„synonymous“
Suchergebnisse
1.000+ Treffer
-
X-linked Alport syndrome associated with a synonymous p.Gly292Gly mutation alters the splicing donor site of the type IV collagen alpha chain 5 gene
-
Recent and Long-Term Selection Across Synonymous Sites in Drosophila ananassae
-
Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk
-
The non-random clustering of non-synonymous substitutions and its relationship to evolutionary rate
-
A non-synonymous coding change in the CYP19A1 gene Arg264Cys (rs700519) does not affect circulating estradiol, bone structure or fracture
-
Additive sex-specific influence of common non-synonymous DISC1 variants on amygdala, basal ganglia, and white cortical surface area in healthy young adults
-
A synonymous EGFR polymorphism predicting responsiveness to anti-EGFR therapy in metastatic colorectal cancer patients
-
The relationship between five non-synonymous polymorphisms within three XRCC genes and gastric cancer risk in a Han Chinese population
-
Synonymous codon usage bias is correlative to intron number and shows disequilibrium among exons in plants
-
Synonymous mutation gene design to overexpress ACCase in creeping bentgrass to obtain resistance to ACCase-inhibiting herbicides
-
Homozygous synonymous FAM111A variant underlies an autosomal recessive form of Kenny-Caffey syndrome
-
Molecular Evolution of Duplicated Ray Finned Fish HoxA Clusters – Increased Synonymous Substitution Rate and Asymmetrical Co-divergence of Coding and Non-coding Sequences
-
MLH1 c.27G>A (p.Arg9=) is a synonymous likely/pathogenic variant underlying variably mosaic constitutional MLH1 methylation in Lynch syndrome
-
CACNA1A gene non-synonymous single nucleotide polymorphisms and common migraine in Italy: a case-control association study with a micro-array technology
-
Genetic association analyses of non-synonymous single nucleotide polymorphisms in diabetic nephropathy
-
Novel synonymous substitution in POMGNT1 promotes exon skipping in a patient with congenital muscular dystrophy
-
Soluble overexpression of a flagellin derivative from Salmonella enterica using synonymous codon substitutions of 5′-coding region in Escherichia coli
-
Synonymous mutations that regulate translation speed might play a non-negligible role in liver cancer development
-
Massively parallel gene expression variation measurement of a synonymous codon library
-
A non-synonymous variant rs12614 of complement factor B associated with risk of chronic hepatitis B in a Korean population