Keyphrases
Dystrophin Gene
99%
Schizophrenia
93%
Duchenne muscular Dystrophy
76%
Charcot-Marie-Tooth Disease
74%
DNA Diagnosis
62%
Exon
60%
Gene Expression
57%
Dystrophin
56%
RNA Sequencing (RNA-seq)
51%
Wilson Disease
49%
Disease Genes
46%
Neural Stem Cells
46%
Autosomal Dominant
45%
Autism Spectrum Disorder
45%
Mdx Mice
44%
Single-cell RNA Sequencing (scRNA-seq)
43%
Growth Hormone Deficiency
40%
Splicing mutation
38%
Pituitary Hormone Deficiency
37%
Panic Disorder
37%
Major Depressive Disorder
37%
Mouse Skeletal muscle
37%
Autism
37%
Spinal muscular Atrophy
37%
Ballistic
37%
Prenatal Diagnosis
35%
Neuropsychiatric Disorders
34%
Single nucleotide Polymorphism
34%
Etiology
32%
Transcription Factor 4 (TCF4)
31%
Pseudogene
31%
Russian children
30%
Neurofilament Light (NF-L)
30%
Human Neural Stem Cells (hNSCs)
29%
Gene mutation
29%
Missense mutation
29%
Middle Turbinate
29%
Olfactory Neuroepithelium
29%
Y Chromosome
29%
Polymerase Chain Reaction
29%
Early Onset
26%
Russian Patients
26%
Neuronal Cells
25%
Dual Signal Amplification
24%
Amplification Method
24%
Liposomes
24%
Oligopeptides
24%
Complex Vector
24%
Non-coding RNA (ncRNA)
24%
Bashkortostan
24%
Biochemistry, Genetics and Molecular Biology
Haplotype
100%
Exon
99%
Genetics
74%
Gene Linkage
71%
RNA
69%
Progenitor Cell
64%
Dystrophin
49%
RNA Sequencing
48%
Gene Linkage Disequilibrium
44%
Pedigree
43%
Polymerase Chain Reaction
41%
Y Chromosome
40%
Gene Expression
38%
Pituitary Hormone
37%
Isolated Growth Hormone Deficiency
37%
Allele
37%
Single-Nucleotide Polymorphism
35%
Mouse
33%
Neurofilament
33%
Autosomal Dominant Inheritance
32%
Missense Mutation
32%
Molecular Genetics
31%
TCF4
29%
Pseudogene
29%
Intron
28%
RNA Sequence
28%
DNA Analysis
28%
Pituitary-Specific Positive Transcription Factor 1
27%
Receptor Tyrosine Kinase
26%
Long Noncoding RNA
24%
Epigenomics
24%
Nijmegen Breakage Syndrome
24%
Antisense
24%
Moesin
24%
Non-Coding RNA
24%
Gene Mutation
24%
Candidate Gene
24%
Microsatellite DNA
23%
Tyrosine Kinase
22%
Transcriptome
22%
Multiplex Polymerase Chain Reaction
21%
B Cell
20%
Contig
18%
Light Chain
18%
Lod Score
18%
Genetic Divergence
17%
Human Genome
16%
21-Hydroxylase
16%
DNA Probe
15%
Brain Development
15%
Neuroscience
Dementia Praecox
93%
Gene Expression
71%
Haplotype
67%
Neural Stem Cell
63%
RNA-Seq
58%
Dystrophin
49%
Charcot-Marie-Tooth Disease
49%
Single-Nucleotide Polymorphism
46%
Transcriptome
44%
Pervasive Developmental Disorder
41%
RNA Sequence
39%
Linkage Disequilibrium
39%
Major Depressive Disorder
37%
Microsatellite
36%
Transfection
33%
Etiology of Schizophrenia
29%
In Vitro
25%
Rett Syndrome
24%
Pseudogene
24%
Oligopeptide
24%
Long Non-Coding RNA
24%
Y Chromosome
24%
Moesin
24%
Skeletal Muscle
24%
Panic Disorder
24%
Cell Culture
24%
Transcriptomics
21%
Complementary DNA
20%
Cell Line
19%
Genome-Wide Association Study
19%
Peripheral Neuropathy
17%
Nerve Cell Differentiation
16%
Temporal Lobe
15%
Methyl CpG Binding Protein 2
14%
Neurofilament Light Chain
14%
Neurofilament
14%
Muscular Dystrophy
14%
Brain Development
14%
Turbinate
13%
Missense Mutation
13%
Alzheimer's Disease
12%
GABRA5
12%
Opiate
12%
Bipolar Disorder
12%
Electroporation
12%
Copper Exporting Adenosine Triphosphatase
12%
Spiral Ganglion Neuron
12%
Innervation
12%
Gene Mutation
12%
Cochlea
12%
