ライフサイエンスコーパス: is required for

1 HopO1-1 is required for P. syringae to spread locally to neighboring

2 PQM-1 is required for the longevity of insulin signaling mutants, b

3 controlled by the PGC family of transcriptional activators is required for angiogenic responses.

4 he synthesis of heparan sulfate, we show that this activity is required for efficient infection by SBV.

5 mogenesis of human acute myeloid leukemia (AML), and ALKBH5 is required for maintaining leukemia stem cell (LSC) function

6 alone is necessary for ZNF165 transcriptional activity and is required for TNBC tumor growth in vivo using an orthotopic

7 ritical regulator of atypical mitosis in the gametogony and is required for mosquito transmission.

8 uclear localization signal (NLS) that binds to importin and is required for its function during cytokinesis.

9 P) is an RNA binding protein that regulates translation and is required for normal cognition.

10 Bcl6 is required for the development of T follicular helper cells

11 -implant conditions according to biological characteristics is required for further BTMs validation and appropriate PIMP

12 We hypothesize that VF coalescence is required for the reassortment of the Birnaviridae This stu

13 Thus, Coq10 is required for the function of Q(6) in respiration and as an

14 11 degradation in vitro, and the DNA-binding ability of CST is required for blocking MRE11-mediated nascent-strand degrad

15 stages of T cell differentiation, while their decommission is required for TCRA locus activation and enforced alphabeta

16 Normally, accessibility to DNA is required for their function.

17 The EACBE is required for long-distance regulation of the Ealpha on the

18 e controls on the distribution and magnitude of earthquakes is required for effective earthquake forecasting.

19 resolved question in the field-whether receptor endocytosis is required for Wnt signal transduction.

20 Curli expression is required for E. coli to exacerbate alphaSyn-induced behavi

21 Thus, LOXL1 expression is required for normal IOP control, while ablation results in

22 Previously, we have demonstrated that the 5-HT(3A)-ICD is required for the interaction between 5-HT(3A) and the chap

23 undant with that of RAD51AP1 in FANCD2 deubiquitination, it is required for efficient HR-mediated chromosome damage repai

24 function experiments in vivo or in cellulo indicate that it is required for Pnr- and Srp-dependent gene expression, sugge

25 Our findings reveal that human METTL15 is required for mitochondrial function, delineate the evoluti

26 The initiation of MSCI is required for stage progression, which enables crossover fo

27 chaperone, microsomal triglyceride transfer protein (MTP), is required for the biosynthesis of these lipoproteins, and i

28 truction complex components in multivesicular bodies (MVBs) is required for sustained canonical Wnt signaling.

29 Our results indicate that the endosomal pathway is required for the signaling cascade initiated by BDNF and i

30 This suggests that the MHC-II antigen presentation pathway is required for PIV-mediated protection against C. burnetii i

31 Mechanistically, PGAM5 is required for mitochondrial fission through dephosphorylati

32 Here, we show that the MA region is required for nuclear import of Gag through the TNPO3 pathw

33 of PIP(3) to the pleckstrin homology (PH) domain of P-Rex1 is required for its activation in cells.

34 lide D and lupinacidin A, an additional ketoreductase RslO8 is required for formation of the main products rishirilide A

35 temperature-sensitive allele (Sac1(ts)), we show that Sac1 is required for structural integrity of the Drosophila retina

36 G protein-coupled receptor signaling is required for the navigation of immune cells along chemoatt

37 d transcriptomic analysis we show that intact SA-signalling is required for potato defences against the necrotrophic fung

38 indicate that intact SA signalling, and not JA signalling, is required for potato defences against the necrotrophic path

39 Phosphorylation at other sites is required for PopP2 but not AvrRps4 responsiveness and faci

40 We have previously shown that TBX1 is required for systemic lymphatic vessel development in pren

41 Farnesylation at the C-terminus is required for hGBP1's activity against microbial pathogens,

42 e tetrapyrrole protoporphyrin IX in order to form heme that is required for growth stimulation and survival in vivo Conse

43 ural and functional insights into an essential protein that is required for organelle-specific trafficking and brain deve

44 ls and of the direct orchestration of their cross-talk that is required for optimal anti-tumour immunity.

45 rin -1 is forebrain axons traversing the midbrain, and this is required for proper GABAergic neuronal migration into the

46 e adult brain, vascular endothelial growth factor D (VEGFD) is required for structural integrity of dendrites and cogniti

47 ed for processing of the sperm surface protein ADAM3, which is required for sperm fertilizing ability.

48 ction, and mRNA export occurs in the absence of Fzo1, which is required for mitochondrial dynamics/respiration.

49 e OsSBEIIb gene encoding starch branching enzyme IIb, which is required for amylopectin synthesis in the endosperm.

50 However, coupling between distant electron spins, which is required for quantum error correction, presents a challeng