Biochemistry, Genetics and Molecular Biology
Activin
33%
Autosomal Recessive Disorder
33%
Autosomal Recessive Inheritance
27%
Bayesian Learning
22%
Biodiversity
33%
Blood Brain Barrier
33%
Campylobacter Jejuni
33%
Cell Junction
33%
CHD3
66%
Chromosome 1
33%
Ciprofloxacin
33%
Consanguinity
33%
CYP2D6
33%
DNA Sequence
22%
Dysplasia
33%
Endoglin
66%
Exome
33%
Exome Sequencing
48%
Exon
80%
Fusion Transcript
33%
Gene Linkage
33%
Gene Mutation
33%
Genetics
80%
Genotyping
41%
Helicase
33%
Homozygosity
66%
Inborn Error of Metabolism
33%
Lymphoblast
33%
Messenger RNA
33%
MicroRNA
33%
Missense
73%
Mosaicism
33%
Mouse
40%
Nonsense-Mediated Decay
33%
Occludin
33%
Parental Age
33%
Penetrance
33%
Prenatal Growth
30%
Prevalence
33%
Proband
50%
Proteoglycan
33%
Retrospective Study
25%
Speech and Language
66%
Stop Codon
33%
Ubiquitin
33%
Wild Type
33%
Wilms' Tumor
33%
WNT5A
40%
X Chromosomal Inheritance
33%
Zinc Ion
33%
Keyphrases
BCR-ABL Transcript
33%
Bent Bone Dysplasia
33%
Camptodactyly-arthropathy-coxa Vara-pericarditis
33%
Cell Degradation
33%
CHD3
66%
Corneal Dystrophy
33%
De-novo mutations
33%
Developmental Disorders
100%
Dipeptidyl peptidase-4 Inhibition
33%
ELAC2
33%
Ellis-van Creveld Syndrome
33%
Etoricoxib
33%
GABPA
33%
Genetic Causes
33%
Helicase Domain
66%
HHT2
33%
Human Atherosclerosis
33%
Human Cognition
33%
Impaired Speech
66%
Infantile Onset
33%
JAM3
33%
Junctional Adhesion Molecule
33%
KMT2E
33%
Low-calorie Diet
33%
Macrocephaly
33%
Methyltransferase
33%
Middle Eastern Population
33%
Neonatal Presentation
33%
Neurodevelopmental Syndrome
33%
Null Variants
33%
Overgrowth Syndrome
33%
Phenotypic Data
33%
Phosphatidylinositol 4,5-bisphosphate (PIP2)
33%
Phosphoinositide Signaling
33%
Probabilistic Genotype
33%
Proteoglycan 4 (PRG4)
33%
Redox Dysregulation
33%
Renal Dysplasia
33%
Secondary Associations
33%
Subependymal
33%
Tight Junction Proteins
33%
UBA5
33%
Ubiquitin-fold Modifier 1
33%
Ubiquitin-specific Protease
33%
Useful Patterns
33%
Vascular Redox
33%
Wnt Signaling
33%
Wnt Signaling Pathway
33%
Wnt5a
33%
X-linked
33%
Medicine and Dentistry
Adenosine Phosphate
9%
Adipose Tissue
33%
Awareness
8%
Beta-Ketothiolase Deficiency
8%
Bloody Diarrhea
11%
Bone Mass
11%
Campylobacter Enteritis
33%
Campylobacter Jejuni
11%
Canagliflozin
33%
Cardiomyopathy
33%
Cardiovascular Disease
33%
Care Coordination
8%
Ciprofloxacin
33%
Colchicine
8%
Coronary Artery Bypass Surgery
20%
Delayed Diagnosis
8%
Deubiquitinase
33%
Dipeptidyl Peptidase IV
33%
Etoricoxib
33%
Family History
8%
Gene Mapping
11%
Genetic Screening
8%
Heart Surgery
7%
In Vitro
7%
Intrauterine Growth Retardation
8%
Joint Swelling
8%
Kidney Dysplasia
33%
Macrocephaly
33%
Maple Syrup Urine Disease
8%
Metabolome
7%
Methyltransferase
33%
microRNA
18%
Myocardium
7%
Nicotinamide Adenine Dinucleotide Phosphate
7%
Obstetrics
33%
Osteoarthropathy
33%
Point Mutation
11%
Population
8%
Quinolone
11%
Quinolone Derivative
33%
Redox Signalling
33%
Retrospective Study
8%
Risedronic Acid
8%
Secreted Frizzled Related Protein 5
8%
Silver-Russell Syndrome
33%
Speech and Language
33%
Tamoxifen
8%
Thrombopoietin
11%
Very Low Calorie Diet
33%
Zellweger Syndrome
8%
