Cockayne Syndrome Type 2 Latest Advances

Features of the dentoalveolar system in children with premature aging syndromes

Journal: Stomatologiia

Published: August 12, 2026

CRISPR/Cas9-mediated editing of ERCC6 in iPSCs: A disease model for Cockayne Syndrome type B.

Journal: Stem cell research

Published: June 04, 2026

Immune dysfunction in nucleotide excision repair disorders: an underrecognized clinical phenotype with relevance for inborn errors of immunity.

Journal: Frontiers in immunology

Published: April 26, 2026

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

Cockayne Syndrome Type 2 Latest Advances

Find the Latest Research About Cockayne Syndrome Type 2

Features of the dentoalveolar system in children with premature aging syndromes

Features of the dentoalveolar system in children with premature aging syndromes

CRISPR/Cas9-mediated editing of ERCC6 in iPSCs: A disease model for Cockayne Syndrome type B.

CRISPR/Cas9-mediated editing of ERCC6 in iPSCs: A disease model for Cockayne Syndrome type B.

Immune dysfunction in nucleotide excision repair disorders: an underrecognized clinical phenotype with relevance for inborn errors of immunity.

Immune dysfunction in nucleotide excision repair disorders: an underrecognized clinical phenotype with relevance for inborn errors of immunity.

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.