FAM111A induces nuclear dysfunction in disease and viral restriction-Reference-Cited by-同舟云学术

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FAM111A induces nuclear dysfunction in disease and viral restriction

Published:2020-12-28 Issue:2 Volume:22 Page:
ISSN:1469-221X
Container-title:EMBO reports
language:en
Short-container-title:EMBO Rep

Author:

Nie Minghua¹^ORCID,Oravcová Martina¹,Jami‐Alahmadi Yasaman²,Wohlschlegel James A²^ORCID,Lazzerini‐Denchi Eros³,Boddy Michael N¹^ORCID

Affiliation:

1. Department of Molecular Medicine The Scripps Research Institute La Jolla CA USA

2. Department of Biological Chemistry David Geffen School of Medicine University of California Los Angeles CA USA

3. Laboratory of Genome Integrity National Cancer Institute NIH Bethesda MD USA

Funder

National Institute of General Medical Sciences

Publisher

EMBO

Subject

Genetics,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/embr.202050803

Reference51 articles.

1. Nascent chromatin capture proteomics determines chromatin dynamics during DNA replication and identifies unknown fork components

2. Hsp70 Isoforms Are Essential for the Formation of Kaposi’s Sarcoma-Associated Herpesvirus Replication and Transcription Compartments

3. BRCA2 prevents R-loop accumulation and associates with TREX-2 mRNA export factor PCID2

4. Gene positioning is regulated by phosphorylation of the nuclear pore complex by Cdk1

5. A rabbitpox virus serpin gene controls host range by inhibiting apoptosis in restrictive cells

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1. Interdependence between Nuclear Pore Gatekeepers and Genome Caretakers: Cues from Genome Instability Syndromes;International Journal of Molecular Sciences;2024-08-29

2. E2F3-dependent activation of FAM111B restricts mouse cytomegalovirus replication in primate cells;2024-08-02

3. Mother and daughter with Kenny-Caffey syndrome: the adult phenotype;European Journal of Medical Genetics;2024-06

4. Disruption of the c‐terminal serine protease domain of Fam111a does not alter calcium homeostasis in mice;Physiological Reports;2024-05

5. Further delineation of phenotype and genotype of Kenny–Caffey syndrome type 2 (phenotype and genotype of KCS type 2);Molecular Genetics & Genomic Medicine;2024-04

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