메뉴 건너뛰기




Volumn 126, Issue 3, 2006, Pages 676-679

Monoclonal origin of anatomically distinct basal cell carcinomas

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR;

EID: 32844461076     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/sj.jid.5700130     Document Type: Article
Times cited : (13)

References (17)
  • 1
    • 0026678490 scopus 로고
    • Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation
    • Allen RC, Zoghbi HY, Moseley AB, Rosenblatt HM, Belmont JW (1992) Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation. Am J Hum Genet 51:1229-39
    • (1992) Am J Hum Genet , vol.51 , pp. 1229-1239
    • Allen, R.C.1    Zoghbi, H.Y.2    Moseley, A.B.3    Rosenblatt, H.M.4    Belmont, J.W.5
  • 2
    • 32844460818 scopus 로고    scopus 로고
    • Aston JS, Beasley WR, Thorne HMC (eds) Philadelphia: Lippicott-Raven Publishers
    • Aston JS, Beasley WR, Thorne HMC (eds) (1997) Grabb and Smith's plastic surgery, 5th ed. Philadelphia: Lippicott-Raven Publishers, 112-7
    • (1997) Grabb and Smith's Plastic Surgery, 5th Ed. , pp. 112-117
  • 3
    • 0019201084 scopus 로고
    • Clonal origin and trisomy of chromosome 15 in murine B-cell malignancies
    • Fialkow PJ, Reddy AL, Bryant JI (1980) Clonal origin and trisomy of chromosome 15 in murine B-cell malignancies. Int J Cancer 26:603-8
    • (1980) Int J Cancer , vol.26 , pp. 603-608
    • Fialkow, P.J.1    Reddy, A.L.2    Bryant, J.I.3
  • 4
    • 0026627965 scopus 로고
    • Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9
    • Gailani MR, Bale SJ, Leffell DJ, DiCiovanna JJ, Peck GL, Poliak S et al. (1992) Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9. Cell 69:111-7
    • (1992) Cell , vol.69 , pp. 111-117
    • Gailani, M.R.1    Bale, S.J.2    Leffell, D.J.3    DiCiovanna, J.J.4    Peck, G.L.5    Poliak, S.6
  • 5
    • 0031932141 scopus 로고    scopus 로고
    • Clonality studies in acute myeloid leukemia
    • Gale RE, Linch DC (1998) Clonality studies in acute myeloid leukemia. Leukemia 12:117-20
    • (1998) Leukemia , vol.12 , pp. 117-120
    • Gale, R.E.1    Linch, D.C.2
  • 6
    • 0033140415 scopus 로고    scopus 로고
    • Allele loss on chromosome 9q22.2-22.3 in sporadic basal cell carcinoma in Chinese
    • He C, Zhang X, Wang Y, Sun K, Chen HD (1999) Allele loss on chromosome 9q22.2-22.3 in sporadic basal cell carcinoma in Chinese. Chin Med J 112:497-500
    • (1999) Chin Med J , vol.112 , pp. 497-500
    • He, C.1    Zhang, X.2    Wang, Y.3    Sun, K.4    Chen, H.D.5
  • 7
    • 11144353901 scopus 로고    scopus 로고
    • Loss of heterozygosity on chromosome 9q22.3 in microdissected basal cell carcinomas around the Semipalatinsk Nuclear Testing Site, Kazakhstan
    • Iwata K, Takamura N, Nakashima M, Alipov G, Mine M, Matsumoto N et al. (2004) Loss of heterozygosity on chromosome 9q22.3 in microdissected basal cell carcinomas around the Semipalatinsk Nuclear Testing Site, Kazakhstan. Hum Pathol 35:460-4
    • (2004) Hum Pathol , vol.35 , pp. 460-464
    • Iwata, K.1    Takamura, N.2    Nakashima, M.3    Alipov, G.4    Mine, M.5    Matsumoto, N.6
  • 8
    • 0031055867 scopus 로고    scopus 로고
    • The reciprocal translocation t(9;16)(q22;p13) is a primary chromosome abnormality in basal cell carcinoma
    • Jin Y, Merterns F, Persson B, Warloe T, Gullestad HP, Salemark L et al. (1997) The reciprocal translocation t(9;16)(q22;p13) is a primary chromosome abnormality in basal cell carcinoma. Cancer Res 57:404-6
    • (1997) Cancer Res , vol.57 , pp. 404-406
    • Jin, Y.1    Merterns, F.2    Persson, B.3    Warloe, T.4    Gullestad, H.P.5    Salemark, L.6
  • 9
    • 0001872496 scopus 로고
    • Glucose-6-phosphate dehydrogenase mosaicism: Utilization as a cell marker in the study of leiomyomas
    • Linder D, Gartler SM (1965) Glucose-6-phosphate dehydrogenase mosaicism: utilization as a cell marker in the study of leiomyomas. Science 150:67-9
    • (1965) Science , vol.150 , pp. 67-69
    • Linder, D.1    Gartler, S.M.2
  • 10
    • 0028268439 scopus 로고
    • Chromosome 9 allele loss occurs in both basal and squamous cell carcinomas of the skin
    • Quinn AG, Campbell C, Healy E, Rees JL (1994) Chromosome 9 allele loss occurs in both basal and squamous cell carcinomas of the skin. J Invest Dermatol 102:300-3
    • (1994) J Invest Dermatol , vol.102 , pp. 300-303
    • Quinn, A.G.1    Campbell, C.2    Healy, E.3    Rees, J.L.4
  • 11
    • 0036440689 scopus 로고    scopus 로고
    • Evidence that superficial basal cell carcinoma is monoclonal from analysis of the Ptch1 gene locus
    • Saldanha G, Shaw JA, Fletcher A (2002) Evidence that superficial basal cell carcinoma is monoclonal from analysis of the Ptch1 gene locus. Br J Dermatol 147:931-5
    • (2002) Br J Dermatol , vol.147 , pp. 931-935
    • Saldanha, G.1    Shaw, J.A.2    Fletcher, A.3
  • 12
    • 0033774239 scopus 로고    scopus 로고
    • High frequency of loss of heterozygosity on chromosome region 9p21-p22 but lack of p16INK4a/p19ARF mutations in Greek patients with basal cell carcinoma of the skin
    • Saridaki Z, Koumantaki E, Liloglou T, Sourvinos G, Papadopoulos O, Zoras O et al. (2000) High frequency of loss of heterozygosity on chromosome region 9p21-p22 but lack of p16INK4a/p19ARF mutations in Greek patients with basal cell carcinoma of the skin. J Invest Dermatol 115:719-25
    • (2000) J Invest Dermatol , vol.115 , pp. 719-725
    • Saridaki, Z.1    Koumantaki, E.2    Liloglou, T.3    Sourvinos, G.4    Papadopoulos, O.5    Zoras, O.6
  • 13
    • 0033055954 scopus 로고    scopus 로고
    • Detection of loss of heterozygosity on chromosome 9q22.3 in microdissected sporadic basal cell carcinoma
    • Shen T, Park WS, Boni R, Saini N, Pham T, Lash AE et al. (1999) Detection of loss of heterozygosity on chromosome 9q22.3 in microdissected sporadic basal cell carcinoma. Hum Pathol 30:247-84
    • (1999) Hum Pathol , vol.30 , pp. 247-284
    • Shen, T.1    Park, W.S.2    Boni, R.3    Saini, N.4    Pham, T.5    Lash, A.E.6
  • 16
    • 0031909826 scopus 로고    scopus 로고
    • Patterns of X chromosome inactivation in sporadic basal cell carcinoma: Evidence for monoclonality
    • Walsh DC, Peacocke M, Harrington A, James WD, Tsou HC (1998) Patterns of X chromosome inactivation in sporadic basal cell carcinoma: evidence for monoclonality. J Am Acad Dermatol 38:49-55
    • (1998) J Am Acad Dermatol , vol.38 , pp. 49-55
    • Walsh, D.C.1    Peacocke, M.2    Harrington, A.3    James, W.D.4    Tsou, H.C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.