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

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.

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 Type 1 Latest Advances

Find the Latest Research About Cockayne Syndrome Type 1

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

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

Cockayne syndrome mutation in XPG activate the integrated stress response.

Cockayne syndrome mutation in XPG activate the integrated stress response.

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.