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DNA repair deficiency in neurodegeneration
Dennis Kjølhede Jeppesen,
Vilhelm A Bohr
, Tinna V. Stevnsner
Molecular Aging Program
Individualized Health
200
Citations (Scopus)
Overview
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Dive into the research topics of 'DNA repair deficiency in neurodegeneration'. Together they form a unique fingerprint.
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Keyphrases
Neurodegeneration
100%
Neurodegenerative Diseases
60%
DNA Lesions
40%
Mitochondrial DNA Damage
40%
Progressive Neurodegeneration
20%
Werner Syndrome
20%
Age-related Illnesses
20%
Ataxia Telangiectasia
20%
Premature Aging
20%
Oxygen Metabolism
20%
Alzheimer's Disease
20%
Non-homologous End Joining
20%
Nucleotide Excision Repair
20%
WRN Gene
20%
Helix
20%
Aging
20%
Spinocerebellar Ataxia
20%
Age-associated
20%
Huntington's Disease
20%
Base Lesions
20%
Amyotrophic Lateral Sclerosis
20%
DNA Double-strand Breaks
20%
Trinucleotide Repeats
20%
Single-strand Breaks
20%
DNA Repair Pathways
20%
Nuclear DNA Damage
20%
Base Excision Repair
20%
Parkinson's Disease
20%
Risk Factors
20%
Oxidative DNA Damage
20%
Homologous Recombination
20%
Cockayne Syndrome
20%
Cellular Pathways
20%
Early childhood
20%
Mismatch Repair
20%
DNA Damage
20%
Related Disorders
20%
Neurodegenerative
20%
Medicine and Dentistry
DNA Damage
100%
DNA Repair
100%
Neurodegeneration
100%
Diseases
50%
Neurodegenerative Disorder
33%
Base
33%
Mitochondrial DNA
33%
Base Excision Repair
33%
Werner Syndrome
16%
Double-Strand DNA Break
16%
Ataxia Telangiectasia
16%
Oculomotor Apraxia
16%
Trinucleotide Repeat
16%
Spinocerebellar Ataxia
16%
Ataxia
16%
Parkinson's Disease
16%
Premature Aging
16%
Helix
16%
Amyotrophic Lateral Sclerosis
16%
Huntington's Disease
16%
Non-Homologous End Joining
16%
Cell Nucleus DNA
16%
Xeroderma pigmentosum
16%
Cockayne Syndrome
16%
Homologous Recombination
16%
Degenerative Disease
16%
Neuropathy
16%
Werner Syndrome ATP Dependent Helicase
16%
DNA Mismatch Repair
16%
Alzheimer's Disease
16%
Disease
16%
Biochemistry, Genetics and Molecular Biology
DNA Damage
100%
DNA Repair
100%
Mitochondrial DNA
33%
Base Excision Repair
33%
Werner Syndrome
16%
Trinucleotide Repeat Expansion
16%
Metabolic Pathway
16%
Non-Homologous End Joining
16%
Cockayne Syndrome
16%
Nucleotide Excision Repair
16%
Double-Strand DNA Break
16%
Nuclear DNA
16%
Homologous Recombination
16%
DNA Mismatch Repair
16%
Xeroderma pigmentosum
16%
Neuroscience
Apraxia
16%
Nucleotide Excision Repair
16%
Werner Syndrome ATP Dependent Helicase
16%
Non-Homologous End Joining
16%