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Lymphoid-specific helicase in epigenetics, DNA repair and cancer

Lymphoid-specific helicase in epigenetics, DNA repair and cancer

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8770686

Lymphoid-specific helicase in epigenetics, DNA repair and cancer

About this item

Full title

Lymphoid-specific helicase in epigenetics, DNA repair and cancer

Publisher

London: Nature Publishing Group UK

Journal title

British journal of cancer, 2022-02, Vol.126 (2), p.165-173

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Lymphoid-specific helicase (LSH) is a member of the SNF2 helicase family of chromatin-remodelling proteins. Dysfunctions or mutations in LSH causes an autosomal recessive disease known as immunodeficiency-centromeric instability-facial anomaly (ICF) syndrome. Interestingly, LSH participates in various aspects of epigenetic regulation, including nuc...

Alternative Titles

Full title

Lymphoid-specific helicase in epigenetics, DNA repair and cancer

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8770686

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8770686

Other Identifiers

ISSN

0007-0920

E-ISSN

1532-1827

DOI

10.1038/s41416-021-01543-2

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