(Q47990305)

7 February 2018

title

Recent amplification of the human FRG1 gene during primate evolution. (English)

1 reference

7 February 2018

author name string

Grewal PK

1

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7 February 2018

van Geel M

2

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7 February 2018

Frants RR

3

1 reference

7 February 2018

de Jong P

4

1 reference

7 February 2018

Hewitt JE

5

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7 February 2018

language of work or name

English

0 references

publication date

1 February 1999

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7 February 2018

published in

Gene

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7 February 2018

volume

227

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7 February 2018

page(s)

79-88

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7 February 2018

issue

1

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7 February 2018

Sequence diversity and chromosomal distribution of "young" Alu repeats.

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

1 reference

7 January 2021

Analysis of the organisation and localisation of the FSHD-associated tandem array in primates: implications for the origin and evolution of the 3.3 kb repeat family

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

A novel mechanism of aberrant pre-mRNA splicing in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

Duplication and distribution of repetitive elements and non-unique regions in the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

Origin of the Alu family: a family of Alu-like monomers gave birth to the left and the right arms of the Alu elements

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

Emergence and scattering of multiple neurofibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

An intronic (A/U)GGG repeat enhances the splicing of an alternative intron of the chicken beta-tropomyosin pre-mRNA

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

Genomic analysis of a NF1-related pseudogene on human chromosome 21.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

Sequence and gene content in 52 kb including and centromeric to the G6PD gene in Xq28

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900587-3

7 January 2021

10.1016/S0378-1119(98)00587-3

Identifiers

DOI

1 reference

7 February 2018

PubMed ID

9931447

1 reference

7 February 2018