ライフサイエンスコーパス: not required

1 ile the folded N-terminal domain and the C-terminal IDR are not required.

2 Randomization was not required.

3 of L-TGF-beta and the release and diffusion of TGF-beta are not required.

4 bon source, such as marine methane clathrates, is therefore not required.

5 efined as a consecutive period in months when treatment was not required because the patient did not meet protocol retrea

6 Other engines that could produce fast radio bursts are not required, but are also not impossible.

7 In contrast, BPN drives straight, forward walking and is not required during courtship.

8 V-1 replication, but in the MT-4 T-cell line the gp41 CT is not required for a spreading infection.

9 Also, N-glycans attached to misfolded AAT are not required for accelerated degradation mediated by the unco

10 s required for full activation of XBP1 targets, but XBP1 is not required for activation of ATF6alpha targets.

11 Avr2 also targets Rcr3 paralog Pip1, which is not required for Avr2 recognition but contributes to basal re

12 Ror was not required for axon regeneration or normal dendrite develop

13 -) recipients, demonstrating that IRF4 expression by cDC is not required for CD4(+) regulatory T cell-mediated control of

14 Our experiment demonstrates that high vacuum is not required for energetic ion acceleration, which relaxes ta

15 development and mating experiments indicate that prokr1b is not required for fertility in zebrafish, although its loss de

16 l or HDAC3/6-selective HDACi, and new protein synthesis was not required for gene suppression by HDACi.

17 the regulation of HPR1 activity in planta, although it was not required for growth under ambient air controlled conditio

18 ude that unlike for host cellular mRNAs, the entire eIF3 is not required for HCV RNA translation, favoring viral expressi

19 ught to be required for the tolerance of abiotic stress, is not required for high rates of photosynthesis and woody bioma

20 ence polarization microscopy to show that cadherin order is not required for hyperadhesion induced by pharmacologic and g

21 ng that transcriptional reprogramming at this time point is not required for immunity to stem rust.

22 Recipient CD4+ T cells were not required for immunoprophylaxis efficacy at baseline, and

23 buted to both CD8+ and CD4+ CAR T cell cytotoxicity but was not required for in vitro or in vivo leukemia clearance.

24 and stability, those that bind to alternate scaffold sites not required for LLPS or that have higher-than-scaffold valen

25 These findings demonstrate that APP family is not required for neuronal survival and suggest that APP famil

26 ESCRT-III components accumulate at the opening but are not required for nuclear closure on their own.

27 TEX15 is predominantly a nuclear protein that is not required for piRNA biogenesis but is essential for piRNA-

28 DEPS-1 is not required for piRNA biogenesis but piRNA-dependent silenci

29 kaging signal (PS), mutagenesis experiments show that PS is not required for production of infectious SFV or Chikungunya

30 xperiments with IL-10(-/-) mice demonstrated that IL-10 was not required for protection against anaphylaxis.

31 required for the displacement of the DETC and that DETC are not required for recruitment of CD8(+) T(RM) cells to the epi

32 Importantly, MASTL kinase activity was not required for regulation of cell spreading or MRTF-A/SRF t

33 hat posttranslational modification by ISG15 (ISGylation) is not required for regulation of the type I IFN response.

34 ctedly, the LC3-lipidation-related functions of ATG16L1 are not required for restricting inclusion development.

35 Moreover, zebrafish Crb1 is not required for retinal morphogenesis and photoreceptor patt

36 Palmitoylation of STING was not required for RV-A16 replication, nor was the C-terminal t

37 vents likely require limited end resection, whereas RNF8 is not required for single-strand annealing repair involving ext

38 ggests that a well-ordered C-terminal beta-barrel domain is not required for TerS(P76-26) to carry out its matchmaking fu

39 The Ctf3 complex (Ctf3c), which is not required for the assembly of most other Ctf19c factors, d

40 assembly in the absence of flwt-Smn, indicating exon 2B is not required for the essential function of Smn.

41 We conclude that SRSF6 is not required for the incomplete splicing of HTT in Huntington

42 CRISPR-mediated gene editing revealed that PKA and AMPK are not required for the starvation-dependent increase in lysosom

43 pharmaceutical inhibition experiments show that H3K27me3 is not required for their silencing in non-2i conditions.

44 Quantitative analysis indicates that the beta3-subunit is not required for this clustering but beta3 does significantly

45 in SCN neurons, but also reveal that diurnal modulation is not required for time-of-day-specific effects on firing and c

46 Localization to P granules is not required for translational repression but is required to

47 howed that the ability to induce a rod-shaped structure was not required for viral replication and spread in cell culture

48 re, in contrast to previous observations, WOX5 mobility was not required to inhibit CSC differentiation.

49 owered transport, however, the proton motive force (PMF) is not required to keep P(i) in the periplasm.

50 Testing is not required to release most patients from isolation.