Fragile sites in human and Macaca fascicularis chromosomes are breakpoints in chromosome evolution.

scientific article published in January 2002

Fragile sites in human and Macaca fascicularis chromosomes are breakpoints in chromosome evolution. is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1002934593
P356DOI10.1023/A:1014261909613
P698PubMed publication ID11863068

P50authorAurora Ruiz-HerreraQ42112937
Montserrat PonsaQ68849042
P2093author name stringM García
F García
J Egozcue
P2860cites workThe origin of man: a chromosomal pictorial legacyQ22299401
Evolutionary conservation of fragile sites induced by 5-azacytidine and 5-azadeoxycytidine in man, gorilla, and chimpanzeeQ28236365
Genes encoding human caveolin-1 and -2 are co-localized to the D7S522 locus (7q31.1), a known fragile site (FRA7G) that is frequently deleted in human cancersQ28287729
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2Q28292748
Homologies in human and Macaca fuscata chromosomes revealed by in situ suppression hybridization with human chromosome specific DNA librariesQ33212904
Fragile sites-cytogenetic similarity with molecular diversityQ34388758
Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogeneticsQ35203122
Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.Q36169197
Cancer-specific chromosome alterations in the constitutive fragile region FRA3B.Q36396981
Expression of common fragile sites in two Ceboidea species: Saimiri boliviensis and Alouatta caraya (Primates: Platyrrhini).Q37253114
Expression of fragile sites triggers intrachromosomal mammalian gene amplification and sets boundaries to early ampliconsQ41115353
Diagrammatic representation for chromosomal mutagenesis studies. III. Radiation-induced rearrangements in Pan troglodytes (chimpanzee).Q52849760
Constitutive fragile sites and cancer.Q52849884
Chromosomal homologies between humans and Cebus apella (Primates) revealed by ZOO-FISHQ60287322
Chromosome abnormalities in peripheral blood lymphocytes from Macaca fascicularis and Erythrocebus patas (Cercopithecidae, Catarrhini) after X-ray irradiationQ61818851
Human gene mapping 11. London Conference (1991). Eleventh International Workshop on Human Gene Mapping. London, UK, August 18-22, 1991Q68330970
Fragile sites are targets of diverse mutagens and carcinogensQ68675516
Common fragile sites in man and three closely related primate speciesQ68748844
Fragile sites, chromosome evolution, and human neoplasiaQ68990916
A comparative mapping study of fragile sites in the human and murine genomesQ69398557
Cytogenetic effects of radiotherapy. Breakpoint distribution in induced chromosome aberrationsQ69694513
Site-specific chromosomal rearrangements induced in human diploid cells by x-irradiationQ69994966
Diagrammatic representation for chromosomal mutagenesis studies. II. Radiation-induced rearrangements in Macaca fascicularisQ71280353
Risk of chromosomal disease due to radiation. Tentative estimate from the study of radiation-induced translocations in human fibroblastsQ71670790
Identifying chromosomal fragile sites from individuals: a multinomial statistical modelQ72573352
How common are common fragile sites: variation of aphidicolin-induced chromosomal fragile sites in a population of the deer mouse (Peromyscus maniculatus)Q73582274
P433issue1
P921main subjectcrab-eating macaqueQ301676
P304page(s)33-44
P577publication date2002-01-01
P1433published inChromosome ResearchQ15765850
P1476titleFragile sites in human and Macaca fascicularis chromosomes are breakpoints in chromosome evolution
P478volume10

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cites work (P2860)
Q39149580A high resolution map of mammalian X chromosome fragile regions assessed by large-scale comparative genomics
Q89113405Association between Genomic Instability and Evolutionary Chromosomal Rearrangements in Neotropical Primates
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Q28755885Chromosomal instability in Afrotheria: fragile sites, evolutionary breakpoints and phylogenetic inference from genome sequence assemblies
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Q51802495Chromosome instability on children with asthma.
Q35056705Common fragile sites are conserved features of human and mouse chromosomes and relate to large active genes
Q58426207Comprehensive genome and transcriptome analysis of the 11q13 amplicon in human oral cancer and synteny to the 7F5 amplicon in murine oral carcinoma
Q45124914Conservation of aphidicolin-induced fragile sites in Papionini (Primates) species and humans.
Q45151925Evolutionary breakpoints are co-localized with fragile sites and intrachromosomal telomeric sequences in primates.
Q52841640Evolutionary conserved chromosomal segments in the human karyotype are bounded by unstable chromosome bands.
Q51131222Feeder layer- and serum-free culture of rhesus monkey embryonic stem cells.
Q35146467Human and mouse genomic sequences reveal extensive breakpoint reuse in mammalian evolution
Q35629768Is mammalian chromosomal evolution driven by regions of genome fragility?
Q42025587Karyotype structure and chromosome fragility in the grass Phleum echinatum Host.
Q33309970Mapping cynomolgus monkey MHC class I district on chromosome 6p13 using pooled cDNAs
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Q37091846Molecular mechanisms of chromosomal rearrangement during primate evolution
Q57304613Murine segmental duplications are hot spots for chromosome and gene evolution
Q33848834Unraveling the effect of genomic structural changes in the rhesus macaque - implications for the adaptive role of inversions

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