Biochemistry, Genetics and Molecular Biology
Mutation
100%
Nested Gene
46%
Hearing
41%
Podocyte
34%
Protein
29%
Steroid
27%
Cystic Fibrosis Transmembrane Conductance Regulator
26%
Genetics
23%
Phenotype
20%
KCNQ4
18%
Cilium
16%
Zebra Fish
15%
Mouse
15%
Mutant
14%
Exome Sequencing
13%
Wild Type
13%
Primary Ciliary Dyskinesia
11%
Exome
10%
Data Base
9%
Electric Potential
9%
Autosomal Recessive Inheritance
8%
Cystic Fibrosis
8%
Age
7%
Association
7%
Cell Membrane
7%
Secretion (Process)
7%
Membrane Protein
7%
PLCE1
6%
Kinase
6%
Homozygosity
6%
RAC1
6%
Cholesterol
6%
Suspension
6%
Membrane
6%
Secretory Pathway
6%
Development
6%
Introspection
6%
Ciliogenesis
6%
Autosomal Dominant Inheritance
5%
Surface Property
5%
Sequencing
5%
Prevalence
5%
Medicine and Dentistry
Gene
42%
Congenital Nephrotic Syndrome
29%
Diseases
24%
Family
20%
Patient
19%
Hearing Impairment
18%
Ciliopathy
18%
Podocyte
16%
Nephronophthisis
15%
Kidney
13%
Exome Sequencing
12%
Protein
12%
Chronic Kidney Disease
12%
Diagnosis
11%
Cells
10%
Analysis
8%
Urinary Tract
8%
Inpatient
8%
Child
7%
Syndrome
7%
Congenital Malformation
6%
Phenotype
6%
Next Generation Sequencing
6%
Kidney Stone
6%
Mutant
5%
Nephropathy
5%
Adult
5%
Therapeutic Procedure
5%
Pathogenesis
5%
Age
5%
Introspection
5%
Nephrotic Syndrome
5%
Association
5%