Concerted evolution of the tandem array encoding primate U2 snRNA occurs in situ, without changing the cytological context of the RNU2 locus (Q24568372)

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English	Concerted evolution of the tandem array encoding primate U2 snRNA occurs in situ, without changing the cytological context of the RNU2 locus	scientific article

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26 October 2019

Concerted evolution of the tandem array encoding primate U2 snRNA occurs in situ, without changing the cytological context of the RNU2 locus (English)

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26 October 2019

A. Gregory Matera

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26 October 2019

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T Pavelitz

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26 October 2019

L Rusché

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26 October 2019

J M Scharf

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26 October 2019

A M Weiner

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1 January 1995

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26 October 2019

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26 October 2019

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26 October 2019

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26 October 2019

169-177

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26 October 2019

Human Genes for U2 Small Nuclear RNA Are Tandemly Repeated

1 reference

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Human U1 small nuclear RNA genes: extensive conservation of flanking sequences suggests cycles of gene amplification and transposition

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Generation of a new adenovirus type 12-inducible fragile site by insertion of an artificial U2 locus in the human genome

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Developmental differences in methylation of human Alu repeats

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Fine-resolution mapping of spontaneous and double-strand break-induced gene conversion tracts in Saccharomyces cerevisiae reveals reversible mitotic conversion polarity

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Human U1 RNA genes contain an unusually sensitive nuclease S1 cleavage site within the conserved 3' flanking region

1 reference

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Genes and pseudogenes for human U2 RNA. Implications for the mechanism of pseudogene formation

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27 September 2017

Clustered genes for human U2 RNA

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27 September 2017

Pseudogenes for human U2 small nuclear RNA do not have a fixed site of 3′ truncation

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27 September 2017

Fungal recombination

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27 September 2017

Human U1 small nuclear RNA pseudogenes do not map to the site of the U1 genes in 1p36 but are clustered in 1q12-q22

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27 September 2017

A fragile site in the human U2 small nuclear RNA gene cluster is revealed by adenovirus type 12 infection

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27 September 2017

Linkage disequilibrium in human ribosomal genes: implications for multigene family evolution

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Sequences flanking the repeat arrays of human minisatellites: association with tandem and dispersed repeat elements.

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27 September 2017

Normal diploid human and rodent cells lack a detectable frequency of gene amplification

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27 September 2017

Chromosomal damage induced by human adenovirus type 12 requires expression of the E1B 55-kilodalton viral protein

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27 September 2017

Molecular cytotaxonomy of primates by chromosomal in situ suppression hybridization

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27 September 2017

Structure and evolution of the U2 small nuclear RNA multigene family in primates: gene amplification under natural selection?

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Fine mapping of human 5S rRNA genes to chromosome 1q42.11→q42.13

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27 September 2017

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27 September 2017

Formation of heteroduplex DNA during mammalian intrachromosomal gene conversion

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Human ribosomal RNA intergenic spacer sequence

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30 May 2018

Early dihydrofolate reductase gene amplification events in CHO cells usually occur on the same chromosome arm as the original locus

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30 May 2018

Human genes for U2 small nuclear RNA map to a major adenovirus 12 modification site on chromosome 17.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=398064

30 May 2018

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30 May 2018

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30 May 2018

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30 May 2018

Isolation of an active human transposable element

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Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7.

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Experimental determination of rates of concerted evolution

1 reference

https://pubmed.ncbi.nlm.nih.gov/7828589

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

https://pubmed.ncbi.nlm.nih.gov/7828589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complex gene conversion events in germline mutation at human minisatellites

1 reference

https://pubmed.ncbi.nlm.nih.gov/7828589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unequal crossover and the evolution of multigene families

1 reference

https://pubmed.ncbi.nlm.nih.gov/7828589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolution of Repeated DNA Sequences by Unequal Crossover

1 reference

https://pubmed.ncbi.nlm.nih.gov/7828589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Either Gene Amplification or Gene Conversion May Maintain the Homogeneity of the Multigene Family Encoding Human U1 Small Nuclear RNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/7828589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile sites, chromosome evolution, and human neoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7828589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct factors with Sp1 and NF-A specificities bind to adjacent functional elements of the human U2 snRNA gene enhancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/7828589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common fragile sites in man and three closely related primate species

1 reference

https://pubmed.ncbi.nlm.nih.gov/7828589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolutionary transience of hypervariable minisatellites in man and the primates

1 reference

https://pubmed.ncbi.nlm.nih.gov/7828589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synergism between aphidicolin and adenoviruses in the induction of breaks at fragile sites on human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7828589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered cell cycle arrest and gene amplification potential accompany loss of wild-type p53

1 reference

https://pubmed.ncbi.nlm.nih.gov/7828589

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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Identifiers

10.1002/J.1460-2075.1995.TB06987.X

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26 October 2019

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26 October 2019

PubMed publication ID

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26 October 2019

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