메뉴 건너뛰기




Volumn 35, Issue 1, 1996, Pages 79-86

The construction of a yeast artificial chromosome (YAC) contig in the vicinity of the Usher syndrome type IIa (USH2A) gene in 1q41

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 1Q; CLINICAL FEATURE; GENE LOCATION; HEARING IMPAIRMENT; HUMAN; MARKER GENE; MOLECULAR CLONING; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; SEQUENCE ANALYSIS; USHER SYNDROME; YEAST ARTIFICIAL CHROMOSOME;

EID: 0030201074     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0325     Document Type: Article
Times cited : (27)

References (41)
  • 1
    • 0025368589 scopus 로고
    • Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents
    • Albertson, O. H., et al. (1990). Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents. Proc. Natl. Acad. Sci. USA 87: 4256-4260.
    • (1990) Proc. Natl. Acad. Sci. USA , vol.87 , pp. 4256-4260
    • Albertson, O.H.1
  • 2
    • 0028262286 scopus 로고
    • Genetic mapping of the gene for Usher syndrome: Linkage analysis in a large samaritan kindred
    • Bonné-Tamir, B., Korostishevsky, M., Kalinsky, H., et al. (1994). Genetic mapping of the gene for Usher syndrome: Linkage analysis in a large Samaritan kindred. Genomics 20: 36-42.
    • (1994) Genomics , vol.20 , pp. 36-42
    • Bonné-Tamir, B.1    Korostishevsky, M.2    Kalinsky, H.3
  • 3
    • 0020619770 scopus 로고
    • Usher syndrome: Definition and estimate of prevalance from two high risk populations
    • Boughman, J. A., Vernon, M., and Shaver, K. (1983). Usher syndrome: Definition and estimate of prevalance from two high risk populations. J. Chronic Dis. 36: 595-603.
    • (1983) J. Chronic Dis. , vol.36 , pp. 595-603
    • Boughman, J.A.1    Vernon, M.2    Shaver, K.3
  • 4
    • 0023349389 scopus 로고
    • Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors
    • Burke, D. T., et al. (1987). Cloning of large segments of exogenous DNA into yeast by means of artificial chromosome vectors. Science 236: 806-812.
    • (1987) Science , vol.236 , pp. 806-812
    • Burke, D.T.1
  • 5
    • 0026738541 scopus 로고
    • Continuum of overlapping clones spanning the entire human chromosome 21q
    • Chumakov, I., Rigault, P., Guillou, S., et al. (1992). Continuum of overlapping clones spanning the entire human chromosome 21q. Nature 359: 380-387.
    • (1992) Nature , vol.359 , pp. 380-387
    • Chumakov, I.1    Rigault, P.2    Guillou, S.3
  • 6
    • 0027604577 scopus 로고
    • Chromosome bands: Flavours to savour
    • Craig, J. M., and Bickmore, W. A. (1993). Chromosome bands: Flavours to savour. BioEssays 15: 349-354.
    • (1993) BioEssays , vol.15 , pp. 349-354
    • Craig, J.M.1    Bickmore, W.A.2
  • 7
    • 0021381028 scopus 로고
    • Addendum: A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
    • Feinberg, A. P., and Vogelstein, B. (1984). Addendum: A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem. 137: 266-267.
    • (1984) Anal. Biochem. , vol.137 , pp. 266-267
    • Feinberg, A.P.1    Vogelstein, B.2
  • 9
    • 0023216891 scopus 로고
    • CpG islands in vertebrate genomes
    • Gardiner-Garden, M., and Frommer, M. (1987). CpG islands in vertebrate genomes. J. Mol. Biol. 196: 261-282.
    • (1987) J. Mol. Biol. , vol.196 , pp. 261-282
    • Gardiner-Garden, M.1    Frommer, M.2
  • 10
    • 0025016822 scopus 로고
    • Systematic screening of yeast artificial chromosome libraries by use of the polymerase chain reaction
    • Green, E. D., and Olson, M. V. (1990). Systematic screening of yeast artificial chromosome libraries by use of the polymerase chain reaction. Proc. Natl. Acad. Sci. USA 87: 1213-1217.
    • (1990) Proc. Natl. Acad. Sci. USA , vol.87 , pp. 1213-1217
    • Green, E.D.1    Olson, M.V.2
  • 11
    • 0028231090 scopus 로고
    • The 1993-94 généthon human genetic linkage map
    • Gyapay, G., Morissette, J., Vignal, A., et al. (1994). The 1993-94 Généthon human genetic linkage map. Nature Genet. 7: 246-339.
    • (1994) Nature Genet. , vol.7 , pp. 246-339
    • Gyapay, G.1    Morissette, J.2    Vignal, A.3
  • 12
    • 7944229728 scopus 로고
    • Retinitis pigmentosa combined with congenital deafness, with vestibulo-cerebellar ataxia and neural abnormality in a proportion of cases
    • Hallgren, B. (1959). Retinitis pigmentosa combined with congenital deafness, with vestibulo-cerebellar ataxia and neural abnormality in a proportion of cases. Acta Psychiatr. Scand. 138(Suppl.): 1-101.
    • (1959) Acta Psychiatr. Scand. , vol.138 , Issue.SUPPL. , pp. 1-101
    • Hallgren, B.1
  • 13
    • 0025088613 scopus 로고
    • Usher syndrome type I is not linked to D1S81 (pTHH 33): Evidence for genetic heterogeneity
    • Kaplan, J., et al. (1990). Usher syndrome type I is not linked to D1S81 (pTHH 33): Evidence for genetic heterogeneity. Ann. Genet. 33: 105-108.
    • (1990) Ann. Genet. , vol.33 , pp. 105-108
    • Kaplan, J.1
  • 14
    • 0027058632 scopus 로고
    • A gene for Usher syndrome type I (USH1A) maps to chromosome 14q
    • Kaplan, J., Gerber, S., Bonneau, D., et al. (1992). A gene for Usher syndrome type I (USH1A) maps to chromosome 14q. Genomics 14: 979-987.
    • (1992) Genomics , vol.14 , pp. 979-987
    • Kaplan, J.1    Gerber, S.2    Bonneau, D.3
  • 15
    • 0028226978 scopus 로고
    • Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11
    • Keats, B. J. B., Nouri, N., Palias, M. Z., Deininger, P. L., and Litt, M. (1994). Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11. Am. J. Hum. Genet. 54: 681-686.
    • (1994) Am. J. Hum. Genet. , vol.54 , pp. 681-686
    • Keats, B.J.B.1    Nouri, N.2    Palias, M.Z.3    Deininger, P.L.4    Litt, M.5
  • 16
    • 0026440240 scopus 로고
    • Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts
    • Kere, J., Nagaraja, R., Mumm, S., Ciccodicola, A., D'Urso, M., and Schlessinger, D. (1992). Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts. Genomics 14: 241-248.
    • (1992) Genomics , vol.14 , pp. 241-248
    • Kere, J.1    Nagaraja, R.2    Mumm, S.3    Ciccodicola, A.4    D'Urso, M.5    Schlessinger, D.6
  • 17
    • 0025308736 scopus 로고
    • Localization of Usher syndrome type II to chromosome 1q
    • Kimberling, W. J., et al. (1990). Localization of Usher syndrome type II to chromosome 1q. Genomics 7: 245-249.
    • (1990) Genomics , vol.7 , pp. 245-249
    • Kimberling, W.J.1
  • 19
    • 0027058412 scopus 로고
    • Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11
    • Kimberling, W. J., Möller, C. G., Davenport, S., et al. (1992). Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11. Genomics 14: 988-994.
    • (1992) Genomics , vol.14 , pp. 988-994
    • Kimberling, W.J.1    Möller, C.G.2    Davenport, S.3
  • 20
    • 0028795018 scopus 로고
    • Gene mapping of Usher syndrome type IIa: Localization of the gene to a 2.1 cM segment on chromosome 1q41
    • Kimberling, W. J., Weston, M. D., Moller, C., et al. (1995). Gene mapping of Usher syndrome type IIa: Localization of the gene to a 2.1 cM segment on chromosome 1q41. Am. J. Hum. Genet. 56: 216-223.
    • (1995) Am. J. Hum. Genet. , vol.56 , pp. 216-223
    • Kimberling, W.J.1    Weston, M.D.2    Moller, C.3
  • 21
    • 0028284847 scopus 로고
    • Genetic heterogeneity of Usher syndrome type I in French families
    • Larget-Piet, D., Gerber, S., Bonneau, D., et al. (1994). Genetic heterogeneity of Usher syndrome type I in French families. Genomics 21: 138-143.
    • (1994) Genomics , vol.21 , pp. 138-143
    • Larget-Piet, D.1    Gerber, S.2    Bonneau, D.3
  • 22
    • 0025323589 scopus 로고
    • Mapping recessive ophthalmic diseases: Linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q
    • Lewis, R. A., et al. (1990). Mapping recessive ophthalmic diseases: Linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q. Genomics 7: 250-256.
    • (1990) Genomics , vol.7 , pp. 250-256
    • Lewis, R.A.1
  • 23
    • 0026410409 scopus 로고
    • Comparative gene mapping, genome duplication and genetics of hearing
    • Nadeau, J. H., Kosovsky, M., and Steel, K. P. (1991). Comparative gene mapping, genome duplication and genetics of hearing. Ann. N.Y. Acad. Sci. 630: 49-67.
    • (1991) Ann. N.Y. Acad. Sci. , vol.630 , pp. 49-67
    • Nadeau, J.H.1    Kosovsky, M.2    Steel, K.P.3
  • 24
    • 1542471167 scopus 로고
    • Alu polymerase chain reaction: A method for rapid isolation of human-specific sequences from complex DNA sources
    • Nelson, D. L., Ledbetter, S. A., Corbo, L., et al. (1989). Alu polymerase chain reaction: A method for rapid isolation of human-specific sequences from complex DNA sources. Proc. Natl. Acad. Sci. USA 86: 6686-6690.
    • (1989) Proc. Natl. Acad. Sci. USA , vol.86 , pp. 6686-6690
    • Nelson, D.L.1    Ledbetter, S.A.2    Corbo, L.3
  • 25
    • 0014780501 scopus 로고
    • Dystrophia retinae pigmentosa-dysacusis syndrome (DRD): A study of the Usher or Hallgren syndrome
    • Nuutila, A. (1970). Dystrophia retinae pigmentosa-dysacusis syndrome (DRD): A study of the Usher or Hallgren syndrome. J. Genet. Hum. 18: 57-58.
    • (1970) J. Genet. Hum. , vol.18 , pp. 57-58
    • Nuutila, A.1
  • 26
    • 0027261513 scopus 로고
    • Isochores and CpG islands in YAC contigs in human Xq26.1-qter
    • Pilia, G., Little, R. D., Aissani, B., Bernardi, G., and Schlessinger, D. (1993). Isochores and CpG islands in YAC contigs in human Xq26.1-qter. Genomics 17: 456-462.
    • (1993) Genomics , vol.17 , pp. 456-462
    • Pilia, G.1    Little, R.D.2    Aissani, B.3    Bernardi, G.4    Schlessinger, D.5
  • 27
    • 0025339588 scopus 로고
    • A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones
    • Riley, J., Butter, R., Ogilvie, D., et al. (1990). A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones. Nucleic Acids Res. 18: 2887-2890.
    • (1990) Nucleic Acids Res. , vol.18 , pp. 2887-2890
    • Riley, J.1    Butter, R.2    Ogilvie, D.3
  • 28
    • 0028836898 scopus 로고
    • Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q
    • Sankila, E-M., Pakarinen, L., Kääriäinen, H., et al. (1995). Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q. Hum. Mol. Genet. 4: 93-98.
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 93-98
    • Sankila, E.-M.1    Pakarinen, L.2    Kääriäinen, H.3
  • 29
    • 0002062060 scopus 로고
    • Pulsed-field gel electrophoresis and the technology of large DNA molecules
    • K. E. Davies, Ed., IRL Press, Oxford
    • Smith, C. L., Klco, S. R., and Cantor, C. R. (1988). Pulsed-field gel electrophoresis and the technology of large DNA molecules. In "Genome Analysis: A Practical Approach" (K. E. Davies, Ed.), pp. 41-72, IRL Press, Oxford.
    • (1988) Genome Analysis: A Practical Approach , pp. 41-72
    • Smith, C.L.1    Klco, S.R.2    Cantor, C.R.3
  • 30
    • 0027058291 scopus 로고
    • Localization of two genes for Usher syndrome type I to chromosome 11
    • Smith, R. J. H., Lee, C., Kimberling, W. J., et al. (1992). Localization of two genes for Usher syndrome type I to chromosome 11. Genomics 14: 995-1002.
    • (1992) Genomics , vol.14 , pp. 995-1002
    • Smith, R.J.H.1    Lee, C.2    Kimberling, W.J.3
  • 31
  • 32
    • 0028982232 scopus 로고
    • Construction and characterization of a NotI linking library from human chromosome region 1q25-qter
    • Talmadge, C. B., Zhen, D-K., Wang, J-Y., et al. (1995). Construction and characterization of a NotI linking library from human chromosome region 1q25-qter. Genomics 29: 105-114.
    • (1995) Genomics , vol.29 , pp. 105-114
    • Talmadge, C.B.1    Zhen, D.-K.2    Wang, J.-Y.3
  • 33
    • 0028897394 scopus 로고
    • YAC contigs covering an 8-megabase region of 3p deleted in the small cell lung cancer cell line U2020
    • Todd, S., Roche, J., Hahner, L., Bolin, R., Drabkin, H. A., and Gremmil, R. M. (1995). YAC contigs covering an 8-megabase region of 3p deleted in the small cell lung cancer cell line U2020. Genomics 25: 19-28.
    • (1995) Genomics , vol.25 , pp. 19-28
    • Todd, S.1    Roche, J.2    Hahner, L.3    Bolin, R.4    Drabkin, H.A.5    Gremmil, R.M.6
  • 34
    • 0001164478 scopus 로고
    • The Bowman lecture: On a few hereditary eye afflictions
    • Usher (1935). The Bowman lecture: On a few hereditary eye afflictions. Trans. Ophthalmol. Soc. UK 55: 164.
    • (1935) Trans. Ophthalmol. Soc. UK , vol.55 , pp. 164
    • Usher1
  • 35
    • 0014561109 scopus 로고
    • Usher's syndrome: Deafness and progressive blindness. Clinical cases, prevention, theory and literature survey
    • Vernon, M. (1969). Usher's syndrome: Deafness and progressive blindness. Clinical cases, prevention, theory and literature survey. J. Chronic Dis. 22: 133-151.
    • (1969) J. Chronic Dis. , vol.22 , pp. 133-151
    • Vernon, M.1
  • 36
    • 0001645884 scopus 로고
    • Exceptionelles verhelten des gesichsfeldes bei pigmententarung der netzhaut von Graefe's acrch
    • von Graefe (1858). Exceptionelles verhelten des gesichsfeldes bei pigmententarung der netzhaut von Graefe's acrch. Klin. Exp. Ophtalmol. 4: 250-253.
    • (1858) Klin. Exp. Ophtalmol. , vol.4 , pp. 250-253
    • Von Graefe1
  • 37
    • 0028212037 scopus 로고
    • Somatic cell hybrid panel and NotI linking clones for physical mapping of human chromosome 3
    • Wang, J-Y., Zabarovsky, E. R., Talmadge, C., et al. (1994). Somatic cell hybrid panel and NotI linking clones for physical mapping of human chromosome 3. Genomics 20: 105-113.
    • (1994) Genomics , vol.20 , pp. 105-113
    • Wang, J.-Y.1    Zabarovsky, E.R.2    Talmadge, C.3
  • 38
    • 0028815440 scopus 로고
    • Defective myosin UHA gene responsible for Usher syndrome 1b
    • Weil, D., Branchard, S., Kaplan, J., et al. (1995). Defective myosin UHA gene responsible for Usher syndrome 1b. Nature 374: 60-61.
    • (1995) Nature , vol.374 , pp. 60-61
    • Weil, D.1    Branchard, S.2    Kaplan, J.3
  • 40
    • 0028356013 scopus 로고
    • Dinucleotide repeat polymorphism for D1S70 (CRI L461) on chromosome 1q41
    • Weston, M. D., and Kimberling, W. J. (1994b). Dinucleotide repeat polymorphism for D1S70 (CRI L461) on chromosome 1q41. Hum. Mol. Genet. 3: 1212.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1212
    • Weston, M.D.1    Kimberling, W.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.