Cockayne Syndrome Type 1 Latest Advances

Find the Latest Research About Cockayne Syndrome Type 1

Last Updated: 04/28/2026

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Found 983 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

ercc6 deficient zebrafish exhibit UV and metronidazole sensitivity, increased oxygen consumption, and impaired hair cell mechanoelectrical transduction which can be restored by the superoxide dismutase mimetic MnTBAP.

ercc6 deficient zebrafish exhibit UV and metronidazole sensitivity, increased oxygen consumption, and impaired hair cell mechanoelectrical transduction which can be restored by the superoxide dismutase mimetic MnTBAP.

Journal: Human molecular genetics

Published: September 05, 2025

Exploring the interaction between nucleotide excision repair pathways and Huntington disease: Implications for neurodegeneration and phenotypic overlap.

Exploring the interaction between nucleotide excision repair pathways and Huntington disease: Implications for neurodegeneration and phenotypic overlap.

Journal: Parkinsonism & related disorders

Published: June 30, 2025

Cockayne syndrome: peculiarities of clinical manifestations and algorithm of observation in childhood

Cockayne syndrome: peculiarities of clinical manifestations and algorithm of observation in childhood

Journal: Problemy endokrinologii

Published: June 30, 2025

Amy and Friends: improving the lives of individuals affected by DNA repair disorders.

Amy and Friends: improving the lives of individuals affected by DNA repair disorders.

Journal: FEBS letters

Published: April 14, 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

Showing 1-12 of 983

Last Updated: 04/28/2026