메뉴 건너뛰기




Volumn 12, Issue 3, 1996, Pages 288-297

A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; GENE REARRANGEMENT; GENE SEQUENCE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; SEQUENCE ANALYSIS; TRANSPOSON;

EID: 0029962292     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0396-288     Document Type: Article
Times cited : (280)

References (65)
  • 1
    • 0027972378 scopus 로고
    • Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17
    • Chance, P.F. et al. Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17. Hum. Mol. Genet. 3, 223-228 (1994)
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 223-228
    • Chance, P.F.1
  • 2
    • 0001910626 scopus 로고
    • Charcot-Marie-Tooth polyneuropathy syndrome: Clinical electrophysiologic and genetic aspects
    • ed. Appel, S Mosby Yearbook, Chicago
    • Lupski, J.R., Garcia, C A., Parry, G.J & Patel, PI Charcot-Marie-Tooth polyneuropathy syndrome: clinical electrophysiologic and genetic aspects. In Current Neurology (ed. Appel, S) 1-25 (Mosby Yearbook, Chicago, 1991).
    • (1991) Current Neurology , pp. 1-25
    • Lupski, J.R.1    Garcia, C.A.2    Parry, G.J.3    Patel, P.I.4
  • 3
    • 0027518166 scopus 로고
    • Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy associated with a segmental duplication of chromosome 17
    • Kaku, D.A., Parry, G.J., Malamut, R., Lupski, J.R. & Garcia, C.A. Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy associated with a segmental duplication of chromosome 17. Neurology 43, 1806-1808 (1993)
    • (1993) Neurology , vol.43 , pp. 1806-1808
    • Kaku, D.A.1    Parry, G.J.2    Malamut, R.3    Lupski, J.R.4    Garcia, C.A.5
  • 4
    • 84957371233 scopus 로고
    • Over families met hereditaire dispositie tot het optreden van neuritiden gecorreleered met migraine
    • De Jong, J.G.Y. Over families met hereditaire dispositie tot het optreden van neuritiden gecorreleered met migraine Psychiat. Neurol Bull. 50, 60-76 (1947).
    • (1947) Psychiat. Neurol Bull. , vol.50 , pp. 60-76
    • De Jong, J.G.Y.1
  • 5
    • 34447275152 scopus 로고
    • Recurrent peripheral-nerve palsies in a family
    • Davis, D.M. Recurrent peripheral-nerve palsies in a family. Lancet 2, 266-268 (1954).
    • (1954) Lancet , vol.2 , pp. 266-268
    • Davis, D.M.1
  • 6
    • 0027366552 scopus 로고
    • Inherited primary peripheral neuropathies: Molecular genetics and clinical implications of CMT1A and HNPP
    • Lupski, J.R., Chance, P.F. & Garcia, C.A. Inherited primary peripheral neuropathies: molecular genetics and clinical implications of CMT1A and HNPP. JAMA 17, 2326-2330 (1993).
    • (1993) JAMA , vol.17 , pp. 2326-2330
    • Lupski, J.R.1    Chance, P.F.2    Garcia, C.A.3
  • 7
    • 0028610199 scopus 로고
    • Molecular genetics of Charcot-Marie-Tooth neuropathy
    • (eds Harns, H. & Hirschhorn, K.) Plenum Press, New York
    • Roa, B.B. & Lupski, J.R. Molecular genetics of Charcot-Marie-Tooth neuropathy. In Advances in Human Genetics (eds Harns, H. & Hirschhorn, K.) 117-152 (Plenum Press, New York, 1994).
    • (1994) Advances in Human Genetics , pp. 117-152
    • Roa, B.B.1    Lupski, J.R.2
  • 8
    • 0025868571 scopus 로고
    • DNA duplication associated with Charcot-Marie-Tooth disease type 1A
    • Lupski, J.R. et al. DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell 66, 219-232 (1991).
    • (1991) Cell , vol.66 , pp. 219-232
    • Lupski, J.R.1
  • 9
    • 0025997898 scopus 로고
    • Duplication in chromosome 17p11.2 in Charcot-Marie- Tooth neuropathy type 1a (CMT1a)
    • Raeymaekers, P. et al. Duplication in chromosome 17p11.2 in Charcot-Marie- Tooth neuropathy type 1a (CMT1a). Neuromusc. Diosord. 1, 93-97 (1991).
    • (1991) Neuromusc. Diosord. , vol.1 , pp. 93-97
    • Raeymaekers, P.1
  • 10
    • 0026564694 scopus 로고
    • Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMTIa)
    • Raeymaekers, P. et al. Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMTIa). J. Med. Genet. 29, 5-11 (1992).
    • (1992) J. Med. Genet. , vol.29 , pp. 5-11
    • Raeymaekers, P.1
  • 11
    • 0027359513 scopus 로고
    • Screening of dominantly inherited Charcot-Marie-Tooth neuropathies
    • Ionasescu, V.V., Ionasescu, R. & Searby, C. Screening of dominantly inherited Charcot-Marie-Tooth neuropathies. Muscle Nerve 16, 1232-1238 (1993).
    • (1993) Muscle Nerve , vol.16 , pp. 1232-1238
    • Ionasescu, V.V.1    Ionasescu, R.2    Searby, C.3
  • 12
    • 0027464397 scopus 로고
    • Stable inheritance of the CMT1A DNA duplication in two patients with CMT1 and NF1
    • Lupski, J.R., Pentao, L., Williams, L.L. & Patel, P.I. Stable inheritance of the CMT1A DNA duplication in two patients with CMT1 and NF1. Am. J. Med. Genet. 45, 92-96 (1993).
    • (1993) Am. J. Med. Genet. , vol.45 , pp. 92-96
    • Lupski, J.R.1    Pentao, L.2    Williams, L.L.3    Patel, P.I.4
  • 13
    • 0027374931 scopus 로고
    • Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMT1A duplication
    • Wise, C.A. et al. Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMT1A duplication. Am J. Hum. Genet. 53, 853-863 (1993).
    • (1993) Am J. Hum. Genet. , vol.53 , pp. 853-863
    • Wise, C.A.1
  • 14
    • 13344287941 scopus 로고    scopus 로고
    • Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 (CMT1) and hereditary neuropathy with liability to pressure palsies (HNPP) a European collaborative study
    • in the press
    • Nelis, E. et al. Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 (CMT1) and hereditary neuropathy with liability to pressure palsies (HNPP) a European collaborative study. Eur. J. Hum. Genet. (in the press)
    • Eur. J. Hum. Genet.
    • Nelis, E.1
  • 15
    • 0027017033 scopus 로고
    • Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit
    • Pentao, L., Wise, C.A., Chinault, A.C., Patel, P.I. & Lupski, J.R. Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit. Nature Genet 2, 292-300 (1992).
    • (1992) Nature Genet , vol.2 , pp. 292-300
    • Pentao, L.1    Wise, C.A.2    Chinault, A.C.3    Patel, P.I.4    Lupski, J.R.5
  • 17
    • 0027108731 scopus 로고
    • De-novo mutation in hereditary motor and sensory neuropathy type 1
    • Hoogendijk, J.E. et al. De-novo mutation in hereditary motor and sensory neuropathy type 1. Lancet 339, 1081-1082 (1992).
    • (1992) Lancet , vol.339 , pp. 1081-1082
    • Hoogendijk, J.E.1
  • 18
    • 0027509953 scopus 로고
    • DNA deletion associated with hereditary neuropathy with liability to pressure palsies
    • Chance, P.F. et al. DNA deletion associated with hereditary neuropathy with liability to pressure palsies Cell 72, 143-151 (1993).
    • (1993) Cell , vol.72 , pp. 143-151
    • Chance, P.F.1
  • 19
    • 0028872907 scopus 로고
    • A 1.5 Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies
    • Lorenzetti, D. et al. A 1.5 Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies. Am. J. Hum. Genet. 56, 91-98 (1995).
    • (1995) Am. J. Hum. Genet. , vol.56 , pp. 91-98
    • Lorenzetti, D.1
  • 21
    • 0026879838 scopus 로고
    • Protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A
    • Matsunami, N. et al. Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A Nature Genet. 1, 176-179 (1992).
    • (1992) Nature Genet. , vol.1 , pp. 176-179
    • Matsunami, N.1
  • 22
    • 0026879614 scopus 로고
    • The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A
    • Patel, P.I. et al The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A. Nature Genet 1, 159-165 (1992).
    • (1992) Nature Genet , vol.1 , pp. 159-165
    • Patel, P.I.1
  • 23
    • 0026879615 scopus 로고
    • The peripheral myelin protein gene PMP22 is contained within the Charcot-Marie-Tooth disease type 1A duplication
    • Timmerman, V. et al. The peripheral myelin protein gene PMP22 is contained within the Charcot-Marie-Tooth disease type 1A duplication. Nature Genet 1, 171-175 (1992).
    • (1992) Nature Genet , vol.1 , pp. 171-175
    • Timmerman, V.1
  • 24
    • 0026879648 scopus 로고
    • The peripheral myelin gene PMP22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A
    • Valentijn, L.J. et al. The peripheral myelin gene PMP22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A. Nature Genet. 1, 166-170 (1992).
    • (1992) Nature Genet. , vol.1 , pp. 166-170
    • Valentijn, L.J.1
  • 25
    • 0028231331 scopus 로고
    • Charcot-Marie-Tooth disease: A new paradigm for the mechanism of inhented disease
    • Patel, P.I. & Lupski, J.R. Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inhented disease. Trends Genet. 10, 128-133 (1994).
    • (1994) Trends Genet. , vol.10 , pp. 128-133
    • Patel, P.I.1    Lupski, J.R.2
  • 26
    • 0027759563 scopus 로고
    • Origin of the de novo duplication in Charcot-Marie-Tooth disease type 1A: Unequal nonsister chromatid exchange during spermatogenesis
    • Patau, F. et al. Origin of the de novo duplication in Charcot-Marie-Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis. Hum. Mol. Genet 2, 2031-2035 (1993).
    • (1993) Hum. Mol. Genet , vol.2 , pp. 2031-2035
    • Patau, F.1
  • 27
    • 0027949179 scopus 로고
    • Charcot-Marie-Tooth disease type 1A: The parental origin of a de novo 17p11.2-p12 duplication
    • Hertz, J.M., Børglum, A.D., Brandt, C.A , Flint, T. & Bisgaard, C. Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplication. Clinical Genet. 46, 291-294 (1994).
    • (1994) Clinical Genet. , vol.46 , pp. 291-294
    • Hertz, J.M.1    Børglum, A.D.2    Brandt, C.A.3    Flint, T.4    Bisgaard, C.5
  • 28
    • 0029120562 scopus 로고
    • Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: A study of 30 unrelated cases
    • LeGuern, E. et al. Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: A study of 30 unrelated cases. Hum. Mol. Genet 4, 1673-1674 (1995).
    • (1995) Hum. Mol. Genet , vol.4 , pp. 1673-1674
    • LeGuern, E.1
  • 29
    • 13344260003 scopus 로고    scopus 로고
    • Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP)
    • Timmerman, V. et al. Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP). Hum Genet. 97, 26-34 (1996).
    • (1996) Hum Genet. , vol.97 , pp. 26-34
    • Timmerman, V.1
  • 30
    • 0028810444 scopus 로고
    • Analysis of the CMT1A-REP repeat: Mapping crossover breakpoints in CMT1A and HNPP
    • Kiyosawa, H., Lensch, M.W. & Chance, P.F. Analysis of the CMT1A-REP repeat: mapping crossover breakpoints in CMT1A and HNPP Hum. Mol. Genet. 4, 2327-2334 (1995).
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 2327-2334
    • Kiyosawa, H.1    Lensch, M.W.2    Chance, P.F.3
  • 31
    • 0027489565 scopus 로고
    • Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1A
    • Roa, B. et al. Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1A. Nature Genet. 5, 189-194 (1993)
    • (1993) Nature Genet. , vol.5 , pp. 189-194
    • Roa, B.1
  • 32
    • 0028209722 scopus 로고
    • Adaptor-based uracil DNA gtycosylase cloning simplifies shotgun library construction for large-scale sequencing
    • Andersson, B. et al Adaptor-based uracil DNA gtycosylase cloning simplifies shotgun library construction for large-scale sequencing. Anal. Biochem. 218, 300-308 (1994).
    • (1994) Anal. Biochem. , vol.218 , pp. 300-308
    • Andersson, B.1
  • 33
    • 0021760092 scopus 로고
    • A comprehensive set of sequence analysis programs for the VAX
    • Devereux, J., Haeberli, P. & Smithies, O A comprehensive set of sequence analysis programs for the VAX Nucl. Acids Res. 12, 387-395 (1984)
    • (1984) Nucl. Acids Res. , vol.12 , pp. 387-395
    • Devereux, J.1    Haeberli, P.2    Smithies, O.3
  • 34
    • 0028920059 scopus 로고
    • Ancestral, mammalian-wide subfamilies of LINE-1 repetitive sequences
    • Smit, A.F A., Tóth, G., Riggs, A D. & Jurka, J. Ancestral, mammalian-wide subfamilies of LINE-1 repetitive sequences. J. Mol Biol. 246, 401-417 (1995).
    • (1995) J. Mol Biol. , vol.246 , pp. 401-417
    • Smit, A.F.A.1    Tóth, G.2    Riggs, A.D.3    Jurka, J.4
  • 35
    • 13344272652 scopus 로고    scopus 로고
    • CENSOR - A program for identification and elimination of repetitive elements from DNA sequences
    • in the press
    • Jurka, J , Klonowski, P., Dagman, V. & Pelton, P. CENSOR - a program for identification and elimination of repetitive elements from DNA sequences. Comp. Chem. (in the press)
    • Comp. Chem.
    • Jurka, J.1    Klonowski, P.2    Dagman, V.3    Pelton, P.4
  • 36
    • 0025174082 scopus 로고
    • Novel families of intespersed repetitive elements from the human genome
    • Jurka, J. Novel families of intespersed repetitive elements from the human genome. Nucl. Acids Res 18, 137-141 (1990).
    • (1990) Nucl. Acids Res , vol.18 , pp. 137-141
    • Jurka, J.1
  • 37
    • 0025730979 scopus 로고
    • Homology requirements for unequal crossing over in humans
    • Metzenberg, A.B., Wurzer, G., Huisman, T H.J. & Smithies, O. Homology requirements for unequal crossing over in humans Genetics 128, 143-161 (1991).
    • (1991) Genetics , vol.128 , pp. 143-161
    • Metzenberg, A.B.1    Wurzer, G.2    Huisman, T.H.J.3    Smithies, O.4
  • 38
    • 0026351408 scopus 로고
    • Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach
    • Uberbacher, E.C. & Mural, R.J. Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach. Proc. Natl. Acad Sci. USA 88, 11261-11265 (1991)
    • (1991) Proc. Natl. Acad Sci. USA , vol.88 , pp. 11261-11265
    • Uberbacher, E.C.1    Mural, R.J.2
  • 39
    • 0028835212 scopus 로고
    • BEAUTY: An enhanced BLAST-based search tool that integrates multiple biological information resources into sequence similarity search results
    • Worley, K.C., Wiese, B.A. & Smith, R.A. BEAUTY: an enhanced BLAST-based search tool that integrates multiple biological information resources into sequence similarity search results Genome Res. 5, 173-184 (1995).
    • (1995) Genome Res. , vol.5 , pp. 173-184
    • Worley, K.C.1    Wiese, B.A.2    Smith, R.A.3
  • 41
    • 0027968068 scopus 로고
    • CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
    • Thompson, J.D , Higgins, D.G & Gibson, T.J. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucl. Acids Res. 22, 4673-4680 (1994).
    • (1994) Nucl. Acids Res. , vol.22 , pp. 4673-4680
    • Thompson, J.D.1    Higgins, D.G.2    Gibson, T.J.3
  • 42
    • 0027398902 scopus 로고
    • The mariner transposable element is widespread in insects
    • Robertson, H.M The mariner transposable element is widespread in insects. Nature 362, 241-245 (1993).
    • (1993) Nature , vol.362 , pp. 241-245
    • Robertson, H.M.1
  • 43
    • 13344257525 scopus 로고    scopus 로고
    • Tiggers and other DNA transposon fossils in the human genome Proc
    • in the press
    • Smit, A.F.A. & Riggs, A.D. Tiggers and other DNA transposon fossils in the human genome Proc. Natl Acad Sci USA (in the press)
    • Natl Acad Sci USA
    • Smit, A.F.A.1    Riggs, A.D.2
  • 44
    • 13344284657 scopus 로고
    • Mariner transposons in humans
    • Oosumi, T., Belknap, W. R & Garlick, B. Mariner transposons in humans. Nature 378, 672 (1995).
    • (1995) Nature , vol.378 , pp. 672
    • Oosumi, T.1    Belknap, W.R.2    Garlick, B.3
  • 45
    • 0029656003 scopus 로고    scopus 로고
    • Chromosomal duplications in bacteria, fruit flies, and humans
    • Lupski, J R., Roth, J.R. & Weinstock, G.M Chromosomal duplications in bacteria, fruit flies, and humans. Am. J. Hum Genet 58, 21-27 (1996)
    • (1996) Am. J. Hum Genet , vol.58 , pp. 21-27
    • Lupski, J.R.1    Roth, J.R.2    Weinstock, G.M.3
  • 46
    • 0025280088 scopus 로고
    • Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements
    • Yen, P.H. et al. Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements. Cell 61, 603-610 (1990).
    • (1990) Cell , vol.61 , pp. 603-610
    • Yen, P.H.1
  • 47
    • 0025167556 scopus 로고
    • Two families of low-copy-number repeats are interspersed on Xp22.3 Implications for the high frequency of deletions in this region
    • Ballabio, A , Bardoni, B , Guioli, S., Basler, E & Camerino, G. Two families of low-copy-number repeats are interspersed on Xp22.3 Implications for the high frequency of deletions in this region. Genomics 3, 263-270 (1990).
    • (1990) Genomics , vol.3 , pp. 263-270
    • Ballabio, A.1    Bardoni, B.2    Guioli, S.3    Basler, E.4    Camerino, G.5
  • 48
    • 0026548122 scopus 로고
    • Characterization of a low copy repetitive element S232 involved in the generation of frequenct deletions of the distal short arm of the human X chromosome
    • Li, X.-M., Yen, P.H. & Shapiro, L. Characterization of a low copy repetitive element S232 involved in the generation of frequenct deletions of the distal short arm of the human X chromosome. Nucl. Acids Res. 20, 1117-1122 (1992).
    • (1992) Nucl. Acids Res. , vol.20 , pp. 1117-1122
    • Li, X.-M.1    Yen, P.H.2    Shapiro, L.3
  • 49
    • 0025190946 scopus 로고
    • Hypervariable minisatellite DNA is a hotspot for homologus recombination in human cells
    • Wahls, W P., Wallace, L J. & Moore, P.D. Hypervariable minisatellite DNA is a hotspot for homologus recombination in human cells Cell 60, 95-103 (1990).
    • (1990) Cell , vol.60 , pp. 95-103
    • Wahls, W.P.1    Wallace, L.J.2    Moore, P.D.3
  • 50
    • 0027520025 scopus 로고
    • Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A
    • Lakich, D., Kazazian, H.H., Jr., Antonarakis, S E. & Gitschier, J Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A. Nature Genet 5, 236-241 (1993)
    • (1993) Nature Genet , vol.5 , pp. 236-241
    • Lakich, D.1    Kazazian Jr., H.H.2    Antonarakis, S.E.3    Gitschier, J.4
  • 51
    • 0027174559 scopus 로고
    • Identification of a new, abundant superfamily of mammalian LTR- Transposons
    • Smit, A.F.A. Identification of a new, abundant superfamily of mammalian LTR- transposons. Nucl Acids Res. 21, 1863-1872 (1993).
    • (1993) Nucl Acids Res. , vol.21 , pp. 1863-1872
    • Smit, A.F.A.1
  • 53
    • 0027137962 scopus 로고
    • Five major subfamilies of mariner transposable elements in insects, including the Mediterranean fruit fly, and related arthropods
    • Robertson, H.M. & MacLeod, E G Five major subfamilies of mariner transposable elements in insects, including the Mediterranean fruit fly, and related arthropods. Insect. Mol. Biol 2, 125-139 (1993)
    • (1993) Insect. Mol. Biol , vol.2 , pp. 125-139
    • Robertson, H.M.1    MacLeod, E.G.2
  • 54
    • 0028329790 scopus 로고
    • Drosophila P element transposase induces male recombination addititvely and without a requirement for P element excision or insertion
    • McCarron, M , Duttaroy, A., Doughty, G. & Chovnick, A Drosophila P element transposase induces male recombination addititvely and without a requirement for P element excision or insertion. Genetics 136, 1013-1023 (1994)
    • (1994) Genetics , vol.136 , pp. 1013-1023
    • McCarron, M.1    Duttaroy, A.2    Doughty, G.3    Chovnick, A.4
  • 55
    • 0027308738 scopus 로고
    • The transposable element mariner mediates germline transformation in Drosophila melanogaster
    • Lidholm, D -A., Lohe, A.R & Hartl, D.L. The transposable element mariner mediates germline transformation in Drosophila melanogaster. Genetics 134, 859-868 (1993).
    • (1993) Genetics , vol.134 , pp. 859-868
    • Lidholm, D.-A.1    Lohe, A.R.2    Hartl, D.L.3
  • 56
    • 0026015008 scopus 로고
    • Introduction of the transposable element mariner into the germline of Drosophila melanogaster
    • Garza, D., Medhora, M., Koga, A & Hartl, D.L Introduction of the transposable element mariner into the germline of Drosophila melanogaster. Genetics 128, 303-310 (1991).
    • (1991) Genetics , vol.128 , pp. 303-310
    • Garza, D.1    Medhora, M.2    Koga, A.3    Hartl, D.L.4
  • 57
    • 0026322114 scopus 로고
    • Evidence for interspecific transfer of the transposable element mariner between Drosophila and Zaprionus
    • Maruyama, K & Hartl, D L. Evidence for interspecific transfer of the transposable element mariner between Drosophila and Zaprionus J Mol Evol. 33, 514-524 (1991)
    • (1991) J Mol Evol. , vol.33 , pp. 514-524
    • Maruyama, K.1    Hartl, D.L.2
  • 58
    • 0027022771 scopus 로고
    • Evolution of the transposable element mariner in the Drosophila melanogaster species group
    • Capy, P., David, J.R. & Hartl, D L. Evolution of the transposable element mariner in the Drosophila melanogaster species group. Genetics 86, 37-46 (1992).
    • (1992) Genetics , vol.86 , pp. 37-46
    • Capy, P.1    David, J.R.2    Hartl, D.L.3
  • 59
    • 0028815959 scopus 로고
    • Horizontal transmission, vertical inactivation, and stochastic loss of mariner-like transposable elements
    • Lohe, A R., Monyama, E.N., Lindholm, D -A & Hartl, D.L Horizontal transmission, vertical inactivation, and stochastic loss of mariner-like transposable elements. Mol Biol Evol. 12, 62-72 (1995)
    • (1995) Mol Biol Evol. , vol.12 , pp. 62-72
    • Lohe, A.R.1    Monyama, E.N.2    Lindholm, D.-A.3    Hartl, D.L.4
  • 60
    • 0028965055 scopus 로고
    • Genotypic effects, maternal effects and grand-maternal effects of immobilized derivatives of the transposable element mariner
    • Lohe, A.R., Lindholm, D -A & Hartl, D.L. Genotypic effects, maternal effects and grand-maternal effects of immobilized derivatives of the transposable element mariner Genomics 140, 183-192 (1995).
    • (1995) Genomics , vol.140 , pp. 183-192
    • Lohe, A.R.1    Lindholm, D.-A.2    Hartl, D.L.3
  • 61
    • 0028285133 scopus 로고
    • A sporadic form of hereditary neuropathy with liability to pressure palsies: Clinical, electrodiagnostic, and molecular genetic findings
    • Reisecker, F et al A sporadic form of hereditary neuropathy with liability to pressure palsies: clinical, electrodiagnostic, and molecular genetic findings. Neurology 44, 753-755 (1994)
    • (1994) Neurology , vol.44 , pp. 753-755
    • Reisecker, F.1
  • 62
    • 0028180964 scopus 로고
    • Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells
    • Rossiter, J.P et al. Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells. Hum. Mol. Genet. 3, 1035-1039 (1994).
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1035-1039
    • Rossiter, J.P.1
  • 63
    • 0028201453 scopus 로고
    • Physical mapping of chromosome 17 cosmids by fluorescence in situ hybridization and digital image analysis
    • Kallioniemi, O.-P. et al. Physical mapping of chromosome 17 cosmids by fluorescence in situ hybridization and digital image analysis. Genomics 20, 125-128 (1994)
    • (1994) Genomics , vol.20 , pp. 125-128
    • Kallioniemi, O.-P.1
  • 65
    • 0012054629 scopus 로고
    • PCR based strategies for gap closure an large-scale sequencing projects
    • (ed. Adams, M A.) Academic Press, London
    • Muzny, D M , Richards, S., Shen, Y & Gibbs, R A PCR based strategies for gap closure an large-scale sequencing projects In Automated DNA Sequencing and Analysis (ed. Adams, M A.) 182-190 (Academic Press, London, 1994).
    • (1994) Automated DNA Sequencing and Analysis , pp. 182-190
    • Muzny, D.M.1    Richards, S.2    Shen, Y.3    Gibbs, R.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.