ライフサイエンスコーパス: molecular motor protein

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1 osite orientation are spatially separated by molecular motor proteins.

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

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

4 ndent chromatin remodeling by four different molecular motor proteins.

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

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

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

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

9 Molecular motor proteins are crucial for the proper dist

10 Molecular motor proteins are responsible for long-range

11 Kinesin molecular motor proteins are responsible for many of the

12 Molecular motor proteins are ubiquitous in nature and ha

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

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

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

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

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

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

19 Because molecular motor proteins have been implicated in a wide

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

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

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

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

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

25 The molecular motor protein myosin VI moves toward the minus

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

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

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

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

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

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

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

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

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

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

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

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

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

39 DBPs are molecular motor proteins that utilize chemical energy in

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

41 Molecular motor proteins use the energy released from AT

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