Skip to main navigation
Skip to search
Skip to main content
Sort by
Keyphrases
Autosomal Dominant Polycystic Kidney Disease (ADPKD)
80%
Meckel Syndrome
77%
Genetic Analysis
77%
Ciliopathy
77%
Fibrocystin
63%
PKHD1
62%
Disease Syndrome
47%
Autosomal Recessive
38%
Polycystic Kidney Disease
37%
PKHD1 Gene
34%
Syndromic
31%
TMEM67
21%
Disease Mechanisms
19%
Non-syndromic
19%
Common Diseases
19%
Cilia
19%
Kidney
17%
Hypomorphic mutation
17%
Zebrafish
16%
Ciliary
16%
Etiology
15%
Mouse Model
14%
Primary Cilia
14%
Protein Family
14%
Basal Body
14%
Liver Disease
14%
Pathogenicity
12%
Variants of Uncertain Significance
12%
Mutation Screening
12%
Allelic Heterogeneity
12%
Cellular Assay
11%
Meckelin
11%
Digenic
11%
Whole Exome Sequencing
11%
Cellular Systems
10%
Oligogenic Inheritance
10%
Ciliopathy Gene
10%
PKD1
10%
Caenorhabditis Elegans
9%
Exon
9%
Diseased Population
9%
Joubert Syndrome
7%
Kidney Epithelial Cells
7%
Associated Proteins
7%
Cell Phenotype
7%
Antibody Constructs
7%
Functional Studies
7%
Developing Zebrafish
7%
Subcellular Localization
7%
Functional Information
7%
Pronephric Duct
7%
Convergent Extension Movements
7%
In Situ Hybridization
7%
Associated Genes
7%
Molecular Study
7%
Chlamydomonas
7%
Genotype-phenotype Correlation
7%
Short Hairpin RNA (shRNA)
7%
Knockdown
7%
Developmental Pathways
7%
Mutation Studies
7%
Perinatal Death
7%
Body Axis
7%
Morphant
7%
Morpholino
7%
Monoclonal Antibody
7%
Expression Construct
7%
Genotype
7%
Membrane-bound
7%
Motility
7%
Flagella
7%
Adult-onset
7%
Disease-related Proteins
7%
Genetic Disease
6%
True Complexity
6%
Liver
6%
Genetic Interaction
5%
Genome Complexity
5%
3D Modeling
5%
Screening Protocol
5%
Modeling Approaches
5%
Including 3D
5%
Cas9 Protein
5%
Sanger Sequencing
5%
Autosomal Dominant
5%
RNA Sequencing (RNA-seq)
5%
Low Temperature
5%
Membrane Protein
5%
Protein Maturation
5%
Complex mutations
5%
Protein Folding
5%
Genetic Heterogeneity
5%
Adult Phenotype
5%
Phenotypic Value
5%
Chemical Chaperone
5%
Early Lethality
5%
Expression Profile
5%
Gene Panel
5%
In Silico
5%
Null Model
5%
Surface Proteins
5%
Surface Localization
5%
Explosives
5%
Phenotypic Profiling
5%
Folding Defect
5%
Cas9 Gene
5%
Monogenic Disease
5%
Chaperone
5%
Gene Editing
5%
Gene/protein
5%
Penetrance
5%
IFT140
5%
Biochemistry, Genetics and Molecular Biology
Autosomal Recessive Inheritance
100%
Genetics
83%
Fibrocystin
70%
Cilium
49%
TMEM67
48%
Allele
33%
Exome Sequencing
25%
Mouse Model
22%
Zebra Fish
22%
Inheritance
17%
Maturation
16%
Next Generation Sequencing
12%
Autosomal Dominant Inheritance
12%
RNA Sequencing
12%
Membrane Protein
12%
Chemical Chaperone
12%
Posttranslational Modification
12%
CRISPR/Cas9
12%
Dideoxynucleotide Sequencing
12%
Protein Folding
12%
Penetrance
12%
Protein Family
12%
Basal Body
12%
Paralogy
11%
Animal Model
10%
IFT140
9%
Caenorhabditis Elegans
9%
Exon
9%
Gene Interaction
8%
Autosomal Dominant Polycystic Kidney
8%
Genetic Disorder
7%
Autosomal Recessive Disorder
7%
Monoclonal Antibody
6%
Convergent Extension
6%
In Situ Hybridization
6%
Subcellular Localization
6%
Genotype Phenotype Correlation
6%
Chlamydomonas
6%
Small Hairpin RNA
6%
Isolated Liver
6%
Morphant
6%
Flagellum
6%
Small Interfering RNA
6%
Genotyping
6%
Morpholino
6%
Chaperone
6%
Medicine and Dentistry
Fibrocystin
58%
Diseases
46%
Polycystic Kidney Disease
39%
Meckel Syndrome
38%
Ciliopathy
38%
Autosomal Recessive Inheritance
38%
Genetic Analysis
38%
Autosomal Recessive Polycystic Kidney Disease
27%
Allele
23%
Genetics
18%
Liver Disease
12%
Protein Family
12%
Basal Body
12%
Cilium
12%
Paralogy
11%
Next Generation Sequencing
10%
Etiology
9%
Caenorhabditis Elegans
9%
Exon
9%
Primary Cilium
8%
Genetic Disorder
6%
Epithelial Cell
6%
Monoclonal Antibody
6%
Short Hairpin RNA
6%
Genotype Phenotype Correlation
6%
Perinatal Death
6%
Flagellum
6%
In Situ Hybridization
6%
Gene Interaction
5%