Biochemistry, Genetics and Molecular Biology
Antisense
15%
Autosomal Recessive Inheritance
62%
Brain Development
62%
Clinical Study
10%
Disease Modeling
31%
Dopaminergic
31%
Electron Microscopy
20%
Enhancer Region
72%
Exon
15%
Fibroblast
41%
Fibroblast Culture
15%
Gene Control
41%
Gene Expression
10%
Gene Mutation
17%
Genetic Disorder
20%
Genetics
96%
HOPS Complex
62%
Human Genetics
17%
Intergenic Region
10%
Intron
15%
Lipid Droplet
20%
Lipid Homeostasis
20%
Lipid Metabolism
20%
Macromolecule
31%
Membrane Trafficking
62%
Mental Retardation
82%
Messenger RNA
15%
Methylation
31%
Motor Neuron
62%
Nerve Cell Differentiation
93%
Oligonucleotide
15%
Penetrance
31%
Peripheral Blood Mononuclear Cell
15%
Posttranslational Modification
31%
Protease
62%
Protein Function
62%
Protein Targeting
31%
Quantitative Reverse Transcription Polymerase Chain Reaction
15%
Regulatory Element
96%
Reverse Transcription Polymerase Chain Reaction
62%
SMN2
31%
Statin
62%
Stem Cell
48%
Tamsulosin
62%
Transport Protein
31%
Ubiquitin
62%
Ubiquitin-Conjugating Enzyme
20%
Vacuolar Protein Sorting
62%
Whole Genome Sequencing
20%
Zebra Fish
100%
Neuroscience
Antisense Oligonucleotide
62%
Ataxia
62%
Autism
31%
Brain Disease
62%
Cell Culture
62%
Cognitive Disorders
20%
Disease Modeling
20%
Dopaminergic Neuron
20%
Dystonia
20%
Electron Microscopy
10%
Endoplasmic Reticulum
20%
Enhancer Region
20%
Exon
62%
Fat Droplet
10%
Fibroblast
82%
Flavivirus
12%
Gene Control
41%
Gene Expression
20%
Gene Mutation
20%
Hereditary Spastic Paraplegia
62%
Hypoplasia
20%
In Vitro
93%
In Vivo
10%
Intellectual and Developmental Disabilities
72%
Intergenic Region
20%
Intron
62%
Language Delay
62%
Messenger RNA
62%
Metabolic Pathway
10%
Methylation
31%
Nerve Cell Differentiation
31%
Nervous System Disorder
24%
Neural Stem Cell
20%
Neurodevelopmental Disorder
51%
Paraplegia
62%
Parkinson's Disease
20%
Peripheral Blood Mononuclear Cell
62%
Posttranslational Modification
20%
Protein Function
41%
Protein Targeting
62%
Psychopathology
10%
Real-Time Polymerase Chain Reaction
62%
Spinal Muscular Atrophy
62%
Statin
62%
Stem Cell
24%
Stereotypic Movement Disorder
31%
Transport Protein
20%
Ubiquitin Protein Ligase E3
10%
West Nile Virus
62%
Whole Genome Sequencing
10%
