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Volumn 58, Issue 18, 1998, Pages 4155-4159

Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; RNA;

EID: 0032530827     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (44)

References (15)
  • 1
    • 0028706337 scopus 로고
    • A developmental context for multiple genetic alterations in Wilms' tumor
    • Feinberg, A. P. A developmental context for multiple genetic alterations in Wilms' tumor. J. Cell Sci., 18: 7-12, 1994.
    • (1994) J. Cell Sci. , vol.18 , pp. 7-12
    • Feinberg, A.P.1
  • 2
    • 0027231784 scopus 로고
    • Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from human chromosome 11
    • Washington DC
    • Koi. M., Johnson, L. A., Kalikin, L. M., Little, P. F. R., Nakamura, Y., and Feinberg, A. P. Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from human chromosome 11. Science (Washington DC), 260; 361-364, 1993.
    • (1993) Science , vol.260 , pp. 361-364
    • Koi, M.1    Johnson, L.A.2    Kalikin, L.M.3    Little, P.F.R.4    Nakamura, Y.5    Feinberg, A.P.6
  • 3
    • 0031573423 scopus 로고    scopus 로고
    • A 2.5 Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes
    • Hu, R-J. R, Lee, M. P., Conners, T. D., Johnson, L. A., Su, K., Burn, T. C., Landes, G. M., and Feinberg, A. P. A 2.5 Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes. Genomics, 46: 9-17, 1997.
    • (1997) Genomics , vol.46 , pp. 9-17
    • Hu, R.-J.R.1    Lee, M.P.2    Conners, T.D.3    Johnson, L.A.4    Su, K.5    Burn, T.C.6    Landes, G.M.7    Feinberg, A.P.8
  • 6
    • 0031046285 scopus 로고    scopus 로고
    • VLQT1 shows tissue-specific imprinting and is physically disrupted by Beckwith-Wiedemann syndrome chromosomal rearrangements
    • VLQT1 shows tissue-specific imprinting and is physically disrupted by Beckwith-Wiedemann syndrome chromosomal rearrangements. Nat. Genet., 15: 181-185, 1997.
    • (1997) Nat. Genet. , vol.15 , pp. 181-185
    • Lee, M.P.1    Hu, R.-J.2    Johnson, L.A.3    Feinberg, A.P.4
  • 7
    • 9844265406 scopus 로고    scopus 로고
    • The IPL gene on chromosome 11p15.5 is imprinted in human and mice and is similar to TDAG51, implicated in Fas expression and apoptosis
    • Qian, N., Frank, D., O'Keefe, D., Dao, D., Zhao, D., Yuan, L., Wang, Q., Keating, M., Walsh, C., and Tycko, B. The IPL gene on chromosome 11p15.5 is imprinted in human and mice and is similar to TDAG51, implicated in Fas expression and apoptosis. Hum. Mol. Genet., 6: 2021-2029, 1997.
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 2021-2029
    • Qian, N.1    Frank, D.2    O'Keefe, D.3    Dao, D.4    Zhao, D.5    Yuan, L.6    Wang, Q.7    Keating, M.8    Walsh, C.9    Tycko, B.10
  • 8
    • 0032032697 scopus 로고    scopus 로고
    • Genomic imprinting of a human apoptosis gene homologue, TSSC3
    • Lee, M. P., and Feinberg, A. P. Genomic imprinting of a human apoptosis gene homologue, TSSC3. Cancer Res., 58: 1052-1056, 1998.
    • (1998) Cancer Res. , vol.58 , pp. 1052-1056
    • Lee, M.P.1    Feinberg, A.P.2
  • 10
    • 0028356544 scopus 로고
    • Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour
    • Steenman, M. J. C., Rainier, S., Dobry, C., Grundy, P., Horon, I., and Feinberg, A. P. Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour. Nat. Genet., 7: 433-439, 1994.
    • (1994) Nat. Genet. , vol.7 , pp. 433-439
    • Steenman, M.J.C.1    Rainier, S.2    Dobry, C.3    Grundy, P.4    Horon, I.5    Feinberg, A.P.6
  • 11
    • 0020793569 scopus 로고
    • A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
    • Feinberg, A. P., and Vogelstein, B. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem., 132: 6-13, 1983.
    • (1983) Anal. Biochem. , vol.132 , pp. 6-13
    • Feinberg, A.P.1    Vogelstein, B.2
  • 13
    • 0031924628 scopus 로고    scopus 로고
    • IMPT1, an imprinted gene similar to polyspecific transporter and multidrug resistance genes
    • Dao, D., Frank, D., Qian, N., O'Keefe, D., Vosatka, R. J., Walsh, C. P., and Tycko, B. IMPT1, an imprinted gene similar to polyspecific transporter and multidrug resistance genes. Hum. Mol. Genet., 7: 597-608, 1998.
    • (1998) Hum. Mol. Genet. , vol.7 , pp. 597-608
    • Dao, D.1    Frank, D.2    Qian, N.3    O'Keefe, D.4    Vosatka, R.J.5    Walsh, C.P.6    Tycko, B.7
  • 14
    • 0030854026 scopus 로고    scopus 로고
    • Aberrant splicing but not mutations of TSG101 in human breast cancer
    • Lee, M. P., and Feinberg, A. P. Aberrant splicing but not mutations of TSG101 in human breast cancer. Cancer Res., 57: 3131-3134, 1997.
    • (1997) Cancer Res. , vol.57 , pp. 3131-3134
    • Lee, M.P.1    Feinberg, A.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.