Cockayne Syndrome Type 1 Latest Advances

The role of transcription-coupled nucleotide excision repair (TC-NER) during mammalian forebrain development.

Journal: Developmental biology

Published: December 31, 2025

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

Journal: The Journal of clinical investigation

Published: November 17, 2025

Swallowing and Communication in Cockayne Syndrome: Clinical Characteristics and Management.

Journal: American journal of medical genetics. Part A

Published: October 08, 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.

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.

Journal: Parkinsonism & related disorders

Published: June 30, 2025

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.

Journal: FEBS letters

Published: April 14, 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

Cockayne Syndrome Type 1 Latest Advances

Find the Latest Research About Cockayne Syndrome Type 1

The role of transcription-coupled nucleotide excision repair (TC-NER) during mammalian forebrain development.

The role of transcription-coupled nucleotide excision repair (TC-NER) during mammalian forebrain development.

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

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

Swallowing and Communication in Cockayne Syndrome: Clinical Characteristics and Management.

Swallowing and Communication in Cockayne Syndrome: Clinical Characteristics and Management.

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.

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.

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

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

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.

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.