Mutation of FOXC and PITX induces cerebral small-vessel disease

Biochemistry, Genetics and Molecular Biology

• Genome Wide Association Study 100%
• Genetics 50%
• Magnetic Resonance Imaging 50%
• Single Nucleotide Polymorphism 50%
• Low Copy Repeats 50%
• Zebra Fish 50%
• Missense Mutation 50%
• Nonsense Mutation 50%
• Forkhead Transcription Factor 50%
• Morpholino 50%
• Mural Cell 50%
• Transcription Factors 50%
• Platelet-Derived Growth Factor 50%
• Neural Crest 50%
• Growth Factor Signaling 50%

Keyphrases

• Cerebral Small Vessel Disease (cSVD) 100%
• Genome-wide Association Analysis 40%
• FoxC 40%
• Growth Factor Signaling 20%
• Transcription Factor 20%
• SNP 20%
• Nonsense mutation 20%
• Cerebral Hemorrhage 20%
• Overexpression 20%
• Neural Crest Cell Migration 20%
• Missense mutation 20%
• Cerebrovascular Disease 20%
• FMRI Analysis 20%
• Platelet-derived Growth factor-BB (PDGF-BB) 20%
• Zebrafish Model 20%
• Transcript Level 20%
• Genetic Etiology 20%
• White Matter Hyperintensities 20%
• Forkhead Transcription Factors 20%
• Vascular Phenotype 20%
• Morpholino 20%
• Segmental Duplication 20%
• Mural Cells 20%
• Lacunar Infarction 20%
• Stroke Etiology 20%
• Age-related Cognitive Impairment 20%
• Pitx 20%
• Dilated Perivascular Spaces 20%
• Vascular Stability 20%
• Segmental Deletion 20%

Neuroscience

• Cerebrovascular Disease 100%
• Cerebrovascular Accident 33%
• Magnetic Resonance Imaging 16%
• Transcription Factors 16%
• Platelet-Derived Growth Factor 16%
• Morpholino 16%
• Missense Mutation 16%
• Segmental Duplication 16%
• Nonsense Mutation 16%
• Forkhead Transcription Factor 16%
• Cerebral Hemorrhage 16%
• Neural Crest 16%
• Lacunar Stroke 16%