Pages that link to "Q72372652"
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The following pages link to Simple repeat DNA is not replicated simply (Q72372652):
Displaying 50 items.
- Replication slippage involves DNA polymerase pausing and dissociation (Q24535283) (← links)
- Simple tandem DNA repeats and human genetic disease (Q24561717) (← links)
- FREP: a database of functional repeats in mouse cDNAs (Q24599014) (← links)
- Structure of a single-cytidine hairpin loop formed by the DNA triplet GCA (Q27729729) (← links)
- Identification of RTG2 as a modifier gene for CTG*CAG repeat instability in Saccharomyces cerevisiae (Q27934694) (← links)
- Study of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 Gene (Q28077015) (← links)
- Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update (Q28116963) (← links)
- The fragile X gene and its function (Q28201533) (← links)
- Analysis of strand slippage in DNA polymerase expansions of CAG/CTG triplet repeats associated with neurodegenerative disease (Q28262967) (← links)
- Incision-dependent and error-free repair of (CAG)(n)/(CTG)(n) hairpins in human cell extracts (Q30356382) (← links)
- Huntington disease expansion mutations in humans can occur before meiosis is completed (Q30962381) (← links)
- The intrinsically unstable life of DNA triplet repeats associated with human hereditary disorders (Q31497967) (← links)
- Genetic mechanisms in squamous cell carcinoma of the head and neck (Q31889996) (← links)
- Development of microsatellite markers and analysis of intraspecific genetic variability in chickpea (Cicer arietinum L.). (Q33236335) (← links)
- Meiotic instability associated with the CAGR1 trinucleotide repeat at 13q13. (Q33678843) (← links)
- The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing (Q33679225) (← links)
- Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats (Q33680162) (← links)
- Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases (Q33750656) (← links)
- Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism (Q33958980) (← links)
- Destabilization of simple repetitive DNA sequences by transcription in yeast. (Q33967667) (← links)
- Microsatellites: consensus and controversy (Q34057384) (← links)
- Evaluation of CAG repeat length of androgen receptor expressing cells in human testes showing different pictures of spermatogenic impairment (Q34061672) (← links)
- Identification, cross-taxon transferability and application of full-length cDNA SSR markers in Phyllostachys pubescens. (Q34168131) (← links)
- Hairpins are formed by the single DNA strands of the fragile X triplet repeats: structure and biological implications (Q34297548) (← links)
- Fragile sites-cytogenetic similarity with molecular diversity (Q34388758) (← links)
- Triplet repeats, over-expanded in neuromuscular diseases, are under-represented in mammalian DNA: a survey of models (Q34446575) (← links)
- Structure and dynamics of the DNA hairpins formed by tandemly repeated CTG triplets associated with myotonic dystrophy (Q34589868) (← links)
- Solution structures of the individual single strands of the fragile X DNA triplets (GCC)n.(GGC)n (Q34590948) (← links)
- Stability of intrastrand hairpin structures formed by the CAG/CTG class of DNA triplet repeats associated with neurological diseases (Q34599367) (← links)
- Cis-elements governing trinucleotide repeat instability in Saccharomyces cerevisiae. (Q34612185) (← links)
- Enrichment of oligo(dG).oligo(dC)-containing fragments from human genomic DNA by Mg 2+-dependent triplex affinity capture (Q34628194) (← links)
- Simple sequence repeats as a source of quantitative genetic variation (Q34738348) (← links)
- Triplet repeats form secondary structures that escape DNA repair in yeast (Q34995821) (← links)
- Microsatellites in different eukaryotic genomes: survey and analysis (Q35028489) (← links)
- The Role of XPG in Processing (CAG)n/(CTG)n DNA Hairpins (Q35073945) (← links)
- The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge (Q35170163) (← links)
- Trinucleotide repeat instability: a hairpin curve at the crossroads of replication, recombination, and repair (Q35550042) (← links)
- Simple sequence repeats (microsatellites): mutational mechanisms and contributions to bacterial pathogenesis. A meeting review. (Q35634103) (← links)
- Postreplication repair inhibits CAG.CTG repeat expansions in Saccharomyces cerevisiae. (Q35641701) (← links)
- Population dynamics of a meiotic/mitotic expansion model for the fragile X syndrome (Q35644120) (← links)
- Length heteroplasmy in the first hypervariable segment of the human mtDNA control region (Q35644511) (← links)
- Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations (Q35659075) (← links)
- Repeat instability during DNA repair: Insights from model systems (Q35680075) (← links)
- In vitro repair of DNA hairpins containing various numbers of CAG/CTG trinucleotide repeats (Q35974610) (← links)
- An empirical review: Characteristics of plant microsatellite markers that confer higher levels of genetic variation (Q35975666) (← links)
- Microsatellite instability in squamous cell carcinomas of the head and neck related to field cancerization phenomena. (Q36115031) (← links)
- LAR tyrosine phosphatase receptor: alternative splicing is preferential to the nervous system, coordinated with cell growth and generates novel isoforms containing extensive CAG repeats (Q36235220) (← links)
- Dp412e: a novel human embryonic dystrophin isoform induced by BMP4 in early differentiated cells. (Q36278519) (← links)
- The role of SOS and flap processing in microsatellite instability in Escherichia coli. (Q36282861) (← links)
- DNA polymerase kappa produces interrupted mutations and displays polar pausing within mononucleotide microsatellite sequences (Q36457026) (← links)