Pages that link to "Q36791809"

The following pages link to Playing hide and seek with mammalian meiotic crossover hotspots (Q36791809):

Displaying 35 items.

• Genome-wide analysis reveals novel molecular features of mouse recombination hotspots (Q24611454) (← links)
• What determines the localisation of spots of meiotic recombination? (Q27029091) (← links)
• Evidence that Cd101 is an autoimmune diabetes gene in nonobese diabetic mice (Q28509117) (← links)
• Mouse PRDM9 DNA-binding specificity determines sites of histone H3 lysine 4 trimethylation for initiation of meiotic recombination (Q28590930) (← links)
• Cis- and trans-acting elements regulate the mouse Psmb9 meiotic recombination hotspot (Q33288732) (← links)
• Global analysis of genetic, epigenetic and transcriptional polymorphisms in Arabidopsis thaliana using whole genome tiling arrays (Q33325903) (← links)
• Genome-wide control of the distribution of meiotic recombination (Q33410335) (← links)
• Genetic crossovers are predicted accurately by the computed human recombination map (Q33529042) (← links)
• Is homologous recombination really an error-free process? (Q33736829) (← links)
• Conservation of recombination hotspots in yeast (Q33842690) (← links)
• Analysis of human meiotic recombination events with a parent-sibling tracing approach (Q34002968) (← links)
• PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice (Q34090633) (← links)
• Fine scale analysis of crossover and non-crossover and detection of recombination sequence motifs in the honeybee (Apis mellifera) (Q34261759) (← links)
• Suppression of genetic recombination in the pseudoautosomal region and at subtelomeres in mice with a hypomorphic Spo11 allele (Q34840536) (← links)
• Variation in patterns of human meiotic recombination (Q35018030) (← links)
• Mammalian recombination hot spots: properties, control and evolution. (Q35311047) (← links)
• Altered LINE-1 Methylation in Mothers of Children with Down Syndrome. (Q35643414) (← links)
• Meiosis-specific proteins MEIOB and SPATA22 cooperatively associate with the single-stranded DNA-binding replication protein A complex and DNA double-strand breaks (Q36358073) (← links)
• Regulating double-stranded DNA break repair towards crossover or non-crossover during mammalian meiosis. (Q36900915) (← links)
• Population genomic inference of recombination rates and hotspots (Q37159047) (← links)
• Detecting Recombination Hotspots from Patterns of Linkage Disequilibrium. (Q37162954) (← links)
• Distinct histone modifications define initiation and repair of meiotic recombination in the mouse (Q37334927) (← links)
• Genomic analysis of hESC pedigrees identifies de novo mutations and enables determination of the timing and origin of mutational events (Q37488070) (← links)
• Initiation of meiotic recombination in mammals (Q37664062) (← links)
• The choice in meiosis – defining the factors that influence crossover or non-crossover formation (Q37833845) (← links)
• MareyMap Online: A User-Friendly Web Application and Database Service for Estimating Recombination Rates Using Physical and Genetic Maps (Q42695050) (← links)
• Meiotic crossovers are associated with open chromatin and enriched with Stowaway transposons in potato (Q45071361) (← links)
• The consequences of sequence erosion in the evolution of recombination hotspots. (Q45987483) (← links)
• Variation in crossover rates across a 3-Mb contig of bread wheat (Triticum aestivum) reveals the presence of a meiotic recombination hotspot (Q46854267) (← links)
• Genetic and evolutionary correlates of fine-scale recombination rate variation in Drosophila persimilis. (Q52710043) (← links)
• Interrogating the Functions of PRDM9 Domains in Meiosis. (Q52718185) (← links)
• [What defines the genetic map? The specification of meiotic recombination sites]. (Q53269777) (← links)
• Combining results of forensic STR kits: HDplex validation including allelic association and linkage testing with NGM and Identifiler loci (Q60232986) (← links)
• A comprehensive study revealed SNP–SNP interactions and a sex-dependent relationship between polymorphisms of the CYP2J2 gene and hypertension risk (Q64004939) (← links)
• Potential of 13 linked autosomal short tandem repeat loci in pairwise kinship analysis (Q88477332) (← links)