Published in Nat Rev Mol Cell Biol on March 01, 2010
Maintaining genome stability at the replication fork. Nat Rev Mol Cell Biol (2010) 5.88
Practical Aspects of microRNA Target Prediction. Curr Mol Med (2011) 2.64
PCNA function in the activation and strand direction of MutLα endonuclease in mismatch repair. Proc Natl Acad Sci U S A (2010) 2.09
Histone deacetylase complexes promote trinucleotide repeat expansions. PLoS Biol (2012) 1.93
DNA replication fidelity and cancer. Semin Cancer Biol (2010) 1.69
Accurate human microsatellite genotypes from high-throughput resequencing data using informed error profiles. Nucleic Acids Res (2012) 1.65
On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease. Hum Mutat (2011) 1.53
Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues. Hum Mol Genet (2010) 1.46
R-loops associated with triplet repeat expansions promote gene silencing in Friedreich ataxia and fragile X syndrome. PLoS Genet (2014) 1.46
CAG repeats mimic CUG repeats in the misregulation of alternative splicing. Nucleic Acids Res (2011) 1.42
RNA mis-splicing in disease. Nat Rev Genet (2015) 1.41
Activation-induced cytidine deaminase induces reproducible DNA breaks at many non-Ig Loci in activated B cells. Mol Cell (2011) 1.39
Partners in crime: bidirectional transcription in unstable microsatellite disease. Hum Mol Genet (2010) 1.37
Mismatch repair balances leading and lagging strand DNA replication fidelity. PLoS Genet (2012) 1.34
Mechanism of mismatch recognition revealed by human MutSβ bound to unpaired DNA loops. Nat Struct Mol Biol (2011) 1.31
Repeat associated non-ATG translation initiation: one DNA, two transcripts, seven reading frames, potentially nine toxic entities! PLoS Genet (2011) 1.25
Global DNA methylation is associated with insulin resistance: a monozygotic twin study. Diabetes (2011) 1.24
Splicing biomarkers of disease severity in myotonic dystrophy. Ann Neurol (2013) 1.22
Isolated short CTG/CAG DNA slip-outs are repaired efficiently by hMutSbeta, but clustered slip-outs are poorly repaired. Proc Natl Acad Sci U S A (2010) 1.20
Bidirectional transcription stimulates expansion and contraction of expanded (CTG)*(CAG) repeats. Hum Mol Genet (2010) 1.19
Compound loss of muscleblind-like function in myotonic dystrophy. EMBO Mol Med (2013) 1.19
The DNA replication program is altered at the FMR1 locus in fragile X embryonic stem cells. Mol Cell (2013) 1.16
Overcoming natural replication barriers: differential helicase requirements. Nucleic Acids Res (2011) 1.14
Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia. Dis Model Mech (2012) 1.13
Convergent transcription through a long CAG tract destabilizes repeats and induces apoptosis. Mol Cell Biol (2010) 1.12
Stress-induced modulators of repeat instability and genome evolution. J Mol Microbiol Biotechnol (2012) 1.10
Stabilization of expanded (CTG)•(CAG) repeats by antisense oligonucleotides. Mol Ther (2011) 1.10
Therapeutics development in myotonic dystrophy type 1. Muscle Nerve (2011) 1.07
The mismatch repair protein MSH2 is rate limiting for repeat expansion in a fragile X premutation mouse model. Hum Mutat (2014) 1.07
Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeats. PLoS Genet (2014) 1.06
The balancing act of DNA repeat expansions. Curr Opin Genet Dev (2013) 1.05
Incidence and persistence of 8-oxo-7,8-dihydroguanine within a hairpin intermediate exacerbates a toxic oxidation cycle associated with trinucleotide repeat expansion. DNA Repair (Amst) (2011) 1.04
Involvement of long noncoding RNAs in diseases affecting the central nervous system. RNA Biol (2012) 1.04
Analysis of microsatellite variation in Drosophila melanogaster with population-scale genome sequencing. PLoS One (2012) 1.02
MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice. PLoS Genet (2013) 1.02
New insights into repeat instability: role of RNA•DNA hybrids. RNA Biol (2010) 1.01
Transcription elongation and tissue-specific somatic CAG instability. PLoS Genet (2012) 1.01
The mismatch repair system protects against intergenerational GAA repeat instability in a Friedreich ataxia mouse model. Neurobiol Dis (2012) 1.00
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A repetitive elements perspective in Polycomb epigenetics. Front Genet (2012) 0.97
DNA mismatch repair complex MutSβ promotes GAA·TTC repeat expansion in human cells. J Biol Chem (2012) 0.97
Transcription-induced DNA toxicity at trinucleotide repeats: double bubble is trouble. Cell Cycle (2011) 0.97
CAG repeat RNA as an auxiliary toxic agent in polyglutamine disorders. RNA Biol (2011) 0.97
Repeat instability during DNA repair: Insights from model systems. Crit Rev Biochem Mol Biol (2015) 0.97
Out of balance: R-loops in human disease. PLoS Genet (2014) 0.97
Accurate typing of short tandem repeats from genome-wide sequencing data and its applications. Genome Res (2015) 0.96
G-quadruplexes in viruses: function and potential therapeutic applications. Nucleic Acids Res (2014) 0.95
AGG interruptions in (CGG)(n) DNA repeat tracts modulate the structure and thermodynamics of non-B conformations in vitro. Biochemistry (2010) 0.95
Regulation of recombination at yeast nuclear pores controls repair and triplet repeat stability. Genes Dev (2015) 0.95
The Yin and Yang of R-loop biology. Curr Opin Cell Biol (2015) 0.94
Role of DNA polymerases in repeat-mediated genome instability. Cell Rep (2012) 0.94
Inhibition of DNA synthesis facilitates expansion of low-complexity repeats: is strand slippage stimulated by transient local depletion of specific dNTPs? Bioessays (2013) 0.94
Extrahelical (CAG)/(CTG) triplet repeat elements support proliferating cell nuclear antigen loading and MutLα endonuclease activation. Proc Natl Acad Sci U S A (2013) 0.93
Topoisomerase 1 and single-strand break repair modulate transcription-induced CAG repeat contraction in human cells. Mol Cell Biol (2011) 0.93
Length-dependent CTG·CAG triplet-repeat expansion in myotonic dystrophy patient-derived induced pluripotent stem cells. Hum Mol Genet (2013) 0.93
Suppression of Somatic Expansion Delays the Onset of Pathophysiology in a Mouse Model of Huntington's Disease. PLoS Genet (2015) 0.92
MutSβ and histone deacetylase complexes promote expansions of trinucleotide repeats in human cells. Nucleic Acids Res (2012) 0.92
The molecular basis of α-thalassemia. Cold Spring Harb Perspect Med (2013) 0.92
The nucleotide sequence, DNA damage location, and protein stoichiometry influence the base excision repair outcome at CAG/CTG repeats. Biochemistry (2012) 0.91
A regulatory path associated with X-linked intellectual disability and epilepsy links KDM5C to the polyalanine expansions in ARX. Am J Hum Genet (2012) 0.90
Pms2 suppresses large expansions of the (GAA·TTC)n sequence in neuronal tissues. PLoS One (2012) 0.90
RNA-protein interactions in unstable microsatellite diseases. Brain Res (2014) 0.89
Trinucleotide repeats: a structural perspective. Front Neurol (2013) 0.89
Inferring short tandem repeat variation from paired-end short reads. Nucleic Acids Res (2013) 0.89
The Repeat Expansion Diseases: The dark side of DNA repair. DNA Repair (Amst) (2015) 0.88
Structure of even/odd trinucleotide repeat sequences modulates persistence of non-B conformations and conversion to duplex. Biochemistry (2011) 0.88
Histone deacetylase complexes as caretakers of genome stability. Epigenetics (2012) 0.88
The role of the mammalian DNA end-processing enzyme polynucleotide kinase 3'-phosphatase in spinocerebellar ataxia type 3 pathogenesis. PLoS Genet (2015) 0.88
DNA triplet repeat expansion and mismatch repair. Annu Rev Biochem (2015) 0.88
The dual nature of mismatch repair as antimutator and mutator: for better or for worse. Front Genet (2014) 0.88
Trinucleotide repeat deletion via a unique hairpin bypass by DNA polymerase β and alternate flap cleavage by flap endonuclease 1. Nucleic Acids Res (2012) 0.88
A brief history of triplet repeat diseases. Methods Mol Biol (2013) 0.88
Unusual structures are present in DNA fragments containing super-long Huntingtin CAG repeats. PLoS One (2011) 0.87
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions. J Neurol (2012) 0.87
Role of transcript and interplay between transcription and replication in triplet-repeat instability in mammalian cells. Nucleic Acids Res (2010) 0.87
Expanded complexity of unstable repeat diseases. Biofactors (2012) 0.87
Cis-acting DNA sequence at a replication origin promotes repeat expansion to fragile X full mutation. J Cell Biol (2014) 0.86
Sequence length dictates repeated CAG folding in three-way junctions. Biochemistry (2010) 0.86
Environmental stress induces trinucleotide repeat mutagenesis in human cells. Proc Natl Acad Sci U S A (2015) 0.86
Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damage-response pathway in SCA3. PLoS Genet (2015) 0.85
Instability of CTG repeats is governed by the position of a DNA base lesion through base excision repair. PLoS One (2013) 0.85
Processing of double-R-loops in (CAG)·(CTG) and C9orf72 (GGGGCC)·(GGCCCC) repeats causes instability. Nucleic Acids Res (2014) 0.85
Interconverting conformations of slipped-DNA junctions formed by trinucleotide repeats affect repair outcome. Biochemistry (2013) 0.85
In vitro repair of DNA hairpins containing various numbers of CAG/CTG trinucleotide repeats. DNA Repair (Amst) (2011) 0.85
Modifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes. Hum Genet (2014) 0.84
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases. Ann Neurol (2016) 0.84
Expression levels of DNA replication and repair genes predict regional somatic repeat instability in the brain but are not altered by polyglutamine disease protein expression or age. Hum Mol Genet (2013) 0.84
Transcriptionally Repressive Chromatin Remodelling and CpG Methylation in the Presence of Expanded CTG-Repeats at the DM1 Locus. J Nucleic Acids (2013) 0.84
The expanding biology of the C9orf72 nucleotide repeat expansion in neurodegenerative disease. Nat Rev Neurosci (2016) 0.84
Genomic deletions and point mutations induced in Saccharomyces cerevisiae by the trinucleotide repeats (GAA·TTC) associated with Friedreich's ataxia. DNA Repair (Amst) (2012) 0.83
Long-range correlations in the mechanics of small DNA circles under topological stress revealed by multi-scale simulation. Nucleic Acids Res (2016) 0.83
Energy landscapes of dynamic ensembles of rolling triplet repeat bulge loops: implications for DNA expansion associated with disease states. J Am Chem Soc (2012) 0.83
Triptycene-based small molecules modulate (CAG)·(CTG) repeat junctions. Chem Sci (2015) 0.83
RAN translation and frameshifting as translational challenges at simple repeats of human neurodegenerative disorders. Nucleic Acids Res (2014) 0.83
Large expansion of CTG•CAG repeats is exacerbated by MutSβ in human cells. Sci Rep (2015) 0.82
Different roles of eukaryotic MutS and MutL complexes in repair of small insertion and deletion loops in yeast. PLoS Genet (2013) 0.82
Human mismatch repair protein hMutLα is required to repair short slipped-DNAs of trinucleotide repeats. J Biol Chem (2012) 0.82
The transcription-coupled repair protein ERCC6/CSB also protects against repeat expansion in a mouse model of the fragile X premutation. Hum Mutat (2015) 0.82
Microsatellite interruptions stabilize primate genomes and exist as population-specific single nucleotide polymorphisms within individual human genomes. PLoS Genet (2014) 0.82
Expandable DNA repeats and human disease. Nature (2007) 5.50
Repeat instability: mechanisms of dynamic mutations. Nat Rev Genet (2005) 5.37
Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos. Cell Stem Cell (2007) 2.87
(CAG)(n)-hairpin DNA binds to Msh2-Msh3 and changes properties of mismatch recognition. Nat Struct Mol Biol (2005) 2.71
CREB-binding protein modulates repeat instability in a Drosophila model for polyQ disease. Science (2007) 2.45
Unstable tandem repeats in promoters confer transcriptional evolvability. Science (2009) 2.41
An antisense transcript spanning the CGG repeat region of FMR1 is upregulated in premutation carriers but silenced in full mutation individuals. Hum Mol Genet (2007) 2.25
The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissues. Hum Mol Genet (2007) 2.22
Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model. Gene (2007) 2.01
Slipped (CTG)*(CAG) repeats can be correctly repaired, escape repair or undergo error-prone repair. Nat Struct Mol Biol (2005) 1.97
Transcription promotes contraction of CAG repeat tracts in human cells. Nat Struct Mol Biol (2006) 1.93
CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination. PLoS Genet (2008) 1.72
R loops stimulate genetic instability of CTG.CAG repeats. Proc Natl Acad Sci U S A (2009) 1.64
A persistent RNA.DNA hybrid formed by transcription of the Friedreich ataxia triplet repeat in live bacteria, and by T7 RNAP in vitro. Nucleic Acids Res (2007) 1.63
Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients. Hum Mol Genet (2010) 1.61
DNA instability in postmitotic neurons. Proc Natl Acad Sci U S A (2008) 1.61
Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice. Hum Genet (2006) 1.55
Large-scale expansions of Friedreich's ataxia GAA repeats in yeast. Mol Cell (2009) 1.52
Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset. Hum Mol Genet (2009) 1.51
The contribution of cis-elements to disease-associated repeat instability: clinical and experimental evidence. Cytogenet Genome Res (2003) 1.49
CTG trinucleotide repeat "big jumps": large expansions, small mice. PLoS Genet (2007) 1.46
Stoichiometry of base excision repair proteins correlates with increased somatic CAG instability in striatum over cerebellum in Huntington's disease transgenic mice. PLoS Genet (2009) 1.37
Expanded repeat in canine epilepsy. Science (2005) 1.37
Coordination between polymerase beta and FEN1 can modulate CAG repeat expansion. J Biol Chem (2009) 1.37
SRS2 and SGS1 prevent chromosomal breaks and stabilize triplet repeats by restraining recombination. Nat Struct Mol Biol (2009) 1.32
Dnmt1 deficiency promotes CAG repeat expansion in the mouse germline. Hum Mol Genet (2008) 1.28
Replication inhibitors modulate instability of an expanded trinucleotide repeat at the myotonic dystrophy type 1 disease locus in human cells. Am J Hum Genet (2003) 1.24
MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice. PLoS Genet (2009) 1.22
Structure-dependent DNA damage and repair in a trinucleotide repeat sequence. Biochemistry (2009) 1.22
Chromatin remodeling in the noncoding repeat expansion diseases. J Biol Chem (2008) 1.22
A genetic defect caused by a triplet repeat expansion in Arabidopsis thaliana. Science (2009) 1.20
DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients. J Med Genet (2008) 1.20
Highly unstable sequence interruptions of the CTG repeat in the myotonic dystrophy gene. Am J Med Genet A (2009) 1.14
Mrc1, Tof1 and Csm3 inhibit CAG.CTG repeat instability by at least two mechanisms. DNA Repair (Amst) (2008) 1.14
Incision-dependent and error-free repair of (CAG)(n)/(CTG)(n) hairpins in human cell extracts. Nat Struct Mol Biol (2009) 1.12
Zinc-finger directed double-strand breaks within CAG repeat tracts promote repeat instability in human cells. Proc Natl Acad Sci U S A (2009) 1.12
Mutagenic roles of DNA "repair" proteins in antibody diversity and disease-associated trinucleotide repeat instability. DNA Repair (Amst) (2008) 1.09
Slipping while sleeping? Trinucleotide repeat expansions in germ cells. Trends Mol Med (2003) 1.07
Checkpoint responses to unusual structures formed by DNA repeats. Mol Carcinog (2009) 1.07
ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice. Nucleic Acids Res (2009) 1.06
Mismatch recognition protein MutSbeta does not hijack (CAG)n hairpin repair in vitro. J Biol Chem (2009) 1.04
Chemotherapeutic deletion of CTG repeats in lymphoblast cells from DM1 patients. Nucleic Acids Res (2004) 1.01
Human embryonic stem cell models of Huntington disease. Reprod Biomed Online (2009) 0.99
Chemically induced increases and decreases in the rate of expansion of a CAG*CTG triplet repeat. Nucleic Acids Res (2004) 0.97
CTG/CAG repeat instability is modulated by the levels of human DNA ligase I and its interaction with proliferating cell nuclear antigen: a distinction between replication and slipped-DNA repair. J Biol Chem (2009) 0.97
A Z-DNA sequence reduces slipped-strand structure formation in the myotonic dystrophy type 2 (CCTG) x (CAGG) repeat. Proc Natl Acad Sci U S A (2009) 0.91
Rapid unwinding of triplet repeat hairpins by Srs2 helicase of Saccharomyces cerevisiae. Nucleic Acids Res (2008) 0.90
CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutation. Mol Hum Reprod (2008) 0.88
SCA8 CAG/CTG expansions, a tale of two TOXICities: a unique or common case? PLoS Genet (2009) 0.85
Huntingtin triplet-repeat locus is stable under long-term Fen1 knockdown in human cells. J Neurosci Methods (2008) 0.85
Repeat instability: mechanisms of dynamic mutations. Nat Rev Genet (2005) 5.37
Effect of Candida glabrata FKS1 and FKS2 mutations on echinocandin sensitivity and kinetics of 1,3-beta-D-glucan synthase: implication for the existing susceptibility breakpoint. Antimicrob Agents Chemother (2009) 3.13
A randomized and blinded multicenter trial of high-dose fluconazole plus placebo versus fluconazole plus amphotericin B as therapy for candidemia and its consequences in nonneutropenic subjects. Clin Infect Dis (2003) 2.84
RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila. Neuron (2003) 2.81
Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells. Nat Genet (2002) 2.81
The disease-associated r(GGGGCC)n repeat from the C9orf72 gene forms tract length-dependent uni- and multimolecular RNA G-quadruplex structures. J Biol Chem (2013) 1.97
Slipped (CTG)*(CAG) repeats can be correctly repaired, escape repair or undergo error-prone repair. Nat Struct Mol Biol (2005) 1.97
Genome-wide expression profiling of the response to polyene, pyrimidine, azole, and echinocandin antifungal agents in Saccharomyces cerevisiae. J Biol Chem (2003) 1.94
CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination. PLoS Genet (2008) 1.72
Slipped-strand DNAs formed by long (CAG)*(CTG) repeats: slipped-out repeats and slip-out junctions. Nucleic Acids Res (2002) 1.64
Implementation and refinement of a problem-based learning model: a ten-year experience. Am J Pharm Educ (2007) 1.60
Voriconazole: a new triazole antifungal agent. Ann Pharmacother (2003) 1.47
Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues. Hum Mol Genet (2010) 1.46
Triplet repeat DNA structures and human genetic disease: dynamic mutations from dynamic DNA. J Biosci (2002) 1.37
Replication fork dynamics and dynamic mutations: the fork-shift model of repeat instability. Trends Genet (2005) 1.33
Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier? Am J Hum Genet (2005) 1.32
Determinants of R-loop formation at convergent bidirectionally transcribed trinucleotide repeats. Nucleic Acids Res (2010) 1.32
Delivery of antifungal agents using bioactive and nonbioactive bone cements. Ann Pharmacother (2009) 1.31
Replication inhibitors modulate instability of an expanded trinucleotide repeat at the myotonic dystrophy type 1 disease locus in human cells. Am J Hum Genet (2003) 1.24
Tissue- and age-specific DNA replication patterns at the CTG/CAG-expanded human myotonic dystrophy type 1 locus. Nat Struct Mol Biol (2010) 1.24
MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice. PLoS Genet (2009) 1.22
Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation. Hum Mol Genet (2010) 1.21
Repeat-associated non-ATG (RAN) translation in neurological disease. Hum Mol Genet (2013) 1.20
Isolated short CTG/CAG DNA slip-outs are repaired efficiently by hMutSbeta, but clustered slip-outs are poorly repaired. Proc Natl Acad Sci U S A (2010) 1.20
Bidirectional transcription stimulates expansion and contraction of expanded (CTG)*(CAG) repeats. Hum Mol Genet (2010) 1.19
TMPyP4 porphyrin distorts RNA G-quadruplex structures of the disease-associated r(GGGGCC)n repeat of the C9orf72 gene and blocks interaction of RNA-binding proteins. J Biol Chem (2013) 1.15
Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice. Hum Mol Genet (2003) 1.14
Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia. Dis Model Mech (2012) 1.13
Mutagenic roles of DNA "repair" proteins in antibody diversity and disease-associated trinucleotide repeat instability. DNA Repair (Amst) (2008) 1.09
In vitro (CTG)*(CAG) expansions and deletions by human cell extracts. J Biol Chem (2002) 1.06
Role of replication and CpG methylation in fragile X syndrome CGG deletions in primate cells. Am J Hum Genet (2004) 1.06
MSH3 polymorphisms and protein levels affect CAG repeat instability in Huntington's disease mice. PLoS Genet (2013) 1.02
CpG methylation modifies the genetic stability of cloned repeat sequences. Genome Res (2002) 0.98
In search of the holy grail of antifungal therapy. Trans Am Clin Climatol Assoc (2008) 0.97
CTG/CAG repeat instability is modulated by the levels of human DNA ligase I and its interaction with proliferating cell nuclear antigen: a distinction between replication and slipped-DNA repair. J Biol Chem (2009) 0.97
Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches. PLoS Genet (2013) 0.95
Maternal germline-specific effect of DNA ligase I on CTG/CAG instability. Hum Mol Genet (2011) 0.92
Genetic diversity of Trichomonas vaginalis clinical isolates determined by EcoRI restriction fragment length polymorphism of heat-shock protein 70 genes. Am J Trop Med Hyg (2009) 0.91
The nucleotide sequence, DNA damage location, and protein stoichiometry influence the base excision repair outcome at CAG/CTG repeats. Biochemistry (2012) 0.91
Fidelity of primate cell repair of a double-strand break within a (CTG).(CAG) tract. Effect of slipped DNA structures. J Biol Chem (2003) 0.90
Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome. J Biol Chem (2004) 0.90
Slipped (CTG).(CAG) repeats of the myotonic dystrophy locus: surface probing with anti-DNA antibodies. J Mol Biol (2003) 0.87
The human cruciform-binding protein, CBP, is involved in DNA replication and associates in vivo with mammalian replication origins. J Biol Chem (2002) 0.87
Atypical tuberculosis skin test reaction. Ann Pharmacother (2003) 0.86
Tissue-specific mismatch repair protein expression: MSH3 is higher than MSH6 in multiple mouse tissues. DNA Repair (Amst) (2012) 0.86
The ATTCT repeats of spinocerebellar ataxia type 10 display strong nucleosome assembly which is enhanced by repeat interruptions. Gene (2008) 0.86
Cardiac toxicity of some echinocandin antifungals. Expert Opin Drug Saf (2013) 0.86
Interconverting conformations of slipped-DNA junctions formed by trinucleotide repeats affect repair outcome. Biochemistry (2013) 0.85
Modifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes. Hum Genet (2014) 0.84
Expression levels of DNA replication and repair genes predict regional somatic repeat instability in the brain but are not altered by polyglutamine disease protein expression or age. Hum Mol Genet (2013) 0.84
The interaction of mannose binding lectin (MBL) with mannose containing glycopeptides and the resultant potential impact on invasive fungal infection. Med Mycol (2008) 0.83
Illuminating CNS and cognitive issues in myotonic dystrophy: Workshop report. Neuromuscul Disord (2013) 0.83
RAN translation: fragile X in the running. Neuron (2013) 0.82
Identification of restriction endonucleases sensitive to 5-cytosine methylation at non-CpG sites, including expanded (CAG)n/(CTG)n repeats. Epigenetics (2011) 0.82
Human mismatch repair protein hMutLα is required to repair short slipped-DNAs of trinucleotide repeats. J Biol Chem (2012) 0.82
Response to Falush: a role for cis-element polymorphisms in HD. Am J Hum Genet (2009) 0.80
Blue digits: cyanosis resulting from norepinephrine treatment. Ann Pharmacother (2005) 0.79
Differential expression of genes encoding immunomodulatory proteins in response to amphotericin B in human mononuclear cells identified by cDNA microarray analysis. J Antimicrob Chemother (2002) 0.79
Deletion hotspot in the argininosuccinate lyase gene: association with topoisomerase II and DNA polymerase alpha sites. Hum Mutat (2006) 0.79
Replacement of the myotonic dystrophy type 1 CTG repeat with 'non-CTG repeat' insertions in specific tissues. J Med Genet (2011) 0.79
Clinical roundtable monograph: safety and efficacy of lipid-based amphotericin B. Clin Adv Hematol Oncol (2009) 0.78
Steroid-induced avascular necrosis. Ann Pharmacother (2002) 0.78
Diced triplets expose neurons to RISC. PLoS Genet (2012) 0.78
Buffalo hump in an HIV-infected patient. Ann Pharmacother (2002) 0.78
Medication-induced adverse effects: important concepts for the hand therapist. J Hand Ther (2010) 0.77
The contribution of Raman scattering to the fluorescence of the polyene antibiotic amphotericin B. J Fluoresc (2010) 0.76
Toll-like receptor 4 polymorphisms and aspergillosis. N Engl J Med (2009) 0.75
Herpes simplex virus encephalitis pharmacotherapy: alternative treatment options. Ann Pharmacother (2013) 0.75
Evidence that impurities contribute to the fluorescence of the polyene antibiotic amphotericin B. J Antimicrob Chemother (2009) 0.75
Co-opting endogenous microRNAs for therapy. Nat Med (2012) 0.75
T. asahii pulmonary infection as a complication of TNF-inhibitor and steroids: posaconazole pharmacotherapy and risk analysis. J Miss State Med Assoc (2011) 0.75
Acyclovir-induced crystalluria. Ann Pharmacother (2002) 0.75
Clinical research in the lay press: irresponsible journalism raises a huge dose of doubt. Clin Infect Dis (2006) 0.75
Evaluation of a positive yeast-in-blood service. Am J Med Sci (2014) 0.75
Bioavailability of promethazine in a topical pluronic lecithin organogel: a pilot study. Int J Pharm Compd (2013) 0.75
Thrombocytosis during antifungal therapy of candidemia. Ann Pharmacother (2005) 0.75