ライフサイエンスコーパス: is required

1 CaMKI is required and serves as both a PINK1 and Parkin kinase.

2 o substantial interannual variability, a 25% load reduction is required before there is 95% certainty of observing any hy

3 esulting from multiple interdependent phosphorylation sites is required for a GC-A conformation capable of transmitting t

4 KL controls the expression of 3BP2, an adapter protein that is required for activation of SRC tyrosine kinase and simulta

5 BPTF is required for anterior-posterior axis formation of the mous

6 Coordination between osteoblasts and osteoclasts is required for bone health and homeostasis.

7 unit of the mammalian SWI/SNF chromatin-remodeling enzymes, is required for both myoblast proliferation and differentiati

8 PRC2 is required for chromatin reprogramming in the germline, and

9 namic induction of DLL4 transcription and that this pathway is required for DLL4 expression.

10 ific but necessarily weak binding of tropomyosin to F-actin is required for effective thin filament function.

11 s not essential for H3-H4 tetrasome deposition in vitro, it is required for efficient DNA synthesis-coupled nucleosome as

12 Together, these data demonstrate that H2A.Z is required for efficient pre-mRNA splicing and indicate a ro

13 Our results altogether suggest that MSRB8 function is required for ETI and containment of stress-induced cell de

14 out the need for collimated or polarised incident light, as is required for existing methods.

15 Thus, mTORC1 activation is required for fueling B cells prior to DZ proliferation rat

16 ata suggest that controlled but not constitutive activation is required for gonococcal infection in mice.

17 chores mature through Ska complex recruitment and that this is required for improved load-bearing capacity and silencing

18 ugh dispensable for homeostatic Th17 cell development, JunB is required for induction and maintenance of Th17 effector re

19 fic ablation of eIF2alphaP and demonstrated that eIF2alphaP is required for induction of ATF4 protein synthesis in vivo i

20 mentation test results suggest that phosphorylation of EMS1 is required for its function in anther development.

21 Mechanistically, CD2AP is required for mechanosensitive ICAM-1 downstream signaling

22 One such nuclear receptor is DAF-12, which is required for normal nematode development, including the al

23 Finally, we found that ST8Sia-IV autopolysialylation is required for NRP-2 polysialylation and that ST8Sia-II auto

24 Here we show that the INO80 chromatin remodeling complex is required for oncogenic transcription and tumor growth in n

25 activity of SWR, whereas an acidic region at the N-terminus is required for optimal SWR function.

26 coactivator with PDZ-binding motif (TAZ) expression, which is required for osteoblast proliferation and differentiation

27 First, after DSB formation, Mer2 is required for pairing by mediating homolog spatial juxtapos

28 Thus, we sought to determine if intrinsic MAVS signaling is required for participation of Tregs in anti-WNV immunity.

29 We show that signalling through the TrpA1 thermo-sensor is required for PMW, and that TrpA1 specifically impacts sies

30 al recordings show that Sema-1a-dependent R axon lamination is required for preventing the spread of synaptic inhibition

31 d DNA is determined by its ATPase domain, that this binding is required for processing protein substrates in nucleoprotei

32 a C2B surface implicated in SNARE complex interaction that is required for rapid synchronization and Ca(2+) cooperativit

33 omal protein uS10 by the E3 ubiquitin ligase Hel2 (or RQT1) is required for RQC.

34 Copper is required for the activity of cytochrome c oxidase (COX), t

35 Ls is an integral component of axon-glial communication and is required for the function and maturation of OLs to promote

36 We also found that the extracellular domain of IL1RAPL1 is required for this effect, independently of the interaction

37 Positive transmural pressure is required for this suction, providing the energy required t

38 e, we show that the Arabidopsis (Arabidopsis thaliana) ADF3 is required in the phloem for controlling infestation by Myzu

39 owever, in applications where a small fluorescence reporter is required or desirable, the choice of fluorophores is rathe

40 ntial dispersion of V. velutina, we conclude that vigilance is required over a large area to prevent the establishment of

41 Because no library preparation is required, the technology permits very efficient use of the

42 MUS81 nucleolytic activity is required to activate compensatory DNA synthesis during mit

43 This study is the first demonstration that an SRRP is required to bind beta-1,4-linked galactose and the first t

44 easonal inundation can account for the emission source that is required to close the Amazon CH4 budget.

45 cardiovascular differences both at baseline and in disease is required to effectively consider and treat all patients wi

46 (Irf4) is highly expressed in murine thymic epithelium and is required to prime thymic epithelial cells (TEC) for effect

47 A borane (e.g., pinacolborane) is required to promote CAH.

48 Our findings indicate that a combination of factors is required to sensitize these regions.

49 n an association between the two groups, although more work is required to show this definitively.

50 Further study is required to test effects of agents that target the NO path