Cockayne Syndrome Type 2 Latest Advances

Find the Latest Research About Cockayne Syndrome Type 2

Last Updated: 02/24/2026

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Found 977 publications

Expanding the landscape of nucleotide excision repair disorders: from discovery to therapy.

Expanding the landscape of nucleotide excision repair disorders: from discovery to therapy.

Journal: The Journal of clinical investigation
Published: November 17, 2025

Cockayne syndrome mutation in XPG activate the integrated stress response.

Cockayne syndrome mutation in XPG activate the integrated stress response.

Journal: Human genetics
Published: March 27, 2025

Protective role of Cockayne Syndrome B (CSB) protein in maintaining genome integrity in human cells under oxidative stress.

Protective role of Cockayne Syndrome B (CSB) protein in maintaining genome integrity in human cells under oxidative stress.

Journal: Mutation research. Genetic toxicology and environmental mutagenesis
Published: March 26, 2025

Altered pathways in Cockayne syndrome: Involvement of MAPK, PI3K-Akt, extracellular matrix, inflammation, and neuronal signaling.

Altered pathways in Cockayne syndrome: Involvement of MAPK, PI3K-Akt, extracellular matrix, inflammation, and neuronal signaling.

Journal: DNA repair
Published: February 18, 2025

Insights Into Cockayne Syndrome Type B: What Underlies Its Pathogenesis?

Insights Into Cockayne Syndrome Type B: What Underlies Its Pathogenesis?

Journal: Aging cell
Published: January 23, 2025

ATP-Dependent Chromatin Remodeler CSB Couples DNA Repair Pathways to Transcription with Implications for Cockayne Syndrome and Cancer Therapy.

ATP-Dependent Chromatin Remodeler CSB Couples DNA Repair Pathways to Transcription with Implications for Cockayne Syndrome and Cancer Therapy.

Journal: Cells
Published: January 10, 2025

Transcription-coupled repair: tangled up in convoluted repair.

Transcription-coupled repair: tangled up in convoluted repair.

Journal: The FEBS journal
Published: December 13, 2024

The aflatoxin B1-induced formamidopyrimidine adduct is repaired by transcription-coupled nucleotide excision repair in human cells.

The aflatoxin B1-induced formamidopyrimidine adduct is repaired by transcription-coupled nucleotide excision repair in human cells.

Journal: NAR cancer
Published: November 27, 2024

PML Nuclear Bodies and Cellular Senescence: A Comparative Study of Healthy and Premature Aging Syndrome Donors' Cells.

PML Nuclear Bodies and Cellular Senescence: A Comparative Study of Healthy and Premature Aging Syndrome Donors' Cells.

Journal: Cells
Published: October 31, 2024

Perspectives in the investigation of Cockayne syndrome group B neurological disease: the utility of patient-derived brain organoid models.

Perspectives in the investigation of Cockayne syndrome group B neurological disease: the utility of patient-derived brain organoid models.

Journal: Journal of Zhejiang University. Science. B
Published: October 18, 2024

Clinical and molecular genetic analysis of a Chinese patient with Cockayne syndrome caused by ERCC8 gene synonymous variant at splicing site and exon 1 deletion.

Clinical and molecular genetic analysis of a Chinese patient with Cockayne syndrome caused by ERCC8 gene synonymous variant at splicing site and exon 1 deletion.

Journal: Orphanet journal of rare diseases
Published: September 18, 2024

Transcription-coupled repair of DNA-protein crosslinks.

Transcription-coupled repair of DNA-protein crosslinks.

Journal: Trends in cell biology
Published: August 14, 2024
Showing 1-12 of 977

Last Updated: 02/24/2026