Keyphrases
Gene-deficient Mice
100%
Forebrain
100%
Cholesterol Biosynthesis
100%
ERCC1
100%
Biosynthesis Gene
100%
Nucleotide Excision Repair
50%
Transcription Factor
25%
Reduced Expression
25%
Failed Repair
25%
Growth Development
12%
Synapse
12%
MRNA Expression
12%
Cerebellum
12%
Knock-in Mouse Model
12%
Hippocampus
12%
Mouse Strain
12%
Neurodevelopmental
12%
Neocortex
12%
Rodents
12%
Purkinje Cell
12%
Cockayne Syndrome
12%
Cell Loss
12%
Central Nervous System Anomalies
12%
Master Regulator
12%
Adult Mice
12%
Microcephaly
12%
Complementation Group
12%
Genetic Defects
12%
Delayed Development
12%
Purkinje Cell Degeneration
12%
Gliosis
12%
Premature Aging
12%
Inherited Defect
12%
Impaired Growth
12%
Sterol Regulatory Element
12%
Hippocampal Transcriptome
12%
Cerebellum Development
12%
Biochemistry, Genetics and Molecular Biology
ERCC1
100%
down Regulation
100%
Cholesterol Synthesis
100%
Nucleotide Excision Repair
80%
Base Excision Repair
80%
Deficiency
80%
Purkinje Cell
40%
Genetics
20%
Synapse
20%
Upregulation
20%
Knockout Mouse
20%
Mouse Strain
20%
Cell Loss
20%
Cell Degeneration
20%
Excision Repair Cross-Complementing
20%
Sterol Regulatory Element Binding Protein 2
20%
Transcription Factors
20%
Cockayne Syndrome
20%
Gliosis
20%
Messenger RNA
20%
Transcriptome
20%
Immunology and Microbiology
Excision Repair
100%
down Regulation
100%
Cholesterol Synthesis
100%
Prosencephalon
100%
Cerebellum
40%
Purkinje Cell
40%
Transcriptome
20%
Synapse
20%
Central Nervous System
20%
Knockout Mouse
20%
Hippocampus
20%
Mouse Strain
20%
Cell Loss
20%
Upregulation
20%
Cell Degeneration
20%
Neocortex
20%
Sterol Regulatory Element Binding Protein 2
20%
Transcription Factors
20%
Neuroscience
Anabolism
100%
Base Excision Repair
80%
Nucleotide Excision Repair
80%
Purkinje Cell
40%
Cerebellum
40%
Synapse
20%
Hippocampus
20%
Transcription Factors
20%
Transcriptome
20%
Central Nervous System
20%
Microcephaly
20%
Cell Loss
20%
Cell Degeneration
20%
Sterol Regulatory Element Binding Protein 2
20%
Excision Repair Cross-Complementing
20%
Gliosis
20%
Cockayne Syndrome
20%
Messenger RNA
20%