Neuroscience
Actin
33%
Astrocyte
33%
Axon
93%
Axon Guidance
78%
Basal Metabolic Rate
5%
Brainstem
28%
Branchial Arch
6%
Cell Membrane
5%
Cell Migration
16%
Chimerin
66%
Congenital Disorder
16%
Cytoskeleton
50%
Drebrin
33%
Eicosanoid Receptor
20%
ELISA
5%
Extraocular Muscle
17%
Eye Movement Disorder
25%
Gain of Function Mutation
5%
Gene Regulatory Network
16%
Glucose Transport
5%
Glucose Transporter 1
5%
Growth Cone
6%
Guanosine
11%
Head Muscle
16%
Hindbrain
33%
In Situ Hybridization
6%
In Vitro
11%
In Vivo
5%
Innervation
5%
Lipopolysaccharide
33%
Metabolic Pathway
33%
Microtubule
33%
Missense Mutation
5%
Mitochondrial Respiration
5%
Morphogenesis
6%
Motor Neuron
22%
Neural Crest
33%
Neural Tube
6%
Neurite Outgrowth
18%
Neuromuscular
16%
Neuropilin
66%
Oxidative Phosphorylation
16%
Regulator Protein
16%
Semaphorin
100%
Strabismus
33%
Transcription Factors
16%
Western Blot
5%
Biochemistry, Genetics and Molecular Biology
Animal Model
16%
Autosomal Recessive Inheritance
33%
Axon
73%
Axon Guidance
77%
Candidate Gene
33%
Cell Membrane
11%
Chick
11%
Clinical Research
16%
Clinical Trial
16%
Cytoskeleton
16%
Eicosanoid Receptor
16%
Eye Movement
41%
Frameshift Mutation
16%
Gain of Function Mutation
11%
Gene Regulatory Network
16%
Genetic Evaluation
16%
Genetics
16%
Growth Cone
13%
Guanosine
22%
Hepatocyte Growth Factor
6%
Innervation
11%
Loss of Function Mutation
33%
Missense Mutation
27%
Motor Neuron
27%
Mouse
11%
Neurite Outgrowth
16%
Nonsense Mutation
16%
Regulatory Network
16%
RNA Interference
6%
Sanger Sequencing
16%
Semaphorin
33%
Signal Transduction
6%
Signaling Protein
17%
Surface Property
16%
Transcription Factors
16%
TUBB3
16%
Medicine and Dentistry
Autosomal Recessive Inheritance
33%
Axon
50%
Axon Guidance
38%
Brainstem
27%
Cell Membrane
5%
Cell Surface
11%
Cellular Model
11%
Chick Embryo
5%
Chimerin
33%
Clinical Genetics
11%
Clinical Research
11%
Congenital Blepharoptosis
11%
Congenital Disorder
22%
Cranial Nerve
15%
Cytoskeleton
11%
Developmental Abnormality
15%
Diseases
80%
Duane Syndrome
44%
Extraocular Muscle
11%
Eye Movement Disorder
16%
Facial Nerve Paralysis
44%
Fibrosis
11%
Gain of Function Mutation
5%
Gene Regulatory Network
11%
Guanosine
11%
Head Muscle
11%
In Vitro
5%
Innervation
5%
Loss of Function Mutation
33%
Missense Mutation
9%
Molecular Model
11%
Motor Nerve
11%
Neurite Outgrowth
11%
Receptor
11%
Regulator Protein
11%
Signaling Protein
5%
Strabismus
22%
Transcription Factors
11%
