Biochemistry, Genetics and Molecular Biology
Missense
100%
Angiopoietin
100%
Exome Sequencing
91%
Genetics
83%
Linkage Analysis
75%
Gene Linkage
75%
Intraocular Pressure
73%
Gene Expression
71%
Mental Retardation
66%
Angiopoietin Receptor
66%
CRISPR/Cas9
62%
Aqueous Humor Outflow
58%
Autosomal Recessive Inheritance
57%
Genomics
57%
UBE3A
50%
Chromosomal Rearrangement
50%
Nuclear Export
50%
Protein Expression
50%
Posttranslational Modification
50%
Enzyme
50%
Wild Type
50%
Infancy
50%
Metabotropic Glutamate Receptor 1
50%
Pedigree
50%
Angiopoietin 1
50%
Repressor
50%
Intron
50%
Exon
50%
LTBP2
50%
Transdifferentiation
50%
RNA
50%
Transactivation
50%
Growth Hormone
50%
Messenger RNA
50%
Autosomal Dominant Inheritance
41%
Gene Dosage
41%
Bovine Somatotropin
37%
Haploinsufficiency
36%
Fibroblast
35%
Single-Nucleotide Polymorphism
33%
ANGPT2
33%
Protein Function
33%
Allele
33%
Isoform
32%
Proband
27%
Genetic Divergence
25%
Minor Spliceosome
25%
Metabotropic Receptor
25%
Thyroid-Stimulating Hormone
25%
Gonad Function
25%
Medicine and Dentistry
Diseases
93%
Congenital Glaucoma
90%
Pedigree
75%
Angiopoietin Receptor
60%
Schlemm's Canal
58%
Stereotypic Movement Disorder
50%
Silver-Russell Syndrome
50%
Diarrhea
50%
Lactic Acidosis
50%
Primary Ovarian Insufficiency
50%
DeJerine-Sottas Disease
50%
Epilepsy Syndromes
50%
Mosaicism
50%
Angiopoietin 1
50%
Hypopituitarism
50%
Gene Linkage
50%
Temporal Lobe Epilepsy
50%
Partial Epilepsy
50%
Arginine
50%
Heterozygote Detection
50%
Angiopoietin
46%
Clinical Method
41%
Genome Sequencing
41%
Epileptic Seizure
37%
In Silico
35%
Gonad Function
33%
Growth Hormone Deficiency
33%
Dystonia
33%
Thyrotropin
33%
Growth Hormone
33%
Autosomal Recessive Inheritance
33%
Aqueous Humor Outflow
28%
Intraocular Pressure
26%
Genetic Variability
25%
Clinical Finding
25%
Pregnancy
25%
Growth Retardation
25%
Medicine
25%
Postnatal Growth
25%
Prenatal Growth
25%
Base
25%
Fibroblast
25%
Trabecular Meshwork
18%
Exome Sequencing
16%
Hormone Deficiency
16%
Protein
16%
Next Generation Sequencing
16%
Ovary Function
16%
Genotype Phenotype Correlation
16%
Human Embryo
16%
Neuroscience
Ataxia
66%
Minor Spliceosome
50%
Coding Region
50%
Temporal Lobe Epilepsy
50%
Partial Epilepsy
50%
In Vitro
50%
Amino Acid Transport
50%
Metabotropic Glutamate Receptor 1
50%
Thyroid-Stimulating Hormone
50%
Hypopituitarism
50%
Growth Hormone Deficiency
50%
Neuropathy
50%
Growth Hormone
50%
CRISPR
41%
Hypoplasia
37%
Exome Sequencing
29%
Exon
25%
Intron
25%
Clinical Method
25%
Anterior Pituitary
25%
Protein
25%
In Situ Hybridization
25%
Bovine Somatotropin
25%
Hypothalamus
25%
Receptor
25%
Posttranslational Modification
16%
Stereotypic Movement Disorder
16%
Protein Expression
16%
Peripheral Nerve
16%
Central Nervous System
16%
Dysarthria
12%
Metabotropic Receptor
12%
Dysmetria
12%
Alternative Splicing
12%
Mutated Genes
12%
Synaptic Plasticity
12%
Purkinje Cell
12%
Brain Imaging
12%
Tremor
12%
Dysdiadochokinesia
12%
Cell Line
12%
Splicing Defect
12%
Metabotropic Glutamate Receptor
12%
