Cockayne Syndrome Type 1 Latest Advances

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

Journal: The Journal of clinical investigation

Published: November 17, 2025

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.

Journal: DNA repair

Published: February 18, 2025

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.

Journal: Cells

Published: January 10, 2025

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.

Journal: NAR cancer

Published: November 27, 2024

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.

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.

Journal: Orphanet journal of rare diseases

Published: September 18, 2024

Transcription-coupled repair of DNA-protein crosslinks.

Journal: Trends in cell biology

Published: August 14, 2024

Cockayne syndrome mice reflect human kidney disease and are defective in de novo NAD biosynthesis.

Journal: Cell death and differentiation

Published: August 08, 2024

Filters

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

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

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.

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.

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

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

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.

Transcription-coupled repair: tangled up in convoluted repair.

Transcription-coupled repair: tangled up in convoluted repair.

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.

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.

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.

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.

Transcription-coupled repair of DNA-protein crosslinks.

Transcription-coupled repair of DNA-protein crosslinks.

Cockayne syndrome mice reflect human kidney disease and are defective in de novo NAD biosynthesis.

Cockayne syndrome mice reflect human kidney disease and are defective in de novo NAD biosynthesis.