969
    • Heimdal, K.1    Olsson, H.2    Tretli, S.3
  • 193
    • 2642531956 scopus 로고    scopus 로고
    • Familial risk in testicular cancer as a clue to a heritable and environmental aetiology
    • Hemminki K., Li X. Familial risk in testicular cancer as a clue to a heritable and environmental aetiology. Br J Cancer 2004, 90:1765-1770.
    • (2004) Br J Cancer , vol.90 , pp. 1765-1770
    • Hemminki, K.1    Li, X.2
  • 194
    • 0029934098 scopus 로고    scopus 로고
    • Cancer risk in fathers and brothers of testicular cancer patients in Denmark. A population-based study
    • Westergaard T., Olsen J.H., Frisch M., et al. Cancer risk in fathers and brothers of testicular cancer patients in Denmark. A population-based study. Int J Cancer 1996, 66:627-631.
    • (1996) Int J Cancer , vol.66 , pp. 627-631
    • Westergaard, T.1    Olsen, J.H.2    Frisch, M.3
  • 195
    • 67649841601 scopus 로고    scopus 로고
    • A mini-review of familial ovarian germ cell tumors: an additional manifestation of the familial testicular germ cell tumor syndrome
    • Giambartolomei C., Mueller C.M., Greene M.H., et al. A mini-review of familial ovarian germ cell tumors: an additional manifestation of the familial testicular germ cell tumor syndrome. Cancer Epidemiol 2009, 33:31-36.
    • (2009) Cancer Epidemiol , vol.33 , pp. 31-36
    • Giambartolomei, C.1    Mueller, C.M.2    Greene, M.H.3
  • 196
    • 31544460668 scopus 로고    scopus 로고
    • Genome-wide linkage screen for testicular germ cell tumour susceptibility loci
    • Crockford G.P., Linger R., Hockley S., et al. Genome-wide linkage screen for testicular germ cell tumour susceptibility loci. Hum Mol Genet 2006, 15:443-451.
    • (2006) Hum Mol Genet , vol.15 , pp. 443-451
    • Crockford, G.P.1    Linger, R.2    Hockley, S.3
  • 197
    • 0015499388 scopus 로고
    • Possible carcinoma-in-situ of the testis
    • Skakkebaek N.E. Possible carcinoma-in-situ of the testis. Lancet 1972, 2:516-517.
    • (1972) Lancet , vol.2 , pp. 516-517
    • Skakkebaek, N.E.1
  • 198
    • 67649867946 scopus 로고    scopus 로고
    • Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer
    • Kanetsky P.A., Mitra N., Vardhanabhuti S., et al. Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer. Nat Genet 2009, 41:811-815.
    • (2009) Nat Genet , vol.41 , pp. 811-815
    • Kanetsky, P.A.1    Mitra, N.2    Vardhanabhuti, S.3
  • 199
    • 67649876131 scopus 로고    scopus 로고
    • A genome-wide association study of testicular germ cell tumor
    • Rapley E.A., Turnbull C., Al Olama A.A., et al. A genome-wide association study of testicular germ cell tumor. Nat Genet 2009, 41:807-810.
    • (2009) Nat Genet , vol.41 , pp. 807-810
    • Rapley, E.A.1    Turnbull, C.2    Al Olama, A.A.3
  • 200
    • 0028207444 scopus 로고
    • Expression of the c-kit protein product in carcinoma-in-situ and invasive testicular germ cell tumours
    • Rajpert-De Meyts E., Skakkebaek N.E. Expression of the c-kit protein product in carcinoma-in-situ and invasive testicular germ cell tumours. Int J Androl 1994, 17:85-92.
    • (1994) Int J Androl , vol.17 , pp. 85-92
    • Rajpert-De Meyts, E.1    Skakkebaek, N.E.2
  • 201
    • 0029962516 scopus 로고    scopus 로고
    • Prevalence of contralateral testicular intraepithelial neoplasia in patients with testicular germ cell neoplasms
    • Dieckmann K.P., Loy V. Prevalence of contralateral testicular intraepithelial neoplasia in patients with testicular germ cell neoplasms. J Clin Oncol 1996, 14:3126-3132.
    • (1996) J Clin Oncol , vol.14 , pp. 3126-3132
    • Dieckmann, K.P.1    Loy, V.2
  • 202
    • 0038613087 scopus 로고    scopus 로고
    • Mammalian Sprouty4 suppresses Ras-independent ERK activation by binding to Raf1
    • Sasaki A., Taketomi T., Kato R., et al. Mammalian Sprouty4 suppresses Ras-independent ERK activation by binding to Raf1. Nat Cell Biol 2003, 5:427-432.
    • (2003) Nat Cell Biol , vol.5 , pp. 427-432
    • Sasaki, A.1    Taketomi, T.2    Kato, R.3
  • 203
    • 0347256705 scopus 로고    scopus 로고
    • Response markers and the molecular mechanisms of action of Gleevec in gastrointestinal stromal tumors
    • Frolov A., Chahwan S., Ochs M., et al. Response markers and the molecular mechanisms of action of Gleevec in gastrointestinal stromal tumors. Mol Cancer Ther 2003, 2:699-709.
    • (2003) Mol Cancer Ther , vol.2 , pp. 699-709
    • Frolov, A.1    Chahwan, S.2    Ochs, M.3
  • 204
    • 0036163135 scopus 로고    scopus 로고
    • Testicular tumors in Carney's complex
    • Washecka R., Dresner M.I., Honda S.A. Testicular tumors in Carney's complex. J Urol 2002, 167:1299-1302.
    • (2002) J Urol , vol.167 , pp. 1299-1302
    • Washecka, R.1    Dresner, M.I.2    Honda, S.A.3
  • 205
    • 0019160686 scopus 로고
    • Large-cell calcifying Sertoli cell tumor of the testis
    • Proppe K.H., Scully R.E. Large-cell calcifying Sertoli cell tumor of the testis. Am J Clin Pathol 1980, 74:607-619.
    • (1980) Am J Clin Pathol , vol.74 , pp. 607-619
    • Proppe, K.H.1    Scully, R.E.2
  • 206
    • 0028215545 scopus 로고
    • Gonadal tumors in disorders of sexual differentiation
    • Gourlay W.A., Johnson H.W., Pantzar J.T., et al. Gonadal tumors in disorders of sexual differentiation. Urology 1994, 43:537-540.
    • (1994) Urology , vol.43 , pp. 537-540
    • Gourlay, W.A.1    Johnson, H.W.2    Pantzar, J.T.3
  • 207
    • 0000152018 scopus 로고
    • Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits; a syndrome of diagnostic significance
    • Jeghers H., Mc K.V., Katz K.H. Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits; a syndrome of diagnostic significance. N Engl J Med 1949, 241:1031-1036.
    • (1949) N Engl J Med , vol.241 , pp. 1031-1036
    • Jeghers, H.1    Mc, K.V.2    Katz, K.H.3
  • 208
    • 34447342867 scopus 로고    scopus 로고
    • Intratubular large cell hyalinizing Sertoli cell neoplasia of the testis: a report of 8 cases of a distinctive lesion of the Peutz-Jeghers syndrome
    • Ulbright T.M., Amin M.B., Young R.H. Intratubular large cell hyalinizing Sertoli cell neoplasia of the testis: a report of 8 cases of a distinctive lesion of the Peutz-Jeghers syndrome. Am J Surg Pathol 2007, 31:827-835.
    • (2007) Am J Surg Pathol , vol.31 , pp. 827-835
    • Ulbright, T.M.1    Amin, M.B.2    Young, R.H.3
  • 209
    • 33845360697 scopus 로고    scopus 로고
    • Carney complex: the first 20 years
    • Boikos S.A., Stratakis C.A. Carney complex: the first 20 years. Curr Opin Oncol 2007, 19:24-29.
    • (2007) Curr Opin Oncol , vol.19 , pp. 24-29
    • Boikos, S.A.1    Stratakis, C.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.