Pages that link to "Q58992790"
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The following pages link to Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism (Q58992790):
Displaying 50 items.
- Factors affecting levels of genetic diversity in natural populations (Q22065927) (← links)
- Human minisatellite mutation rate after the Chernobyl accident (Q22337273) (← links)
- PRDM9 variation strongly influences recombination hot-spot activity and meiotic instability in humans (Q24595214) (← links)
- Germ-line mutations, DNA damage, and global hypermethylation in mice exposed to particulate air pollution in an urban/industrial location (Q24648996) (← links)
- Evidence for widespread convergent evolution around human microsatellites (Q24798682) (← links)
- Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat (Q28304011) (← links)
- Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1 (Q28307006) (← links)
- Differential Structuring of Human Populations for Homologous X and Y Microsatellite Loci (Q28764585) (← links)
- Nuclear pseudogenes of mitochondrial DNA as a variable part of the human genome (Q30831922) (← links)
- Sexual selection does not influence minisatellite mutation rate (Q33398648) (← links)
- Microsatellite and trinucleotide-repeat evolution: evidence for mutational bias and different rates of evolution in different lineages (Q33703945) (← links)
- Human minisatellites, repeat DNA instability and meiotic recombination (Q33704277) (← links)
- Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms (Q33802755) (← links)
- Repeat instability at human minisatellites arising from meiotic recombination (Q33889147) (← links)
- Two modes of germline instability at human minisatellite MS1 (locus D1S7): complex rearrangements and paradoxical hyperdeletion. (Q33904840) (← links)
- Patterns of instability of expanded CAG repeats at the ERDA1 locus in general populations (Q34390843) (← links)
- Triplet repeats, over-expanded in neuromuscular diseases, are under-represented in mammalian DNA: a survey of models (Q34446575) (← links)
- Heterogeneity of microsatellite mutations within and between loci, and implications for human demographic histories (Q34603478) (← links)
- Complex minisatellite rearrangements generated in the total or partial absence of Rad27/hFEN1 activity occur in a single generation and are Rad51 and Rad52 dependent. (Q35071154) (← links)
- Somatic mutations and ageing in silico (Q35078370) (← links)
- Hypermutable minisatellites, a human affair? (Q35099496) (← links)
- 2 Meiotic Recombination Hotspots: Shaping the Genome and Insights into Hypervariable Minisatellite DNA Change (Q35152335) (← links)
- Meiotic recombination hot spots and human DNA diversity. (Q35213819) (← links)
- Homopolymeric tract heteroplasmy in mtDNA from tissues and single oocytes: support for a genetic bottleneck (Q35238386) (← links)
- The contribution of <i>cis</i>-elements to disease-associated repeat instability: clinical and experimental evidence (Q35550046) (← links)
- Mutation rate in the hypervariable VNTR g3 (D7S22) is affected by allele length and a flanking DNA sequence polymorphism near the repeat array (Q35881955) (← links)
- The rate of nonallelic homologous recombination in males is highly variable, correlated between monozygotic twins and independent of age (Q37622310) (← links)
- Variable germline and embryonic instability of the human minisatellite MS32 (D1S8) in transgenic mice. (Q37639338) (← links)
- Monitoring for induced heritable mutations in natural populations: application of minisatellite DNA screening. (Q39471611) (← links)
- Comparative sequence analysis of human minisatellites showing meiotic repeat instability. (Q40413312) (← links)
- Evolutionary fate of an unstable human minisatellite deduced from sperm-mutation spectra of individual alleles (Q40725040) (← links)
- Mutation processes at human minisatellites. (Q40959180) (← links)
- DNA diagnosis of human genetic individuality (Q41073241) (← links)
- Trinucleotide Repeat Instability: Genetic Features and Molecular Mechanisms (Q41527084) (← links)
- Influences of array size and homogeneity on minisatellite mutation. (Q41974604) (← links)
- Multiple levels of single-strand slippage at cetacean tri- and tetranucleotide repeat microsatellite loci. (Q42565443) (← links)
- Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28 (Q45295470) (← links)
- Inhibitory effects of expanded GAA.TTC triplet repeats from intron I of the Friedreich ataxia gene on transcription and replication in vivo (Q48034382) (← links)
- FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis. (Q48036449) (← links)
- Distribution of tandem repeat polymorphism within minisatellite MS621 (D5S110). (Q48067400) (← links)
- Distinguishing minisatellite mutation from non-paternity by MVR-PCR. (Q52925453) (← links)
- Minisatellite diversity supports a recent African origin for modern humans (Q57718889) (← links)
- Local Mutagenic Impact of Insertions of LTR Retrotransposons on the Mouse Genome (Q61658996) (← links)
- Pathogenic expansions of the SCA6 locus are associated with a common CACNA1A haplotype across the globe: founder effect or predisposing chromosome? (Q62024060) (← links)
- Meiotic interallelic conversion at the human minisatellite MS32 in yeast triggers recombination in several chromatids (Q64388736) (← links)
- Meiotic instability of human minisatellite CEB1 in yeast requires DNA double-strand breaks (Q64388755) (← links)
- Dose—response of a Radiation Induction of a Germline Mutation at a Hypervariable Mouse Minisatellite Locus (Q72018290) (← links)
- Direct analysis by small-pool PCR of MS205 minisatellite mutation rates in sperm after mutagenic therapies (Q73083693) (← links)
- GAA instability in Friedreich's Ataxia shares a common, DNA-directed and intraallelic mechanism with other trinucleotide diseases (Q74771975) (← links)
- High-resolution mapping of crossovers in human sperm defines a minisatellite-associated recombination hotspot (Q77231600) (← links)