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1 ouse (Peromyscus maniculatus), infected with Sin Nombre virus.
2 other HPS-associated hantaviruses, including Sin Nombre virus.
3 ntaviruses, including Andes virus (ANDV) and Sin Nombre virus, cause a distinct zoonotic disease, han
4 cessfully passaged a mouse-adapted strain of Sin Nombre virus from deer mice (Peromyscus maniculatus)
5 ombinant PCMV was constructed that contained Sin Nombre virus glycoprotein G1 (SNV-G1) fused in frame
6 d to clarify the involvement of Cdc42 in the Sin Nombre virus internalization and the signaling pathw
7 of virus assembly was recently described for Sin Nombre virus, it is likely that all of the new Ameri
11 served nucleotides of the panhandle, whereas Sin Nombre virus N requires the first 23 nucleotides for
13 he Andes, Puumala, Prospect Hill, Seoul, and Sin Nombre viruses recognize their individual homologous
14 ibition of host autophagy machinery inhibits Sin Nombre virus replication in cells, suggesting that a
15 e deer mouse with its homologous hantavirus, Sin Nombre virus, results in low levels of immune gene e
16 rdiopulmonary syndrome (HCPS), we quantified Sin Nombre virus S segment viral RNA in plasma samples f
18 f the core domains of NP (NPcore) encoded by Sin Nombre virus (SNV) and Andes virus (ANDV), which are
23 sid (N) proteins of hantaviruses such as the Sin Nombre virus (SNV) bind to membranes and viral RNAs,
25 a zoonotic disease caused by transmission of Sin Nombre virus (SNV) from chronically infected deer mi
26 , a laboratory animal model for the study of Sin Nombre virus (SNV) infection or associated disease h
35 ing of inactivated and fluorescently labeled Sin Nombre virus (SNV) to the integrin PSI domain stimul
37 n with HPS-associated hantaviruses, NY-1 and Sin Nombre virus (SNV), is inhibited by antibodies to be
38 s maniculatus) are the natural reservoirs of Sin Nombre virus (SNV), the etiologic agent of most HCPS
39 e we show that rhesus macaques infected with Sin Nombre virus (SNV), the primary etiological agent of
40 igate early events in the innate response to Sin Nombre virus (SNV), the principal etiologic agent of
41 cases of HCPS in North America are caused by Sin Nombre virus (SNV), which is carried asymptomaticall
42 ar responses in both Andes virus (ANDV)- and Sin Nombre virus (SNV)-infected A549 and Huh7-TLR3 cells
46 er mice are the principal reservoir hosts of Sin Nombre virus, the etiologic agent of most hantavirus
47 eer mice can be experimentally infected with Sin Nombre virus, which now allows provocative examinati