Cockayne Syndrome Latest Advances

Advancing Obstetric Care: The Role of Targeted Next-Generation Sequencing in Pregnancies with Structurally Normal Fetuses.

Journal: Journal of the Chinese Medical Association : JCMA

Published: January 27, 2026

Repurposing Alkylating Agents in Melanoma via ERCC8 Silencing: A Novel Therapeutic Strategy.

Journal: Cancers

Published: January 13, 2026

The Role of Transcription-Coupled Nucleotide Excision Repair (TC-NER) during Mammalian Forebrain Development.

Journal: Developmental biology

Published: December 31, 2025

Molecular basis for CSB stimulation of the SNM1A DNA repair nuclease.

Journal: Research square

Published: December 03, 2025

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

Journal: The Journal of clinical investigation

Published: November 17, 2025

Metronidazole-Induced Hepatotoxicity in Children with Cockayne Syndrome.

Journal: Indian journal of pediatrics

Published: October 23, 2025

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

Journal: American journal of medical genetics. Part A

Published: October 08, 2025

Neuroimages of an Adult Cockayne Syndrome Patient.

Journal: Internal medicine (Tokyo, Japan)

Published: October 01, 2025

Mechanisms of transcription-coupled repair and DNA damage surveillance in health and disease.

Journal: Nature reviews. Molecular cell biology

Published: September 29, 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

Studies on the functionality of the TC-NER ERCC6-M1097V protein variant frequently found in Louisiana patients with PCa upon UV damage.

Journal: Frontiers in oncology

Published: August 04, 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 Latest Advances

Find the Latest Research About Cockayne Syndrome

Advancing Obstetric Care: The Role of Targeted Next-Generation Sequencing in Pregnancies with Structurally Normal Fetuses.

Advancing Obstetric Care: The Role of Targeted Next-Generation Sequencing in Pregnancies with Structurally Normal Fetuses.

Repurposing Alkylating Agents in Melanoma via ERCC8 Silencing: A Novel Therapeutic Strategy.

Repurposing Alkylating Agents in Melanoma via ERCC8 Silencing: A Novel Therapeutic Strategy.

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.

Molecular basis for CSB stimulation of the SNM1A DNA repair nuclease.

Molecular basis for CSB stimulation of the SNM1A DNA repair nuclease.

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

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

Metronidazole-Induced Hepatotoxicity in Children with Cockayne Syndrome.

Metronidazole-Induced Hepatotoxicity in Children with Cockayne Syndrome.

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

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

Neuroimages of an Adult Cockayne Syndrome Patient.

Neuroimages of an Adult Cockayne Syndrome Patient.

Mechanisms of transcription-coupled repair and DNA damage surveillance in health and disease.

Mechanisms of transcription-coupled repair and DNA damage surveillance in health and disease.

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.

Studies on the functionality of the TC-NER ERCC6-M1097V protein variant frequently found in Louisiana patients with PCa upon UV damage.

Studies on the functionality of the TC-NER ERCC6-M1097V protein variant frequently found in Louisiana patients with PCa upon UV damage.

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.