-
1
-
-
10744230604
-
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2
-
Moreira MC, Klur S, Watanabe M, Nemeth AH, Le Ber I, et al. (2004) Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. Nat Genet 36: 225-227.
-
(2004)
Nat Genet
, vol.36
, pp. 225-227
-
-
Moreira, M.C.1
Klur, S.2
Watanabe, M.3
Nemeth, A.H.4
Le Ber, I.5
-
2
-
-
70349957925
-
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients
-
Anheim M, Monga B, Fleury M, Charles P, Barbot C, et al. (2009) Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients. Brain 132 (Pt 10): 2688-2698.
-
(2009)
Brain
, vol.132
, Issue.PART 10
, pp. 2688-2698
-
-
Anheim, M.1
Monga, B.2
Fleury, M.3
Charles, P.4
Barbot, C.5
-
3
-
-
2442658908
-
DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)
-
Chen YZ, Bennett CL, Huynh HM, Blair IP, Puls I, et al. (2004) DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). Am J Hum Genet 74: 1128-1135.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1128-1135
-
-
Chen, Y.Z.1
Bennett, C.L.2
Huynh, H.M.3
Blair, I.P.4
Puls, I.5
-
4
-
-
2342453900
-
Multiple protein/protein and protein/RNA interactions suggest roles for yeast DNA/RNA helicase Sen1p in transcription, transcription-coupled DNA repair and RNA processing
-
Ursic D, Chinchilla K, Finkel JS, Culbertson MR, (2004) Multiple protein/protein and protein/RNA interactions suggest roles for yeast DNA/RNA helicase Sen1p in transcription, transcription-coupled DNA repair and RNA processing. Nucleic Acids Res 32: 2441-2452.
-
(2004)
Nucleic Acids Res
, vol.32
, pp. 2441-2452
-
-
Ursic, D.1
Chinchilla, K.2
Finkel, J.S.3
Culbertson, M.R.4
-
5
-
-
34250775522
-
Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage
-
Suraweera A, Becherel OJ, Chen P, Rundle N, Woods R, et al. (2007) Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage. J Cell Biol 177: 969-979.
-
(2007)
J Cell Biol
, vol.177
, pp. 969-979
-
-
Suraweera, A.1
Becherel, O.J.2
Chen, P.3
Rundle, N.4
Woods, R.5
-
6
-
-
69449101422
-
Functional role for senataxin, defective in ataxia oculomotor apraxia type 2, in transcriptional regulation
-
Suraweera A, Lim Y, Woods R, Birrell GW, Nasim T, et al. (2009) Functional role for senataxin, defective in ataxia oculomotor apraxia type 2, in transcriptional regulation. Hum Mol Genet 18: 3384-3396.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 3384-3396
-
-
Suraweera, A.1
Lim, Y.2
Woods, R.3
Birrell, G.W.4
Nasim, T.5
-
7
-
-
79959345878
-
Human Senataxin Resolves RNA/DNA Hybrids Formed at Transcriptional Pause Sites to Promote Xrn2-Dependent Termination
-
Skourti-Stathaki K, Proudfoot NJ, Gromak N, (2011) Human Senataxin Resolves RNA/DNA Hybrids Formed at Transcriptional Pause Sites to Promote Xrn2-Dependent Termination. Mol Cell 42: 794-805.
-
(2011)
Mol Cell
, vol.42
, pp. 794-805
-
-
Skourti-Stathaki, K.1
Proudfoot, N.J.2
Gromak, N.3
-
8
-
-
0141819093
-
Cotranscriptionally formed DNA:RNA hybrids mediate transcription elongation impairment and transcription-associated recombination
-
Huertas P, Aguilera A, (2003) Cotranscriptionally formed DNA:RNA hybrids mediate transcription elongation impairment and transcription-associated recombination. Mol Cell 12: 711-721.
-
(2003)
Mol Cell
, vol.12
, pp. 711-721
-
-
Huertas, P.1
Aguilera, A.2
-
9
-
-
23744455164
-
Inactivation of the SR protein splicing factor ASF/SF2 results in genomic instability
-
Li X, Manley JL, (2005) Inactivation of the SR protein splicing factor ASF/SF2 results in genomic instability. Cell 122: 365-378.
-
(2005)
Cell
, vol.122
, pp. 365-378
-
-
Li, X.1
Manley, J.L.2
-
10
-
-
78650727733
-
Yeast Sen1 helicase protects the genome from transcription-associated instability
-
Mischo HE, Gomez-Gonzalez B, Grzechnik P, Rondon AG, Wei W, et al. (2011) Yeast Sen1 helicase protects the genome from transcription-associated instability. Mol Cell 41: 21-32.
-
(2011)
Mol Cell
, vol.41
, pp. 21-32
-
-
Mischo, H.E.1
Gomez-Gonzalez, B.2
Grzechnik, P.3
Rondon, A.G.4
Wei, W.5
-
11
-
-
84871861757
-
Senataxin, defective in the neurogenerative disorder AOA-2, lies at the interface of transcription and the DNA damage response
-
doi:10.1128/MCB.01195-12
-
Yüce-Petronczki O, West SC, (2012) Senataxin, defective in the neurogenerative disorder AOA-2, lies at the interface of transcription and the DNA damage response. Mol Cell Biol doi:10.1128/MCB.01195-12.
-
(2012)
Mol Cell Biol
-
-
Yüce-Petronczki, O.1
West, S.C.2
-
12
-
-
84869026790
-
Senataxin Associates with Replication Forks to Protect Fork Integrity across RNA-Polymerase-II-Transcribed Genes
-
Alzu A, Bermejo R, Begnis M, Lucca C, Piccini D, et al. (2012) Senataxin Associates with Replication Forks to Protect Fork Integrity across RNA-Polymerase-II-Transcribed Genes. Cell 151: 835-46.
-
(2012)
Cell
, vol.151
, pp. 835-846
-
-
Alzu, A.1
Bermejo, R.2
Begnis, M.3
Lucca, C.4
Piccini, D.5
-
13
-
-
80055101576
-
A simple composite phenotype scoring system for evaluating mouse models of cerebellar ataxia
-
doi:pii: 1787. 10.3791/1787
-
Guyenet SJ, Furrer SA, Damian VM, Baughan TD, La Spada AR, et al. (2010) A simple composite phenotype scoring system for evaluating mouse models of cerebellar ataxia. J Vis Exp pp. 21 doi:pii: 1787. 10.3791/1787.
-
(2010)
J Vis Exp
, pp. 21
-
-
Guyenet, S.J.1
Furrer, S.A.2
Damian, V.M.3
Baughan, T.D.4
La Spada, A.R.5
-
14
-
-
15844426692
-
Atm-deficient mice: a paradigm of ataxia telangiectasia
-
Barlow C, Hirotsune S, Paylor R, Liyanage M, Eckhaus M, et al. (1996) Atm-deficient mice: a paradigm of ataxia telangiectasia. Cell 86: 159-171.
-
(1996)
Cell
, vol.86
, pp. 159-171
-
-
Barlow, C.1
Hirotsune, S.2
Paylor, R.3
Liyanage, M.4
Eckhaus, M.5
-
15
-
-
0029844048
-
Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma
-
Xu Y, Ashley T, Brainerd EE, Bronson RT, Meyn MS, et al. (1996) Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma. Genes Dev 10: 2411-2422.
-
(1996)
Genes Dev
, vol.10
, pp. 2411-2422
-
-
Xu, Y.1
Ashley, T.2
Brainerd, E.E.3
Bronson, R.T.4
Meyn, M.S.5
-
16
-
-
0035202120
-
Regulation of meiotic recombination and prophase I progression in mammals
-
Cohen PE, Pollard JW, (2001) Regulation of meiotic recombination and prophase I progression in mammals. Bioessays 23: 996-1009.
-
(2001)
Bioessays
, vol.23
, pp. 996-1009
-
-
Cohen, P.E.1
Pollard, J.W.2
-
17
-
-
0034538075
-
Conversion from mitosis to meiosis: morphology and expression of proliferating cell nuclear antigen (PCNA) and Dmc1 during newt spermatogenesis
-
Yazawa T, Yamamoto T, Nakayama T, Hamada S, Abe S, (2000) Conversion from mitosis to meiosis: morphology and expression of proliferating cell nuclear antigen (PCNA) and Dmc1 during newt spermatogenesis. Dev Growth Differ 42: 603-611.
-
(2000)
Dev Growth Differ
, vol.42
, pp. 603-611
-
-
Yazawa, T.1
Yamamoto, T.2
Nakayama, T.3
Hamada, S.4
Abe, S.5
-
18
-
-
4243175916
-
Nucleoprotein transitions during spermiogenesis in mice with transition nuclear protein Tnp1 and Tnp2 mutations
-
Zhao M, Shirley CR, Mounsey S, Meistrich MI, (2004) Nucleoprotein transitions during spermiogenesis in mice with transition nuclear protein Tnp1 and Tnp2 mutations. Biol Reprod 71: 1016-1025.
-
(2004)
Biol Reprod
, vol.71
, pp. 1016-1025
-
-
Zhao, M.1
Shirley, C.R.2
Mounsey, S.3
Meistrich, M.I.4
-
19
-
-
0035223878
-
Mechanism and control of meiotic recombination initiation
-
Keeney S, (2001) Mechanism and control of meiotic recombination initiation. Curr Top Dev Biol 52: 1-53.
-
(2001)
Curr Top Dev Biol
, vol.52
, pp. 1-53
-
-
Keeney, S.1
-
20
-
-
0032861343
-
Megabase chromatin domains involved in DNA double-strand breaks in vivo
-
Rogakou E, Boon P, Redon C, Bonner WM, (1999) Megabase chromatin domains involved in DNA double-strand breaks in vivo. J Cell Biol 146: 905-916.
-
(1999)
J Cell Biol
, vol.146
, pp. 905-916
-
-
Rogakou, E.1
Boon, P.2
Redon, C.3
Bonner, W.M.4
-
21
-
-
0035096507
-
Gamma-H2AX illuminates meiosis
-
Hunter N, Borner GV, Lichten M, Kleckner R, (2001) Gamma-H2AX illuminates meiosis. Nat Genet 27: 236-238.
-
(2001)
Nat Genet
, vol.27
, pp. 236-238
-
-
Hunter, N.1
Borner, G.V.2
Lichten, M.3
Kleckner, R.4
-
22
-
-
10344264478
-
BRCA1, histone H2AX phosphorylation, and male meiotic sex chromosome inactivation
-
Turner J M, Aprelikova O, Xu X, Wang R, Kim S, et al. (2004) BRCA1, histone H2AX phosphorylation, and male meiotic sex chromosome inactivation. Curr Biol 14: 2135-2142.
-
(2004)
Curr Biol
, vol.14
, pp. 2135-2142
-
-
Turner, J.M.1
Aprelikova, O.2
Xu, X.3
Wang, R.4
Kim, S.5
-
23
-
-
0036860728
-
Meiotic sex chromosome inactivation in male mice with targeted disruptions of Xist
-
Turner JM, Mahadevaiah SK, Elliott DJ, Garchon HJ, Pehrson JR, et al. (2002) Meiotic sex chromosome inactivation in male mice with targeted disruptions of Xist. J Cell Sci 115 (Pt 21): 4097-4105.
-
(2002)
J Cell Sci
, vol.115
, Issue.PART 21
, pp. 4097-4105
-
-
Turner, J.M.1
Mahadevaiah, S.K.2
Elliott, D.J.3
Garchon, H.J.4
Pehrson, J.R.5
-
24
-
-
11244350100
-
Silencing of unsynapsed meiotic chromosomes in the mouse
-
Turner JM, Mahadevaiah SK, Fernandez-Capetillo O, Nussenzweig A, Xu X, et al. (2005) Silencing of unsynapsed meiotic chromosomes in the mouse. Nat Genet 37: 41-47.
-
(2005)
Nat Genet
, vol.37
, pp. 41-47
-
-
Turner, J.M.1
Mahadevaiah, S.K.2
Fernandez-Capetillo, O.3
Nussenzweig, A.4
Xu, X.5
-
25
-
-
0028807903
-
Dynamic changes in Rad51 distribution on chromatin during meiosis in male and female vertebrates
-
Ashley T, Plug AW, Xu J, Solari AJ, Reddy G, et al. (1995) Dynamic changes in Rad51 distribution on chromatin during meiosis in male and female vertebrates. Chromosoma 104: 19-28.
-
(1995)
Chromosoma
, vol.104
, pp. 19-28
-
-
Ashley, T.1
Plug, A.W.2
Xu, J.3
Solari, A.J.4
Reddy, G.5
-
26
-
-
8944232867
-
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over
-
Baker SM, Plug AW, Prolla TA, Bronner CE, Harris AC, et al. (1996) Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nat Genet 13: 336-342.
-
(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
-
27
-
-
0030906684
-
Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis
-
Hunter N, Borts RH, (1997) Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis. Genes Dev 11: 1573-1582.
-
(1997)
Genes Dev
, vol.11
, pp. 1573-1582
-
-
Hunter, N.1
Borts, R.H.2
-
28
-
-
0032918559
-
Distribution of crossing over on mouse synaptonemal complexes using immunofluorescent localization of MLH1 protein
-
Anderson LK, Reeves A, Webb LM, Ashley T, (1999) Distribution of crossing over on mouse synaptonemal complexes using immunofluorescent localization of MLH1 protein. Genetics 151: 1569-79.
-
(1999)
Genetics
, vol.151
, pp. 1569-1579
-
-
Anderson, L.K.1
Reeves, A.2
Webb, L.M.3
Ashley, T.4
-
29
-
-
0022516464
-
Characterization of monoclonal antibody to DNA:RNA and its application to immunodetection of hybrids
-
Boguslawski SJ, Smith DE, Michalak MA, Mickelson KE, Yehle CO, et al. (1986) Characterization of monoclonal antibody to DNA:RNA and its application to immunodetection of hybrids. J Immunol Methods 89: 123-130.
-
(1986)
J Immunol Methods
, vol.89
, pp. 123-130
-
-
Boguslawski, S.J.1
Smith, D.E.2
Michalak, M.A.3
Mickelson, K.E.4
Yehle, C.O.5
-
30
-
-
33645805622
-
An antibody-based microarray assay for small RNA detection
-
Hu Z, Zhang A, Storz G, Gottesman S, Leppla SH, (2006) An antibody-based microarray assay for small RNA detection. Nucleic Acids Res 34: e52.
-
(2006)
Nucleic Acids Res
, vol.34
-
-
Hu, Z.1
Zhang, A.2
Storz, G.3
Gottesman, S.4
Leppla, S.H.5
-
31
-
-
84864872064
-
Inactivation or non-reactivation: what accounts better for the silence of sex chromosomes during mammalian male meiosis?
-
Page J, de la Fuente R, Manterola M, Parra MT, Viera MT, et al. (2012) Inactivation or non-reactivation: what accounts better for the silence of sex chromosomes during mammalian male meiosis? Chromosoma 121: 307-326.
-
(2012)
Chromosoma
, vol.121
, pp. 307-326
-
-
Page, J.1
de la Fuente, R.2
Manterola, M.3
Parra, M.T.4
Viera, M.T.5
-
32
-
-
0346634937
-
H2AX is required for chromatin remodeling and inactivation of sex chromosomes in male mouse meiosis
-
Fernandez-Capetillo O, Mahadevaiah SK, Celeste A, Romanienko PJ, Camerini-Otero RT, et al. (2003) H2AX is required for chromatin remodeling and inactivation of sex chromosomes in male mouse meiosis. Dev Cell 4: 497-508.
-
(2003)
Dev Cell
, vol.4
, pp. 497-508
-
-
Fernandez-Capetillo, O.1
Mahadevaiah, S.K.2
Celeste, A.3
Romanienko, P.J.4
Camerini-Otero, R.T.5
-
33
-
-
79955690241
-
MDC1 directs chromosome-wide silencing of the sex chromosomes in male germ cells
-
Ichijima Y, Ichijima M, Lou Z, Nussenzweig A, Camerini-Otero RD, et al. (2011) MDC1 directs chromosome-wide silencing of the sex chromosomes in male germ cells. Genes Dev 25: 959-971.
-
(2011)
Genes Dev
, vol.25
, pp. 959-971
-
-
Ichijima, Y.1
Ichijima, M.2
Lou, Z.3
Nussenzweig, A.4
Camerini-Otero, R.D.5
-
34
-
-
2142822506
-
The XY body: a specialized meiotic chromatin domain
-
Handel MA, (2004) The XY body: a specialized meiotic chromatin domain. Exp Cell Res 296: 57-63.
-
(2004)
Exp Cell Res
, vol.296
, pp. 57-63
-
-
Handel, M.A.1
-
35
-
-
26444490659
-
Differential expression of sex-linked and autosomal germ-cell-specific genes during spermatogenesis in the mouse
-
Wang PJ, Page DC, McCarrey JR, (2005) Differential expression of sex-linked and autosomal germ-cell-specific genes during spermatogenesis in the mouse. Hum Mol Genet 14: 2911-2918.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 2911-2918
-
-
Wang, P.J.1
Page, D.C.2
McCarrey, J.R.3
-
36
-
-
78650144544
-
Evidence that meiotic sex chromosome inactivation is essential for male fertility
-
Royo H, Polikiewicz G, Mahadevaiah SK, Prosser H, Mitchell M, et al. (2010) Evidence that meiotic sex chromosome inactivation is essential for male fertility. Curr Biol 20: 2117-2123.
-
(2010)
Curr Biol
, vol.20
, pp. 2117-2123
-
-
Royo, H.1
Polikiewicz, G.2
Mahadevaiah, S.K.3
Prosser, H.4
Mitchell, M.5
-
37
-
-
12844280588
-
Silencing of unpaired chromatin and histone H2A ubiquitination in mammalain meiosis
-
Baarends WM, Wassenaar E, van der Laan R, Hoogerbrugge J, Sleddens-Linkels E, et al. (2005) Silencing of unpaired chromatin and histone H2A ubiquitination in mammalain meiosis. Mol Cell Biol 25: 1041-1053.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 1041-1053
-
-
Baarends, W.M.1
Wassenaar, E.2
van der Laan, R.3
Hoogerbrugge, J.4
Sleddens-Linkels, E.5
-
38
-
-
0033634652
-
The mouse Spo11 gene is required for meiotic chromosome synapsis
-
Romanienko PJ, Camerini-Otero RD, (2000) The mouse Spo11 gene is required for meiotic chromosome synapsis. Mol Cell 6: 975-987.
-
(2000)
Mol Cell
, vol.6
, pp. 975-987
-
-
Romanienko, P.J.1
Camerini-Otero, R.D.2
-
39
-
-
0032039077
-
Meiotic prophase arrest with failure of chromosome synapsis in mice deficient for Dmc1, a germline-specific RecA homolog
-
Pittman DL, Cobb J, Schimenti KJ, Wilson LA, Cooper DM, et al. (1998) Meiotic prophase arrest with failure of chromosome synapsis in mice deficient for Dmc1, a germline-specific RecA homolog. Mol Cell 1: 697-705.
-
(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
-
40
-
-
0032823314
-
Growth retardation, DNA repair defects, and lack of spermatogenesis in BRCA1-deficient mice
-
Cressman VL, Backlund DC, Avrutskaya AV, Leadon SA, Godfrey V, et al. (1999) Growth retardation, DNA repair defects, and lack of spermatogenesis in BRCA1-deficient mice. Mol Cell Biol 19: 7061-7075.
-
(1999)
Mol Cell Biol
, vol.19
, pp. 7061-7075
-
-
Cressman, V.L.1
Backlund, D.C.2
Avrutskaya, A.V.3
Leadon, S.A.4
Godfrey, V.5
-
41
-
-
0032900534
-
Mammalian MutS homologue 5 is required for chromosome pairing in meiosis
-
Edelmann W, Cohen PE, Kneitz B, Winand N, Lia M, et al. (1999) Mammalian MutS homologue 5 is required for chromosome pairing in meiosis. Nat Genet 21: 123-127.
-
(1999)
Nat Genet
, vol.21
, pp. 123-127
-
-
Edelmann, W.1
Cohen, P.E.2
Kneitz, B.3
Winand, N.4
Lia, M.5
-
42
-
-
0034192849
-
MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice
-
Kneitz B, Cohen PE, Avdievich E, Zhu L, Kane MF, et al. (2000) MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice. Genes Dev 14: 1085-1097.
-
(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
-
43
-
-
27744579794
-
Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I
-
Kolas NK, Svetlanov A, Lenzi ML, Macaluso FP, Lipkin SM, et al. (2005) Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I. J Cell Biol 171: 447-458.
-
(2005)
J Cell Biol
, vol.171
, pp. 447-458
-
-
Kolas, N.K.1
Svetlanov, A.2
Lenzi, M.L.3
Macaluso, F.P.4
Lipkin, S.M.5
-
44
-
-
0038296998
-
Impaired meiotic DNA-damage repair and lack of crossing-over during spermatogenesis in BRCA1 full-length isoform deficient mice
-
Xu X, Aprelikova OI, Moens P, Deng CX, Furth PA, (2003) Impaired meiotic DNA-damage repair and lack of crossing-over during spermatogenesis in BRCA1 full-length isoform deficient mice. Development 130: 2001-2012.
-
(2003)
Development
, vol.130
, pp. 2001-2012
-
-
Xu, X.1
Aprelikova, O.I.2
Moens, P.3
Deng, C.X.4
Furth, P.A.5
-
45
-
-
26944477491
-
mRNA processing and genomic instability
-
Aguilera A, (2005) mRNA processing and genomic instability. Nat Struct Mol Biol 12: 737-738.
-
(2005)
Nat Struct Mol Biol
, vol.12
, pp. 737-738
-
-
Aguilera, A.1
-
46
-
-
84867021526
-
R-loops cause replication impairment and genome instability during meiosis
-
Castellano-Pozo M, Garcia-Muse T, Aguilera A, (2012) R-loops cause replication impairment and genome instability during meiosis. EMBO Reports 13: 923-929.
-
(2012)
EMBO Reports
, vol.13
, pp. 923-929
-
-
Castellano-Pozo, M.1
Garcia-Muse, T.2
Aguilera, A.3
-
47
-
-
80053645721
-
R-loop meidated genomic instability is caused by impairement of replication fork progression
-
Gan W, Guan Z, Liu J, Gui T, Shen K, et al. (2011) R-loop meidated genomic instability is caused by impairement of replication fork progression. Genes Dev 25: 2041-2056.
-
(2011)
Genes Dev
, vol.25
, pp. 2041-2056
-
-
Gan, W.1
Guan, Z.2
Liu, J.3
Gui, T.4
Shen, K.5
-
48
-
-
74949110813
-
DNA double-strand breaks and ATM activation by transcription-blocking DNA lesions
-
Sordet O, Nakamura AJ, Redon CE, Pommier Y, (2010) DNA double-strand breaks and ATM activation by transcription-blocking DNA lesions. Cell Cycle 9: 274-278.
-
(2010)
Cell Cycle
, vol.9
, pp. 274-278
-
-
Sordet, O.1
Nakamura, A.J.2
Redon, C.E.3
Pommier, Y.4
-
49
-
-
34250626425
-
Meiotic sex chromosome inactivation
-
Turner JM, (2007) Meiotic sex chromosome inactivation. Development 134: 1823-1831.
-
(2007)
Development
, vol.134
, pp. 1823-1831
-
-
Turner, J.M.1
-
50
-
-
0027511117
-
Sex chromosomes, recombination, and chromatin conformation
-
McKee BD, Handel MA, (1993) Sex chromosomes, recombination, and chromatin conformation. Chromosoma 102: 71-80.
-
(1993)
Chromosoma
, vol.102
, pp. 71-80
-
-
McKee, B.D.1
Handel, M.A.2
-
51
-
-
0035097808
-
Recombinational DNA double-strand breaks in mice precede synapsis
-
Mahadevaiah SK, Turner JM, Baudat F, Rogakou EP, de Boer P, et al. (2001) Recombinational DNA double-strand breaks in mice precede synapsis. Nat Genet 27: 271-276.
-
(2001)
Nat Genet
, vol.27
, pp. 271-276
-
-
Mahadevaiah, S.K.1
Turner, J.M.2
Baudat, F.3
Rogakou, E.P.4
de Boer, P.5
-
53
-
-
80052567822
-
BRCA1 tumour suppression occurs via heterochromatin-mediated silencing
-
Zhu Q, Pao GM, Huynh AM, Suh H, Tonnu N, et al. (2011) BRCA1 tumour suppression occurs via heterochromatin-mediated silencing. Nature 7363: 179-184.
-
(2011)
Nature
, vol.7363
, pp. 179-184
-
-
Zhu, Q.1
Pao, G.M.2
Huynh, A.M.3
Suh, H.4
Tonnu, N.5
-
54
-
-
34250315750
-
A recombineering based approach for high-throughput conditional knockout targeting vector construction
-
Chan W, Costantino N, Li R, Lee SC, Su Q, et al. (2007) A recombineering based approach for high-throughput conditional knockout targeting vector construction. Nucleic Acids Res 35: e64.
-
(2007)
Nucleic Acids Res
, vol.35
-
-
Chan, W.1
Costantino, N.2
Li, R.3
Lee, S.C.4
Su, Q.5
-
55
-
-
45049085458
-
Polyglutamine-expanded ataxin-3 causes cerebellar dysfunction of SCA3 transgenic mice by inducing transcriptional dysregulation
-
Chou AH, (2008) Polyglutamine-expanded ataxin-3 causes cerebellar dysfunction of SCA3 transgenic mice by inducing transcriptional dysregulation. Neurobiol Dis 31: 89-101.
-
(2008)
Neurobiol Dis
, vol.31
, pp. 89-101
-
-
Chou, A.H.1
-
56
-
-
33745592187
-
Loss of endogenous androgen receptor protein accelerates motor neuron degeneration and accentuates androgen insensitivity in a mouse model of X-linked spinal and bulbar muscular atrophy
-
Thomas PS Jr, (2006) Loss of endogenous androgen receptor protein accelerates motor neuron degeneration and accentuates androgen insensitivity in a mouse model of X-linked spinal and bulbar muscular atrophy. Hum Mol Genet 15: 2225-2238.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2225-2238
-
-
Thomas Jr., P.S.1
-
57
-
-
45549084641
-
A Rapid Neurobehavioral Assessment Reveals that FK506 Delays Symptom Onset in R6/2 Huntington's Disease Mice
-
Ditzler S, Stoeck J, LeBlanc M, Kooperberg C, Hansen S, et al. (2003) A Rapid Neurobehavioral Assessment Reveals that FK506 Delays Symptom Onset in R6/2 Huntington's Disease Mice. Preclinica Research Articles 1: 115-126.
-
(2003)
Preclinica Research Articles
, vol.1
, pp. 115-126
-
-
Ditzler, S.1
Stoeck, J.2
LeBlanc, M.3
Kooperberg, C.4
Hansen, S.5
-
58
-
-
0036377472
-
Male Germ cell gene expression
-
Eddy EM, (2002) Male Germ cell gene expression. Recent Prog Horm Res 57: 103-28.
-
(2002)
Recent Prog Horm Res
, vol.57
, pp. 103-128
-
-
Eddy, E.M.1
|