Biochemistry, Genetics and Molecular Biology
Allele
100%
Candidate Gene
100%
Sodium-Hydrogen Antiporter
100%
Infancy
100%
Platelet
100%
ATPase
100%
Carrier Protein
75%
Protein Repeat
50%
Protein-Protein Interaction
50%
Autosomal Recessive Disorder
50%
Sodium-Iodide Symporter
50%
Single-Nucleotide Polymorphism
50%
Genetics
50%
Brush Border
50%
Lipid
50%
Gene Linkage
50%
Microsatellite Marker
50%
Aquaporin
50%
Hepatocyte
50%
Platelet Alpha-Granule
50%
Ion Transporter
50%
TPR Domain
50%
Bioinformatics
50%
Genetic Architecture
25%
Transport Protein
25%
Mitochondrial Membrane Transport Protein
25%
Keyphrases
Trichohepatoenteric Syndrome
100%
TTC21B
100%
TTC37
100%
Diarrhea
100%
Ciliopathy
100%
Adenosine Triphosphatase
28%
Causal Genes
20%
Ciliary Dysfunction
20%
IFT139
20%
Intraflagellar Transport Protein
20%
Nephronophthisis
20%
Modifier Alleles
20%
Genetic Overlap
20%
Disease Genes
20%
In Vitro Evaluation
20%
Inherited Disorders
20%
Genetic Lesions
20%
Jeune's Asphyxiating Thoracic Dystrophy
20%
Functional Analysis
20%
Syndromic
20%
Genetic Architecture
20%
Overlapping Phenotypes
20%
Trichorrhexis Nodosa
14%
Sodium-hydrogen Exchanger 3
14%
Sodium-hydrogen Exchanger
14%
Tetratricopeptide Repeat Proteins
14%
Aquaporin 7
14%
Protein Chaperone
14%
Mutation Effect
14%
AIMS™
14%
Liver Disease
14%
Bioinformatics Analysis
14%
Cardiac Defects
14%
Protein-protein Interaction
14%
SNP Array
14%
Autozygosity Mapping
14%
Multisystem
14%
Autosomal Recessive
14%
Human Sodium Iodide Symporter (hNIS)
14%
Ion Transporter Protein
14%
Immunohistochemistry
14%
Intestinal Epithelial Cells
14%
Hepatocytes
14%
Life-threatening
14%
Microsatellite Markers
14%
Microtubules
14%
Immunodeficiency
14%
Brush Border
14%
Intracellular Localization
14%
Hypopigmentation
14%
Reduced Expression
14%
Lipid Inclusions
14%
Potassium
14%
Consanguineous Family
14%
α-granules
14%
Facial Dysmorphism
14%
Protein Production
14%
Na-K
14%
Platelet Alpha Granules
14%
Enterocyte
14%
Delocalization
14%
Platelets
14%
Platelet Dysfunction
14%