Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains. (Q48038450)

7 February 2018

title

Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains. (English)

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7 February 2018

author

Richard J Gibbons

4

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7 February 2018

author name string

D J Picketts

1

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7 February 2018

A O Tastan

2

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7 February 2018

D R Higgs

3

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7 February 2018

publication date

1 May 1998

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7 February 2018

number of pages

4

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inferred from page(s)

published in

Mammalian Genome

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volume

9

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7 February 2018

issue

5

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7 February 2018

page(s)

400-403

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7 February 2018

https://scigraph.springernature.com/pub.10.1007/s003359900781

exact match

0 references

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Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

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Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain

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ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome

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Determination of the genomic structure of the XNP/ATRX gene encoding a potential zinc finger helicase

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Cis-acting sequences regulating expression of the human alpha-globin cluster lie within constitutively open chromatin

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A possible involvement of TIF1 alpha and TIF1 beta in the epigenetic control of transcription by nuclear receptors

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Identifiers

DOI

10.1007/S003359900781

1 reference

7 February 2018

PubMed ID

9545503

1 reference

7 February 2018