Biochemistry, Genetics and Molecular Biology
Autosomal Dominant Polycystic Kidney
100%
Polycystin 2
77%
Polycystic Kidney Disease 2
73%
Exon
59%
Mouse
52%
Amino Acids
51%
Integral Membrane Protein
48%
C-Terminus
40%
Gene Product
32%
PKD1
32%
Oligonucleotide
30%
Calcium Channel
26%
Monospecific Antibody
24%
Orexin
24%
Transposase
24%
DNA Methylation
24%
Stem Cell
24%
Drosophila Melanogaster
24%
Missense
24%
Cell Level
24%
Genotyping
24%
Exon Structure
24%
ATAC-Seq
24%
Chromosomal Localization
24%
Amnion
24%
Autosomal Dominant Inheritance
24%
Myeloid
24%
Whole Genome Sequencing
24%
Molecular Cloning
24%
Induced Mutation
24%
Protein Sequencing
24%
Lead Poisoning
24%
Offspring
24%
Hypovitaminosis D
24%
Immunocompetent Cell
24%
Allele
23%
N-Terminus
21%
Nonsense Mutation
21%
Sodium Channel
20%
Electric Potential
20%
Vitamin D
19%
Lymphoblast
18%
Candidate Gene
18%
Mosaic (Genetics)
16%
Chemical Mutagenesis
16%
Wild Type
16%
Differentially Methylated Regions
14%
Volume
12%
Nucleic Acid Base Substitution
12%
Peptide Sequence
12%
Keyphrases
Autosomal Dominant Polycystic Kidney Disease (ADPKD)
78%
Polycystic Kidney Disease
77%
PKD2
73%
PKD2 Gene
42%
Integral Membrane Protein
38%
Polycystic Liver Disease
34%
HMSH2
24%
Hypocretin
24%
Ectodermal
24%
Chromosomal Localization
24%
Exon Structure
24%
Reduced Expression
24%
Complementary DNA (cDNA)
24%
Lymphoblastoid Cells
24%
19p13.2
24%
Ultrarapid Metabolizer
24%
Tissue Expression
24%
Molecular Cloning
24%
Sequence Analysis
24%
Amino Acids
17%
Polycystin
16%
Amino Acid Similarities
14%
Gene Products
12%
Positional Cloning
12%
PKD1
12%
Demultiplexing
10%
Nonsense mutation
9%
Small Deletion
8%
Transmembrane Domain
7%
Multiplexing Technique
6%
2-plex
6%
Truncated Protein
6%
Systematic mutation
6%
PKHD1 Gene
6%
4q21
6%
Retina
6%
Disease Mapping
6%
Coding Sequence
6%
Testicle
6%
Membrane Glycoproteins
6%
Unknown Function
6%
Gene-gene
6%
Transmembrane
6%
Heart muscle
6%
Exon-intron Structure
6%
Skeletal muscle
6%
Genomic DNA (gDNA)
6%
Recombinant Chromosome
6%
Exon
6%
Rps3
6%