Type |
Details |
Score |
HT Experiment |
|
Experiment Type: |
RNA-Seq |
Study Type: |
Baseline |
Source: |
GEO |
|
•
•
•
•
•
|
HT Experiment |
|
Experiment Type: |
RNA-Seq |
Study Type: |
Baseline |
Source: |
GEO |
|
•
•
•
•
•
|
Publication |
First Author: |
Yang B |
Year: |
2023 |
Journal: |
Cell Discov |
Title: |
A tissue specific-infection mouse model of SARS-CoV-2. |
Volume: |
9 |
Issue: |
1 |
Pages: |
43 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wang LA |
Year: |
2018 |
Journal: |
Neuropharmacology |
Title: |
Coupling corticotropin-releasing-hormone and angiotensin converting enzyme 2 dampens stress responsiveness in male mice. |
Volume: |
133 |
|
Pages: |
85-93 |
|
•
•
•
•
•
|
Publication |
First Author: |
Fukui K |
Year: |
2005 |
Journal: |
Cell Metab |
Title: |
The HNF-1 target collectrin controls insulin exocytosis by SNARE complex formation. |
Volume: |
2 |
Issue: |
6 |
Pages: |
373-84 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
222
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
60
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Leist SR |
Year: |
2020 |
Journal: |
Dis Model Mech |
Title: |
Cell and animal models of SARS-CoV-2 pathogenesis and immunity. |
Volume: |
13 |
Issue: |
9 |
|
|
•
•
•
•
•
|
Strain |
Attribute String: |
transgenic, mutant stock |
|
•
•
•
•
•
|
Publication |
First Author: |
Calvier L |
Year: |
2023 |
Journal: |
Front Immunol |
Title: |
Circulating Reelin promotes inflammation and modulates disease activity in acute and long COVID-19 cases. |
Volume: |
14 |
|
Pages: |
1185748 |
|
•
•
•
•
•
|
Strain |
Attribute String: |
mutant stock, transgenic |
|
•
•
•
•
•
|
Strain |
Attribute String: |
mutant strain, endonuclease-mediated mutation, coisogenic |
|
•
•
•
•
•
|
Allele |
Name: |
transgene insertion 2, Roger E Breitbart |
Allele Type: |
Transgenic |
Attribute String: |
Humanized sequence, Inserted expressed sequence |
|
•
•
•
•
•
|
Strain |
Attribute String: |
coisogenic, mutant strain, transgenic |
|
•
•
•
•
•
|
Allele |
Name: |
angiotensin converting enzyme 2; targeted mutation 1, David Wentworth |
Allele Type: |
Targeted |
Attribute String: |
Humanized sequence, Inserted expressed sequence |
|
•
•
•
•
•
|
Strain |
Attribute String: |
congenic, mutant strain, targeted mutation |
|
•
•
•
•
•
|
Allele |
Name: |
angiotensin converting enzyme 2; targeted mutation 1.1, Michael D Koob |
Allele Type: |
Targeted |
Attribute String: |
Humanized sequence, Inserted expressed sequence |
|
•
•
•
•
•
|
Strain |
Attribute String: |
coisogenic, endonuclease-mediated mutation, mutant strain |
|
•
•
•
•
•
|
Allele |
Name: |
angiotensin converting enzyme 2; endonuclease-mediated mutation 1, Channabasavaiah Gurumurthy |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Humanized sequence |
|
•
•
•
•
•
|
Allele |
Name: |
angiotensin converting enzyme 2; endonuclease-mediated mutation 1, Mark L Kahn |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Conditional ready, Humanized sequence, Inserted expressed sequence, Null/knockout |
|
•
•
•
•
•
|
Allele |
Name: |
angiotensin converting enzyme 2; endonuclease-mediated mutation 2, Mark L Kahn |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Conditional ready, Humanized sequence, Inserted expressed sequence, Null/knockout, Reporter |
|
•
•
•
•
•
|
Allele |
Name: |
angiotensin converting enzyme 2; endonuclease-mediated mutation 2, Mark L Kahn |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Conditional ready, Humanized sequence, Inserted expressed sequence, Null/knockout |
|
•
•
•
•
•
|
Allele |
Name: |
gene trap ROSA 26, Philippe Soriano; endonuclease-mediated mutation 1, Wei Li |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Conditional ready, Epitope tag, Humanized sequence, Inserted expressed sequence |
|
•
•
•
•
•
|
Strain |
Attribute String: |
coisogenic, endonuclease-mediated mutation, mutant strain |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(Nphs1-ACE2)#Kdbu/? |
Background: |
FVB//N-Tg(Nphs1-ACE2)#Kdbu |
Zygosity: |
ot |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(CAG-ACE2)AC70Ctkt/? |
Background: |
either: (involves: BALB/c * C3H/HeJ * C57BL/6J) or (involves: C3H/HeJ * C57BL/6 * C57BL/6J) |
Zygosity: |
ot |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Ace2/Ace2 |
Background: |
C57BL/6-Ace2 |
Zygosity: |
hm |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(CAG-ACE2)AC63Ctkt/? |
Background: |
either: (involves: BALB/c * C3H/HeJ * C57BL/6J) or (involves: C3H/HeJ * C57BL/6 * C57BL/6J) |
Zygosity: |
ot |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(Myh6-ACE2)1Rbre/? |
Background: |
involves: FVB/N |
Zygosity: |
ot |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Tg(Myh6-ACE2)2Rbre/? |
Background: |
involves: FVB/N |
Zygosity: |
ot |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Natoli S |
Year: |
2020 |
Journal: |
Eur J Neurol |
Title: |
Does SARS-Cov-2 invade the brain? Translational lessons from animal models. |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Zhang Z |
Year: |
2024 |
Journal: |
Emerg Microbes Infect |
Title: |
The lethal K18-hACE2 knock-in mouse model mimicking the severe pneumonia of COVID-19 is practicable for antiviral development. |
Volume: |
13 |
Issue: |
1 |
Pages: |
2353302 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lutz C |
Year: |
2020 |
Journal: |
Hum Genomics |
Title: |
COVID-19 preclinical models: human angiotensin-converting enzyme 2 transgenic mice. |
Volume: |
14 |
Issue: |
1 |
Pages: |
20 |
|
•
•
•
•
•
|
Strain |
Attribute String: |
mutant strain, targeted mutation |
|
•
•
•
•
•
|
Allele |
Name: |
gene trap ROSA 26, Philippe Soriano; endonuclease-mediated mutation 25, Michael V Wiles |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Epitope tag, Humanized sequence, Inserted expressed sequence |
|
•
•
•
•
•
|
Strain |
Attribute String: |
congenic, endonuclease-mediated mutation, targeted mutation, mutant strain, spontaneous mutation |
|
•
•
•
•
•
|
Publication |
First Author: |
Yoshikawa N |
Year: |
2009 |
Journal: |
J Virol |
Title: |
Differential virological and immunological outcome of severe acute respiratory syndrome coronavirus infection in susceptible and resistant transgenic mice expressing human angiotensin-converting enzyme 2. |
Volume: |
83 |
Issue: |
11 |
Pages: |
5451-65 |
|
•
•
•
•
•
|
Strain |
Attribute String: |
coisogenic, endonuclease-mediated mutation, mutant strain |
|
•
•
•
•
•
|
Strain |
Attribute String: |
coisogenic, endonuclease-mediated mutation, mutant strain |
|
•
•
•
•
•
|
Allele |
Name: |
angiotensin converting enzyme 2; endonuclease-mediated mutation 1, Synbal |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Humanized sequence, Inserted expressed sequence, Null/knockout |
|
•
•
•
•
•
|
Allele |
Name: |
angiotensin converting enzyme 2; endonuclease-mediated mutation 2.1, Synbal |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Humanized sequence, Inserted expressed sequence, Null/knockout |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
805
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
265
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
521
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
557
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
787
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
805
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
The CoV Spike (S) protein is an envelope glycoprotein that plays the most important role in viral attachment, fusion, and entry into host cells, and serves as a major target for the development of neutralizing antibodies, inhibitors of viral entry, and vaccines. It is synthesised as a precursor protein that is cleaved into an N-terminal S1 subunit (~700 amino acids) and a C-terminal S2 subunit (~600 amino acids) that mediates attachment and membrane fusion, respectively. Three S1/S2 heterodimers assemble to form a trimer spike protruding from the viral envelope. The S1 subunit contains a receptor-binding domain (RBD), while the S2 subunit contains a hydrophobic fusion peptide and two heptad repeat regions. S1 contains two structurally independent domains, the N-terminal domain (NTD) and the C-terminal domain (C-domain). Depending on the virus, either the NTD or the C-domain can serve as the receptor-binding domain (RBD). Most CoVs, including SARS-CoV-2, SARS-CoV, and MERS-CoV use the C-domain to bind their receptors. However, CoV such as mouse hepatitis virus (MHV) uses the NTD to bind its receptor, mouse carcinoembryonic antigen related cell adhesion molecule 1a (mCEACAM1a). The S1 NTD contributes to the Spike trimer interface [, , , , ].This entry represents the RBD domain of Spike protein S1 subunit from SARS-CoV-2, which binds the extracellular peptidase domain of angiotensin-converting enzyme 2 (ACE2). It has been shown that the receptor binding induces the dissociation of the S1 with ACE2, prompting the S2 to transit from a metastable pre-fusion to a more-stable post-fusion state that is essential for membrane fusion [, , , ]. Recent structures revealed that only a single RBD is necessary for ACE2 binding and it is not yet clear if protrusion of the RBD from the S protein trimer is necessary for binding to ACE2 or the interconversion of the RBD between closed and open states represents an intrinsic property of the S protein []. During the pandemic, many amino acid substitutions have been reported in the S1 segment, being D614G the most commonly observed amino acid change from the reference sequence. Although it was estimated to be slightly destabilizing, it was hypothesized that it increases virus infectivity by increasing the total amount of S protein incorporated into virions. The most prevalent RBD substitution in the RBD is the T478I, located in a portion of a loop that contacts ACE2. However, most substitutions in the interface with ACE2 appear to be neutral or destabilizing, with none improving binding affinity [].SARS-CoV-2 RBD has a core formed by a twisted five-stranded antiparallel β-sheet (β1-7) with short helices and loops connecting them. Between the β4 and β7 strands in the core, there is an extended insertion, the receptor-binding motif (RBM), containing the short β5 and β6 strands, α4 and α5 helices and loops, which contains most of the contacting residues for binding to ACE2. There are nine cysteine residues in the RBD, eight of which form four pairs of disulfide bonds. Among these four pairs, three are in the core which help to stabilise the β-sheet structure, while the remaining pair connects the loops in the distal end of the RBM []. |
|
•
•
•
•
•
|
Strain |
Attribute String: |
congenic, mutant strain, targeted mutation, spontaneous mutation |
|
•
•
•
•
•
|
Strain |
Attribute String: |
congenic, endonuclease-mediated mutation, mutant strain, transgenic, targeted mutation |
|
•
•
•
•
•
|
Publication |
First Author: |
Tseng CT |
Year: |
2007 |
Journal: |
J Virol |
Title: |
Severe acute respiratory syndrome coronavirus infection of mice transgenic for the human Angiotensin-converting enzyme 2 virus receptor. |
Volume: |
81 |
Issue: |
3 |
Pages: |
1162-73 |
|
•
•
•
•
•
|
Strain |
Attribute String: |
coisogenic, endonuclease-mediated mutation, mutant strain |
|
•
•
•
•
•
|
Strain |
Attribute String: |
endonuclease-mediated mutation, mutant strain |
|
•
•
•
•
•
|
Publication |
First Author: |
Fraga-Silva RA |
Year: |
2008 |
Journal: |
Mol Med |
Title: |
The antithrombotic effect of angiotensin-(1-7) involves mas-mediated NO release from platelets. |
Volume: |
14 |
Issue: |
1-2 |
Pages: |
28-35 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ward K |
Year: |
1993 |
Journal: |
Nat Genet |
Title: |
A molecular variant of angiotensinogen associated with preeclampsia. |
Volume: |
4 |
Issue: |
1 |
Pages: |
59-61 |
|
•
•
•
•
•
|
Publication |
First Author: |
Donoghue M |
Year: |
2000 |
Journal: |
Circ Res |
Title: |
A novel angiotensin-converting enzyme-related carboxypeptidase (ACE2) converts angiotensin I to angiotensin 1-9. |
Volume: |
87 |
Issue: |
5 |
Pages: |
E1-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ehlers MR |
Year: |
1989 |
Journal: |
Biochemistry |
Title: |
Angiotensin-converting enzyme: new concepts concerning its biological role. |
Volume: |
28 |
Issue: |
13 |
Pages: |
5311-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Fuchs S |
Year: |
2004 |
Journal: |
Curr Hypertens Rep |
Title: |
Newly recognized physiologic and pathophysiologic actions of the angiotensin-converting enzyme. |
Volume: |
6 |
Issue: |
2 |
Pages: |
124-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Goodfriend TL |
Year: |
1975 |
Journal: |
Circ Res |
Title: |
Angiotensin III: (DES-Aspartic Acid-1)-Angiotensin II. Evidence and speculation for its role as an important agonist in the renin - angiotensin system. |
Volume: |
36 |
Issue: |
6 Suppl 1 |
Pages: |
38-48 |
|
•
•
•
•
•
|
Publication |
First Author: |
Flohr H |
Year: |
1975 |
Journal: |
Arzneimittelforschung |
Title: |
Effect of etafenone on total and regional myocardial blood flow. |
Volume: |
25 |
Issue: |
9 |
Pages: |
1400-3 |
|
•
•
•
•
•
|
Publication |
First Author: |
Marniemi J |
Year: |
1975 |
Journal: |
Biochem Pharmacol |
Title: |
Radiochemical assay of glutathione S-epoxide transferase and its enhancement by phenobarbital in rat liver in vivo. |
Volume: |
24 |
Issue: |
17 |
Pages: |
1569-72 |
|
•
•
•
•
•
|
Publication |
First Author: |
Agardh CD |
Year: |
1979 |
Journal: |
Diabetes |
Title: |
The effect of pronounced hypoglycemia on monoamine metabolism in rat brain. |
Volume: |
28 |
Issue: |
9 |
Pages: |
804-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lewis J |
Year: |
1976 |
Journal: |
J Stud Alcohol |
Title: |
Washington report. |
Volume: |
37 |
Issue: |
3 |
Pages: |
409-14 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
Angiotensinogen is a component of the renin-angiotensin system (RAS), a hormone system that regulates blood pressure and fluid balance. It is also known as the renin substrate, and is a non-inhibitory member of the serpin family of proteinase inhibitors (MEROPS inhibitor family I4, clan ID, MEROPS identifier I04.953).Angiotensinogen is catalytically cleaved by renin to produce angiotensin I in response to lowered blood pressure. Angiotensin converting enzyme (ACE), subsequently removes a dipeptide to produce angiotensin II, the physiologically active peptide, which functions in the regulation of volume and mineral balance of body fluids [, ]. Angiotensin I and angiotensin II can be further processed to generate angiotensin III, which stimulates aldosterone release [], and angiotensin IV. Angiotensin 1-9 is cleaved from angiotensin-1 by ACE2 []and can be further processed by ACE to produce angiotensin 1-7, angiotensin 1-5 and angiotensin 1-4 [, ].Angiotensinogen is synthesised in the liver and secreted in plasma [, , , ]. Angiotensinogen appears to be associated with a predisposition to essential hypertension; it is also associated with pregnancy-induced hypertension (pih) (preeclampsia), a heterogeneous disorder that complicates 5-7% of all pregnancies and remains a leading cause of maternal, foetal and neonatal morbidity and mortality [].The entry represents the full precursor sequence of angiotensinogen. |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
Angiotensinogen is a component of the renin-angiotensin system (RAS), a hormone system that regulates blood pressure and fluid balance. It is also known as the renin substrate, and is a non-inhibitory member of the serpin family of proteinase inhibitors (MEROPS inhibitor family I4, clan ID, MEROPS identifier I04.953).Angiotensinogen is catalytically cleaved by renin to produce angiotensin I in response to lowered blood pressure. Angiotensin converting enzyme (ACE), subsequently removes a dipeptide to produce angiotensin II, the physiologically active peptide, which functions in the regulation of volume and mineral balance of body fluids [, ]. Angiotensin I and angiotensin II can be further processed to generate angiotensin III, which stimulates aldosterone release [], and angiotensin IV. Angiotensin 1-9 is cleaved from angiotensin-1 by ACE2 []and can be further processed by ACE to produce angiotensin 1-7, angiotensin 1-5 and angiotensin 1-4 [, ].Angiotensinogen is synthesised in the liver and secreted in plasma [, , , ]. Angiotensinogen appears to be associated with a predisposition to essential hypertension; it is also associated with pregnancy-induced hypertension (pih) (preeclampsia), a heterogeneous disorder that complicates 5-7% of all pregnancies and remains a leading cause of maternal, foetal and neonatal morbidity and mortality [].This entry represents the serpin domain of angiotensinogen. |
|
•
•
•
•
•
|
Publication |
First Author: |
Kowalczuk S |
Year: |
2008 |
Journal: |
FASEB J |
Title: |
A protein complex in the brush-border membrane explains a Hartnup disorder allele. |
Volume: |
22 |
Issue: |
8 |
Pages: |
2880-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Fairweather SJ |
Year: |
2015 |
Journal: |
J Biol Chem |
Title: |
Molecular basis for the interaction of the mammalian amino acid transporters B0AT1 and B0AT3 with their ancillary protein collectrin. |
Volume: |
290 |
Issue: |
40 |
Pages: |
24308-25 |
|
•
•
•
•
•
|
Publication |
First Author: |
Danilczyk U |
Year: |
2006 |
Journal: |
Nature |
Title: |
Essential role for collectrin in renal amino acid transport. |
Volume: |
444 |
Issue: |
7122 |
Pages: |
1088-91 |
|
•
•
•
•
•
|
Publication |
First Author: |
Sun J |
Year: |
2020 |
Journal: |
Cell |
Title: |
Generation of a Broadly Useful Model for COVID-19 Pathogenesis, Vaccination, and Treatment. |
Volume: |
182 |
Issue: |
3 |
Pages: |
734-743.e5 |
|
•
•
•
•
•
|
Publication |
First Author: |
Hassan AO |
Year: |
2020 |
Journal: |
Cell |
Title: |
A SARS-CoV-2 Infection Model in Mice Demonstrates Protection by Neutralizing Antibodies. |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Brann DH |
Year: |
2020 |
Journal: |
Sci Adv |
Title: |
Non-neuronal expression of SARS-CoV-2 entry genes in the olfactory system suggests mechanisms underlying COVID-19-associated anosmia. |
Volume: |
6 |
Issue: |
31 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Biering SB |
Year: |
2022 |
Journal: |
Nat Genet |
Title: |
Genome-wide bidirectional CRISPR screens identify mucins as host factors modulating SARS-CoV-2 infection. |
Volume: |
54 |
Issue: |
8 |
Pages: |
1078-1089 |
|
•
•
•
•
•
|
Publication |
First Author: |
Fumagalli V |
Year: |
2024 |
Journal: |
Nat Immunol |
Title: |
Antibody-independent protection against heterologous SARS-CoV-2 challenge conferred by prior infection or vaccination. |
Volume: |
25 |
Issue: |
4 |
Pages: |
633-643 |
|
•
•
•
•
•
|
Publication |
First Author: |
Spalinger MR |
Year: |
2020 |
Journal: |
bioRxiv |
Title: |
Identification of a Novel Susceptibility Marker for SARS-CoV-2 Infection in Human Subjects and Risk Mitigation with a Clinically Approved JAK Inhibitor in Human/Mouse Cells. |
|
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Benjakul S |
Year: |
2023 |
Journal: |
PNAS Nexus |
Title: |
A pan-SARS-CoV-2-specific soluble angiotensin-converting enzyme 2-albumin fusion engineered for enhanced plasma half-life and needle-free mucosal delivery. |
Volume: |
2 |
Issue: |
12 |
Pages: |
pgad403 |
|
•
•
•
•
•
|
Publication |
First Author: |
Abdelfattah AS |
Year: |
2023 |
Journal: |
Neuron |
Title: |
Sensitivity optimization of a rhodopsin-based fluorescent voltage indicator. |
Volume: |
111 |
Issue: |
10 |
Pages: |
1547-1563.e9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chong Z |
Year: |
2022 |
Journal: |
Cell Rep |
Title: |
Nasally delivered interferon-λ protects mice against infection by SARS-CoV-2 variants including Omicron. |
Volume: |
39 |
Issue: |
6 |
Pages: |
110799 |
|
•
•
•
•
•
|
Publication |
First Author: |
Wu CT |
Year: |
2023 |
Journal: |
Cell |
Title: |
SARS-CoV-2 replication in airway epithelia requires motile cilia and microvillar reprogramming. |
Volume: |
186 |
Issue: |
1 |
Pages: |
112-130.e20 |
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•
•
•
•
•
|
Publication |
First Author: |
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2022 |
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Front Immunol |
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2022 |
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bioRxiv |
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2021 |
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Cell Rep |
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2022 |
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Cell Rep |
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2021 |
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iScience |
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2022 |
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PLoS Pathog |
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Cell Rep |
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Front Microbiol |
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Year: |
2022 |
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PLoS Pathog |
Title: |
A broadly neutralizing monoclonal antibody overcomes the mutational landscape of emerging SARS-CoV-2 variants of concern. |
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18 |
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Cell Rep |
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37 |
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2021 |
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J Exp Med |
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218 |
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2021 |
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Elife |
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10 |
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2022 |
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Cell Rep |
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Viral E protein neutralizes BET protein-mediated post-entry antagonism of SARS-CoV-2. |
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