| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Mitas M | |
| P2860 | cites work | Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13 | Q24336093 |
| Simple tandem DNA repeats and human genetic disease | Q24561717 | ||
| Genomic sequencing reveals a positive correlation between the kinetics of strand-specific DNA demethylation of the overlapping estradiol/glucocorticoid-receptor binding sites and the rate of avian vitellogenin mRNA synthesis | Q24629611 | ||
| G . T base-pairs in a DNA helix: the crystal structure of d(G-G-G-G-T-C-C-C) | Q27729054 | ||
| Solution structure of a DNA quadruplex containing the fragile X syndrome triplet repeat | Q27729324 | ||
| The crystal structure of Haelll methyltransferase covalently complexed to DNA: An extrahelical cytosine and rearranged base pairing | Q27729758 | ||
| Solution structure of a parallel-stranded G-quadruplex DNA | Q27731509 | ||
| Crystal structure of the HhaI DNA methyltransferase complexed with S-adenosyl-L-methionine | Q27731970 | ||
| Genetically unstable CXG repeats are structurally dynamic and have a high propensity for folding. An NMR and UV spectroscopic study | Q27734113 | ||
| Mutation of a mutL homolog in hereditary colon cancer | Q28114939 | ||
| Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox | Q28235115 | ||
| Binding of mismatched microsatellite DNA sequences by the human MSH2 protein | Q28241673 | ||
| The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
| Genetic mapping of a locus predisposing to human colorectal cancer | Q28268634 | ||
| Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome | Q28273791 | ||
| Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion | Q28275699 | ||
| Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene | Q28285882 | ||
| Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel | Q28300848 | ||
| Trinucleotide repeats that expand in human disease form hairpin structures in vitro | Q28301826 | ||
| Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat | Q28304011 | ||
| Biological implications of the mechanism of action of human DNA (cytosine-5)methyltransferase | Q28307510 | ||
| Human strand-specific mismatch repair occurs by a bidirectional mechanism similar to that of the bacterial reaction | Q28610824 | ||
| Monovalent cation-induced structure of telomeric DNA: the G-quartet model | Q30459609 | ||
| Relationship between transient DNA hypomethylation and erythroid differentiation of murine erythroleukemia cells | Q33678578 | ||
| Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines | Q33720790 | ||
| Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases | Q33750656 | ||
| Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member. | Q33968674 | ||
| Hairpins are formed by the single DNA strands of the fragile X triplet repeats: structure and biological implications | Q34297548 | ||
| High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome | Q34346939 | ||
| An unstable triplet repeat in a gene related to myotonic muscular dystrophy | Q34355359 | ||
| Structure and dynamics of the DNA hairpins formed by tandemly repeated CTG triplets associated with myotonic dystrophy | Q34589868 | ||
| Solution structures of the individual single strands of the fragile X DNA triplets (GCC)n.(GGC)n | Q34590948 | ||
| Stability of intrastrand hairpin structures formed by the CAG/CTG class of DNA triplet repeats associated with neurological diseases | Q34599367 | ||
| Chemical reactivity of potassium permanganate and diethyl pyrocarbonate with B DNA: specific reactivity with short A-tracts | Q68472026 | ||
| Dynamics of demethylation and activation of the alpha-actin gene in myoblasts | Q68636634 | ||
| A guide for probing native small nuclear RNA and ribonucleoprotein structures | Q69268139 | ||
| Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci | Q71145616 | ||
| Trinucleotide repeat expansion and human disease | Q71576495 | ||
| The trinucleotide repeat sequence d(CGG)15 forms a heat-stable hairpin containing Gsyn. Ganti base pairs | Q71715523 | ||
| Triad-DNA: a model for trinucleotide repeats | Q72345831 | ||
| At physiological pH, d(CCG)15 forms a hairpin containing protonated cytosines and a distorted helix | Q73299175 | ||
| The selective degradation of pyrimidines in nucleic acids by permanganate oxidation | Q82640916 | ||
| Hairpin properties of single-stranded DNA containing a GC-rich triplet repeat: (CTG)15. | Q34743394 | ||
| HhaI and HpaII DNA methyltransferases bind DNA mismatches, methylate uracil and block DNA repair | Q34746885 | ||
| Methylation of slipped duplexes, snapbacks and cruciforms by human DNA(cytosine-5)methyltransferase | Q34749202 | ||
| The purine-rich trinucleotide repeat sequences d(CAG)15 and d(GAC)15 form hairpins | Q34775992 | ||
| CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro | Q34777507 | ||
| DNA CTG triplet repeats involved in dynamic mutations of neurologically related gene sequences form stable duplexes | Q34778233 | ||
| The essentials of DNA methylation | Q35326024 | ||
| Replacement of 5-methylcytosine by cytosine: a possible mechanism for transient DNA demethylation during differentiation | Q35602033 | ||
| A mismatch recognition defect in colon carcinoma confers DNA microsatellite instability and a mutator phenotype | Q35753566 | ||
| Variations in DNA methylation during mouse cell differentiation in vivo and in vitro | Q36256690 | ||
| 5'-CGA sequence is a strong motif for homo base-paired parallel-stranded DNA duplex as revealed by NMR analysis | Q36344574 | ||
| Helix formation by guanylic acid | Q36397431 | ||
| Demethylation of somatic and testis-specific histone H2A and H2B genes in F9 embryonal carcinoma cells | Q36699908 | ||
| Methyl-directed repair of DNA base-pair mismatches in vitro | Q37344016 | ||
| DNA determinants and substrate specificities of Escherichia coli MutY. | Q38290583 | ||
| hMSH2-independent DNA mismatch recognition by human proteins | Q38362634 | ||
| M.HhaI binds tightly to substrates containing mismatches at the target base | Q40393755 | ||
| Compact structures of d(CNG)noligonucleotides in solution and their possible relevance to Fragile X and related human genetic diseases | Q40394217 | ||
| The trinucleotide repeat sequence d(GTC)15adopts ahairpin conformation | Q40394976 | ||
| On base flipping | Q40442261 | ||
| Mismatch repair, genetic stability, and cancer | Q40556409 | ||
| Hypermethylation of telomere-like foldbacks at codon 12 of the human c-Ha-ras gene and the trinucleotide repeat of the FMR-1 gene of fragile X. | Q40636136 | ||
| The expanding world of trinucleotide repeats | Q40966903 | ||
| DNA demethylation in vitro: involvement of RNA. | Q41168637 | ||
| Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome | Q41178713 | ||
| Trinucleotide repeat disorders in humans: discussions of mechanisms and medical issues | Q41323569 | ||
| Methylation patterns of the human apoA-I/C-III/A-IV gene cluster in adult and embryonic tissues suggest dynamic changes in methylation during development | Q41652746 | ||
| Absence of expression of the FMR-1 gene in fragile X syndrome | Q41669091 | ||
| Demethylation of CpG islands in embryonic cells | Q41961577 | ||
| Cation-dependent transition between the quadruplex and Watson-Crick hairpin forms of d(CGCG3GCG) | Q44857238 | ||
| Mispair specificity of methyl-directed DNA mismatch correction in vitro | Q44909730 | ||
| Structure, dynamics, and thermodynamics of mismatched DNA oligonucleotide duplexes d(CCCAGGG)2 and d(CCCTGGG)2. | Q45968929 | ||
| Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation | Q46049171 | ||
| Telomeric DNA oligonucleotides form novel intramolecular structures containing guanine-guanine base pairs | Q46058606 | ||
| Recognition of foldback DNA by the human DNA (cytosine-5-) methyltransferase | Q46694742 | ||
| Recognition of unusual DNA structures by human DNA (cytosine-5)methyltransferase | Q47574035 | ||
| Distribution of trinucleotide microsatellites in different categories of mammalian genomic sequence: implications for human genetic diseases | Q48082852 | ||
| Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
| Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line | Q50792932 | ||
| DNA methylation represses FMR-1 transcription in fragile X syndrome | Q52042005 | ||
| Microsatellite instability and other molecular abnormalities in human prostate cancer. | Q54161978 | ||
| CTG triplet repeats from the myotonic dystrophy gene are expanded in Escherichia coli distal to the replication origin as a single large event. | Q54588463 | ||
| CTG triplet repeats from human hereditary diseases are dominant genetic expansion products in Escherichia coli. | Q54595038 | ||
| Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli | Q54611269 | ||
| Solution Structure of two Mismatches A . A and T . T in the K-ras Gene Context by Nuclear Magnetic Resonance and Molecular Dynamics | Q58022362 | ||
| Unusual DNA conformation at low pH revealed by NMR: parallel-stranded DNA duplex with homo base pairs | Q67570946 | ||
| Metal ions cause the isomerization of certain intramolecular triplexes | Q67841193 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 10 | |
| P304 | page(s) | 2245-2254 | |
| P577 | publication date | 1997-06-01 | |
| P1433 | published in | Nucleic Acids Research | Q135122 |
| P1476 | title | Trinucleotide repeats associated with human disease | |
| P478 | volume | 25 |
| Q74070924 | (CGA)(4): parallel, anti-parallel, right-handed and left-handed homoduplexes of a trinucleotide repeat DNA |
| Q47781807 | A B-Z junction induced by an A … A mismatch in GAC repeats in the gene for cartilage oligomeric matrix protein promotes binding with the hZαADAR1 protein |
| Q35043910 | A GAG trinucleotide-repeat polymorphism in the gene for glutathione biosynthetic enzyme, GCLC, affects gene expression through translation |
| Q78008264 | A fast polymerase chain reaction-mediated strategy for introducing repeat expansions into CAG-repeat containing genes |
| Q38314380 | A high mobility group protein binds to long CAG repeat tracts and establishes their chromatin organization in Saccharomyces cerevisiae |
| Q28273955 | A mutant Drosophila homolog of mammalian Clock disrupts circadian rhythms and transcription of period and timeless |
| Q40603655 | AGG interruptions in (CGG)(n) DNA repeat tracts modulate the structure and thermodynamics of non-B conformations in vitro |
| Q78207888 | Abasic sites induce triplet-repeat expansion during DNA replication in vitro |
| Q24816457 | Advances in mechanisms of genetic instability related to hereditary neurological diseases |
| Q38454927 | Allelic alterations at the STR markers in the buccal tissue cells of oral cancer patients and the oral epithelial cells of healthy betel quid-chewers: an evaluation of forensic applicability |
| Q74825113 | Amplification of GAA/TTC triplet repeat in vitro: preferential expansion of (TTC)n strand |
| Q35642112 | An origin of DNA replication in the promoter region of the human fragile X mental retardation (FMR1) gene |
| Q28262967 | Analysis of strand slippage in DNA polymerase expansions of CAG/CTG triplet repeats associated with neurodegenerative disease |
| Q34083269 | Androgen receptor polymorphisms and mutations in male infertility |
| Q33688372 | Automated mutation analysis |
| Q41740863 | Base stacking and even/odd behavior of hairpin loops in DNA triplet repeat slippage and expansion with DNA polymerase |
| Q40764515 | Base-Pairing Energies of Proton-Bound Dimers and Proton Affinities of 1-Methyl-5-Halocytosines: Implications for the Effects of Halogenation on the Stability of the DNA i-Motif. |
| Q50584942 | Base-Pairing Energies of Protonated Nucleoside Base Pairs of dCyd and m(5)dCyd: Implications for the Stability of DNA i-Motif Conformations. |
| Q34464221 | Biological aspects of DNA/RNA quadruplexes |
| Q41844296 | Biological implications of the DNA structures associated with disease-causing triplet repeats |
| Q35130388 | CAG*CTG repeat instability in cultured human astrocytes |
| Q37975286 | Chemical and biological consequences of oxidatively damaged guanine in DNA. |
| Q40485534 | Chemotherapeutic deletion of CTG repeats in lymphoblast cells from DM1 patients |
| Q44179098 | Chemotherapeutically induced deletion of expanded triplet repeats |
| Q34615584 | Chromosomal elements evolve at different rates in the Drosophila genome |
| Q78230840 | Circular dichroism spectroscopy analysis of conformational transitions of a 54 base pair DNA duplex composed of alternating CGCGCG and TATATA blocks |
| Q34612185 | Cis-elements governing trinucleotide repeat instability in Saccharomyces cerevisiae. |
| Q24650948 | Comparative genomics and molecular dynamics of DNA repeats in eukaryotes |
| Q34378999 | Conformational energetics of stable and metastable states formed by DNA triplet repeat oligonucleotides: implications for triplet expansion diseases |
| Q39724094 | Conformational properties of DNA dodecamers containing four tandem repeats of the CNG triplets |
| Q43141835 | Context dependence of trinucleotide repeat structures |
| Q34289810 | Context of deletions and insertions in human coding sequences. |
| Q37518254 | DNA elements important for CAG*CTG repeat thresholds in Saccharomyces cerevisiae. |
| Q33733162 | DNA methylation in eukaryotic chromosome stability revisited: DNA methyltransferase in the management of DNA conformation space |
| Q73357737 | DNA polymerase III proofreading mutants enhance the expansion and deletion of triplet repeat sequences in Escherichia coli |
| Q34603989 | DNA polymerase fidelity: from genetics toward a biochemical understanding |
| Q42137431 | DNA repair and DNA triplet repeat expansion: the impact of abasic lesions on triplet repeat DNA energetics |
| Q26996542 | DNA triplet repeat expansion and mismatch repair |
| Q42637855 | DNABIT Compress - Genome compression algorithm |
| Q35808034 | Detecting microsatellites within genomes: significant variation among algorithms |
| Q41892688 | Energetic coupling between clustered lesions modulated by intervening triplet repeat bulge loops: allosteric implications for DNA repair and triplet repeat expansion |
| Q41842676 | Energy landscapes of dynamic ensembles of rolling triplet repeat bulge loops: implications for DNA expansion associated with disease states |
| Q34670846 | Epigenetic mechanisms for primary differentiation in mammalian embryos |
| Q38726913 | Ethidium Bromide Modifies The Agarose Electrophoretic Mobility of CAG•CTG Alternative DNA Structures Generated by PCR. |
| Q77912145 | Expansion and deletion of triplet repeat sequences in Escherichia coli occur on the leading strand of DNA replication |
| Q42086935 | Expansion of CAG repeats in Escherichia coli is controlled by single-strand DNA exonucleases of both polarities. |
| Q48036449 | FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis. |
| Q34502500 | Flexible and efficient genome tiling design with penalized uniqueness score |
| Q34674298 | Fluorescent dyes specific for quadruplex DNA |
| Q52641453 | Frequency and coverage of trinucleotide repeats in eukaryotes. |
| Q36924430 | Functional significance of the GAG trinucleotide-repeat polymorphism in the gene for the catalytic subunit of gamma-glutamylcysteine ligase. |
| Q43984153 | Genetic assays for measuring rates of (CAG).(CTG) repeat instability in Escherichia coli |
| Q34589589 | Genetic instability induced by overexpression of DNA ligase I in budding yeast |
| Q36700171 | Genome-wide analysis of microsatellite polymorphism in chicken circumventing the ascertainment bias |
| Q28478458 | HPLC-UV, MALDI-TOF-MS and ESI-MS/MS analysis of the mechlorethamine DNA crosslink at a cytosine-cytosine mismatch pair |
| Q30962381 | Huntington disease expansion mutations in humans can occur before meiosis is completed |
| Q33837555 | Identification of a unique library of complex, but ordered, arrays of repetitive elements in the human genome and implication of their potential involvement in pathobiology |
| Q37577365 | Impact of bulge loop size on DNA triplet repeat domains: Implications for DNA repair and expansion |
| Q35136598 | Incidence and persistence of 8-oxo-7,8-dihydroguanine within a hairpin intermediate exacerbates a toxic oxidation cycle associated with trinucleotide repeat expansion |
| Q54478897 | Increased negative superhelical density in vivo enhances the genetic instability of triplet repeat sequences. |
| Q41974604 | Influences of array size and homogeneity on minisatellite mutation. |
| Q37149212 | Inhibition of DNA synthesis facilitates expansion of low-complexity repeats: is strand slippage stimulated by transient local depletion of specific dNTPs? |
| Q48034382 | Inhibitory effects of expanded GAA.TTC triplet repeats from intron I of the Friedreich ataxia gene on transcription and replication in vivo |
| Q27619180 | Interlocked mismatch-aligned arrowhead DNA motifs |
| Q74044878 | Involvement of the nucleotide excision repair protein UvrA in instability of CAG*CTG repeat sequences in Escherichia coli |
| Q46602626 | Isolation and characterization of simple repeat sequences from the yellow fin sea bream Acanthopagrus latus (Sparidae). |
| Q24813983 | Length-dependent energetics of (CTG)n and (CAG)n trinucleotide repeats. |
| Q64387814 | Long CTG.CAG repeats from myotonic dystrophy are preferred sites for intermolecular recombination |
| Q34608413 | Long inverted repeats are an at-risk motif for recombination in mammalian cells |
| Q28294940 | Mechanism of trinucleotide repeats instabilities: the necessities of repeat non-B secondary structure formation and the roles of cellular trans-acting factors |
| Q33824924 | Mechanistic studies of hairpin to duplex conversion for trinucleotide repeat sequences |
| Q35049665 | Meiotic instability of CAG repeat tracts occurs by double-strand break repair in yeast |
| Q28080022 | Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells |
| Q77536532 | Modelling studies on neurodegenerative disease-causing triplet repeat sequences d(GGC/GCC)n and d(CAG/CTG)n |
| Q37362336 | Models for chromosomal replication-independent non-B DNA structure-induced genetic instability |
| Q52538313 | Molecular basis of androgen receptor diseases. |
| Q52048591 | Molecular dynamics studies of trinucleotide repeat DNA involved in neurodegenerative disorders. |
| Q93371579 | Mrc1 and Tof1 prevent fragility and instability at long CAG repeats by their fork stabilizing function |
| Q34433268 | MsDetector: toward a standard computational tool for DNA microsatellites detection |
| Q39940361 | Mutations in Yeast Replication Proteins That Increase CAG/CTG Expansions Also Increase Repeat Fragility |
| Q34473652 | Non-B DNA structure-induced genetic instability and evolution |
| Q52574399 | Nucleotide sequences flanking dinucleotide microsatellites in the human, mouse and Drosophila genomes. |
| Q42858144 | Optimal computation of all tandem repeats in a weighted sequence |
| Q36524919 | Orientation-dependent and sequence-specific expansions of CTG/CAG trinucleotide repeats in Saccharomyces cerevisiae |
| Q34446607 | Pharmacological reactivation of inactive genes: the fragile X experience |
| Q40821912 | Polar alteration of short tandem repeats (STRs) in mammalian cells |
| Q42609875 | Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains |
| Q35613535 | Premutation huntingtin allele adopts a non-B conformation and contains a hot spot for DNA damage |
| Q33939780 | Pseudoachondroplastic dysplasia: an Iowa review from human to mouse |
| Q35978312 | Rate-determining Step of Flap Endonuclease 1 (FEN1) Reflects a Kinetic Bias against Long Flaps and Trinucleotide Repeat Sequences |
| Q40749079 | Recombination-induced CAG trinucleotide repeat expansions in yeast involve the MRE11-RAD50-XRS2 complex |
| Q24535283 | Replication slippage involves DNA polymerase pausing and dissociation |
| Q62399665 | Resolution of Overlapped Reduction Signals in Short Hetero-oligonucleotides by Elimination Voltammetry |
| Q38450378 | RiDs db: Repeats in diseases database |
| Q32060860 | Screening of a highly polymorphic microsatellite for microheterogeneity in human identification. |
| Q46324287 | Sedimentation Velocity Analysis with Fluorescence Detection of Mutant Huntingtin Exon 1 Aggregation in Drosophila melanogaster and Caenorhabditis elegans. |
| Q44758127 | Self-assembling of cytosine nucleoside into triply-bound dimers in acid media. A comprehensive evaluation of proton-bound pyrimidine nucleosides by electrospray tandem mass spectrometry, X-rays diffractometry, and theoretical calculations |
| Q34520527 | Sequence length dictates repeated CAG folding in three-way junctions |
| Q27641299 | Sheared-type G(anti).C(syn) base-pair: a unique d(GXC) loop closure motif |
| Q24548611 | Short-sequence DNA repeats in prokaryotic genomes |
| Q54481127 | Srs2 helicase of Saccharomyces cerevisiae selectively unwinds triplet repeat DNA. |
| Q33958980 | Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism |
| Q46025063 | Statistical mechanics of secondary structures formed by random RNA sequences. |
| Q39722798 | Structural analysis of slipped-strand DNA (S-DNA) formed in (CTG)n. (CAG)n repeats from the myotonic dystrophy locus |
| Q28202114 | Structural and functional characterization of the human PAX7 5'-flanking regulatory region |
| Q77946552 | Structural properties of Friedreich's ataxia d(GAA) repeats |
| Q24803215 | Structural roles of CTG repeats in slippage expansion during DNA replication |
| Q26851232 | Structural studies of CNG repeats |
| Q46146519 | Structural studies of a trinucleotide repeat sequence using 2-aminopurine. |
| Q52607744 | Structure and Dynamics of DNA and RNA Double Helices Obtained from the CCG and GGC Trinucleotide Repeats. |
| Q35004374 | Structure of even/odd trinucleotide repeat sequences modulates persistence of non-B conformations and conversion to duplex |
| Q92846766 | Structures and stability of simple DNA repeats from bacteria |
| Q36749672 | Studying polyglutamine aggregation in Caenorhabditis elegans using an analytical ultracentrifuge equipped with fluorescence detection. |
| Q73947948 | Tandem duplication. A novel type of triplet repeat instability |
| Q35193278 | The androgen receptor: structure, mutations, and antiandrogens |
| Q39488976 | The fragile X chromosome (GCC) repeat folds into a DNA tetraplex at neutral pH. |
| Q34466844 | The human RIL gene: mapping to human chromosome 5q31.1, genomic organization and alternative transcripts |
| Q31497967 | The intrinsically unstable life of DNA triplet repeats associated with human hereditary disorders |
| Q42572300 | The role of nucleotide cofactor binding in cooperativity and specificity of MutS recognition |
| Q34218124 | Theoretical analysis of mutation hotspots and their DNA sequence context specificity |
| Q34291180 | Transcription and nuclear transport of CAG/CTG trinucleotide repeats in yeast |
| Q37509279 | Transcription influences the types of deletion and expansion products in an orientation-dependent manner from GAC*GTC repeats |
| Q73428107 | Trinucleotide (CAG) repeat polymorphisms in the androgen receptor gene: molecular markers of risk for male infertility |
| Q35663496 | Trinucleotide repeat DNA alters structure to minimize the thermodynamic impact of 8-oxo-7,8-dihydroguanine |
| Q33836548 | Trinucleotide repeats and other microsatellites in yeasts |
| Q77858213 | Triplet repeat DNA structures and human genetic disease: dynamic mutations from dynamic DNA |
| Q34995821 | Triplet repeats form secondary structures that escape DNA repair in yeast |
| Q34446575 | Triplet repeats, over-expanded in neuromuscular diseases, are under-represented in mammalian DNA: a survey of models |
| Q27319575 | Twisting right to left: A…A mismatch in a CAG trinucleotide repeat overexpansion provokes left-handed Z-DNA conformation |
| Q36896574 | Unique Length-Dependent Biophysical Properties of Repetitive DNA. |
| Q73009397 | Unpaired structures in SCA10 (ATTCT)n.(AGAAT)n repeats |
| Q35018181 | Unusual DNA duplex and hairpin motifs. |
| Q30487862 | Visualization of long human telomere mimics by single-molecule fluorescence imaging |
| Q36569447 | When secondary comes first--the importance of non-canonical DNA structures. |
| Q73013123 | X-linked mental retardation |
| Q74825051 | Yeast ARMs (DNA at-risk motifs) can reveal sources of genome instability |
| Q35211583 | mreps: Efficient and flexible detection of tandem repeats in DNA |
| Q92493276 | p53 Binds Preferentially to Non-B DNA Structures Formed by the Pyrimidine-Rich Strands of GAA·TTC Trinucleotide Repeats Associated with Friedreich's Ataxia |
| Q38319824 | tumor suppressor p53 binds with high affinity to CTG.CAG trinucleotide repeats and induces topological alterations in mismatched duplexes |
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