Biochemistry, Genetics and Molecular Biology
ABCC9
9%
Allele
25%
Amino Acids
8%
Aquaporin 2
28%
Arginine Vasopressin
17%
ATPase
14%
Autosomal Dominant Inheritance
22%
Autosomal Recessive Disorder
9%
Autosomal Recessive Inheritance
39%
Bartter Syndrome
24%
Base Excess
9%
Body Height
11%
Candidate Gene
19%
Cell Membrane
14%
Cilium
14%
Cotransporter
41%
Deep Sequencing
12%
Dysplasia
15%
Eicosanoid Receptor
51%
Exome Sequencing
33%
Exon
16%
Fibroblast
14%
FXYD2
13%
Gene Linkage
21%
Genetic Counseling
13%
Genetic Disorder
14%
Genetic Screening
27%
Genetics
100%
Genotyping
18%
Haploinsufficiency
9%
Haplotype
13%
Hypokalemia
8%
Hypomagnesemia
61%
Intellectual Disability
17%
Intraflagellar Transport
15%
Linkage Analysis
10%
LMX1B
19%
Microdeletion Syndrome
10%
Missense Mutation
19%
Mosaicism
9%
Mouse
12%
Next Generation Sequencing
34%
Proband
10%
Receptor Gene
15%
RNA
11%
Single-Nucleotide Polymorphism
22%
Transient Receptor Potential Channels
13%
Vasopressin
55%
Wild Type
24%
X Chromosome
11%
Medicine and Dentistry
Aquaporin 2
26%
Argipressin
21%
Autosomal Dominant Inheritance
7%
Autosomal Recessive Inheritance
14%
Bartter Syndrome
10%
Basolateral Membrane
5%
Case-Control Study
9%
Chronic Kidney Disease
20%
Ciliopathy
22%
Clinician
5%
Collecting Duct
13%
Congenital Malformation
18%
Cotransporter
8%
Counseling
8%
Diagnosis
31%
Disease
83%
Dysplasia
6%
Emergency Medical Technician
6%
Epileptic Seizure
9%
Epithelial Cell
6%
Exome Sequencing
10%
Fibroblast
8%
Focal Segmental Glomerulosclerosis
7%
Genetic Counseling
13%
Genetic Disorder
25%
Genetic Screening
13%
Gitelman Syndrome
13%
Glomerulus Basement Membrane
5%
Hypomagnesemia
14%
Kidney Tubule Disorder
7%
Magnesium
6%
Magnesium Ion
6%
Nail Patella Syndrome
10%
Nephrocalcinosis
6%
Nephrogenic Diabetes Insipidus
71%
Nephronophthisis
16%
Nephropathy
41%
Next Generation Sequencing
10%
Pediatrics
9%
Polycystic Kidney Disease
7%
Primary Cilium
5%
Receptor
18%
Receptor Gene
6%
Renal Failure
12%
Severe Myoclonic Epilepsy of Infancy
7%
Symptom
13%
Urinary System
5%
Urinary Tract
16%
Vasopressin
25%
Vasopressin V2 Receptor
24%
Keyphrases
Antidiuretic Hormone
5%
Aquaporin-2 (AQP2)
19%
Aquaporin-2 Water Channel
16%
Arginine
11%
Arginine Vasopressin
19%
Chronic Kidney Disease
7%
Chronic Kidney Disease of Unknown Etiology (CKDu)
7%
Clinical Outcomes
5%
Diabetes Insipidus
71%
Diagnostic Performance
8%
Dravet Syndrome
6%
FXYD2
8%
Genetic Defects
8%
Genetic Testing
7%
Gitelman Syndrome
12%
Hypocalciuria
6%
Hypomagnesemia
14%
Hypospadias
6%
Intellectual Disability
6%
K-Cl Cotransporter
10%
Kidney
19%
Kidney Disease
11%
Linkage Analysis
6%
LMX1B
5%
Long Arm
5%
Magnesium
5%
Massively Parallel Sequencing
5%
Misrouting
6%
Nail-patella Syndrome
6%
Next-generation Sequencing
6%
Odds Ratio
5%
Pathophysiology
5%
Receptor 2
7%
Receptor Gene
8%
Renal Collecting Ducts
5%
SCN1A
9%
Single nucleotide Polymorphism
6%
Thiazides
6%
Unsolicited Findings
5%
Urinary Tract
8%
V2 Receptor
12%
Vasopressin
10%
Vasopressin V2 Receptor
24%
Water Channel
6%
Water Reabsorption
5%
Whole Exome Sequencing
10%
X Chromosome
5%
Xq28
6%
