Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText.
Kick-your-searchterm to multiple Engines kick-your-query now !>
A dictionary by aggregated review articles of nephrology, medicine and the life sciences
Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

suck abstract from ncbi


10.1002/jmv.26548

http://scihub22266oqcxt.onion/10.1002/jmv.26548
suck pdf from google scholar
32970329!7537117!32970329
unlimited free pdf from europmc32970329    free
PDF from PMC    free
html from PMC    free

suck abstract from ncbi


Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534
pmid32970329      J+Med+Virol 2021 ; 93 (3): 1702-1721
Nephropedia Template TP

gab.com Text

Twit Text FOAVip

Twit Text #

English Wikipedia


  • Genomic and proteomic mutation landscapes of SARS-CoV-2 #MMPMID32970329
  • Badua CLDC; Baldo KAT; Medina PMB
  • J Med Virol 2021[Mar]; 93 (3): 1702-1721 PMID32970329show ga
  • The ongoing pandemic caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), affects thousands of people every day worldwide. Hence, drugs and vaccines effective against all variants of SARS-CoV-2 are crucial today. Viral genome mutations exist commonly which may impact the encoded proteins, possibly resulting to varied effectivity of detection tools and disease treatment. Thus, this study surveyed the SARS-CoV-2 genome and proteome and evaluated its mutation characteristics. Phylogenetic analyses of SARS-CoV-2 genes and proteins show three major clades and one minor clade (P6810S; ORF1ab). The overall frequency and densities of mutations in the genes and proteins of SARS-CoV-2 were observed. Nucleocapsid exhibited the highest mutation density among the structural proteins while the spike D614G was the most common, occurring mostly in genomes outside China and United States. ORF8 protein had the highest mutation density across all geographical areas. Moreover, mutation hotspots neighboring and at the catalytic site of RNA-dependent RNA polymerase were found that might challenge the binding and effectivity of remdesivir. Mutation coldspots may present as conserved diagnostic and therapeutic targets were found in ORF7b, ORF9b, and ORF14. These findings suggest that the virion's genotype and phenotype in a specific population should be considered in developing diagnostic tools and treatment options.
  • |*Genome, Viral[MESH]
  • |*Mutation[MESH]
  • |*Phylogeny[MESH]
  • |*Proteome[MESH]
  • |COVID-19/virology[MESH]
  • |China[MESH]
  • |Evolution, Molecular[MESH]
  • |Genomics[MESH]
  • |Humans[MESH]
  • |Open Reading Frames[MESH]
  • |Proteomics[MESH]
  • |SARS-CoV-2/*genetics[MESH]
  • |Spike Glycoprotein, Coronavirus/genetics[MESH]
  • |United States[MESH]


  • DeepDyve
  • Pubget Overpricing
  • suck abstract from ncbi

    Linkout box