ライフサイエンスコーパス: CAEV

コーパス検索結果 (left1)

通し番号をクリックするとPubMedの該当ページを表示します

1 eutralizing antibody titers against CAEV-63, CAEV-Co, and CAEV-1g5 compared to titers of SU-W-immuniz

2 oss-reactive neutralizing antibodies against CAEV-Co, a virus isolate closely related to CAEV-63, and

3 ease in neutralizing antibody titers against CAEV-63, CAEV-Co, and CAEV-1g5 compared to titers of SU-

4 irus isolate closely related to CAEV-63, and CAEV-1g5, an isolate geographically distinct from CAEV-6

5 ntibody titers against CAEV-63, CAEV-Co, and CAEV-1g5 compared to titers of SU-W-immunized goats.

6 structural and functional parallels between CAEV gp135 and HIV-1 gp120 that may be more broadly appl

7 Replication-defective CAEV proviral constructs lacking the env, tat, and vif g

8 proviral constructs and plasmids expressing CAEV, MVV, or vesicular stomatitis virus envelope glycop

9 1g5, an isolate geographically distinct from CAEV-63, were determined.

10 Epitope mapping of sera from CAEV-infected goats localized immunodominant linear epit

11 FN-gamma in the context of both a functional CAEV LTR and a heterologous promoter.

12 ith the envelope glycoproteins of MVV K1514, CAEV CO, and lytic and nonlytic North American MVV strai

13 f caprine arthritis-encephalitis lentivirus (CAEV-63).

14 trast, functional receptors for the nonlytic CAEV CO are absent from human cells.

15 ptomatic goats have a dominant population of CAEV SU-reactive T-helper 1 (Th1)-like lymphocytes in PB

16 c MVV receptors and the narrow host range of CAEV.

17 es in the putative virion-proximal region of CAEV gp135 comprising putative beta-strands 4, 5, and 25

18 following in vitro stimulation with purified CAEV gp135 surface protein (SU).

19 tis-encephalitis virus long terminal repeat (CAEV LTR).

20 d-type and modified SU-induced type-specific CAEV-63 neutralizing antibodies and cross-reactive neutr

21 expression of IFN-gamma cDNA promoted by the CAEV LTR was confirmed by the intramuscular (IM) injecti

22 nstrate that the putative GAS element in the CAEV LTR binds specifically to a cellular factor induced

23 Thus, the GAS sequence in the CAEV LTR is essential for the response to IFN-gamma and

24 the nuclear factor to the GAS element in the CAEV LTR is inhibited by antibody directed against STAT1

25 at least one mechanism for activation of the CAEV LTR by IFN-gamma in monocytes.

26 ssary and sufficient for the response of the CAEV LTR to this cytokine.

27 CAEV-Co, a virus isolate closely related to CAEV-63, and CAEV-1g5, an isolate geographically distinc

28 ted, unlike the Icelandic MVV and similar to CAEV, were limited to cells of ruminant species, regardl

29 wo modified SU (SU-M and SU-T) and wild-type CAEV-63 SU (SU-W) were produced in vaccinia virus and ut

30 us and caprine arthritis-encephalitis virus (CAEV) and human immunodeficiency virus type 1 (HIV-1) gp

31 V) and caprine arthritis-encephalitis virus (CAEV) cause encephalitis, progressive pneumonia, arthrit

32 The caprine arthritis-encephalitis virus (CAEV) long terminal repeat (LTR) is activated by gamma i

33 ivirus caprine arthritis-encephalitis virus (CAEV) were evaluated by semiquantitative reverse transcr

WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。