Microsatellite evolution--evidence for directionality and variation in rate between species (Q72048133)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670473%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

title

Microsatellite evolution--evidence for directionality and variation in rate between species (English)

1 reference

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23 October 2019

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Rubinsztein DC

1

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23 October 2019

Amos W

2

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23 October 2019

Leggo J

3

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23 October 2019

Goodburn S

4

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23 October 2019

Jain S

5

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23 October 2019

Li SH

6

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23 October 2019

Margolis RL

7

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23 October 2019

Ross CA

8

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23 October 2019

Ferguson-Smith MA

9

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23 October 2019

publication date

1 July 1995

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23 October 2019

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23 October 2019

volume

10

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23 October 2019

page(s)

337-343

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23 October 2019

issue

3

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https://scigraph.springernature.com/pub.10.1038/ng0795-337

23 October 2019

exact match

0 references

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Dynamic mutations hit double figures

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence.

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

High resolution of human evolutionary trees with polymorphic microsatellites

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Conservation of human chromosome 13 polymorphic microsatellite (CA)n repeats in chimpanzees

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Survey of human and rat microsatellites.

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Mutation of human short tandem repeats

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

New alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Complex gene conversion events in germline mutation at human minisatellites

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Evolutionary transience of hypervariable minisatellites in man and the primates

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Evolution of genetic redundancy for advanced players

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Simple repeat DNA is not replicated simply

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Complex recombination events at the hypermutable minisatellite CEB1 (D2S90).

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Trinucleotide repeat length instability and age of onset in Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

B37 repeats are normal in most schizophrenic patients

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Construction of a GT polymorphism map of human 9q

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Isolation and characterization of 19 dinucleotide repeat polymorphisms on chromosome 3p.

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Human GluR6 kainate receptor (GRIK2): molecular cloning, expression, polymorphism, and chromosomal assignment

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Genetic and physical mapping around the properdin P gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Dinucleotide repeat polymorphism at the human dopamine beta-hydroxylase (DBH) locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Polymorphic dinucleotide repeat at the DXS3 locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

A highly informative CACA repeat polymorphism upstream of the human dystrophin gene (DMD).

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Dinucleotide repeat polymorphism near the RP3 locus in Xp21 (DXS1110)

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q.

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

A polymorphic dinucleotide repeat at the DXS7 locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

An STR polymorphism at the CYBB locus.

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

https://api.crossref.org/works/10.1038%2FNG0795-337

7 January 2021

Identifiers

DOI

10.1038/NG0795-337

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7670473%20AND%20SRC:MED&resulttype=core&format=json

23 October 2019

1 reference