-
1
-
-
34250878426
-
Expandable DNA repeats and human disease
-
Mirkin SM (2007) Expandable DNA repeats and human disease. Nature 447:932-940.
-
(2007)
Nature
, vol.447
, pp. 932-940
-
-
Mirkin, S.M.1
-
2
-
-
0027742295
-
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
-
DOI 10.1016/0092-8674(93)90546-3
-
Fishel R, et al. (1993) The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell 75:1027-1038. (Pubitemid 24014559)
-
(1993)
Cell
, vol.75
, Issue.5
, pp. 1027-1038
-
-
Fishel, R.1
Lescoe, M.K.2
Rao, M.R.S.3
Copeland, N.G.4
Jenkins, N.A.5
Garber, J.6
Kane, M.7
Kolodner, R.8
-
3
-
-
0024148621
-
Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: A survey of 50 patients
-
Jaspers NG, Gatti RA, Baan C, Linssen PC, Bootsma D (1988) Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: A survey of 50 patients. Cytogenet Cell Genet 49:259-263. (Pubitemid 19154985)
-
(1988)
Cytogenetics and Cell Genetics
, vol.49
, Issue.4
, pp. 259-263
-
-
Jaspers, N.G.J.1
Gatti, R.A.2
Baan, C.3
Linssen, P.C.M.L.4
Bootsma, D.5
-
4
-
-
29244489543
-
Fanconi anemia (cross)linked to DNA repair
-
DOI 10.1016/j.cell.2005.12.009, PII S0092867405013917
-
Niedernhofer LJ, Lalai AS, Hoeijmakers JHJ (2005) Fanconi anemia (cross)linked to DNA repair. Cell 123:1191-1198. (Pubitemid 41821778)
-
(2005)
Cell
, vol.123
, Issue.7
, pp. 1191-1198
-
-
Niedernhofer, L.J.1
Lalai, A.S.2
Hoeijmakers, J.H.J.3
-
5
-
-
0027514825
-
Trinucleotide repeat expansions in neurological disease
-
DOI 10.1016/0959-4388(93)90149-S
-
Warren ST, Nelson DL (1993) Trinucleotide repeat expansions in neurological disease. Curr Opin Neurobiol 3:752-759. (Pubitemid 23303381)
-
(1993)
Current Opinion in Neurobiology
, vol.3
, Issue.5
, pp. 752-759
-
-
Warren, S.T.1
Nelson, D.L.2
-
6
-
-
0242718930
-
Trinucleotide repeat instability: A hairpin curve at the crossroads of replication, recombination, and repair
-
DOI 10.1159/000072836
-
Lenzmeier BA, Freudenreich CH (2003) Trinucleotide repeat instability: A hairpin curve at the crossroads of replication, recombination, and repair. Cytogenet Genome Res 100:7-24. (Pubitemid 37467788)
-
(2003)
Cytogenetic and Genome Research
, vol.100
, Issue.1-4
, pp. 7-24
-
-
Lenzmeier, B.A.1
Freudenreich, C.H.2
-
7
-
-
0033514926
-
DNA secondary structure: A common and causative factor for expansion in human disease
-
McMurray CT (1999) DNA secondary structure: A common and causative factor for expansion in human disease. Proc Natl Acad Sci USA 96:1823-1825.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 1823-1825
-
-
McMurray, C.T.1
-
8
-
-
0033771685
-
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
-
Matsuura T, et al. (2000) Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nat Genet 26:191-194.
-
(2000)
Nat Genet
, vol.26
, pp. 191-194
-
-
Matsuura, T.1
-
9
-
-
0037470576
-
Unpaired structures in SCA10 (ATTCT)n.(AGAAT)n repeats
-
Potaman VN, et al. (2003) Unpaired structures in SCA10 (ATTCT)n.(AGAAT)n repeats. J Mol Biol 326:1095-1111.
-
(2003)
J Mol Biol
, vol.326
, pp. 1095-1111
-
-
Potaman, V.N.1
-
10
-
-
36048954457
-
Unstable spinocerebellar ataxia type 10 (ATTCT)*(AGAAT) repeats are associated with aberrant replication at the ATX10 locus and replication origin-dependent expansion at an ectopic site in human cells
-
DOI 10.1128/MCB.01276-07
-
Liu G, Bissler JJ, Sinden RR, Leffak M (2007) Unstable spinocerebellar ataxia type 10 (ATTCT*(AGAAT) repeats are associated with aberrant replication at the ATX10 locus and replication origin-dependent expansion at an ectopic site in human cells. Mol Cell Biol 27:7828-7838. (Pubitemid 350086416)
-
(2007)
Molecular and Cellular Biology
, vol.27
, Issue.22
, pp. 7828-7838
-
-
Liu, G.1
Bissler, J.J.2
Sinden, R.R.3
Leffak, M.4
-
11
-
-
71849083831
-
Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n
-
Sato N, et al. (2009) Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n. Am J Hum Genet 85:544-557.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 544-557
-
-
Sato, N.1
-
12
-
-
0344100057
-
SCA10 and ATTCT repeat expansion: Clinical features and molecular aspects
-
DOI 10.1159/000072853
-
Lin X, Ashizawa T (2003) SCA10 and ATTCT repeat expansion: Clinical features and molecular aspects. Cytogenet Genome Res 100:184-188. (Pubitemid 37467805)
-
(2003)
Cytogenetic and Genome Research
, vol.100
, Issue.1-4
, pp. 184-188
-
-
Lin, X.1
Ashizawa, T.2
-
13
-
-
0036340277
-
Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10
-
DOI 10.1001/archneur.59.8.1285
-
Grewal RP, et al. (2002) Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10. Arch Neurol 59:1285-1290. (Pubitemid 34856382)
-
(2002)
Archives of Neurology
, vol.59
, Issue.8
, pp. 1285-1290
-
-
Grewal, R.P.1
Achari, M.2
Matsuura, T.3
Durazo, A.4
Tayag, E.5
Zu, L.6
Pulst, S.M.7
Ashizawa, T.8
-
14
-
-
0034902760
-
Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10
-
DOI 10.1002/ana.1081
-
Rasmussen A, et al. (2001) Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10. Ann Neurol 50:234-239. (Pubitemid 32738149)
-
(2001)
Annals of Neurology
, vol.50
, Issue.2
, pp. 234-239
-
-
Rasmussen, A.1
Matsuura, T.2
Ruano, L.3
Yescas, P.4
Ochoa, A.5
Ashizawa, T.6
Alonso, E.7
-
15
-
-
77954171034
-
Inactivation of hnRNP K by expanded intronic AUUCU repeat induces apoptosis via translocation of PKCdelta to mitochondria in spinocerebellar ataxia 10
-
White MC, et al. (2010) Inactivation of hnRNP K by expanded intronic AUUCU repeat induces apoptosis via translocation of PKCdelta to mitochondria in spinocerebellar ataxia 10. PLoS Genet 6:e1000984.
-
(2010)
PLoS Genet
, vol.6
-
-
White, M.C.1
-
16
-
-
17844394198
-
Recent progress in spinocerebellar ataxia type-10 (SCA10)
-
DOI 10.1080/14734220510007897
-
Lin X, Ashizawa T (2005) Recent progress in spinocerebellar ataxia type-10 (SCA10). Cerebellum 4:37-42. (Pubitemid 40592807)
-
(2005)
Cerebellum
, vol.4
, Issue.1
, pp. 37-42
-
-
Lin, X.1
Ashizawa, T.2
-
17
-
-
67649639511
-
Large-scale expansions of Friedreich's ataxia GAA repeats in yeast
-
Shishkin AA, et al. (2009) Large-scale expansions of Friedreich's ataxia GAA repeats in yeast. Mol Cell 35:82-92.
-
(2009)
Mol Cell
, vol.35
, pp. 82-92
-
-
Shishkin, A.A.1
-
18
-
-
14744299899
-
Uncoupling of unwinding from DNA synthesis implies regulation of MCM helicase by Tof1/Mrc1/Csm3 checkpoint complex
-
DOI 10.1016/j.jmb.2005.01.041
-
Nedelcheva MN, et al. (2005) Uncoupling of unwinding from DNA synthesis implies regulation of MCM helicase by Tof1/Mrc1/Csm3 checkpoint complex. J Mol Biol 347: 509-521. (Pubitemid 40332361)
-
(2005)
Journal of Molecular Biology
, vol.347
, Issue.3
, pp. 509-521
-
-
Nedelcheva, M.N.1
Roguev, A.2
Dolapchiev, L.B.3
Shevchenko, A.4
Taskov, H.B.5
Shevchenko, A.6
Stewart, A.F.7
Stoynov, S.S.8
-
19
-
-
24044552287
-
Mrc1 and Tof1 promote replication fork progression and recovery independently of Rad53
-
DOI 10.1016/j.molcel.2005.07.028, PII S1097276505015133
-
Tourrière H, Versini G, Cordón-Preciado V, Alabert C, Pasero P (2005) Mrc1 and Tof1 promote replication fork progression and recovery independently of Rad53. Mol Cell 19:699-706. (Pubitemid 41219445)
-
(2005)
Molecular Cell
, vol.19
, Issue.5
, pp. 699-706
-
-
Tourriere, H.1
Versini, G.2
Cordon-Preciado, V.3
Alabert, C.4
Pasero, P.5
-
20
-
-
35348933781
-
Reversal of fortune: Rad5 to the rescue
-
Klein HL (2007) Reversal of fortune: Rad5 to the rescue. Mol Cell 28:181-183.
-
(2007)
Mol Cell
, vol.28
, pp. 181-183
-
-
Klein, H.L.1
-
21
-
-
0033578017
-
Dna repair: Rad52 - The means to an end
-
Hiom K (1999) Dna repair: Rad52 - the means to an end. Curr Biol 9:R446-R448.
-
(1999)
Curr Biol
, vol.9
-
-
Hiom, K.1
-
22
-
-
0033231558
-
Patching broken chromosomes with extranuclear cellular DNA
-
Yu X, Gabriel A (1999) Patching broken chromosomes with extranuclear cellular DNA. Mol Cell 4:873-881.
-
(1999)
Mol Cell
, vol.4
, pp. 873-881
-
-
Yu, X.1
Gabriel, A.2
-
24
-
-
34547681831
-
Chromosome fragility: Molecular mechanisms and cellular consequences
-
Freudenreich CH (2007) Chromosome fragility: Molecular mechanisms and cellular consequences. Front Biosci 12:4911-4924.
-
(2007)
Front Biosci
, vol.12
, pp. 4911-4924
-
-
Freudenreich, C.H.1
-
25
-
-
0142027842
-
Mutations in Yeast Replication Proteins That Increase CAG/CTG Expansions Also Increase Repeat Fragility
-
DOI 10.1128/MCB.23.21.7849-7860.2003
-
Callahan JL, Andrews KJ, Zakian VA, Freudenreich CH (2003) Mutations in yeast replication proteins that increase CAG/CTG expansions also increase repeat fragility. Mol Cell Biol 23:7849-7860. (Pubitemid 37271481)
-
(2003)
Molecular and Cellular Biology
, vol.23
, Issue.21
, pp. 7849-7860
-
-
Callahan, J.L.1
Andrews, K.J.2
Zakian, V.A.3
Freudenreich, C.H.4
-
26
-
-
77949654751
-
The Rtt109 histone acetyltransferase facilitates error-free replication to prevent CAG/CTG repeat contractions
-
Yang JH, Freudenreich CH (2010) The Rtt109 histone acetyltransferase facilitates error-free replication to prevent CAG/CTG repeat contractions. DNA Repair (Amst) 9: 414-420.
-
(2010)
DNA Repair (Amst)
, vol.9
, pp. 414-420
-
-
Yang, J.H.1
Freudenreich, C.H.2
-
27
-
-
74249111370
-
Double-strand break repair pathways protect against CAG/CTG repeat expansions, contractions and repeat-mediated chromosomal fragility in Saccharomyces cerevisiae
-
Sundararajan R, Gellon L, Zunder RM, Freudenreich CH (2010) Double-strand break repair pathways protect against CAG/CTG repeat expansions, contractions and repeat-mediated chromosomal fragility in Saccharomyces cerevisiae. Genetics 184: 65-77.
-
(2010)
Genetics
, vol.184
, pp. 65-77
-
-
Sundararajan, R.1
Gellon, L.2
Zunder, R.M.3
Freudenreich, C.H.4
-
28
-
-
0033059981
-
Formation of mRNA 3' ends in eukaryotes: Mechanism, regulation, and interrelationships with other steps in mRNA synthesis
-
Zhao J, Hyman L, Moore C (1999) Formation of mRNA 3′ ends in eukaryotes: Mechanism, regulation, and interrelationships with other steps in mRNA synthesis. Microbiol Mol Biol Rev 63:405-445. (Pubitemid 29264977)
-
(1999)
Microbiology and Molecular Biology Reviews
, vol.63
, Issue.2
, pp. 405-445
-
-
Zhao, J.1
Hyman, L.2
Moore, C.3
-
29
-
-
40649114958
-
Mrc1, Tof1 and Csm3 inhibit CAG.CTG repeat instability by at least two mechanisms
-
Razidlo DF, Lahue RS (2008) Mrc1, Tof1 and Csm3 inhibit CAG.CTG repeat instability by at least two mechanisms. DNA Repair (Amst) 7:633-640.
-
(2008)
DNA Repair (Amst)
, vol.7
, pp. 633-640
-
-
Razidlo, D.F.1
Lahue, R.S.2
-
30
-
-
0042865938
-
S-phase checkpoint proteins Tof1 and Mrc1 form a stable replication-pausing complex
-
DOI 10.1038/nature01900
-
Katou Y, et al. (2003) S-phase checkpoint proteins Tof1 and Mrc1 form a stable replication-pausing complex. Nature 424:1078-1083. (Pubitemid 37064311)
-
(2003)
Nature
, vol.424
, Issue.6952
, pp. 1078-1083
-
-
Katou, Y.1
Kanoh, Y.2
Bando, M.3
Noguchi, H.4
Tanaka, H.5
Ashikari, T.6
Sugimoto, K.7
Shirahige, K.8
-
31
-
-
33344463137
-
DNA repeat rearrangements mediated by DnaK-dependent replication fork repair
-
DOI 10.1016/j.molcel.2006.01.025, PII S1097276506000475
-
Goldfless SJ, Morag AS, Belisle KA, Sutera VA, Jr., Lovett ST (2006) DNA repeat rearrangements mediated by DnaK-dependent replication fork repair. Mol Cell 21: 595-604. (Pubitemid 43290727)
-
(2006)
Molecular Cell
, vol.21
, Issue.5
, pp. 595-604
-
-
Goldfless, S.J.1
Morag, A.S.2
Belisle, K.A.3
Sutera Jr., V.A.4
Lovett, S.T.5
-
32
-
-
33845651294
-
Replication fork regression in repetitive DNAs
-
DOI 10.1093/nar/gkl757
-
Fouché N, Ozgür S, Roy D, Griffith JD (2006) Replication fork regression in repetitive DNAs. Nucleic Acids Res 34:6044-6050. (Pubitemid 44941182)
-
(2006)
Nucleic Acids Research
, vol.34
, Issue.20
, pp. 6044-6050
-
-
Fouche, N.1
Ozgur, S.2
Roy, D.3
Griffith, J.D.4
-
33
-
-
59649119505
-
SRS2 and SGS1 prevent chromosomal breaks and stabilize triplet repeats by restraining recombination
-
Kerrest A, et al. (2009) SRS2 and SGS1 prevent chromosomal breaks and stabilize triplet repeats by restraining recombination. Nat Struct Mol Biol 16:159-167.
-
(2009)
Nat Struct Mol Biol
, vol.16
, pp. 159-167
-
-
Kerrest, A.1
-
34
-
-
35148847451
-
Yeast Rad5 Protein Required for Postreplication Repair Has a DNA Helicase Activity Specific for Replication Fork Regression
-
DOI 10.1016/j.molcel.2007.07.030, PII S1097276507005473
-
Blastyák A, et al. (2007) Yeast Rad5 protein required for postreplication repair has a DNA helicase activity specific for replication fork regression. Mol Cell 28:167-175. (Pubitemid 47542303)
-
(2007)
Molecular Cell
, vol.28
, Issue.1
, pp. 167-175
-
-
Blastyak, A.1
Pinter, L.2
Unk, I.3
Prakash, L.4
Prakash, S.5
Haracska, L.6
-
35
-
-
0033895728
-
The impact of lagging strand replication mutations on the stability of CAG repeat tracts in yeast
-
Ireland MJ, Reinke SS, Livingston DM (2000) The impact of lagging strand replication mutations on the stability of CAG repeat tracts in yeast. Genetics 155:1657-1665. (Pubitemid 30626386)
-
(2000)
Genetics
, vol.155
, Issue.4
, pp. 1657-1665
-
-
Ireland, M.J.1
Reinke, S.S.2
Livingston, D.M.3
-
36
-
-
0032579440
-
Designer deletion strains derived from Saccharomyces cerevisiae S288C: A useful set of strains and plasmids for PCR-mediated gene disruption and other applications
-
DOI 10.1002/(SICI)1097-0061(19980130)14:2<115::AID-YEA204>3.0.CO;2- 2
-
Brachmann CB, et al. (1998) Designer deletion strains derived from Saccharomyces cerevisiae S288C: A useful set of strains and plasmids for PCR-mediated gene disruption and other applications. Yeast 14:115-132. (Pubitemid 28062863)
-
(1998)
Yeast
, vol.14
, Issue.2
, pp. 115-132
-
-
Brachmann, C.B.1
Davies, A.2
Cost, G.J.3
Caputo, E.4
Li, J.5
Hieter, P.6
Boeke, J.D.7
-
38
-
-
0025886466
-
A constant rate of spontaneous mutation in DNA-based microbes
-
Drake JW (1991) A constant rate of spontaneous mutation in DNA-based microbes. Proc Natl Acad Sci USA 88:7160-7164.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 7160-7164
-
-
Drake, J.W.1
|