scholarly article | Q13442814 |
P356 | DOI | 10.1016/J.VIRUSRES.2007.03.011 |
P8608 | Fatcat ID | release_onghbjnguferld7rblgwbfkype |
P932 | PMC publication ID | 7114319 |
P698 | PubMed publication ID | 17448558 |
P50 | author | Lorne Babiuk | Q6681421 |
P2093 | author name string | Martin Petric | |
Alexander N Zakhartchouk | |||
Igor Moshynskyy | |||
Vladislav Lobanov | |||
Sathiyanarayanan Viswanathan | |||
Natalia Vasilenko | |||
P2860 | cites work | Nuclear envelope permeability | Q22122423 |
CRM1 is an export receptor for leucine-rich nuclear export signals | Q27860453 | ||
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CRM1 is responsible for intracellular transport mediated by the nuclear export signal | Q29547861 | ||
The Genome sequence of the SARS-associated coronavirus | Q29619007 | ||
Leptomycin B is an inhibitor of nuclear export: inhibition of nucleo-cytoplasmic translocation of the human immunodeficiency virus type 1 (HIV-1) Rev protein and Rev-dependent mRNA | Q29620175 | ||
Evidence for a role of CRM1 in signal-mediated nuclear protein export | Q29620231 | ||
B-cell responses in patients who have recovered from severe acute respiratory syndrome target a dominant site in the S2 domain of the surface spike glycoprotein | Q31149856 | ||
A severe acute respiratory syndrome-associated coronavirus-specific protein enhances virulence of an attenuated murine coronavirus | Q33930434 | ||
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Switching species tropism: an effective way to manipulate the feline coronavirus genome | Q34857052 | ||
The severe acute respiratory syndrome | Q35610030 | ||
The nuclear pore complex: the gateway to successful nonviral gene delivery | Q36416930 | ||
Transmissible gastroenteritis coronavirus gene 7 is not essential but influences in vivo virus replication and virulence. | Q40653676 | ||
Heat-stable inhibitors of cAMP-dependent protein kinase carry a nuclear export signal. | Q41408510 | ||
Subcellular localization of CrmA: identification of a novel leucine-rich nuclear export signal conserved in anti-apoptotic serpins. | Q42157217 | ||
The crystal structure of ORF-9b, a lipid binding protein from the SARS coronavirus. | Q42691537 | ||
SARS corona virus peptides recognized by antibodies in the sera of convalescent cases | Q43691969 | ||
Coronaviral hypothetical and structural proteins were found in the intestinal surface enterocytes and pneumocytes of severe acute respiratory syndrome (SARS). | Q44289899 | ||
Cytoplasmic localization of mitogen-activated protein kinase kinase directed by its NH2-terminal, leucine-rich short amino acid sequence, which acts as a nuclear export signal | Q45300833 | ||
Antibody responses to individual proteins of SARS coronavirus and their neutralization activities | Q47801038 | ||
P433 | issue | 1 | |
P921 | main subject | Protein 9b [SARS-Cov] | Q88365865 |
SARS-CoV-1 | Q85438966 | ||
P304 | page(s) | 116-121 | |
P577 | publication date | 2007-04-19 | |
P1433 | published in | Virus Research | Q15749215 |
P1476 | title | Intracellular localization of the SARS coronavirus protein 9b: evidence of active export from the nucleus | |
P478 | volume | 127 |
Q38226293 | Accessory proteins of SARS-CoV and other coronaviruses |
Q38766707 | Continuous and Discontinuous RNA Synthesis in Coronaviruses |
Q33921025 | SARS-CoV 9b protein diffuses into nucleus, undergoes active Crm1 mediated nucleocytoplasmic export and triggers apoptosis when retained in the nucleus |
Q30588597 | SARS-coronavirus open reading frame-9b suppresses innate immunity by targeting mitochondria and the MAVS/TRAF3/TRAF6 signalosome |
Q107329242 | Selinexor, a novel selective inhibitor of nuclear export, reduces SARS-CoV-2 infection and protects the respiratory system in vivo |
Q43800914 | Severe acute respiratory syndrome coronavirus accessory proteins 6 and 9b interact in vivo. |
Q36747726 | Severe acute respiratory syndrome coronavirus protein 6 accelerates murine hepatitis virus infections by more than one mechanism. |
Q37099656 | Severe acute respiratory syndrome coronavirus protein 6 is required for optimal replication |
Q24605877 | The role of severe acute respiratory syndrome (SARS)-coronavirus accessory proteins in virus pathogenesis |
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