메뉴 건너뛰기




Volumn 5, Issue 6, 1997, Pages 382-389

Identification and characterization of a novel member of the EXT gene family, EXTL2

Author keywords

Chromosome 1p11 p12; Chromosome 2q24 q31; EXT; EXT like gene 2; EXTL2; EXTL2P; Multiple exostoses

Indexed keywords

PROTEIN;

EID: 13144275255     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000484796     Document Type: Article
Times cited : (89)

References (40)
  • 1
    • 0001524698 scopus 로고
    • Hereditary multiple exostosis
    • Solomon L: Hereditary multiple exostosis. Am J Hum Genet 1964;16:351-363.
    • (1964) Am J Hum Genet , vol.16 , pp. 351-363
    • Solomon, L.1
  • 2
    • 0025810316 scopus 로고
    • Hereditary multiple exostoses
    • Hennekam RCM: Hereditary multiple exostoses. J Med Genet 1991;28:262-266.
    • (1991) J Med Genet , vol.28 , pp. 262-266
    • Hennekam, R.C.M.1
  • 13
    • 0028916693 scopus 로고
    • Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11
    • Raskind WH, Conrad EU, Chansky H, Matsushita M: Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11. Am J Hum Genet 1995;56:1132-1139.
    • (1995) Am J Hum Genet , vol.56 , pp. 1132-1139
    • Raskind, W.H.1    Conrad, E.U.2    Chansky, H.3    Matsushita, M.4
  • 14
    • 0031051305 scopus 로고    scopus 로고
    • Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family
    • Wise CA, Clines GA, Massa H, Trask BJ, Lovett M: Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family. Genome Res 1997;7:10-1 6.
    • (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
  • 15
    • 0029889221 scopus 로고    scopus 로고
    • Local alignment statistics
    • Altschul SF , Gish W: Local alignment statistics. Methods Enzymol 1996;266:460-480.
    • (1996) Methods Enzymol , vol.266 , pp. 460-480
    • Altschul, S.F.1    Gish, W.2
  • 16
    • 0029259085 scopus 로고
    • Maximum discrimination hidden Markov models of sequence consensus
    • Eddy SR, Mitchison G, Durbin R: Maximum discrimination hidden Markov models of sequence consensus. J Comput Biol 1995;2:9-23.
    • (1995) J Comput Biol , vol.2 , pp. 9-23
    • Eddy, S.R.1    Mitchison, G.2    Durbin, R.3
  • 18
    • 0028266032 scopus 로고
    • The human vigilin gene: Identification, chromosomal localization and expression pattern
    • Plenz G, Kügler S, Schnittger S, Rieder H, Fonatsch C, Müller PK: The human vigilin gene: Identification, chromosomal localization and expression pattern. Hum Genet 1994;93:575-582.
    • (1994) Hum Genet , vol.93 , pp. 575-582
    • Plenz, G.1    Kügler, S.2    Schnittger, S.3    Rieder, H.4    Fonatsch, C.5    Müller, P.K.6
  • 22
    • 0002345846 scopus 로고
    • Genetic and physical mapping
    • Davies KE, Tilghman SM (eds): Cold Spring Harbor Labaratory Press
    • Lehrach H: Genetic and physical mapping; in Davies KE, Tilghman SM (eds): Genome analysis Cold Spring Harbor, Cold Spring Harbor Labaratory Press, 1990, vol 1, pp 39-81.
    • (1990) Genome Analysis Cold Spring Harbor , vol.1 , pp. 39-81
    • Lehrach, H.1
  • 23
    • 0023651307 scopus 로고
    • RNA splicing junctions of different classes of eukaryotes: Sequence statistics and functional implications in expression
    • Shapiro MB, Senapathy P: RNA splicing junctions of different classes of eukaryotes: Sequence statistics and functional implications in expression. Nucleic Acids Res 1987;15:7155-7174.
    • (1987) Nucleic Acids Res , vol.15 , pp. 7155-7174
    • Shapiro, M.B.1    Senapathy, P.2
  • 24
    • 0028917663 scopus 로고
    • Hereditary multiple exostosis and chondrosarcoma: Linkage to chromosome 11 and loss of heterozygosity for EXT-linked markers on chromosomes 11 and 8
    • Hecht JT, Hogue D, Strong LC, Hansen MF, Blanton SH, Wagner M: Hereditary multiple exostosis and chondrosarcoma: Linkage to chromosome 11 and loss of heterozygosity for EXT-linked markers on chromosomes 11 and 8. Am J Hum Genet 1995;56:1125-1131.
    • (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
  • 26
    • 0027422876 scopus 로고
    • Biologic and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions
    • Bridge JA, Paramjit SB, Anderson JR, Neff JR: Biologic and clinical significance of cytogenetic and molecular cytogenetic abnormalities in benign and malignant cartilaginous lesions. Cancer Genet Cytogenet 1993;69:79-90.
    • (1993) Cancer Genet Cytogenet , vol.69 , pp. 79-90
    • Bridge, J.A.1    Paramjit, S.B.2    Anderson, J.R.3    Neff, J.R.4
  • 29
    • 0023810844 scopus 로고
    • Chromosome 1 abnormalities in cervical carcinoma
    • Sreekantaiah C, Bhargava KM, Shetty JN: Chromosome 1 abnormalities in cervical carcinoma. Cancer 1988;62:1317-1324.
    • (1988) Cancer , vol.62 , pp. 1317-1324
    • Sreekantaiah, C.1    Bhargava, K.M.2    Shetty, J.N.3
  • 31
    • 0023196534 scopus 로고
    • Cytogenetic studies of four human lung adenocarcinoma cell lines
    • Fan YS, Li P: Cytogenetic studies of four human lung adenocarcinoma cell lines. Cancer Genet Cytogenet 1987;26:317-325.
    • (1987) Cancer Genet Cytogenet , vol.26 , pp. 317-325
    • Fan, Y.S.1    Li, P.2
  • 37
    • 0027363063 scopus 로고
    • Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse
    • Dietrich WF, Lander ES, Smith JS, Moser AR, Gould KA, Luongo C, Borenstein N, Dove W: Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse. Cell 1993;75:631-639.
    • (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
  • 38
    • 0028111570 scopus 로고
    • Frequent genetic alterations at distal regions of chromosome 1p in human hepatocellular carcinomas
    • Yeh SH, Chen PJ, Chen HL, Lai MY, Wang CC, Chen DS: Frequent genetic alterations at distal regions of chromosome 1p in human hepatocellular carcinomas. Cancer Res 1994; 54:4188-4192.
    • (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
  • 39
    • 0028046406 scopus 로고
    • Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors
    • Mathew H, Murty VVVS, Bosl GJ, Chaganti RSK: Loss of heterozygosity identifies multiple sites of allelic deletions on chromosome 1 in human male germ cell tumors. Cancer Res 1994;54:6265-6269.
    • (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
  • 40


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.