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Human imprinted chromosomal regions are historical hot-spots of recombination.
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1487178
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26 December 2019
title
Human imprinted chromosomal regions are historical hot-spots of recombination
(English)
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1487178
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26 December 2019
author
Ionel Sandovici
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1
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1487178
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26 December 2019
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Sacha Kassovska-Bratinova
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2
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1487178
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26 December 2019
Joe E Vaughan
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3
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26 December 2019
Rae Stewart
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26 December 2019
Mark Leppert
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5
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26 December 2019
Carmen Sapienza
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26 December 2019
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22 May 2006
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26 December 2019
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PLOS Genetics
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26 December 2019
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2
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26 December 2019
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7
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26 December 2019
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26 December 2019
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7 July 2006
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A novel STX16 deletion in autosomal dominant pseudohypoparathyroidism type Ib redefines the boundaries of a cis-acting imprinting control element of GNAS
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The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern
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Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor
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Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome
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The fine-scale structure of recombination rate variation in the human genome
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Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations
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Roles of histone acetylation and chromatin remodeling factor in a meiotic recombination hotspot.
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Imprinted chromosomal regions of the human genome have unusually high recombination rates
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Natural Selection and the Evolution of Genome Imprinting
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Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS
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Insulator and silencer sequences in the imprinted region of human chromosome 11p15.5.
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The evolution of sex dimorphism in recombination
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Recombination explains isochores in mammalian genomes
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Properties of linkage disequilibrium (LD) maps
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21 June 2018
Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation
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The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis
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21 June 2018
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21 June 2018
Genomic imprinting: parental influence on the genome
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21 June 2018
Natural selection and the function of genome imprinting: beyond the silenced minority
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H19 and Igf2 monoallelic expression is regulated in two distinct ways by a shared cis acting regulatory region upstream of H19.
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Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region
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21 June 2018
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome
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Relationship between transcription and initiation of meiotic recombination: toward chromatin accessibility
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21 June 2018
Transcription factor Mts1/Mts2 (Atf1/Pcr1, Gad7/Pcr1) activates the M26 meiotic recombination hotspot in Schizosaccharomyces pombe
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21 June 2018
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21 June 2018
Centromere and telomere movements during early meiotic prophase of mouse and man are associated with the onset of chromosome pairing
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21 June 2018
Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population
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21 June 2018
Statistical properties of the number of recombination events in the history of a sample of DNA sequences
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21 June 2018
Polymorphism in the activity of human crossover hotspots independent of local DNA sequence variation.
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31 October 2018
Comparison of fine-scale recombination rates in humans and chimpanzees.
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31 October 2018
Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome
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31 October 2018
The initiation of homologous chromosome synapsis in mouse fetal oocytes is not directly driven by centromere and telomere clustering in the bouquet
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31 October 2018
Gene-specific timing and epigenetic memory in oocyte imprinting
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31 October 2018
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31 October 2018
Relaxation of IGF2 imprinting in Wilms tumours associated with specific changes in IGF2 methylation
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31 October 2018
Genomic imprinting of the insulin-like growth factor 2 gene in sheep
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31 October 2018
Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis.
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31 October 2018
Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies
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31 October 2018
Local Rates of Recombination Are Positively Correlated with GC Content in the Human Genome
1 reference
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12 December 2020
based on heuristic
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Long-range sequence composition mirrors linkage disequilibrium pattern in a 1.13 Mb region of human chromosome 22
1 reference
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PubMed
reference URL
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions
1 reference
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reference URL
https://pubmed.ncbi.nlm.nih.gov/16839189
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Evidence for substantial fine-scale variation in recombination rates across the human genome
1 reference
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reference URL
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Meiosis-induced double-strand break sites determined by yeast chromatin structure
1 reference
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region
1 reference
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reference URL
https://pubmed.ncbi.nlm.nih.gov/16839189
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Interchromosomal Transfer of Epigenetic States in Ascobolus: Transfer of DNA Methylation Is Mechanistically Related to Homologous Recombination
1 reference
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https://pubmed.ncbi.nlm.nih.gov/16839189
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1371/JOURNAL.PGEN.0020101
1 reference
stated in
Europe PubMed Central
PMC publication ID
1487178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839189%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
PMC publication ID
1487178
1 reference
stated in
Europe PubMed Central
PMC publication ID
1487178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839189%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
PubMed publication ID
16839189
1 reference
stated in
Europe PubMed Central
PMC publication ID
1487178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16839189%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
ResearchGate publication ID
6946861
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