메뉴 건너뛰기




Volumn 12, Issue 9, 2002, Pages 1323-1332

Comparative genomic sequence analysis of the human chromosome 21 down syndrome critical region

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA;

EID: 0036739213     PISSN: 10889051     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.153702     Document Type: Review
Times cited : (46)

References (37)
  • 3
    • 0033861549 scopus 로고    scopus 로고
    • Human and mouse gene structure: Comparative analysis and application to exon prediction
    • Batzoglou, S., Pachter, L., Mesirov, J., Berger, B., and Lander, E.S. 2000. Human and mouse gene structure: Comparative analysis and application to exon prediction. Genome Res. 10: 950-958.
    • (2000) Genome Res , vol.10 , pp. 950-958
    • Batzoglou, S.1    Pachter, L.2    Mesirov, J.3    Berger, B.4    Lander, E.S.5
  • 4
    • 0033978891 scopus 로고    scopus 로고
    • Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse
    • Baxter, L.L., Moran, T.H., Richtsmeier, J.T., Troncoso, J., and Reeves, R.H. 2000. Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse. Hum. Mol. Genet. 9: 195-202.
    • (2000) Hum. Mol. Genet , vol.9 , pp. 195-202
    • Baxter, L.L.1    Moran, T.H.2    Richtsmeier, J.T.3    Troncoso, J.4    Reeves, R.H.5
  • 5
    • 0031586003 scopus 로고    scopus 로고
    • Prediction of complete gene structure in human genomic DNA
    • Burge, C. and Karlin, S. 1997. Prediction of complete gene structure in human genomic DNA. J. Mol. Biol. 268: 78-94.
    • (1997) J. Mol. Biol , vol.268 , pp. 78-94
    • Burge, C.1    Karlin, S.2
  • 6
    • 0034128820 scopus 로고    scopus 로고
    • The end of the LINE?: Lack of recent L1 activity in a group of South American rodents
    • Casavant, N.C., Scott, L., Cantrell, M.A., Wiggins, L.E., Baker, R.J., and Wichman, H.A. 2000 The end of the LINE?: Lack of recent L1 activity in a group of South American rodents. Genetics 154: 1809-1817.
    • (2000) Genetics , vol.154 , pp. 1809-1817
    • Casavant, N.C.1    Scott, L.2    Cantrell, M.A.3    Wiggins, L.E.4    Baker, R.J.5    Wichman, H.A.6
  • 11
    • 0031955518 scopus 로고    scopus 로고
    • Base-calling of automated sequencer traces using Phred, I: Accuracy assessment
    • Ewing, B., Hillier, L., Wendl, M.C., and Green, P. 1998. Base-calling of automated sequencer traces using Phred, I: Accuracy assessment. Genome Res. 8: 175-185.
    • (1998) Genome Res , vol.8 , pp. 175-185
    • Ewing, B.1    Hillier, L.2    Wendl, M.C.3    Green, P.4
  • 12
    • 0031732094 scopus 로고    scopus 로고
    • A computer program for aligning a cDNA sequence with a genomic DNA sequence
    • Florea, L., Hartzell, G., Zhang, Z., Rubin, G.M., and Miller, W. 1998. A computer program for aligning a cDNA sequence with a genomic DNA sequence. Genome Res. 8: 967-974.
    • (1998) Genome Res , vol.8 , pp. 967-974
    • Florea, L.1    Hartzell, G.2    Zhang, Z.3    Rubin, G.M.4    Miller, W.5
  • 14
    • 0031955116 scopus 로고    scopus 로고
    • Consed: A graphical tool for sequence finishing
    • Gordon, D., Abajian, C., and Green, P. 1998. Consed: A graphical tool for sequence finishing. Genome Res. 8: 195-202.
    • (1998) Genome Res , vol.8 , pp. 195-202
    • Gordon, D.1    Abajian, C.2    Green, P.3
  • 16
    • 0030825243 scopus 로고    scopus 로고
    • A novel method for making nested deletions and its application for sequencing of a 300 kb region of human APP locus
    • Hattori, M., Tsukahara, F., Furuhata, Y., Tanahashi, H., Hirose, M., Saito, M., Tsukuni, S., and Sakaki, Y. 1997. A novel method for making nested deletions and its application for sequencing of a 300 kb region of human APP locus. Nucleic Acids Res. 25: 1802-1808.
    • (1997) Nucleic Acids Res , vol.25 , pp. 1802-1808
    • Hattori, M.1    Tsukahara, F.2    Furuhata, Y.3    Tanahashi, H.4    Hirose, M.5    Saito, M.6    Tsukuni, S.7    Sakaki, Y.8
  • 19
    • 17444437765 scopus 로고    scopus 로고
    • Integrating genomic homology into gene structure prediction
    • Korf, I., Flicek P., Duan, D., and Brent, M.R. 2001. Integrating genomic homology into gene structure prediction. Bioinformatics 17: S140-S148.
    • (2001) Bioinformatics , vol.17
    • Korf, I.1    Flicek, P.2    Duan, D.3    Brent, M.R.4
  • 21
    • 0034616398 scopus 로고    scopus 로고
    • Identification of a coordinate regulator of interleukins 4, 13, and 5 by cross-species sequence comparisons
    • Loots, G.G., Locksley, R.M., Blankespoor, C.M., Wang, Z.E., Miller, W., Rubin, E.M., and Frazer, K.A. 2000. Identification of a coordinate regulator of interleukins 4, 13, and 5 by cross-species sequence comparisons. Science 288: 136-140.
    • (2000) Science , vol.288 , pp. 136-140
    • Loots, G.G.1    Locksley, R.M.2    Blankespoor, C.M.3    Wang, Z.E.4    Miller, W.5    Rubin, E.M.6    Frazer, K.A.7
  • 22
    • 0034143652 scopus 로고    scopus 로고
    • Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2
    • Lund, J., Chen, F., Hua, A., Roe, B., Budarf, M., Emanuel, B.S., and Reeves, R.H. 2000. Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2. Genomics 63: 374-383.
    • (2000) Genomics , vol.63 , pp. 374-383
    • Lund, J.1    Chen, F.2    Hua, A.3    Roe, B.4    Budarf, M.5    Emanuel, B.S.6    Reeves, R.H.7
  • 24
    • 0033813884 scopus 로고    scopus 로고
    • Comparative genomic sequence analysis of the Williams syndrome region (LIMK1-RFC2) of human chromosome 7q11.23
    • Martindale, D.W., Wilson, M.D., Wang, D., Burke, R.D., Chen, X., Duronio, V., and Koop, B.F. 2000. Comparative genomic sequence analysis of the Williams syndrome region (LIMK1-RFC2) of human chromosome 7q11.23. Mamm. Genome 11: 890-898.
    • (2000) Mamm. Genome , vol.11 , pp. 890-898
    • Martindale, D.W.1    Wilson, M.D.2    Wang, D.3    Burke, R.D.4    Chen, X.5    Duronio, V.6    Koop, B.F.7
  • 27
    • 0033665147 scopus 로고    scopus 로고
    • Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain
    • Onyango, P., Miller, W., Lehoczky, J., Leung, C.T., Birren, B., Wheelan, S., Dewar, K., and Feinberg, A.P. 2000. Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain. Genome Res. 10: 1697-1710.
    • (2000) Genome Res , vol.10 , pp. 1697-1710
    • Onyango, P.1    Miller, W.2    Lehoczky, J.3    Leung, C.T.4    Birren, B.5    Wheelan, S.6    Dewar, K.7    Feinberg, A.P.8
  • 29
    • 0033782989 scopus 로고    scopus 로고
    • Chromosome evolution: The junction of mammalian chromosomes in the formation of mouse chromosome 10
    • Pletcher, M., Roe, B.A., Chen, F., Do, T., Do, A., Malaj, E., and Reeves, R.H. 2000. Chromosome evolution: The junction of mammalian chromosomes in the formation of mouse chromosome 10. Genome Res. 10: 1463-1467.
    • (2000) Genome Res , vol.10 , pp. 1463-1467
    • Pletcher, M.1    Roe, B.A.2    Chen, F.3    Do, T.4    Do, A.5    Malaj, E.6    Reeves, R.H.7
  • 30
    • 0035872772 scopus 로고    scopus 로고
    • Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21
    • Pletcher, M.T., Wiltshire, T., Cabin, D.E., Villanueva, M., and Reeves, R.H. 2001. Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21. Genomics 74: 45-54.
    • (2001) Genomics , vol.74 , pp. 45-54
    • Pletcher, M.T.1    Wiltshire, T.2    Cabin, D.E.3    Villanueva, M.4    Reeves, R.H.5
  • 32
    • 0035252562 scopus 로고    scopus 로고
    • Too much of a good thing: Mechanisms of gene action in Down syndrome
    • Reeves, R.H., Baxter, L.L., and Richtsmeier, J.T. 2001. Too much of a good thing: Mechanisms of gene action in Down syndrome. Trend Genet. 17: 83-88.
    • (2001) Trend Genet , vol.17 , pp. 83-88
    • Reeves, R.H.1    Baxter, L.L.2    Richtsmeier, J.T.3
  • 33
    • 0033980511 scopus 로고    scopus 로고
    • Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice
    • Richtsmeier, J.T., Baxter, L.L., and Reeves, R.H. 2000. Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice. Dev. Dyn. 217: 137-145.
    • (2000) Dev. Dyn , vol.217 , pp. 137-145
    • Richtsmeier, J.T.1    Baxter, L.L.2    Reeves, R.H.3
  • 34
    • 0036467052 scopus 로고    scopus 로고
    • Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome
    • Richtsmeier, J.T., Epstein, C.J., Carlson, E., and Reeves, R.H. 2002. Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome. Am. J. Med. Genet. 107: 317-324.
    • (2002) Am. J. Med. Genet , vol.107 , pp. 317-324
    • Richtsmeier, J.T.1    Epstein, C.J.2    Carlson, E.3    Reeves, R.H.4
  • 36
    • 0034685632 scopus 로고    scopus 로고
    • Isolation of two novel genes, DSCR5 and DSCR6, from Down syndrome critical region on human chromosome 21q22.2
    • Shibuya, K., Kudoh, J., Minoshima, S., Kawasaki, K., Asakawa, S., and Shimizu, N. 2000. Isolation of two novel genes, DSCR5 and DSCR6, from Down syndrome critical region on human chromosome 21q22.2. Biochem. Biophys. Res. Commun. 19: 693-698.
    • (2000) Biochem. Biophys. Res. Commun , vol.19 , pp. 693-698
    • Shibuya, K.1    Kudoh, J.2    Minoshima, S.3    Kawasaki, K.4    Asakawa, S.5    Shimizu, N.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.