-
1
-
-
0020312498
-
Polymorphism in immunoglobulin heavy chains suggesting gene conversion
-
Clarke, S.H., Claflin, J.L. & Rudikoff, S. Polymorphism in immunoglobulin heavy chains suggesting gene conversion. Proc. Natl. Acad. Sci. USA 79, 3280-3284 (1982).
-
(1982)
Proc. Natl. Acad. Sci. USA
, vol.79
, pp. 3280-3284
-
-
Clarke, S.H.1
Claflin, J.L.2
Rudikoff, S.3
-
2
-
-
0342807477
-
High-frequency meiotic gene conversion between repeated genes on nonhomologous chromosomes in yeast
-
Jinks-Robertson, S. & Petes, T.D. High-frequency meiotic gene conversion between repeated genes on nonhomologous chromosomes in yeast. Proc. Natl. Acad. Sci. USA 82, 3350-3354 (1985).
-
(1985)
Proc. Natl. Acad. Sci. USA
, vol.82
, pp. 3350-3354
-
-
Jinks-Robertson, S.1
Petes, T.D.2
-
3
-
-
0022596851
-
Short gene conversions in the human fetal globin gene region: A by-product of chromosome pairing during meiosis?
-
Powers, P.A. & Smithies, O. Short gene conversions in the human fetal globin gene region: a by-product of chromosome pairing during meiosis? Genetics 112, 343-358 (1986).
-
(1986)
Genetics
, vol.112
, pp. 343-358
-
-
Powers, P.A.1
Smithies, O.2
-
4
-
-
0035020152
-
Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes
-
Ogasawara, K. et al. Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes. Immunogenetics 53, 190-199 (2001).
-
(2001)
Immunogenetics
, vol.53
, pp. 190-199
-
-
Ogasawara, K.1
-
5
-
-
0037967231
-
Abundant gene conversion between arms of palindromes in human and ape Y chromosomes
-
Rozen, S. et al. Abundant gene conversion between arms of palindromes in human and ape Y chromosomes. Nature 423, 873-876 (2003).
-
(2003)
Nature
, vol.423
, pp. 873-876
-
-
Rozen, S.1
-
6
-
-
0027477152
-
A de novo pathological point mutation at the 21-hydroxylase locus: Implications for gene conversion in the human genome
-
Collier, S., Tassabehji, M., Sinnott, P. & Strachan, T. A de novo pathological point mutation at the 21-hydroxylase locus: implications for gene conversion in the human genome. Nat. Genet. 3, 260-265 (1993).
-
(1993)
Nat. Genet.
, vol.3
, pp. 260-265
-
-
Collier, S.1
Tassabehji, M.2
Sinnott, P.3
Strachan, T.4
-
7
-
-
0031857758
-
Gene conversion is a likely cause of mutation in PKD1
-
Watnick, T.J., Gandolph, M.A., Weber, H., Neumann, H.P. & Germino, G.G. Gene conversion is a likely cause of mutation in PKD1. Hum. Mol. Genet. 7, 1239-1243 (1998).
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1239-1243
-
-
Watnick, T.J.1
Gandolph, M.A.2
Weber, H.3
Neumann, H.P.4
Germino, G.G.5
-
8
-
-
0034795550
-
Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex
-
Jeffreys, A.J., Kauppi, L. & Neumann, R. Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex. Nat. Genet. 29, 217-222 (2001).
-
(2001)
Nat. Genet.
, vol.29
, pp. 217-222
-
-
Jeffreys, A.J.1
Kauppi, L.2
Neumann, R.3
-
9
-
-
0036648248
-
Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX
-
May, C.A., Shone, A.C., Kalaydjieva, L., Sajantila, A. & Jeffreys, A.J. Crossover clustering and rapid decay of linkage disequilibrium in the Xp/ Yp pseudoautosomal gene SHOX. Nat. Genet. 31, 272-275 (2002).
-
(2002)
Nat. Genet.
, vol.31
, pp. 272-275
-
-
May, C.A.1
Shone, A.C.2
Kalaydjieva, L.3
Sajantila, A.4
Jeffreys, A.J.5
-
10
-
-
0036604253
-
Characterization of a de novo conversion in human complement C4 gene producing a C4B5-like protein
-
Jaatinen, T., Eholuoto, M., Laitinen, T. & Lokki, M.L. Characterization of a de novo conversion in human complement C4 gene producing a C4B5-like protein. J. Immunol. 168, 5652-5658 (2002).
-
(2002)
J. Immunol.
, vol.168
, pp. 5652-5658
-
-
Jaatinen, T.1
Eholuoto, M.2
Laitinen, T.3
Lokki, M.L.4
-
11
-
-
0028841215
-
Analysis of mutational changes at the HLA locus in single human sperm
-
Huang, M.M., Erlich, H.A., Goodman, M.F. & Arnheim, N. Analysis of mutational changes at the HLA locus in single human sperm. Hum. Mutat. 6, 303-310 (1995).
-
(1995)
Hum. Mutat.
, vol.6
, pp. 303-310
-
-
Huang, M.M.1
Erlich, H.A.2
Goodman, M.F.3
Arnheim, N.4
-
12
-
-
0028786666
-
Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms
-
Tusie-Luna, M.T. & White, P.C. Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms. Proc. Natl. Acad. Sci. USA 92, 10796-10800 (1995).
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 10796-10800
-
-
Tusie-Luna, M.T.1
White, P.C.2
-
13
-
-
0034892915
-
Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion
-
Ardlie, K. et al. Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion. Am. J. Hum. Genet. 69, 582-589 (2001).
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 582-589
-
-
Ardlie, K.1
-
14
-
-
0026095133
-
Shared epitopes among HLA class II alleles: Gene conversion, common ancestry and balancing selection
-
Erlich, H.A. & Gyllensten, U.B. Shared epitopes among HLA class II alleles: gene conversion, common ancestry and balancing selection. Immunol. Today 12, 411-414 (1991).
-
(1991)
Immunol. Today
, vol.12
, pp. 411-414
-
-
Erlich, H.A.1
Gyllensten, U.B.2
-
15
-
-
0034701292
-
High-resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot
-
Jeffreys, A.J., Ritchie, A. & Neumann, R. High-resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot. Hum. Mol. Genet. 9, 725-733 (2000).
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 725-733
-
-
Jeffreys, A.J.1
Ritchie, A.2
Neumann, R.3
-
16
-
-
0029120677
-
New HLA-DPB1 alleles generated by interallelic gene conversion detected by analysis of sperm
-
Zangenberg, G., Huang, M.M., Arnheim, N. & Erlich, H. New HLA-DPB1 alleles generated by interallelic gene conversion detected by analysis of sperm. Nat. Genet. 10, 407-414 (1995).
-
(1995)
Nat. Genet.
, vol.10
, pp. 407-414
-
-
Zangenberg, G.1
Huang, M.M.2
Arnheim, N.3
Erlich, H.4
-
17
-
-
0142092536
-
DNA enrichment by allele-specific hybridisation (DEASH): A novel method for haplotyping and for detecting low frequency base substitutional variants and recombinant DNA molecules
-
Jeffreys, A.J. & May, C.A. DNA enrichment by allele-specific hybridisation (DEASH): a novel method for haplotyping and for detecting low frequency base substitutional variants and recombinant DNA molecules. Genome Res. 13, 2316-2324 (2003).
-
(2003)
Genome Res.
, vol.13
, pp. 2316-2324
-
-
Jeffreys, A.J.1
May, C.A.2
-
18
-
-
0020541955
-
The double-strand-break repair model for recombination
-
Szostak, J.W., Orr-Weaver, T.L., Rothstein, R.J. & Stahl, F.W. The double-strand-break repair model for recombination. Cell 33, 25-35 (1983).
-
(1983)
Cell
, vol.33
, pp. 25-35
-
-
Szostak, J.W.1
Orr-Weaver, T.L.2
Rothstein, R.J.3
Stahl, F.W.4
-
19
-
-
0035223878
-
Mechanism and control of meiotic recombination initiation
-
Keeney, S. Mechanism and control of meiotic recombination initiation. Curr. Top. Dev. Biol. 52, 1-53 (2001).
-
(2001)
Curr. Top. Dev. Biol.
, vol.52
, pp. 1-53
-
-
Keeney, S.1
-
20
-
-
0036649022
-
Reciprocal crossover asymmetry and meiotic drive in a human recombination hot spot
-
Jeffreys, A.J. & Neumann, R. Reciprocal crossover asymmetry and meiotic drive in a human recombination hot spot. Nat. Genet. 31, 267-271 (2002).
-
(2002)
Nat. Genet.
, vol.31
, pp. 267-271
-
-
Jeffreys, A.J.1
Neumann, R.2
-
21
-
-
0038799991
-
Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae
-
Paques, F. & Haber, J.E. Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae. Microbiol. Mol. Biol. Rev. 63, 349-404 (1999).
-
(1999)
Microbiol. Mol. Biol. Rev.
, vol.63
, pp. 349-404
-
-
Paques, F.1
Haber, J.E.2
-
22
-
-
0036787813
-
An initiation site for meiotic crossing-over and gene conversion in the mouse
-
Guillon, H. & De Massy, B. An initiation site for meiotic crossing-over and gene conversion in the mouse. Nat. Genet. 32, 296-299 (2002).
-
(2002)
Nat. Genet.
, vol.32
, pp. 296-299
-
-
Guillon, H.1
De Massy, B.2
-
23
-
-
0028146106
-
Meiotic gene conversion tract length distribution within the rosy locus of Drosophila melanogaster
-
Hilliker, A.J. et al. Meiotic gene conversion tract length distribution within the rosy locus of Drosophila melanogaster. Genetics 137, 1019-1026 (1994).
-
(1994)
Genetics
, vol.137
, pp. 1019-1026
-
-
Hilliker, A.J.1
-
24
-
-
0025609159
-
Decreasing gradients of gene conversion on both sides of the initiation site for meiotic recombination at the ARG4 locus in yeast
-
Schultes, N.P. & Szostak, J.W. Decreasing gradients of gene conversion on both sides of the initiation site for meiotic recombination at the ARG4 locus in yeast. Genetics 126, 813-822 (1990).
-
(1990)
Genetics
, vol.126
, pp. 813-822
-
-
Schultes, N.P.1
Szostak, J.W.2
-
25
-
-
0024462116
-
Length and distribution of meiotic gene conversion tracts and crossovers in Saccharomyces cerevisiae
-
Borts, R.H. & Haber, J.E. Length and distribution of meiotic gene conversion tracts and crossovers in Saccharomyces cerevisiae. Genetics 123, 69-80 (1989).
-
(1989)
Genetics
, vol.123
, pp. 69-80
-
-
Borts, R.H.1
Haber, J.E.2
-
26
-
-
0036799145
-
Carriership of a defective tenascin-X gene in steroid 21-hydroxylase deficiency patients: TNXB-TNXA hybrids in apparent large-scale gene conversions
-
Koppens, P.F., Hoogenboezem, T. & Degenhart, H.J. Carriership of a defective tenascin-X gene in steroid 21-hydroxylase deficiency patients: TNXB-TNXA hybrids in apparent large-scale gene conversions. Hum. Mol. Genet. 11, 2581-2590 (2002).
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2581-2590
-
-
Koppens, P.F.1
Hoogenboezem, T.2
Degenhart, H.J.3
-
27
-
-
16944367290
-
Prenatal diagnosis of the fragile X syndrome: Loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus
-
Losekoot, M. et al. Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus. J. Med. Genet. 34, 924-926 (1997).
-
(1997)
J. Med. Genet.
, vol.34
, pp. 924-926
-
-
Losekoot, M.1
-
28
-
-
0043267974
-
Haplotype blocks and linkage disequilibrium in the human genome
-
Wall, J.D. & Pritchard, J.K. Haplotype blocks and linkage disequilibrium in the human genome. Nat. Rev. Genet. 4, 587-597 (2003).
-
(2003)
Nat. Rev. Genet.
, vol.4
, pp. 587-597
-
-
Wall, J.D.1
Pritchard, J.K.2
-
29
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel, S.B. et al. The structure of haplotype blocks in the human genome. Science 296, 2225-2229 (2002).
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
-
30
-
-
0036844238
-
Distribution of recombination crossovers and the origin of haplotype blocks: The interplay of population history, recombination, and mutation
-
Wang, N., Akey, J.M., Zhang, K., Chakraborty, R. & Jin, L. Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation. Am. J. Hum. Genet. 71, 1227-1234 (2002).
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 1227-1234
-
-
Wang, N.1
Akey, J.M.2
Zhang, K.3
Chakraborty, R.4
Jin, L.5
|