ライフサイエンスコーパス: molecular motor protein

1 NF2-like ATP-dependent nucleosome remodeling molecular motor proteins.

2 osite orientation are spatially separated by molecular motor proteins.

3 ndent chromatin remodeling by four different molecular motor proteins.

4 atable forces imposed on the microtubules by molecular motor proteins.

5 ors Bach1 and 2, as well as cytoskeletal and molecular motor proteins.

6 The movement of a molecular motor protein along a cytoskeletal track requi

7 Myosins are a superfamily of actin-dependent molecular motor proteins, among which the bipolar filame

8 affect microtubule-related proteins such as molecular motor proteins and microtubule severing enzyme

9 Both ATP-driven molecular motor proteins are able to translocate nucleos

10 Molecular motor proteins are crucial for the proper dist

11 Molecular motor proteins are responsible for long-range

12 Kinesin molecular motor proteins are responsible for many of the

13 Molecular motor proteins are ubiquitous in nature and ha

14 The reliability by which molecular motor proteins convert undirected energy input

15 e 5 (AdV5) capsid protein hexon recruits the molecular motor protein cytoplasmic dynein in a pH-depen

16 er particles along microtubules requires the molecular motor protein dynein.

17 ransport by reducing the dosage of a kinesin molecular motor protein enhanced the frequency of axonal

18 rete molecular photodynamic steps, action of molecular motors, protein folding, diffusion, etc. down

19 g myosin heavy chain 7 (Myh7), which encodes molecular motor proteins for heart contraction.

20 Evidence suggests that fast molecular motor proteins have a role in slow axonal tran

21 Because molecular motor proteins have been implicated in a wide

22 be adequate to explain observed behavior of molecular motor proteins in the presence of applied forc

23 The myosin superfamily of molecular motor proteins includes conventional myosins a

24 ly requires the combined activity of various molecular motor proteins, including Eg5 and dynein.

25 merization studies, MT-based GLUT4 movement, molecular motor proteins involved in GLUT4 trafficking,

26 Structurally, this molecular motor protein is a tetrameric complex composed

27 dritic localization of ADEPTR is mediated by molecular motor protein Kif2A.

28 r (syd), which has been proposed to link the molecular motor protein kinesin-1 to axonal vesicles.

29 The molecular motor protein myosin VI moves toward the minus

30 We find that the molecular motor protein myosin-1c (Myo1c) regulates the

31 Here, we show that a molecular motor protein, myosin Va, is present in high p

32 enetic variants in the gene that encodes the molecular motor protein nonmuscle myosin 2a (MYH9) with

33 normal amounts of microtubule-associated and molecular motor proteins, organelles, and vesicles.

34 To test the hypothesis that fast anterograde molecular motor proteins power the slow axonal transport

35 patterns may arise from a redistribution of molecular motor proteins previously used for mitosis of

36 iquitous in bacteria and play a dual role as molecular motor proteins responsible for branch migratio

37 Here, we examined the role of KIF16B, the molecular motor protein that directs outward movement of

38 Kinesin-1 is a molecular motor protein that transports cargo along micr

39 nd protein kinase C isozymes and then on the molecular motor proteins that function downstream to dri

40 Kinesins are a group of related molecular motor proteins that have great potential as ta

41 g most members of the kinesin superfamily of molecular motor proteins that is critical for kinesin's

42 in axons and dendrites primarily depends on molecular motor proteins that move along the cytoskeleto

43 ed by a number of microtubule-associated and molecular motor proteins that sort microtubules into bun

44 DBPs are molecular motor proteins that utilize chemical energy in

45 Hexameric helicases are molecular motor proteins that utilize energy obtained fr

46 Molecular motor proteins use the energy released from AT