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Hotspots of mammalian chromosomal evolution
scientific article
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instance of
scholarly article
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title
Hotspots of mammalian chromosomal evolution
(English)
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author
David Haussler
series ordinal
4
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Evan E. Eichler
series ordinal
5
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Robert Baertsch
series ordinal
2
object named as
Robert Baertsch
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Jim Kent
series ordinal
3
object named as
W James Kent
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author name string
Jeffrey A Bailey
series ordinal
1
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language of work or name
English
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publication date
2004
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published in
Genome Biology
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volume
5
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page(s)
R23
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issue
4
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exact match
https://scigraph.springernature.com/pub.10.1186/gb-2004-5-4-r23
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cites work
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7 April 2017
Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p
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7 April 2017
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7 April 2017
Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse
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7 April 2017
Initial sequencing and analysis of the human genome
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7 April 2017
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7 April 2017
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7 April 2017
Initial sequencing and comparative analysis of the mouse genome
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7 April 2017
Genome sequence and comparative analysis of the model rodent malaria parasite Plasmodium yoelii yoelii
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Whole-Genome Shotgun Assembly and Analysis of the Genome of Fugu rubripes
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DNA sequence variation in a non-coding region of low recombination on the human X chromosome
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7 April 2017
Fourfold faster rate of genome rearrangement in nematodes than in Drosophila
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7 April 2017
The mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genome
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7 April 2017
Recent segmental duplications in the human genome
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7 April 2017
Analysis of complex disease association and linkage studies using the University of California Santa Cruz Genome Browser
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Structural dynamics of eukaryotic chromosome evolution
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28 September 2017
Human and mouse genomic sequences reveal extensive breakpoint reuse in mammalian evolution
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28 September 2017
Complex Evolution of 7E Olfactory Receptor Genes in Segmental Duplications
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28 September 2017
Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome
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28 September 2017
Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22.
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28 September 2017
Human chromosome 19 and related regions in mouse: conservative and lineage-specific evolution
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28 September 2017
The evolutionary chromosome translocation 4;19 in Gorilla gorilla is associated with microduplication of the chromosome fragment syntenic to sequences surrounding the human proximal CMT1A-REP
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28 September 2017
Segmental duplications: organization and impact within the current human genome project assembly
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28 September 2017
Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).
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28 September 2017
Lengths of chromosomal segments conserved since divergence of man and mouse
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28 September 2017
Using a pericentromeric interspersed repeat to recapitulate the phylogeny and expansion of human centromeric segmental duplications
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30 May 2018
Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10q.
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=395782
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30 May 2018
Molecular evolution of the human chromosome 15 pericentromeric region.
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PubMed Central
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28 November 2018
Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=395782
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28 November 2018
Chromosome 6 phylogeny in primates and centromere repositioning.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=395782
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28 November 2018
Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletions
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15059256
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1186/GB-2004-5-4-R23
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2813155
Dimensions Publication ID
1025231468
0 references
OpenCitations bibliographic resource ID
2813155
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2813155
PMCID
395782
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2813155
PubMed ID
15059256
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2813155
ResearchGate publication ID
8642678
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