Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Joshua E. Donovan"'
Autor:
Ewelina D. Hejenkowska, Nilay Mitash, Joshua E. Donovan, Anvita Chandra, Carol Bertrand, Chiara De Santi, Catherine M. Greene, Fangping Mu, Agnieszka Swiatecka-Urban
Publikováno v:
Journal of Innate Immunity, Pp 1-1 (2023)
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), responsible for COVID-19, utilizes receptor binding domain (RBD) of spike glycoprotein to interact with angiotensin (Ang)-converting enzyme 2 (ACE2). Altering ACE2 levels may affect en
Externí odkaz:
https://doaj.org/article/e8079fb07a51463c8f78746a32af8a84
Publikováno v:
J Vis Exp
Micro(mi)RNAs are short, non-coding RNAs that mediate the RNA interference (RNAi) by post-transcriptional mechanisms. Specific miRNAs are recruited to the cytoplasmic RNA induced silencing complex (RISC). Argonaute2 (Ago2), an essential component of
Publikováno v:
Journal of Visualized Experiments.
Micro(mi)RNAs are short, non-coding RNAs that mediate the RNA interference (RNAi) by post-transcriptional mechanisms. Specific miRNAs are recruited to the cytoplasmic RNA induced silencing complex (RISC). Argonaute2 (Ago2), an essential component of
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 3848, p 3848 (2020)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Mucociliary clearance, mediated by a coordinated function of cilia bathing in the airway surface liquid (ASL) on the surface of airway epithelium, protects the host from inhaled pathogens and is an essential component of the innate immunity. ASL is c
Autor:
Catherine M. Greene, Sarangarajan Ranganathan, Agnieszka Swiatecka-Urban, Nilay Mitash, Fangping Mu, Joshua E Donovan, Michael M. Myerburg
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 19, p 4933 (2019)
International Journal of Molecular Sciences
Volume 20
Issue 19
International Journal of Molecular Sciences
Volume 20
Issue 19
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Mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (<
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CFTR<
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) gene lead to cystic fibrosis (CF). The most common mutation F508del inhibits folding and processing of CFT
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Mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (<
italic>
CFTR<
/italic>
) gene lead to cystic fibrosis (CF). The most common mutation F508del inhibits folding and processing of CFT