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Volumn 9, Issue 12, 2000, Pages 1881-1889

Unequal exchange at the Charcot-Marie-Tooth disease type 1A recombination hot-spot is not elevated above the genome average rate

(5) Han, Li Ling a Keller, Marcel P b,d Navidi, William c Chance, Phillip F b Arnheim, Norman a

a UNIVERSITY OF SOUTHERN CALIFORNIA (United States)

b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE (United States)

c Department of Geology and Geological Engineering (United States)

d UNIVERSITY HOSPITAL BASEL (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 17; CHROMOSOME DUPLICATION; CONTROLLED STUDY; CROSSING OVER; DNA SEQUENCE; GENE DELETION; GENETIC RECOMBINATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; MALE; PRIORITY JOURNAL; YEAST;

EID: 0033860409 PISSN: 09646906 EISSN: None Source Type: Journal
DOI: 10.1093/hmg/9.12.1881 Document Type: Article

Times cited : (35)

References (52)

1
- 0025868571
- DNA duplication associated with Charcot-Marie-Tooth disease type 1A
- (1991) Cell , vol.66 , pp. 219-232
- Lupski, J.R.¹ de Oca-Luna, R.M.² Slaugenhaupt, S.³ Pentao L⁴ Guzzetta, V.⁵ Trask, B.J.⁶ Saucedo-Cardenas, O.⁷ Barker, D.F.⁸ Killian, J.M.⁹ Garcia, C.A.¹⁰

2
- 0026849499
- Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A
- (1992) Nature Genet. , vol.1 , pp. 29-33
- Lupski, J.R.¹ Wise, C.A.² Kuwano, A.³ Pentao, L.⁴ Parke, J.T.⁵ Glaze, D.G.⁶ Ledbetter, D.H.⁷ Greenberg, F.⁸ Patel, P.I.⁹

3
- 0025997898
- Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group
- (1991) Neuromusc. Disord. , vol.1 , pp. 93-97
- Raeymaekers, P.¹ Timmerman, V.² Nelis, E.³ De Jonghe, P.⁴ Hoogendijk, J.E.⁵ Baas, F.⁶ Barker, D.F.⁷ Martin, J.J.⁸ De Visser, M.⁹ Bolhuis, P.A.¹⁰

4
- 0027017033
- Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit
- (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

5
- 0027374931
- Molecular analyzes of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication
- (1993) Am. J. Hum. Genet. , vol.53 , pp. 853-863
- Wise, C.A.¹ Garcia, C.A.² Davis, S.N.³ Heju, Z.⁴ Pentao, L.⁵ Patel, P.I.⁶ Lupski, J.R.⁷

6
- 0030871024
- The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMTIA-REPs
- (1997) Hum. Mol. Genet. , vol.6 , pp. 1595-1603
- Reiter, L.T.¹ Murakami, T.² Koeuth, T.³ Gibbs, R.A.⁴ Lupski, J.R.⁵

7
- 0029999248
- Primate origin of the CMTIA-REP repeat and analysis of a putative transposon-associated recombinational hot-spot
- (1996) Hum. Mol. Genet. , vol.5 , pp. 745-753
- Kiyosawa, H.¹ Chance, P.F.²

8
- 0027972378
- Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17
- (1994) Hum. Mol. Genet. , vol.3 , pp. 223-228
- Chance, P.F.¹ Abbas, N.² Lensch, M.W.³ Pentao, L.⁴ Roa, B.B.⁵ Patel, P.I.⁶ Lupski, J.R.⁷

9
- 0027509953
- DNA deletion associated with hereditary neuropathy with liability to pressure palsies
- (1993) Cell , vol.72 , pp. 143-151
- Chance, P.F.¹ Alderson, M.K.² Leppig, K.A.³ Lensch, M.W.⁴ Matsunami, N.⁵ Smith, B.⁶ Swanson, P.D.⁷ Odelberg, S.J.⁸ Disteche, C.M.⁹ Bird, T.D.¹⁰

10
- 0028810444
- Analysis of the CMT1A-REP repeat: Mapping crossover breakpoints in CMT1A and HNPP
- (1995) Hum. Mol. Genet. , vol.4 , pp. 2327-2334
- Kiyosawa, H.¹ Lensch, M.W.² Chance, P.F.³

11
- 0031972093
- Human meiotic recombination products revealed by sequencing a hot-spot for homologous strand exchange in multiple HNPP deletion patients
- (1998) Am. J. Hum. Genet. , vol.62 , pp. 1023-1033
- Reiter, L.T.¹ Hastings, P.J.² Nelis, E.³ De Jonghe, P.⁴ Van Broeckhoven, C.⁵ Lupski, J.R.⁶

12
- 0029962292
- A recombination hot-spot responsible for two inherited peripheral neuropathies is located neat a mariner transposon-like element
- [Erratum (1998) Nature Genet., 19, 303.]
- (1996) Nature Genet. , vol.12 , pp. 288-297
- Reiter, L.T.¹ Murakami, T.² Koeuth, T.³ Pentao, L.⁴ Muzny, D.M.⁵ Gibbs, R.A.⁶ Lupski, J.R.⁷

13
- 6844249444
- Clustering of CMT1A duplication breakpoints in a 700 bp interval of the CMTIA-REP repeat
- (1998) Hum. Mutat. , vol.11 , pp. 109-113
- Yamamoto, M.¹ Keller, M.P.² Yasuda, T.³ Hayasaka, K.⁴ Ohnishi, A.⁵ Yoshikawa, H.⁶ Yanagihara, T.⁷ Mitsuma, T.⁸ Chance, P.F.⁹ Sobue, G.¹⁰

14
- 6844239521
- Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination
- (1998) Hum. Mol. Genet. , vol.7 , pp. 141-148
- Lopes, J.¹ Ravise, N.² Vandenberghe, A.³ Palau, F.⁴ Ionasescu, V.⁵ Mayer, M.⁶ Levy, N.⁷ Wood, N.⁸ Tachi, N.⁹ Bouche, P.¹⁰

15
- 0029989649
- New tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group
- (1996) Am. J. Hum. Genet. , vol.58 , pp. 1223-1230
- Lopes, J.¹ LeGuem, E.² Gouider, R.³ Tardieu, S.⁴ Abbas, N.⁵ Birouk, N.⁶ Gugenheim, M.⁷ Bouche, P.⁸ Agid, Y.⁹ Brice, A.¹⁰

16
- 16944365439
- Detection of the CMT1A/HNPP recombination hot-spot in unrelated patients of European descent
- (1997) J. Med. Genet. , vol.34 , pp. 43-49
- Timmerman, V.¹ Rautenstrauss, B.² Reiter, L.T.³ Koeuth, T.⁴ Lofgren, A.⁵ Liehr, T.⁶ Nelis, E.⁷ Bathke, K.D.⁸ De Jonghe, P.⁹ Grehl, H.¹⁰

17
- 0031038297
- Prevalence and parental origin of de novo 1.5-Mb duplication in Charcot-Marie-Tooth disease type 1A [letter]
- (1997) Am. J. Hum. Genet. , vol.60 , pp. 230-233
- Bort, S.¹ Martinez, F.² Palau, F.³

18
- 0027759563
- Origin of the de novo duplication in Charcot-Marie-Tooth disease type 1A: Unequal nonsister chromatid exchange during spermatogenesis
- (1993) Hum. Mol. Genet. , vol.2 , pp. 2031-2035
- Palau, F.¹ Lofgren, A.² De Jonghe, P.³ Bort, S.⁴ Nelis, E.⁵ Sevilla, T.⁶ Martin, J.J.⁷ Vilchez, J.⁸ Prieto, F.⁹ Van Broeckhoven, C.¹⁰

19
- 84984760579
- Sex-dependent rearrangements resulting in CMT1A and HNPP [letter]
- (1997) Nature Genet. , vol.17 , pp. 136-137
- Lopes, J.¹ Vandenberghe, A.² Tardieu, S.³ Ionasescu, V.⁴ Levy, N.⁵ Wood, N.⁶ Tachi, N.⁷ Bouche, P.⁸ Latour, P.⁹ Brice, A.¹⁰ LeGuem, E.¹¹

20
- 0033554364
- Molecular mechanisms for CMT1A duplication and HNPP deletion
- (1999) Ann. N Y Acad. Sci. , vol.883 , pp. 22-35
- Boerkoel, C.F.¹ Inoue, K.² Reiter, L.T.³ Warner, L.E.⁴ Lupski, J.R.⁵

21
- 0025124532
- Human immunodeficiency virus-infected individuals contain provirus in small numbers of peripheral mononuclear cells and at low copy numbers
- (1990) J. Virol. , vol.64 , pp. 864-872
- Simmonds, P.¹ Balfe, P.² Peutherer, J.F.³ Ludlam, C.A.⁴ Bishop, J.O.⁵ Brown, A.J.⁶

22
- 0029817147
- The mutation rate of the human mtDNA deletion mtDNA4977
- (1996) Am. J. Hum. Genet. , vol.59 , pp. 772-780
- Shenkar, R.¹ Navidi, W.² Tavare, S.³ Dang, M.H.⁴ Chomyn, A.⁵ Attardi, G.⁶ Cortopassi, G.⁷ Amheim, N.⁸

23
- 0032695458
- Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: A study of 17p11.2 rearrangements associated with CMT1A and HNPP
- (1999) Hum. Mol. Genet. , vol.8 , pp. 2285-2292
- Lopes, J.¹ Tardieu, S.² Silander, K.³ Blair, I.⁴ Vandenberghe, A.⁵ Palau, F.⁶ Ruberg, M.⁷ Brice, A.⁸ LeGuem, E.⁹

24
- 0033987366
- Molecular mechanism for duplication 17p11.2-the homologous recombination reciprocal of the Smith-Magenis microdeletion
- (2000) Nature Genet , vol.24 , pp. 84-87
- Potocki, L.¹ Chen, K.S.² Park, S.S.³ Osterholm, D.E.⁴ Withers, M.A.⁵ Kimonis, V.⁶ Summers, A.M.⁷ Meschino, W.S.⁸ Anyane-Yeboa, K.⁹ Kashork, C.D.¹⁰

25
- 0016266593
- Genetic and clinical aspects of Charcot-Marie-Tooth's disease
- (1974) Clin. Genet. , vol.6 , pp. 98-118
- Skre, H.¹

26
- 0018949405
- Genetic aspects of hereditary motor and sensory neuropathy (types I and II)
- (1980) J. Med. Genet. , vol.17 , pp. 329-336
- Harding, A.E.¹ Thomas, P.K.²

27
- 0029863589
- Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: A European collaborative study
- (1996) Eur. J. Hum. Genet. , vol.4 , pp. 25-33
- Nelis, E.¹ Van Broeckhoven, C.² De Jonghe, P.³ Lofgren, A.⁴ Vandenberghe, A.⁵ Latour, P.⁶ Le Guern, E.⁷ Brice, A.⁸ Mostacciuolo, M.L.⁹ Schiavon, F.¹⁰

28
- 0030030169
- Prevalence and origin of de novo duplications in Charcot-Marie-Tooth disease type 1A: First report of a de novo duplication with a maternal origin
- (1996) Am. J. Hum. Genet. , vol.58 , pp. 472-476
- Blair, I.P.¹ Nash, J.² Gordon, M.J.³ Nicholson, G.A.⁴

29
- 0029988255
- A metric map of humans: 23,500 loci in 850 bands
- (1996) Proc. Natl Acad. Sci. USA , vol.93 , pp. 14771-14775
- Collins, A.¹ Frezal, J.² Teague, J.³ Morton, N.E.⁴

30
- 0022630729
- A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes
- (1986) Nature , vol.319 , pp. 291-295
- Rouyer, F.¹ Simmler, M.C.² Johnsson, C.³ Vergnaud, G.⁴ Cooke, H.J.⁵ Weissenbach, J.⁶

31
- 0023447909
- Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes
- (1987) Genomics , vol.1 , pp. 243-256
- Page, D.C.¹ Bieker, K.² Brown, L.G.³ Hinton, S.⁴ Leppert, M.⁵ Lalouel, J.M.⁶ Lathrop, M.⁷ Nystrom-Lahti, M.⁸ de la Chapelle, A.⁹ White, R.¹⁰

32
- 0019967273
- Genetic homology and crossing over in the X and Y chromosomes of mammals
- (1982) Hum. Genet. , vol.61 , pp. 85-90
- Burgoyne, P.S.¹

33
- 0033929751
- Evidence for heterogeniety in recombination in the human pseudoautosomal region: High resolution analysis by sperm typing and radiation hybrid mapping
- (2000) Am. J. Hum Genet , vol.66 , pp. 557-566
- Lien, S.¹ Szyda, J.² Schechinger, B.³ Rappold, G.⁴ Arnheim, N.⁵

34
- 0032133324
- High-resolution mapping of crossovers in human sperm defines a minisatellite-associated recombination hot-spot
- (1998) Mol. Cell , vol.2 , pp. 267-273
- Jeffreys, A.J.¹ Murray, J.² Neumann, R.³

35
- 0028786666
- Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms
- (1995) Proc. Natl Acad, Sci. USA , vol.92 , pp. 10796-10800
- Tusie-Luna, M.T.¹ White, P.C.²

36
- 0030054682
- A model for testing recombinogenic sequences in the mouse germ line
- (1996) Hum. Mol. Genet. , vol.5 , pp. 875-886
- Moynahan, M.E.¹ Akgun, E.² Jasin, M.³

37
- 0026764183
- High-frequency germ line gene conversion in transgenic mice
- (1992) Mol. Cell Biol. , vol.12 , pp. 2545-2552
- Murti, J.R.¹ Bumbulis, M.² Schimenti, J.C.³

38
- 0028338678
- Gene conversion between unlinked sequences in the germline of mice
- (1994) Genetics , vol.137 , pp. 837-843
- Murti, J.R.¹ Bumbulis, M.² Schimenti, J.C.³

39
- 0032955550
- Gene conversion can create new MHC alleles
- (1999) Immunol. Rev , vol.167 , pp. 305-317
- Hogstrand, K.¹ Bohme, J.²

40
- 0026087053
- The frequency of meiotic recombination in yeast is independent of the number and position of homologous donor sequences: Implications for chromosome pairing
- (1991) Proc. Natl Acad. Sci. USA , vol.88 , pp. 1120-1124
- Haber, J.E.¹ Leung, W.Y.² Borts, R.H.³ Lichten, M.⁴

41
- 0029745577
- The efficiency of meiotic recombination between dispersed sequences in Saccharomyces cerevisiae depends upon their chromosomal location
- (1996) Genetics , vol.144 , pp. 43-55
- Goldman, A.S.¹ Lichten, M.²

42
- 0023001701
- Chromosomal translocations generated by high-frequency meiotic recombination between repeated yeast genes
- (1986) Genetics , vol.114 , pp. 731-752
- Jinks-Robertson, S.¹ Petes, T.D.²

43
- 0000459439
- Recombination in yeast
- In Broach, J.R., Jones, E. and Pringle, J. (eds), The Molecular and Cellular Biology of the Yeast Saccharomyces: Genome Dynamics, Protein Synthesis and Energetics. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
- (1991) , pp. 407-521
- Petes, T.D.¹ Malone, R.E.² Symington, L.S.³

44
- 0023135574
- Meiotic gene conversion and crossing over between dispersed homologous sequences occurs frequently in Saccharomyces cerevisiae
- (1987) Genetics , vol.115 , pp. 233-246
- Lichten, M.¹ Borts, R.H.² Haber, J.E.³

45
- 0008393544
- Meiotic recombination between dispersed homologous sequences in Saccharomyces cerevisiae
- In Klar, A. and Strathern, J.N. (eds), Mechanisms of Yeast Recombination. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
- (1986) , pp. 123-130
- Lichten, M.¹ Boris, R.H.² Haber, J.E.³

46
- 0025158560
- A genetic map of human chromosome 17p
- (1990) Genomics , vol.7 , pp. 103-109
- Wright, E.C.¹ Goldgar, D.E.² Fain, P.R.³ Barker, D.F.⁴ Skolnick, M.H.⁵

47
- 0026771287
- Highly efficient gene targeting in embryonic stem cells through homologous recombination with isogenic DNA constructs
- (1992) Proc. Natl Acad. Sci. USA , vol.89 , pp. 5128-5132
- te Riele, H.¹ Maandag, E.R.² Berns, A.³

48
- 0023684936
- Dependence of intrachromosomal recombination in mammalian cells on uninterrupted homology
- (1988) Mol. Cell. Biol. , vol.8 , pp. 5350-5357
- Waldman, A.S.¹ Liskay, R.M.²

49
- 0026560826
- Targeted homologous recombination in mammalian cells
- (1992) Crit. Rev. Oncol. Hematol. , vol.12 , pp. 49-64
- Waldman, A.S.¹

50
- 0029935705
- The most unkindest cut of all
- (1996) Nature Genet. , vol.12 , pp. 227-229
- Hartl, D.L.¹

51
- 0033962584
- Self-inflicted wounds, template-directed gap repair and a recombination hot-spot. Effects of the mariner transposase
- (2000) Genetics , vol.154 , pp. 647-656
- Lohe, A.R.¹ Timmons, C.² Beerman, I.³ Lozovskaya, E.R.⁴ Harll, D.L.⁵

52
- 0022344309
- Forensic application of DNA 'fingerprints'
- (1985) Nature , vol.318 , pp. 577-579
- Gill, P.¹ Jeffreys, A.J.² Werrett, D.J.³

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