-
4
-
-
0028261654
-
Homologous recombination in fission yeast: Absence of crossover interference and synaptonemal complex
-
(1994)
Experientia
, vol.50
, pp. 295-306
-
-
Kohli, J.1
Bahler, J.2
-
6
-
-
0033569601
-
A mouse homolog of the Saccharomyces cerevisiae meiotic recombination DNA transesterase Spo11p
-
(1999)
Genomics
, vol.61
, pp. 170-182
-
-
Keeney, S.1
Baudat, F.2
Angeles, M.3
Zhou, Z.H.4
Copeland, N.G.5
Jenkins, N.A.6
Manova, K.7
Jasin, M.8
-
15
-
-
0033594904
-
Disruption of mRad50 causes embryonic stem cell lethality, abnormal embryonic development, and sensitivity to ionizing radiation
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 7376-7381
-
-
Luo, G.1
Yao, M.S.2
Bender, C.F.3
Mills, M.4
Bladl, A.R.5
Bradley, A.6
Petrini, J.H.7
-
16
-
-
0030749867
-
Conditional gene targeted deletion by Cre recombinase demonstrates the requirement for the double-strand break repair Mre11 protein in murine embryonic stem cells
-
(1997)
Nucl Acids Res
, vol.25
, pp. 2985-2991
-
-
Xiao, Y.1
Weaver, D.T.2
-
17
-
-
0033544724
-
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxiatelangieotasia-like disorder
-
(1999)
Cell
, vol.99
, pp. 577-587
-
-
Stewart, G.S.1
Maser, R.S.2
Stankovic, T.3
Bressan, D.A.4
Kaplan, M.I.5
Jaspers, N.G.6
Raams, A.7
Byrd, P.J.8
Petrini, J.H.9
Taylor, A.M.10
-
21
-
-
0026697166
-
DMC1: A meiosis-specific yeast homolog of E. coli recA required for recombination, synaptonemal complex formation, and cell cycle progression
-
(1992)
Cell
, vol.69
, pp. 439-456
-
-
Bishop, D.K.1
Park, D.2
Xu, L.3
Kleckner, N.4
-
22
-
-
0028600050
-
RecA homologs Dmc1 and Rad51 interact to form multiple nuclear complexes prior to meiotic chromosome synapsis
-
(1994)
Cell
, vol.79
, pp. 1081-1092
-
-
Bishop, D.K.1
-
23
-
-
0029909565
-
A mutation in mouse rad51 results in an early embryonic lethal that is suppressed by a mutation in p53
-
(1996)
Mol Cell Biol
, vol.16
, pp. 7133-7143
-
-
Lim, D.S.1
Hasty, P.2
-
24
-
-
0029987450
-
Targeted disruption of the Rad51 gene leads to lethality in embryonic mice
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 6236-6240
-
-
Tsuzuki, T.1
Fujii, Y.2
Sakumi, K.3
Tominaga, Y.4
Nakao, K.5
Sekiguchi, M.6
Matsushiro, A.7
Yoshimura, Y.8
Morita, T.9
-
29
-
-
0032039077
-
Meiotic prophase arrest with failiure of chromosome synapsis in mice deficient for Dmc1, a germline-specific RecA homolog
-
(1998)
Mol Cell
, vol.1
, pp. 697-705
-
-
Pittman, D.L.1
Cobb, J.2
Schimenti, K.J.3
Wilson, L.A.4
Cooper, D.M.5
Brignull, E.6
Handel, M.A.7
Schimenti, J.C.8
-
31
-
-
0028785586
-
The Bloom's syndrome gene product is homologous to RecQ helicases
-
(1995)
Cell
, vol.83
, pp. 655-666
-
-
Ellis, N.A.1
Groden, J.2
Ye, T.Z.3
Straugnen, J.4
Lennon, D.J.5
Ciocci, S.6
Proytcheva, M.7
German, J.8
-
33
-
-
15844409553
-
Positional cloning of the Werner's syndrome gene
-
(1996)
Science
, vol.272
, pp. 258-262
-
-
Yu, C.E.1
Oshima, J.2
Fu, Y.H.3
Wijsman, E.M.4
Hisama, F.5
Alisch, R.6
Matthews, S.7
Nakura, J.8
Miki, T.9
Ouais, S.10
-
35
-
-
0030751354
-
The Werner syndrome protein is a DNA helicase
-
(1997)
Nat Genet
, vol.17
, pp. 100-103
-
-
Gray, M.D.1
Shen, J.C.2
Kamath-Loeb, A.S.3
Blank, A.4
Sopher, B.L.5
Martin, G.M.6
Oshima, J.7
Loeb, L.A.8
-
39
-
-
0034737641
-
The Bloom's syndrome gene product interacts with topoisomerase III
-
(2000)
J Biol Chem
, vol.275
, pp. 9636-9644
-
-
Wu, L.1
Davies, S.L.2
North, P.S.3
Goulaouic, H.4
Riou, J.-F.5
Turley, H.6
Gatter, K.C.7
Hickson, I.D.8
-
40
-
-
0030582673
-
Meiotic recombination in yeast: Coronation of the double-strand-break repair model
-
(1996)
Cell
, vol.87
, pp. 965-968
-
-
Stahl, F.1
-
46
-
-
0027971222
-
An essential gene ESR1, is required for mitotic cell growth, DNA repair and meiotic recombination in Saccharomyces cerevisiae
-
(1994)
Nucl Acids Res
, vol.22
, pp. 3104-3112
-
-
Kato, R.1
Ogawa, H.2
-
47
-
-
0029827367
-
The Schizosaccharomyces pombe rad3 checkpoint gene
-
(1996)
EMBO J
, vol.15
, pp. 6641-6651
-
-
Bentley, N.J.1
Holtzman, D.A.2
Flaggs, G.3
Keegan, K.S.4
DeMaggio, A.5
Ford, J.C.6
Hoekstra, M.7
Carr, A.M.8
-
54
-
-
15844426692
-
Atm-deficient mice: A paradigm of ataxia telangiectasia
-
(1996)
Cell
, vol.86
, pp. 159-171
-
-
Barlow, C.1
Hirotsune, S.2
Paylor, R.3
Liyanage, M.4
Eckhaus, M.5
Collins, F.6
Shiloh, Y.7
Crawley, J.N.8
Ried, T.9
Tagle, D.10
-
55
-
-
18244421978
-
Atm deficiency results in severe meiotic disruption as early as leptonema of prophase I
-
(1998)
Development
, vol.125
, pp. 4007-4017
-
-
Barlow, C.1
Liyanage, M.2
Moens, P.B.3
Tarsounas, M.4
Nagashima, K.5
Brown, K.6
Rottinghaus, S.7
Jackson, S.P.8
Tagle, D.9
Ried, T.10
-
56
-
-
0032898945
-
The association of ATR protein with mouse meiotic chromosome cores
-
(1999)
Chromosoma
, vol.108
, pp. 95-102
-
-
Moens, P.B.1
Tarsounas, M.2
Morita, T.3
Habu, T.4
Rottinghaus, S.T.5
Freire, R.6
Jackson, S.P.7
Barlow, C.8
Wynshaw-Boris, A.9
-
57
-
-
10244227923
-
The Atr and Atm protein kinases associate with different sites along meiotically pairing chromosomes
-
(1996)
Genes Dev
, vol.10
, pp. 2423-2437
-
-
Keegan, K.S.1
Holtzman, D.A.2
Plug, A.W.3
Christenson, E.R.4
Brainerd, E.E.5
Flaggs, G.6
Bentley, N.J.7
Taylor, E.M.8
Meyn, M.S.9
Moss, S.B.10
-
66
-
-
0032900534
-
Mammalian MutS homologue 5 is required for chromosome pairing in meiosis
-
(1999)
Nat Genet
, vol.21
, pp. 123-127
-
-
Edelmann, W.1
Cohen, P.E.2
Kneitz, B.3
Winand, N.4
Lia, M.5
Heyer, J.6
Kolodner, R.7
Pollard, J.W.8
Kucherlapati, R.9
-
67
-
-
0033557912
-
hMSH5: A human MutS homologue that forms a novel heterodimer with hMSH4 and is expressed during spermatogenesis
-
(1999)
Cancer Res
, vol.59
, pp. 816-822
-
-
Bocker, T.1
Barusevicius, A.2
Snowden, T.3
Rasio, D.4
Guerrette, S.5
Robbins, D.6
Schmidt, C.7
Burczak, J.8
Croce, C.M.9
Copeland, T.10
-
69
-
-
0034192849
-
MutS homolog 4 (MSH4) localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice
-
(2000)
Genes Dev
, vol.14
, pp. 1085-1097
-
-
Kneitz, B.1
Cohen, P.E.2
Avdievich, E.3
Zhu, L.4
Kane, M.F.5
Hou, H.6
Koledner, R.D.7
Kucherlapati, R.8
Pollard, J.W.9
Edelmann, W.10
-
73
-
-
8944232867
-
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over
-
(1996)
Nat Genet
, vol.13
, pp. 336-342
-
-
Baker, S.M.1
Plug, A.W.2
Prolla, T.A.3
Bronner, C.E.4
Harris, A.C.5
Yao, X.6
Christie, D.M.7
Monell, C.8
Arnheim, N.9
Bradley, A.10
-
75
-
-
15844367099
-
Meiotic pachytene arrest in MLH-1-deficient mice
-
(1996)
Cell
, vol.85
, pp. 1125-1134
-
-
Edelmann, W.1
Cohen, P.E.2
Kane, M.3
Lau, K.4
Morrow, B.5
Bennett, S.6
Umar, A.7
Kunkel, T.8
Cattoretti, G.9
Chaganti, R.10
-
77
-
-
0029099989
-
Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synopsis in meiosis
-
(1995)
Cell
, vol.82
, pp. 309-319
-
-
Baker, S.M.1
Bronner, C.E.2
Zhang, L.3
Plug, A.K.4
Robatzek, M.5
Warren, G.6
Elliott, E.A.7
Yu, J.8
Ashley, T.9
Arnheim, N.10
-
80
-
-
0033986475
-
MLH3: A DNA mismatch repair gene associated with mammalian microsatellite instability
-
(2000)
Nat Genet
, vol.24
, pp. 27-35
-
-
Lipkin, S.M.1
Wang, V.2
Jacoby, R.3
Banerjee-Basu, S.4
Baxevanis, A.D.5
Lynch, H.T.6
Elliott, R.M.7
Collins, F.S.8
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