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Volumn 47, Issue 2, 1998, Pages 230-237

Identification of a third EXT-like gene (EXTL3) belonging to the EXT gene family

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BREAST CANCER; CANCER GENETICS; CHROMOSOME 8P; EXOSTOSIS; MULTIGENE FAMILY; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; TUMOR SUPPRESSOR GENE;

EID: 0032518417     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1997.5101     Document Type: Article
Times cited : (117)

References (42)
  • 2
    • 0029889221 scopus 로고    scopus 로고
    • Local alignment statistics
    • Altschul S. F., Gish W. Local alignment statistics. Methods Enzymol. 266:1996;460-480.
    • (1996) Methods Enzymol. , vol.266 , pp. 460-480
    • Altschul, S.F.1    Gish, W.2
  • 5
    • 0027422876 scopus 로고
    • Biological and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions
    • Bridge J. A., Parmajit S. B., Anderson J. R., Neff J. R. Biological and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions. Cancer Genet. Cytogenet. 69:1993;79-90.
    • (1993) Cancer Genet. Cytogenet. , vol.69 , pp. 79-90
    • Bridge, J.A.1    Parmajit, S.B.2    Anderson, J.R.3    Neff, J.R.4
  • 8
    • 0027363063 scopus 로고
    • Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse
    • Dietrich W. F., Lander E. S., Smith J. S., Moser A. R., Gould K. A., Luongo C., Borenstein N., Dove W. Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse. Cell. 75:1993;631-639.
    • (1993) Cell , vol.75 , pp. 631-639
    • Dietrich, W.F.1    Lander, E.S.2    Smith, J.S.3    Moser, A.R.4    Gould, K.A.5    Luongo, C.6    Borenstein, N.7    Dove, W.8
  • 9
    • 0029259085 scopus 로고
    • Maximum discrimination hidden Markov models of sequence consensus
    • Eddy S. R., Mitchison G., Durbin R. Maximum discrimination hidden Markov models of sequence consensus. J. Comput. Biol. 2:1995;9-23.
    • (1995) J. Comput. Biol. , vol.2 , pp. 9-23
    • Eddy, S.R.1    Mitchison, G.2    Durbin, R.3
  • 10
    • 0027231756 scopus 로고
    • Cervical cord compression in hereditary multiple exostoses
    • Eder H. G., Oberbauer R. W., Ranner G. Cervical cord compression in hereditary multiple exostoses. J. Neurosurg. Sci. 37:1993;53-56.
    • (1993) J. Neurosurg. Sci. , vol.37 , pp. 53-56
    • Eder, H.G.1    Oberbauer, R.W.2    Ranner, G.3
  • 11
    • 0030218799 scopus 로고    scopus 로고
    • Finding genes by computer: The state of the art
    • Fickett J. W. Finding genes by computer: The state of the art. Trends Genet. 12:1996;316-320.
    • (1996) Trends Genet. , vol.12 , pp. 316-320
    • Fickett, J.W.1
  • 12
    • 0028211586 scopus 로고
    • Deletion of chromosome arm 1p in a Merkel cell carcinoma (MCC)
    • Gibas Z., Weil S., Chen S. T., McCue P. A. Deletion of chromosome arm 1p in a Merkel cell carcinoma (MCC). Genes Chromosomes Cancer. 9:1994;216-220.
    • (1994) Genes Chromosomes Cancer , vol.9 , pp. 216-220
    • Gibas, Z.1    Weil, S.2    Chen, S.T.3    McCue, P.A.4
  • 13
    • 0028917663 scopus 로고
    • Hereditary multiple exostosis and chondrosarcoma: Linkage to chromosome 11 and loss of heterozygosity for EXT-linked markers on chromosome 11 and 8
    • Hecht J. T., Hogue D., Strong L. C., Hansen M. F., Blanton S. H., Wagner M. Hereditary multiple exostosis and chondrosarcoma: Linkage to chromosome 11 and loss of heterozygosity for EXT-linked markers on chromosome 11 and 8. Am. J. Hum. Genet. 56:1995;1125-1131.
    • (1995) Am. J. Hum. Genet. , vol.56 , pp. 1125-1131
    • Hecht, J.T.1    Hogue, D.2    Strong, L.C.3    Hansen, M.F.4    Blanton, S.H.5    Wagner, M.6
  • 15
    • 0025810316 scopus 로고
    • Hereditary multiple exostoses
    • Hennekam R. C. M. Hereditary multiple exostoses. J. Med. Genet. 28:1991;262-266.
    • (1991) J. Med. Genet. , vol.28 , pp. 262-266
    • Hennekam, R.C.M.1
  • 20
    • 0025792297 scopus 로고
    • Structural features in eukaryotic mRNAs that modulate the initiation of translation
    • Kozak M. Structural features in eukaryotic mRNAs that modulate the initiation of translation. J. Biol. Chem. 266:1991;19867-19870.
    • (1991) J. Biol. Chem. , vol.266 , pp. 19867-19870
    • Kozak, M.1
  • 21
    • 0002345846 scopus 로고
    • Genetic and physical mapping
    • Cold Spring Harbor: Cold Spring Harbor Laboratory Press. p. 39-81
    • Lehrach H. Genetic and physical mapping. Genome Analysis. 1990;Cold Spring Harbor Laboratory Press, Cold Spring Harbor. p. 39-81.
    • (1990) Genome Analysis
    • Lehrach, H.1
  • 24
    • 0028046406 scopus 로고
    • Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors
    • Mathew H., Murty V. V. V. S., Bosl G. J., Chaganti R. S. K. Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors. Cancer Res. 54:1994;6265-6269.
    • (1994) Cancer Res. , vol.54 , pp. 6265-6269
    • Mathew, H.1    Murty, V.V.V.S.2    Bosl, G.J.3    Chaganti, R.S.K.4
  • 26
  • 27
    • 0028916693 scopus 로고
    • Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosome 8 and 11
    • Raskind W. H., Conrad E. U., Chansky H., Matsushita M. Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosome 8 and 11. Am. J. Hum. Genet. 56:1995;1132-1139.
    • (1995) Am. J. Hum. Genet. , vol.56 , pp. 1132-1139
    • Raskind, W.H.1    Conrad, E.U.2    Chansky, H.3    Matsushita, M.4
  • 28
  • 29
    • 0031045260 scopus 로고    scopus 로고
    • Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: Linkage in German breast cancer families
    • Seitz S., Rohde K., Bender E., Nothnagel A., Kölbe K., Schlag P. M., Scherneck S. Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: Linkage in German breast cancer families. Oncogene. 14:1997;741-743.
    • (1997) Oncogene , vol.14 , pp. 741-743
    • Seitz, S.1    Rohde, K.2    Bender, E.3    Nothnagel, A.4    Kölbe, K.5    Schlag, P.M.6    Scherneck, S.7
  • 31
    • 0001524698 scopus 로고
    • Hereditary multiple exostoses
    • Solomon L. Hereditary multiple exostoses. Am. J. Hum. Genet. 16:1964;351-363.
    • (1964) Am. J. Hum. Genet. , vol.16 , pp. 351-363
    • Solomon, L.1
  • 33
    • 0027853058 scopus 로고
    • Recurrent deletions of specific chromosomal sites in 1p, 3p, 6q and 9p in human malignant mesothelioma
    • Taguchi T., Jhanwar S. C., Siegfried J. M., Keller S. M., Testa J. R. Recurrent deletions of specific chromosomal sites in 1p, 3p, 6q and 9p in human malignant mesothelioma. Cancer Res. 53:1993;4349-4355.
    • (1993) Cancer Res. , vol.53 , pp. 4349-4355
    • Taguchi, T.1    Jhanwar, S.C.2    Siegfried, J.M.3    Keller, S.M.4    Testa, J.R.5
  • 34
    • 0027484115 scopus 로고
    • High-resolution fluorescence mapping of 46 markers on the short arm of chromosome 1
    • Van Roy N., Laureys G., Versteeg R., Opdenakker G., Speleman F. High-resolution fluorescence mapping of 46 markers on the short arm of chromosome 1. Genomics. 18:1993;71-78.
    • (1993) Genomics , vol.18 , pp. 71-78
    • Van Roy, N.1    Laureys, G.2    Versteeg, R.3    Opdenakker, G.4    Speleman, F.5
  • 36
    • 0031051305 scopus 로고    scopus 로고
    • Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family
    • Wise C. A., Clines G. A., Massa H., Trask B. J., Lovett M. Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family. Genome Res. 7:1997;10-16.
    • (1997) Genome Res. , vol.7 , pp. 10-16
    • Wise, C.A.1    Clines, G.A.2    Massa, H.3    Trask, B.J.4    Lovett, M.5
  • 42
    • 0028111570 scopus 로고
    • Frequent genetic alterations at distal regions of chromosome 1p in human hepatocellular carcinomas
    • Yeh S. H., Chen P. J., Chen H. L., Lai M. Y., Wang C. C., Chen D. S. Frequent genetic alterations at distal regions of chromosome 1p in human hepatocellular carcinomas. Cancer Res. 54:1994;4188-4192.
    • (1994) Cancer Res. , vol.54 , pp. 4188-4192
    • Yeh, S.H.1    Chen, P.J.2    Chen, H.L.3    Lai, M.Y.4    Wang, C.C.5    Chen, D.S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.