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  4. NPC1 as a Modulator of Disease Severity and Viral Entry of SARSCoV- 2
Details

NPC1 as a Modulator of Disease Severity and Viral Entry of SARSCoV- 2

Journal
Current Molecular Medicine
ISSN
1566-5240
Date Issued
2021
Author(s)
VIAL COX, MARIA CECILIA  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
CALDERON GIADROSIC, JUAN FRANCISCO  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
KLEIN POSTERNACK, ANDRES DAVID  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85103608252
WoS ID
WOS:000647674200002
DOI
10.2174/1566524020666200713175426
URL
https://investigadores.udd.cl/handle/123456789/6312
URL Institutional Repository
http://hdl.handle.net/11447/4342
Abstract
<jats:sec>
<jats:title />
<jats:p>The COVID-19 plague is hitting mankind. Several viruses, including SARS-CoV-1,
MERS-CoV, EBOV, and SARS-CoV-2, use the endocytic machinery to enter the cell. Genomic
variants in NPC1, which encodes for the endo-lysosomal Niemann-Pick type C1 protein, restricts
the host-range of viruses in bats and susceptibility to infections in humans. Lack of NPC1 and its
pharmacological suppression inhibits many viral infections including SARS-CoV-1 and Type I Feline
Coronavirus Infection. Antiviral effects of NPC1-inhibiting drugs for COVID-19 treatment should be
explored.</jats:p>
</jats:sec>
Project(s)
Understanding host response to ANDV infection, immunological and transcriptomics approach  
Unraveling the differences between mild and severe hantavirus infected patients: delineating mechanisms to propose novel therapies  
Identifying Genetic Modifiers of Clinical Severity in Chilean Patients with Inheritable Connective Tissue Disordes Through Genotype-Phenotype Correlations And Whole Exome Sequencing  
Uncovering modifier genes of lysosomal biology by exploiting the natural genetic variation of inbred mouse strains  
Subjects
covid-19

; 

sars-cov-2

; 

niemann-pick c1

; 

modifier gene

; 

drug repurposing

; 

virus

; 

infection

; 

antiviral agents

; 

covid-19

; 

drug repositioning

; 

humans

; 

intracellular signaling peptides and proteins

; 

sars-cov-2

; 

severity of illness index

; 

virus internalization

; 

1 benzylpiperazine derivative

; 

amphophile

; 

angiotensin converting enzyme 2

; 

antisense oligonucleotide

; 

clomifene

; 

diamide

; 

hydroxychloroquine

; 

npc intracellular cholesterol transporter 1

; 

terconazole

; 

antivirus agent

; 

npc1 protein, human

; 

signal peptide

; 

antiviral activity

; 

article

; 

chikungunya virus

; 

cholesterol metabolism

; 

coronavirus disease 2019

; 

dengue virus

; 

disease severity

; 

drug repositioning

; 

ebolavirus

; 

endocytosis

; 

feline coronavirus

; 

filovirus

; 

gene silencing

; 

genetic susceptibility

; 

hepatitis c

; 

host range

; 

human

; 

human immunodeficiency virus

; 

lysosome

; 

lysosome storage disease

; 

middle east respiratory syndrome coronavirus

; 

modifier gene

; 

multiple sclerosis

; 

niemann pick disease

; 

nonhuman

; 

plague

; 

protein function

; 

severe acute respiratory syndrome coronavirus 2

; 

single nucleotide polymorphism

; 

virus entry

; 

virus infection

; 

west nile virus

; 

zika fever

; 

zika virus

; 

drug therapy

; 

pathophysiology

; 

physiology

; 

severity of illness index

; 

virology

; 

virus entry
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