메뉴 건너뛰기




Volumn 57, Issue 20, 1997, Pages 4455-4459

Coding region of NKX3.1, a prostate-specific homeobox gene on 8p21, is not mutated in human prostate cancers

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 8P; GENE LOCUS; GENE MUTATION; GENE REPRESSION; HOMEOBOX; HUMAN; HUMAN TISSUE; PRIORITY JOURNAL; PROSTATE CANCER; TUMOR SUPPRESSOR GENE;

EID: 0030822020     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (131)

References (17)
  • 2
    • 0028059899 scopus 로고
    • Deletion mapping of chromosome 8p in prostate cancer by fluorescence in situ hybridization
    • Matsuyama, H., Pan, Y., Skoog, L., and Tribukait, B. Deletion mapping of chromosome 8p in prostate cancer by fluorescence in situ hybridization. Oncogene, 9: 3071-3076, 1994.
    • (1994) Oncogene , vol.9 , pp. 3071-3076
    • Matsuyama, H.1    Pan, Y.2    Skoog, L.3    Tribukait, B.4
  • 3
    • 0028354948 scopus 로고
    • A 3-Mb physical map of the chromosome region 8p21.3-p22, including a 600-kb region commonly deleted in human hepatocellular carcinoma, colorectal cancer, and non-small cell lung cancer
    • Fujiwara, Y., Ohata, H., Emi, M., Okui, K., Koyama, K., Tsuchirya, E., Nakajima, T., Monden, M., Mori, T., Kurimasa, A., Oshimura, M., and Nakamura, Y. A 3-Mb physical map of the chromosome region 8p21.3-p22, including a 600-kb region commonly deleted in human hepatocellular carcinoma, colorectal cancer, and non-small cell lung cancer. Genes Chromosomes Cancer, 10: 7-14, 1994.
    • (1994) Genes Chromosomes Cancer , vol.10 , pp. 7-14
    • Fujiwara, Y.1    Ohata, H.2    Emi, M.3    Okui, K.4    Koyama, K.5    Tsuchirya, E.6    Nakajima, T.7    Monden, M.8    Mori, T.9    Kurimasa, A.10    Oshimura, M.11    Nakamura, Y.12
  • 5
    • 0028862492 scopus 로고
    • Homozygous deletions at 8p22 and 8p21 in prostate cancer implicate these regions as the sites for candidate tumor suppressor genes
    • Kagan, J., Stein, J., Babaian, R. J., Joe, Y. S., Pisters, L. L., Glassman, A. B., von Eschenbach, A. C., and Troncoso, P. Homozygous deletions at 8p22 and 8p21 in prostate cancer implicate these regions as the sites for candidate tumor suppressor genes. Oncogene, 11: 2121-2126, 1995.
    • (1995) Oncogene , vol.11 , pp. 2121-2126
    • Kagan, J.1    Stein, J.2    Babaian, R.J.3    Joe, Y.S.4    Pisters, L.L.5    Glassman, A.B.6    Von Eschenbach, A.C.7    Troncoso, P.8
  • 6
    • 0029007714 scopus 로고
    • Localization of a tumor suppressor gene associated with progression of human prostate cancer within a 1.2 Mb region of 8p22-p21.3
    • Suzuki, H., Emi, M., Komiya, A., Fujiwara, Y., Yatani, R., Nakamura, Y., and Shimazaki, J. Localization of a tumor suppressor gene associated with progression of human prostate cancer within a 1.2 Mb region of 8p22-p21.3. Genes Chromosomes Cancer, 13: 168-174, 1995.
    • (1995) Genes Chromosomes Cancer , vol.13 , pp. 168-174
    • Suzuki, H.1    Emi, M.2    Komiya, A.3    Fujiwara, Y.4    Yatani, R.5    Nakamura, Y.6    Shimazaki, J.7
  • 8
    • 0028340435 scopus 로고
    • Loss of chromosome arm 8p loci in prostate cancer: Mapping by quantitative allelic imbalance
    • MacGrogen, D., Levy, A., Bostwick, D., Wagner, M., Wells, D., and Bookstein, R. Loss of chromosome arm 8p loci in prostate cancer: mapping by quantitative allelic imbalance. Genes Chromosomes Cancer. 10: 151-159, 1994.
    • (1994) Genes Chromosomes Cancer , vol.10 , pp. 151-159
    • MacGrogen, D.1    Levy, A.2    Bostwick, D.3    Wagner, M.4    Wells, D.5    Bookstein, R.6
  • 9
    • 0029768633 scopus 로고    scopus 로고
    • Prostate-specific and androgen-dependent expression of a novel homeobox gene
    • Bieberich, C. J., Fujita, K., He, W. W., and Jay, G. Prostate-specific and androgen-dependent expression of a novel homeobox gene. J. Biol. Chem., 271: 31779-31782, 1996.
    • (1996) J. Biol. Chem. , vol.271 , pp. 31779-31782
    • Bieberich, C.J.1    Fujita, K.2    He, W.W.3    Jay, G.4
  • 13
    • 0023867576 scopus 로고
    • Sensitive high-resolution chromatin and chromosome mapping in situ: Presence and orientation of two closely integrated copies of EBV in a lymphoma line
    • Lawrence, J. B., Villnavae, C. A., and Singer, R. A. Sensitive high-resolution chromatin and chromosome mapping in situ: presence and orientation of two closely integrated copies of EBV in a lymphoma line. Cell, 52: 51-61, 1988.
    • (1988) Cell , vol.52 , pp. 51-61
    • Lawrence, J.B.1    Villnavae, C.A.2    Singer, R.A.3
  • 14
    • 0026303395 scopus 로고
    • Fluorescent detection of nuclear RNA and DNA: Implications for genome organization
    • Johnson, C. V., Singer, R. H., and Lawrence, J. B. Fluorescent detection of nuclear RNA and DNA: implications for genome organization. Methods Cell Biol., 35: 73-99, 1991.
    • (1991) Methods Cell Biol. , vol.35 , pp. 73-99
    • Johnson, C.V.1    Singer, R.H.2    Lawrence, J.B.3
  • 15
    • 44949283339 scopus 로고
    • A simple, rapid technique for precise mapping of multiple sequences in two colors using a single optical fiber set
    • Johnson, C. V., McNeil, J. A., Carter, K. C., and Lawrence, J. B. A simple, rapid technique for precise mapping of multiple sequences in two colors using a single optical fiber set. Genet. Anal. Tech. Appl., 8: 75-76, 1991.
    • (1991) Genet. Anal. Tech. Appl. , vol.8 , pp. 75-76
    • Johnson, C.V.1    McNeil, J.A.2    Carter, K.C.3    Lawrence, J.B.4
  • 16
    • 0022332415 scopus 로고
    • ISCN (1985): An international system for human cytogenetic nomenclature
    • March of Dimes Birth Defects Foundation
    • ISCN (1985): an international system for human cytogenetic nomenclature. In: D. G. Harnden and H. P. Klinger (eds.), Birth Defects: Original Article Series, Vol. 21. March of Dimes Birth Defects Foundation, 1985.
    • (1985) Birth Defects: Original Article Series , vol.21
    • Harnden, D.G.1    Klinger, H.P.2
  • 17
    • 0027456784 scopus 로고
    • A primary genetic linkage map of 14 polymorphic loci for the short arm of human chromosome 8
    • Emi, M., Fujiwara, Y., and Nakamura, Y. A primary genetic linkage map of 14 polymorphic loci for the short arm of human chromosome 8. Genomics, 15: 530-534, 1993.
    • (1993) Genomics , vol.15 , pp. 530-534
    • Emi, M.1    Fujiwara, Y.2    Nakamura, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.