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10.1002/1873-3468.13908

http://scihub22266oqcxt.onion/10.1002/1873-3468.13908
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32880920!7461230!32880920
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suck abstract from ncbi


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pmid32880920      FEBS+Lett 2020 ; 594 (20): 3363-3370
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  • Transcriptomic analyses suggest that mucopolysaccharidosis patients may be less susceptible to COVID-19 #MMPMID32880920
  • Pierzynowska K; Gaffke L; Wegrzyn G
  • FEBS Lett 2020[Oct]; 594 (20): 3363-3370 PMID32880920show ga
  • We used transcriptomic (RNA-seq) analyses to determine whether patients suffering from all types and subtypes of mucopolysaccharidosis (MPS), a severe inherited metabolic disease, may be more susceptible to coronavirus disease 2019 (COVID-19). The expression levels of genes encoding proteins potentially involved in SARS-CoV-2 development were estimated in MPS cell lines. Four genes (GTF2F2, RAB18, TMEM97, PDE4DIP) coding for proteins potentially facilitating virus development were down-regulated, while two genes (FBN1, MFGE8), the products of which potentially interfere with virus propagation, were up-regulated in most MPS types. Although narrowing of respiratory tract and occurrence of thick mucus, characteristic of MPS, are risk factors for COVID-19, transcriptomic analyses suggest that MPS cells might be less, rather than more, susceptible to SARS-CoV-2 infection.
  • |*Virus Internalization[MESH]
  • |Angiotensin-Converting Enzyme 2/genetics/metabolism[MESH]
  • |COVID-19/*genetics/metabolism/pathology/prevention & control[MESH]
  • |Cells, Cultured[MESH]
  • |Fibroblasts/metabolism/pathology/virology[MESH]
  • |Gene Expression Profiling[MESH]
  • |Genetic Predisposition to Disease[MESH]
  • |Humans[MESH]
  • |Mucopolysaccharidoses/*genetics/metabolism/pathology/virology[MESH]
  • |SARS-CoV-2/pathogenicity/*physiology[MESH]
  • |Serine Endopeptidases/genetics/metabolism[MESH]


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