Hominoid chromosomal rearrangements on 17q map to complex regions of segmental duplication. (Q38275855)

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2 January 2020

title

Hominoid chromosomal rearrangements on 17q map to complex regions of segmental duplication (English)

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2 January 2020

5

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2 January 2020

Maria Francesca Cardone

1

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2 January 2020

Pietro D'Addabbo

3

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2 January 2020

Nicoletta Archidiacono

4

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2 January 2020

Mario Ventura

7

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2 January 2020

6

Evan E Eichler

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2 January 2020

2

Zhaoshi Jiang

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2 January 2020

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publication date

7 February 2008

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2 January 2020

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2 January 2020

volume

9

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2 January 2020

issue

2

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2 January 2020

page(s)

R28

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Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15

2 January 2020

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Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy

6 September 2017

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Evolutionary and Biomedical Insights from the Rhesus Macaque Genome

6 September 2017

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Gene duplication: a drive for phenotypic diversity and cause of human disease

6 September 2017

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A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.

6 September 2017

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Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

6 September 2017

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6 September 2017

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6 September 2017

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DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage

6 September 2017

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A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications

6 September 2017

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Dynamics of mammalian chromosome evolution inferred from multispecies comparative maps

6 September 2017

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The evolution of eutherian chromosomes

6 September 2017

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Mammalian phylogenomics comes of age

6 September 2017

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Evolutionary history of chromosome 20.

6 September 2017

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Segmental duplications flank the multiple sclerosis locus on chromosome 17q.

6 September 2017

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Analysis of segmental duplications and genome assembly in the mouse

6 September 2017

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Hotspots of mammalian chromosomal evolution

6 September 2017

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The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats

6 September 2017

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Reconstruction of the ancestral karyotype of eutherian mammals

6 September 2017

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Reciprocal chromosome painting among human, aardvark, and elephant (superorder Afrotheria) reveals the likely eutherian ancestral karyotype

6 September 2017

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Analysis of chromosome conservation in Lemur catta studied by chromosome paints and BAC/PAC probes.

6 September 2017

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Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17

6 September 2017

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Structure and evolution of the Smith-Magenis syndrome repeat gene clusters, SMS-REPs.

6 September 2017

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Divergent origins and concerted expansion of two segmental duplications on chromosome 16

6 September 2017

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Segmental duplications and the evolution of the primate genome

6 September 2017

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Genome-scale evolution: reconstructing gene orders in the ancestral species.

6 September 2017

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Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22.

6 September 2017

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"Bar-coding" primate chromosomes: molecular cytogenetic screening for the ancestral hominoid karyotype

6 September 2017

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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

6 September 2017

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Evolution of mammalian genome organization inferred from comparative gene mapping

6 September 2017

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The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes

6 September 2017

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Centromere emergence in evolution

6 September 2017

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A physical map of the human genome

6 September 2017

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Molecular phylogenetics and the origins of placental mammals

6 September 2017

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Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24.

6 September 2017

1 reference

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Structure of chromosomal duplicons and their role in mediating human genomic disorders

6 September 2017

1 reference

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Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374708

DNA rearrangements on both homologues of chromosome 17 in a mildly delayed individual with a family history of autosomal dominant carpal tunnel syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374708

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374708

The chimpanzee-specific pericentric inversions that distinguish humans and chimpanzees have identical breakpoints in Pan troglodytes and Pan paniscus

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374708

Segmental duplications: organization and impact within the current human genome project assembly

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374708

Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2374708

Ancestral reconstruction of segmental duplications reveals punctuated cores of human genome evolution.

27 September 2017

1 reference

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Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements

31 August 2018

1 reference

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Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22-q24

31 August 2018

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12 December 2020

Evolutionary history of chromosome 10 in primates

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12 December 2020

Shotgun sequence assembly and recent segmental duplications within the human genome

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12 December 2020

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

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12 December 2020

Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

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12 December 2020

Identifiers

DOI

10.1186/GB-2008-9-2-R28

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18257913%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

2 January 2020

0 references

1 reference

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2 January 2020

PubMed publication ID

18257913

1 reference