Keyphrases
Purine nucleoside Phosphorylase
100%
Purine nucleoside Phosphorylase Deficiency
100%
Base Change
100%
Single Base
100%
Mutated Genes
44%
Exon
33%
Single-point mutation
33%
Complementary DNA (cDNA)
11%
Cell Control
11%
Genomic DNA (gDNA)
11%
Peptide Mapping
11%
Transcriptional Regulation
11%
Codon
11%
Nitrocellulose Membrane
11%
Isoelectric Focusing
11%
Consanguineous
11%
In Vitro mutagenesis
11%
Catalytic Function
11%
Coding Region
11%
T Lymphocyte Function
11%
Mapping Data
11%
Type Sequences
11%
HeLa Cells
11%
Mammalian Expression Vector
11%
Immunology and Microbiology
Purine Nucleoside Phosphorylase Deficiency
100%
Exon
100%
Wild Type
66%
Intron
33%
Catalysis
33%
Progeny
33%
Promoter Region
33%
Expression Vector
33%
Lymphocyte Function
33%
T Cell
33%
Codon
33%
Mutagenesis
33%
Biochemistry, Genetics and Molecular Biology
Purine Nucleoside Phosphorylase
100%
Exon
27%
Wild Type
18%
Mutagenesis
9%
Catalysis
9%
Progeny
9%
Promoter Region
9%
Lymphocyte Function
9%
Mating
9%
Coding Region
9%
Intron
9%
Codon
9%
T Cell
9%
Isoelectric Focusing
9%
Expression Vector
9%
Genomics
9%
Nitrocellulose
9%
Neuroscience
Purine Nucleoside Phosphorylase
100%
Exon
27%
Complementary DNA
9%
Coding Region
9%
In Vitro
9%
Oligomer
9%
Promoter Region
9%
Intron
9%
Expression Vector
9%
Genomic DNA
9%
Codon
9%
T Cell
9%
Mutagenesis
9%