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Publications by Cecilie Löe Licht

Cockayne Syndrome Group B Cellular and Biochemical Functions

American Journal of Human Genetics

English

Related publications

Biochemical and Biological Characterization of Wild-Type and ATPase-deficient Cockayne Syndrome B Repair Protein

Journal of Biological Chemistry

Molecular Biology

English

Molecular Characterization of an Acidic Region Deletion Mutant of Cockayne Syndrome Group B Protein

Nucleic Acids Research

English

Cockayne Syndrome Group B Protein Prevents the Accumulation of Damaged Mitochondria by Promoting Mitochondrial Autophagy

Journal of Experimental Medicine

English

Manitoba Aboriginal Kindred With Original Cerebro-Oculo-Facio-Skeletal Syndrome Has a Mutation in the Cockayne Syndrome Group B (CSB) Gene

American Journal of Human Genetics

English

Cockayne Syndrome (Cs) Masquerading as Seckel Syndrome (Ss)

Pediatric Research

English

The Cellular and Physiological Functions of the Lowe Syndrome Protein OCRL1

Molecular Biology

Structural Biology

English

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

Frontiers in Pediatrics

English

Cockayne Syndrome B Protein (CSB): Linking P53, HIF-1 and P300 to Robustness, Lifespan, Cancer and Cell Fate Decisions

Developmental Biology

Molecular Biology

English

GP59 a Rare Cause of ‘Mitochondrial Disorder’: Cockayne Syndrome

English