-
1
-
-
0031794286
-
Molecular mechanism of DNA double strand break repair
-
Kanaar R., et al. Molecular mechanism of DNA double strand break repair. Trends Cell. Biol. 8 (1998) 483-489
-
(1998)
Trends Cell. Biol.
, vol.8
, pp. 483-489
-
-
Kanaar, R.1
-
2
-
-
22244446185
-
Advances in mechanisms of genetic instability related to hereditary neurological diseases
-
Wells R.D., et al. Advances in mechanisms of genetic instability related to hereditary neurological diseases. Nucleic Acids Res. 33 (2005) 3785-3798
-
(2005)
Nucleic Acids Res.
, vol.33
, pp. 3785-3798
-
-
Wells, R.D.1
-
3
-
-
33744807443
-
DNA structure, repeat expansions and human hereditary disorders
-
Mirkin S.M. DNA structure, repeat expansions and human hereditary disorders. Curr. Opin. Struct. Biol. 16 (2006) 351-358
-
(2006)
Curr. Opin. Struct. Biol.
, vol.16
, pp. 351-358
-
-
Mirkin, S.M.1
-
6
-
-
33947265929
-
A common topology for bacterial and eukaryotic transcription initiation?
-
Travers A., and Muskhelishvili G. A common topology for bacterial and eukaryotic transcription initiation?. EMBO 2 (2007) 147-151
-
(2007)
EMBO
, vol.2
, pp. 147-151
-
-
Travers, A.1
Muskhelishvili, G.2
-
7
-
-
25144495578
-
Organization of supercoil domains and their reorganization by transcription
-
Deng S., et al. Organization of supercoil domains and their reorganization by transcription. Molec. Microbiol. 57 (2005) 1511-1521
-
(2005)
Molec. Microbiol.
, vol.57
, pp. 1511-1521
-
-
Deng, S.1
-
8
-
-
0037020238
-
Failure to relax negative supercoiling of DNA is a primary cause of mitotic hyper-recombination in topoisomerase-deficient yeast cells
-
Trigueros S., and Roca J. Failure to relax negative supercoiling of DNA is a primary cause of mitotic hyper-recombination in topoisomerase-deficient yeast cells. J. Biol Chem. 277 (2002) 37207-37211
-
(2002)
J. Biol Chem.
, vol.277
, pp. 37207-37211
-
-
Trigueros, S.1
Roca, J.2
-
9
-
-
0031731487
-
Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits
-
Lupski J.R. Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits. Trends Genet. 14 (1998) 417-422
-
(1998)
Trends Genet.
, vol.14
, pp. 417-422
-
-
Lupski, J.R.1
-
10
-
-
33747654494
-
Non-B DNA structures formed by long DNA repeats of DM1, DM2, and FRDA genes, not the sequences per se, promote mutagenesis in flanking DNA
-
Wojciechowska M., et al. Non-B DNA structures formed by long DNA repeats of DM1, DM2, and FRDA genes, not the sequences per se, promote mutagenesis in flanking DNA. J. Biol Chem. 281 (2006) 24531-24543
-
(2006)
J. Biol Chem.
, vol.281
, pp. 24531-24543
-
-
Wojciechowska, M.1
-
11
-
-
27844482529
-
Increased negative superhelical density in vivo enhances the genetic instability of triplet repeat sequences
-
Napierala M., et al. Increased negative superhelical density in vivo enhances the genetic instability of triplet repeat sequences. J. Biol. Chem. 280 (2005) 37366-37376
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 37366-37376
-
-
Napierala, M.1
-
12
-
-
33750962353
-
SOS Repair and DNA supercoiling influence the genetic instability of DNA triplet repeats in Escherichia coli
-
Majchrzak M., et al. SOS Repair and DNA supercoiling influence the genetic instability of DNA triplet repeats in Escherichia coli. J. Mol. Biol. 364 (2006) 612-624
-
(2006)
J. Mol. Biol.
, vol.364
, pp. 612-624
-
-
Majchrzak, M.1
-
13
-
-
8444231721
-
Non-B DNA conformations, genomic rearrangements, and genetic diseases
-
Bacolla A., and Wells R.D. Non-B DNA conformations, genomic rearrangements, and genetic diseases. J. Biol. Chem. 279 (2004) 47411-47414
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 47411-47414
-
-
Bacolla, A.1
Wells, R.D.2
-
14
-
-
10744220154
-
Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion
-
Saitta S.C., et al. Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion. Hum. Mol Genet. 13 (2004) 417-428
-
(2004)
Hum. Mol Genet.
, vol.13
, pp. 417-428
-
-
Saitta, S.C.1
-
15
-
-
0034161932
-
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis
-
Shaikh T.H., et al. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis. Hum. Mol. Genet. 9 (2000) 489-501
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 489-501
-
-
Shaikh, T.H.1
-
16
-
-
34147119249
-
AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12
-
Babcock M., et al. AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12. Genome Res. 17 (2007) 451-460
-
(2007)
Genome Res.
, vol.17
, pp. 451-460
-
-
Babcock, M.1
-
17
-
-
0347382445
-
Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution
-
Babcock M., et al. Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution. Genome Res. 13 (2003) 2519-2532
-
(2003)
Genome Res.
, vol.13
, pp. 2519-2532
-
-
Babcock, M.1
-
18
-
-
33144472660
-
Genetic variation affects de novo translocation frequency
-
Kato T., et al. Genetic variation affects de novo translocation frequency. Science 311 (2006) 971
-
(2006)
Science
, vol.311
, pp. 971
-
-
Kato, T.1
-
19
-
-
33747874030
-
Palindrome-mediated chromosomal translocations in humans
-
Kurahashi H., et al. Palindrome-mediated chromosomal translocations in humans. DNA Repair 5 (2006) 1136-1145
-
(2006)
DNA Repair
, vol.5
, pp. 1136-1145
-
-
Kurahashi, H.1
-
20
-
-
4544288618
-
Naturally occurring H-DNA- forming sequences are mutagenic in mammalian cells
-
Wang G., and Vasquez K.M. Naturally occurring H-DNA- forming sequences are mutagenic in mammalian cells. Proc. Natl Acad. Sci. 101 (2004) 13448-13453
-
(2004)
Proc. Natl Acad. Sci.
, vol.101
, pp. 13448-13453
-
-
Wang, G.1
Vasquez, K.M.2
-
21
-
-
33644543741
-
Z-DNA-forming sequences generate large-scale deletions in mammalian cells
-
Wang G., et al. Z-DNA-forming sequences generate large-scale deletions in mammalian cells. Proc. Natl. Acad. Sci. 103 (2006) 2677-2682
-
(2006)
Proc. Natl. Acad. Sci.
, vol.103
, pp. 2677-2682
-
-
Wang, G.1
-
22
-
-
0023508506
-
Left-handed DNA in vivo
-
Jaworski A., et al. Left-handed DNA in vivo. Science 238 (1987) 773-777
-
(1987)
Science
, vol.238
, pp. 773-777
-
-
Jaworski, A.1
-
23
-
-
0037803571
-
Z-DNA: the long road to biological function
-
Rich A., and Zhang S. Z-DNA: the long road to biological function. Nat. Reviews Genet. 4 (2003) 566-572
-
(2003)
Nat. Reviews Genet.
, vol.4
, pp. 566-572
-
-
Rich, A.1
Zhang, S.2
-
24
-
-
0033766239
-
Specific mutations induced by triplex-forming oligonucleotides in mice
-
Vasquez K., et al. Specific mutations induced by triplex-forming oligonucleotides in mice. Science 290 (2000) 530-533
-
(2000)
Science
, vol.290
, pp. 530-533
-
-
Vasquez, K.1
-
25
-
-
0035947657
-
Triplex-induced recombination in human cell-free extracts dependence on xpa and hsrad51
-
Datta H.J., et al. Triplex-induced recombination in human cell-free extracts dependence on xpa and hsrad51. J. Biol. Chem 276 (2001) 18018-18023
-
(2001)
J. Biol. Chem
, vol.276
, pp. 18018-18023
-
-
Datta, H.J.1
-
26
-
-
33744944261
-
Non-B DNA structure-induced genetic instability
-
Wang G., and Vasquez K.M. Non-B DNA structure-induced genetic instability. Mutation Res. 598 (2006) 103-119
-
(2006)
Mutation Res.
, vol.598
, pp. 103-119
-
-
Wang, G.1
Vasquez, K.M.2
-
27
-
-
33746923523
-
Triplex-stimulated intermolecular recombination at a single-copy genomic target
-
Knauert M.P., et al. Triplex-stimulated intermolecular recombination at a single-copy genomic target. Molec. Therapy 14 (2006) 392-400
-
(2006)
Molec. Therapy
, vol.14
, pp. 392-400
-
-
Knauert, M.P.1
-
28
-
-
32344447218
-
Targeted cross-linking of the human β- globin gene in living cells mediated by a triple helix forming oligonucleotide
-
Shahid K.A., et al. Targeted cross-linking of the human β- globin gene in living cells mediated by a triple helix forming oligonucleotide. Biochemistry 45 (2006) 1970-1978
-
(2006)
Biochemistry
, vol.45
, pp. 1970-1978
-
-
Shahid, K.A.1
-
29
-
-
33745299348
-
Targeted genome modification via triple helix formation
-
Kalish J.M., and Glazer P.M. Targeted genome modification via triple helix formation. Ann. N. Y. Acad. Sci. 1058 (2005) 151-161
-
(2005)
Ann. N. Y. Acad. Sci.
, vol.1058
, pp. 151-161
-
-
Kalish, J.M.1
Glazer, P.M.2
-
30
-
-
33748138991
-
Roles of nonhomologous DNA end joining, V(D)J recombination, and class switch recombination in chromosomal translocations
-
Lieber M.R., et al. Roles of nonhomologous DNA end joining, V(D)J recombination, and class switch recombination in chromosomal translocations. DNA Repair 5 (2006) 1234-1245
-
(2006)
DNA Repair
, vol.5
, pp. 1234-1245
-
-
Lieber, M.R.1
-
31
-
-
33646359685
-
DNA structures at chromosomal translocation sites
-
Raghavan S.C., and Lieber M.F. DNA structures at chromosomal translocation sites. BioEssays 28 (2006) 480-494
-
(2006)
BioEssays
, vol.28
, pp. 480-494
-
-
Raghavan, S.C.1
Lieber, M.F.2
-
32
-
-
20744431751
-
Evidence for a triplex DNA conformation at the bcl-2 major breakpoint region of the t(14;18) translocation
-
Raghavan S.C., et al. Evidence for a triplex DNA conformation at the bcl-2 major breakpoint region of the t(14;18) translocation. J. Biol. Chem. 280 (2005) 22749-22760
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 22749-22760
-
-
Raghavan, S.C.1
-
33
-
-
33745218951
-
Analysis of a non-B DNA structure at chromosomal sites in the mammalian genome
-
Raghavan S.C., et al. Analysis of a non-B DNA structure at chromosomal sites in the mammalian genome. Methods Enzymol. 409 (2006) 301-316
-
(2006)
Methods Enzymol.
, vol.409
, pp. 301-316
-
-
Raghavan, S.C.1
-
35
-
-
25844487226
-
Diseases of unstable repeat expansion: mechanisms and common principles
-
Gatchel J.R., and Zoghbi H.Y. Diseases of unstable repeat expansion: mechanisms and common principles. Nat. Reviews Genet. 6 (2005) 743-755
-
(2005)
Nat. Reviews Genet.
, vol.6
, pp. 743-755
-
-
Gatchel, J.R.1
Zoghbi, H.Y.2
-
37
-
-
0035947688
-
PKD1 unusual DNA conformations are recognized by nucleotide excision repair
-
Bacolla A., et al. PKD1 unusual DNA conformations are recognized by nucleotide excision repair. J. Biol. Chem. 276 (2001) 18597-18604
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 18597-18604
-
-
Bacolla, A.1
-
38
-
-
4644327494
-
Breakpoints of gross deletions coincide with non-B DNA conformations
-
Bacolla A., et al. Breakpoints of gross deletions coincide with non-B DNA conformations. Proc. Natl. Acad. Sci. 101 (2004) 14162-14167
-
(2004)
Proc. Natl. Acad. Sci.
, vol.101
, pp. 14162-14167
-
-
Bacolla, A.1
-
39
-
-
33747871340
-
-
Bacolla, A. et al. (2006) The involvement of non-B DNA structures in gross chromosomal rearrangements. In DNA Repair (Lieber, M., ed.), p. 5, 1161-1170, Elsevier
-
-
-
-
40
-
-
33751329250
-
Global variation in coy number in the human genome
-
Redon R., et al. Global variation in coy number in the human genome. Nature 444 (2006) 444-454
-
(2006)
Nature
, vol.444
, pp. 444-454
-
-
Redon, R.1
-
41
-
-
19944430730
-
BDNF gene is a risk factor for schizophrenia in a Scottish population
-
Neves-Pereira M., et al. BDNF gene is a risk factor for schizophrenia in a Scottish population. Mol. Psychiatry. 10 (2005) 208-212
-
(2005)
Mol. Psychiatry.
, vol.10
, pp. 208-212
-
-
Neves-Pereira, M.1
-
42
-
-
3042679816
-
Identification of a novel neuregulin I at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype
-
Li T., et al. Identification of a novel neuregulin I at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype. Mol. Psychiatry 9 (2004) 698-704
-
(2004)
Mol. Psychiatry
, vol.9
, pp. 698-704
-
-
Li, T.1
-
43
-
-
3343019031
-
Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population
-
Li T., et al. Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population. Am. J. Med. Genet. B Neuropsychiatr. Genet. 129 (2004) 13-15
-
(2004)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.129
, pp. 13-15
-
-
Li, T.1
-
44
-
-
7444219594
-
Functional effects of a tandem duplication polymorphism in the 5′ flanking region of the DRD4 gene
-
D'Souza U.M., et al. Functional effects of a tandem duplication polymorphism in the 5′ flanking region of the DRD4 gene. Biol. Psychiatry 56 (2004) 691-697
-
(2004)
Biol. Psychiatry
, vol.56
, pp. 691-697
-
-
D'Souza, U.M.1
-
45
-
-
33749458682
-
Episodic memory performance predicted by the 2bp deletion in exon 6 of the 'α7-like' nicotinic receptor subunit gene
-
Dempster E.L., et al. Episodic memory performance predicted by the 2bp deletion in exon 6 of the 'α7-like' nicotinic receptor subunit gene. Am. J. Psychiatry 163 (2006) 1832-1834
-
(2006)
Am. J. Psychiatry
, vol.163
, pp. 1832-1834
-
-
Dempster, E.L.1
-
46
-
-
26444531847
-
Association analysis of the RGS4 gene in Han Chinese and Scottish populations with schizophrenia
-
Zhang F., et al. Association analysis of the RGS4 gene in Han Chinese and Scottish populations with schizophrenia. Genes Brain Behav. 4 (2005) 444-448
-
(2005)
Genes Brain Behav.
, vol.4
, pp. 444-448
-
-
Zhang, F.1
-
47
-
-
33745885945
-
Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples
-
Talkowski M.E., et al. Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biol. Psychiatry 60 (2006) 152-162
-
(2006)
Biol. Psychiatry
, vol.60
, pp. 152-162
-
-
Talkowski, M.E.1
-
48
-
-
33749043929
-
Genomic rearrangements and gene copy-number alterations as a cause for nervous system disorders
-
Lee J.A., and Lupski J.R. Genomic rearrangements and gene copy-number alterations as a cause for nervous system disorders. Neuron 52 (2006) 103-121
-
(2006)
Neuron
, vol.52
, pp. 103-121
-
-
Lee, J.A.1
Lupski, J.R.2
-
49
-
-
30044449524
-
A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice
-
Hiroi N., et al. A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 19132-19137
-
(2005)
Proc. Natl. Acad. Sci. U. S. A.
, vol.102
, pp. 19132-19137
-
-
Hiroi, N.1
-
50
-
-
33645234528
-
A dopamine transporter gene functional variant associated with cocaine abuse in a Brazilian sample
-
Guindalini C., et al. A dopamine transporter gene functional variant associated with cocaine abuse in a Brazilian sample. Proc. Natl. Acad. Sci. 103 (2006) 4552-4557
-
(2006)
Proc. Natl. Acad. Sci.
, vol.103
, pp. 4552-4557
-
-
Guindalini, C.1
-
51
-
-
18844366665
-
Association of genetic variants in alcohol dehydrogenase 4 with alcohol dependence in Brazilian patients
-
Guindalini C., et al. Association of genetic variants in alcohol dehydrogenase 4 with alcohol dependence in Brazilian patients. Am. J. Psychiatry 162 (2005) 1005-1007
-
(2005)
Am. J. Psychiatry
, vol.162
, pp. 1005-1007
-
-
Guindalini, C.1
-
52
-
-
3343003563
-
Association analysis of the DRD4 and COMT genes in methamphetamine abuse
-
Li T., et al. Association analysis of the DRD4 and COMT genes in methamphetamine abuse. Am. J. Med. Genet. B Neuropsychiatr. Genet. 129 (2004) 120-124
-
(2004)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.129
, pp. 120-124
-
-
Li, T.1
-
53
-
-
25444433619
-
Transient expression analysis of allelic variants of a VNTR in the dopamine transporter gene (DAT1)
-
Mill J., et al. Transient expression analysis of allelic variants of a VNTR in the dopamine transporter gene (DAT1). BMC Genet. 6 (2005) 3-13
-
(2005)
BMC Genet.
, vol.6
, pp. 3-13
-
-
Mill, J.1
-
54
-
-
29844456031
-
A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy
-
Brookes K.-J., et al. A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy. Arch. Gen. Psychiatry 63 (2006) 74-81
-
(2006)
Arch. Gen. Psychiatry
, vol.63
, pp. 74-81
-
-
Brookes, K.-J.1
-
55
-
-
33645235486
-
Effects of the D4 dopamine receptor gene variation on behavior problems at 6 years of age
-
Birkas E., et al. Effects of the D4 dopamine receptor gene variation on behavior problems at 6 years of age. Neuropsychopharmacol. Hung. 7 (2005) 125-131
-
(2005)
Neuropsychopharmacol. Hung.
, vol.7
, pp. 125-131
-
-
Birkas, E.1
-
56
-
-
33749076012
-
Association of the dysbindin gene with bipolar affective disorder
-
Breen G., et al. Association of the dysbindin gene with bipolar affective disorder. Am. J. Psychiatry 163 (2006) 1636-1638
-
(2006)
Am. J. Psychiatry
, vol.163
, pp. 1636-1638
-
-
Breen, G.1
-
57
-
-
0036367404
-
Novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene associated with biopolar affective disorder
-
Nyegaard M., et al. Novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene associated with biopolar affective disorder. Mol. Psychiatry 7 (2002) 745-754
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 745-754
-
-
Nyegaard, M.1
-
58
-
-
33745622389
-
A complex polymorphic region in the brain- derived neurotrophic factor (BDNF) gene confers susceptibility to biopolar disorder and affects transcription al activity
-
Okada T., et al. A complex polymorphic region in the brain- derived neurotrophic factor (BDNF) gene confers susceptibility to biopolar disorder and affects transcription al activity. Mol. Psychiatry 11 (2006) 695-703
-
(2006)
Mol. Psychiatry
, vol.11
, pp. 695-703
-
-
Okada, T.1
-
59
-
-
3042736862
-
Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations
-
Ribases M., et al. Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations. Hum. Molec. Genet. 13 (2004) 1205-1212
-
(2004)
Hum. Molec. Genet.
, vol.13
, pp. 1205-1212
-
-
Ribases, M.1
-
60
-
-
34249895353
-
-
Proceedings of the 2nd International Tandem Repeat Consortium Workshop on the Bioinformatics, Genomics, and Functionality of Microsatellites and VNTRs, Budapest, Hungary, 8-11 September, 2006
-
-
-
-
61
-
-
8444225364
-
Hotspots of homologous recombination in the human genome: not all homologous sequences are equal
-
Lupski J.R. Hotspots of homologous recombination in the human genome: not all homologous sequences are equal. Genome Biol. 5 (2004) 242.1-242.4
-
(2004)
Genome Biol.
, vol.5
-
-
Lupski, J.R.1
-
62
-
-
12544250465
-
The myotonic dystrophy type 1 triplet repeat sequence induces gross deletions and inversions
-
Wojciechowska M., et al. The myotonic dystrophy type 1 triplet repeat sequence induces gross deletions and inversions. J. Biol. Chem. 280 (2005) 941-952
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 941-952
-
-
Wojciechowska, M.1
-
63
-
-
0019350114
-
Cruciform structures in supercoiled DNA
-
Panayotatos N., and Wells R.D. Cruciform structures in supercoiled DNA. Nature 289 (1981) 466-470
-
(1981)
Nature
, vol.289
, pp. 466-470
-
-
Panayotatos, N.1
Wells, R.D.2
-
64
-
-
0019087696
-
The inverted repeat as a recognizable structural feature in supercoiled DNA molecules
-
Lilley D.M.J. The inverted repeat as a recognizable structural feature in supercoiled DNA molecules. Proc. Natl. Acad. Sci. U. S. A. 77 (1980) 6468-6472
-
(1980)
Proc. Natl. Acad. Sci. U. S. A.
, vol.77
, pp. 6468-6472
-
-
Lilley, D.M.J.1
-
65
-
-
34249901069
-
-
Wordrow, S. (1996) I Love Me, Palindrome Encyclopedia (Vol. 1) Algonquin Books of Chapel Hill, Division of Workman Publishing
-
-
-
|