ライフサイエンスコーパス: viral membrane fusion

コーパス検索結果 (１語後でソート)

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 ntagonists blocked infection at the level of viral membrane fusion.

2 on at a postendocytic entry step, presumably viral membrane fusion.

3 , thereby lowering the activation energy for viral membrane fusion.

4 iochemical understanding of low-pH-triggered viral membrane fusion.

5 ral role for the N-terminal glycine ridge in viral membrane fusion.

6 disordered (ld) phase boundary to facilitate viral membrane fusion.

7 mbrane ordering is a common prerequisite for viral membrane fusion.

8 To understand the steps in viral membrane fusion, a library of synthetic antibodies

9 p41 envelope glycoprotein, potently inhibits viral membrane fusion and entry.

10 irus envelope, supports the current model of viral membrane fusion and gives insight into the design

11 Since the viral membrane fusion apparatus may open the passages th

12 is required to facilitate the triggering of viral membrane fusion by destabilizing the prefusion con

13 vides an overview of the basic principles of viral membrane fusion common to all enveloped viruses an

14 We observed an inhibition of viral membrane fusion during the entry process by 25HC,

15 lical coiled-coil core relates gB to class I viral membrane fusion glycoproteins; two extended beta h

16 fusion potential of influenza HA, like many viral membrane-fusion glycoproteins, is generated by pro

17 osomal compartment are probably required for viral membrane fusion; however, despite considerable eff

18 oop, a critical and conserved element of the viral membrane fusion machinery, and neutralize viral en

19 that New World arenaviruses exhibit class I viral membrane fusion machinery.

20 nucleopolyhedrovirus (AcMNPV) is a class III viral membrane fusion protein that is triggered by low p

21 (FAST) proteins comprise a unique family of viral membrane fusion proteins dedicated to inducing cel

22 Viral membrane fusion proteins of class I are trimers in

23 The fusion peptides of viral membrane fusion proteins play a key role in the me

24 Structural studies of viral membrane fusion proteins suggest that a "trimer-of

25 ity after PRV infection due to the action of viral membrane fusion proteins, yet it is unclear if suc

26 ardtii HAP2 that reveal homology to class II viral membrane fusion proteins.

27 that the coiled-coil motif occurs in several viral membrane-fusion proteins, including HIV-1 gp41 and

28 overall architecture resembles several other viral membrane-fusion proteins, including those from HIV

29 coil is a common motif found in many diverse viral membrane-fusion proteins.

30 for identifying coiled-coil-like regions in viral membrane-fusion proteins.

31 ace loop at the cleavage site that activates viral membrane fusion reveal structural features primari

32 Despite their diversity, basic principles of viral membrane fusion, simultaneous engagement of both d

33 However, mechanistic viral membrane fusion studies have predominantly focused

34 to a CoRA-dependent decrease in the rate of viral membrane fusion that extends the lifetime of the i

35 HIV-1 glycoprotein Env, which promotes viral membrane fusion through receptor-mediated conforma

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。