<p>(A) Sequence alignment of STING from different species. The four variations in the coding region of hSTING, R71, G230, R232 and R293 are shown in bold and colored in red. The evolutional conservation of R232 and R293 among the species is highlighted. The residue numbers denote those in hSTING. (B) Allele frequency of hSTING. The frequencies derived from 1000 Genome Project database are in the left-most column and the amino acid variations are colored in red. The name of hSTING SNPs and mutants studied in this work are shown in bold and the frequency is calculated in the right-most column. (C) Localization of G230, R232 and R293 in the crystal structure of hSTING in complex with c-di-GMP. A monomer of the hSTING bound to c-di-GMP is sh...
Single nucleotide polymorphisms (SNPs) are the most common form of human genetic variation, with mil...
Single nucleotide polymorphisms (or SNPs, pronounced as “snips”) are DNA se-quence variations that o...
The investigation of genetic di#erences among humans has given evidence that mutations in DNA seque...
<p>A possible evolutionary history of the 12 major human STING haplotypes (ht-1 to ht-12) was inferr...
a<p>First letter indicates common bp at this site, followed by position of SNP in sequence on GenBan...
OAK B188 Single nucleotide polymorphism (SNPs) are the most common form of sequence variation in the...
We assessed the disease-causing potential of single nucleotide polymorphisms (SNPs) based on a simpl...
<p>Abbreviations: pet = <i>H. e. petiverana;</i> fav = <i>H.e. favorinus;</i> mel = <i>H.m.melpomene...
<p>(A) Sequence conservation profile of the Hsp70 residues. The KL conservation score was calculated...
<p>Multiple sequence alignment of the full-length amino acid sequences of the Hsp110/HSPH gene famil...
<p>Multiple sequence alignment of the full-length amino acid sequences of the Hsp70/HSPA gene famili...
The glutathione(GSH)-glutathione-S-transferase(GST) system is a detoxification system capable of ina...
Single nucleotide polymorphisms (SNPs) are places along the chromosomes where the genetic code tends...
<p><b>A.</b> Nucleotide alignment of a fragment of the gC gene from the current passage of HSV-1 <i>...
Single nucleotide polymorphisms (SNPs) are useful for genome-wide mapping and study of disease genes...
Single nucleotide polymorphisms (SNPs) are the most common form of human genetic variation, with mil...
Single nucleotide polymorphisms (or SNPs, pronounced as “snips”) are DNA se-quence variations that o...
The investigation of genetic di#erences among humans has given evidence that mutations in DNA seque...
<p>A possible evolutionary history of the 12 major human STING haplotypes (ht-1 to ht-12) was inferr...
a<p>First letter indicates common bp at this site, followed by position of SNP in sequence on GenBan...
OAK B188 Single nucleotide polymorphism (SNPs) are the most common form of sequence variation in the...
We assessed the disease-causing potential of single nucleotide polymorphisms (SNPs) based on a simpl...
<p>Abbreviations: pet = <i>H. e. petiverana;</i> fav = <i>H.e. favorinus;</i> mel = <i>H.m.melpomene...
<p>(A) Sequence conservation profile of the Hsp70 residues. The KL conservation score was calculated...
<p>Multiple sequence alignment of the full-length amino acid sequences of the Hsp110/HSPH gene famil...
<p>Multiple sequence alignment of the full-length amino acid sequences of the Hsp70/HSPA gene famili...
The glutathione(GSH)-glutathione-S-transferase(GST) system is a detoxification system capable of ina...
Single nucleotide polymorphisms (SNPs) are places along the chromosomes where the genetic code tends...
<p><b>A.</b> Nucleotide alignment of a fragment of the gC gene from the current passage of HSV-1 <i>...
Single nucleotide polymorphisms (SNPs) are useful for genome-wide mapping and study of disease genes...
Single nucleotide polymorphisms (SNPs) are the most common form of human genetic variation, with mil...
Single nucleotide polymorphisms (or SNPs, pronounced as “snips”) are DNA se-quence variations that o...
The investigation of genetic di#erences among humans has given evidence that mutations in DNA seque...