ライフサイエンスコーパス: tethering of @3 to

1 on of the liver, initiating steps leading to tethering of polymorphonuclear neutrophil leukocytes to

2 Tethering of Ctp1 to a flexible Nbs1 arm suggests a mech

3 We show that direct tethering of each Rif protein to a telomere shortens tha

4 se 2B uncover an unexpected observation that tethering of phosphatases to a seven-residue sequence of

5 Tethering of Set2 to a heterologous promoter reveals tha

6 othesis that this step is TFIID recruitment, tethering of TBP to a target promoter via a heterologous

7 Tethering of the SUUR protein to a specific site is insu

8 We speculate that intermittent tethering of claudins to actin may allow for accommodati

9 in the in vitro motility assay caused by the tethering of myosin to actin through binding of both the

10 otein ligand-1 (PSGL-1) mediates the initial tethering of leukocytes to activated platelets and endot

11 of Pcr1 is required for hotspot activity and tethering of Atf1 to ade6 promotes recombination in the

12 n cell is accomplished through intracellular tethering of membrane proteins to an extensive, flexible

13 , indicating that Asp(55) is involved in the tethering of the C1a domain to another part of PKC-alpha

14 Tethering of antibodies to both TLR4 and FcgammaRs prove

15 Tethering of plasminogen to cell surfaces controls plasm

16 ly of condensed mitotic chromosomes and that tethering of chromosomal arm regions to centromeres allo

17 a molecular mechanism for LEDGF/p75-mediated tethering of HIV-1 integrase to chromatin.

18 A recent report on the tethering of MLL1 to chromatin binding factor lens epith

19 Furthermore, via pharmacological tethering of proteasomes to chromatin or the plasma memb

20 The tethering of HC to CMFs is modeled in accordance with th

21 tures of archaeal lipids, such as: 1) single tethering of lipid tails to create fully transmembrane t

22 However, tethering of BICD2-N to different membranes promotes the

23 In an in vitro system, tethering of Fab fragments to DNA ends inhibits MRX-medi

24 We also found that direct tethering of KAP1 to DNA was sufficient to repress trans

25 by in situ transcription and intermolecular tethering of RNA to DNA.

26 spatially distinct protein-protein contacts: tethering of the two proteins to each other and formatio

27 opodia, N-WASP stabilized MT1-MMP via direct tethering of its cytoplasmic tail to F-actin.

28 -terminal GRASP domain and mediate homotypic tethering of Golgi cisternae to form extended Golgi ribb

29 After tethering of ER-derived vesicles to Golgi-acceptor membr

30 Therefore, E2-mediated tethering of viral genomes to host chromatin has multipl

31 Ags (listeriolysin O and p60) revealed that tethering of these Ags to Ii markedly improved the vacci

32 ut has been proposed to involve the indirect tethering of LXRs to inflammatory gene promoters.

33 ssociate in cells, allowing NHERF-2-mediated tethering of P2Y(1)R to key downstream effectors such as

34 We propose a mechanism to explain how tethering of the actin cytoskeleton to leukocyte integri

35 These findings suggest that tethering of CheR to MCPs is a relatively recent event i

36 , an octameric protein complex implicated in tethering of vesicles to membranes.

37 virus-host interaction is important for the tethering of BPV E2 to mitotic chromatin and the stable

38 Thus, E2-mediated tethering of viral genomes to mitotic chromosomes is a c

39 on and suggest a signaling pathway involving tethering of MMP-2 to MT1-MMP as a modulator of MMP-9 ex

40 by supplying an excess of E12, and covalent tethering of E47 to MyoD rendered the E-box-dependent tr

41 results are consistent with a model whereby tethering of actin to myosin by caldesmon may play a rol

42 Enforced tethering of CG9754 to nascent messenger RNA transcripts

43 Tethering of Pcf11 to nascent mRNA is sufficient to enha

44 egative mutants of NPRAP designed to disrupt tethering of ABP to NPRAP-cadherin complexes reduced sur

45 In this paper we show that tethering of heterochromatic regions to nuclear landmark

46 antitative models of ER binding that suggest tethering of ER to one-third of cell-specific sites.

47 ich changes function on apoptosis, promoting tethering of dying cells to phagocytes.

48 Tethering of monocytes to platelets and to purified P-se

49 In vitro, activated platelets enhanced tethering of lymphocytes to PNAd and sustained lymphocyt

50 Moreover, artificial tethering of Polkappa to proliferating cell nuclear anti

51 t data hints at a common targeting mechanism-tethering of integration complexes to proteins bound at

52 the membrane component of exosite-dependent tethering of substrate to prothrombinase and a relaxatio

53 dicating phosphorylated Rpt6 may promote the tethering of proteasomes to scaffolds and cytoskeletal c

54 Strikingly, artificial tethering of Ncoa6 to Sd is sufficient to promote tissue

55 Our observations suggest a role for membrane tethering of p59/GRASP55 to select transmembrane protein

56 dent component of segregation; the symmetric tethering of plasmid sisters to sister chromatids embodi

57 ocyst, which has been implicated in specific tethering of vesicles to sites of polarized exocytosis.

58 Co-immunoprecipitation studies revealed tethering of C/EBPbeta to Sp1 by E(2)-activated ERalpha.

59 protein complex that has been implicated in tethering of secretory vesicles to specific regions on t

60 tibodies blocking Mac-1 function allowed the tethering of PMN to targets with hu14.18/GM-CSF but prev

61 Furthermore, the tethering of p28II directly to tax/rex mRNA resulted in

62 Only tethering of alpha5beta1 to the substrate was required f

63 Tethering of an ammonium group to the hydrogen bond dono

64 y with spliced beta-globin mRNA in vivo, and tethering of any hUpf protein to the 3'UTR of beta-globi

65 binding pocket that results in the stronger tethering of B25-B28 residues to the protein core.

66 tition can be completely blocked by covalent tethering of CaM to the channel.

67 to heterochromatic regions and promotes the tethering of centromeric DNA to the SUN-KASH complex.

68 og pairing is an active process in which the tethering of chromosome sites to the NE may be necessary

69 Mitosis begins with the tethering of chromosomes to the mitotic spindle and thei

70 TRAPPI is a large complex that mediates the tethering of COPII vesicles to the Golgi (heterotypic te

71 L-Cys-AMP formation and subsequent covalent tethering of Cys to the phosphopantetheinyl arm of the t

72 ike Sec35p, which has been implicated in the tethering of ER-derived vesicles to the Golgi, Sec34p is

73 yst, a conserved protein complex involved in tethering of exocytic vesicles to the plasma membrane, r

74 Furthermore, it indicates that the tethering of FtsZ to the membrane shows sufficient plast

75 Here we reconstitute the tethering of FtsZ to the membrane via FtsA's C-terminal

76 en together, these results indicate that the tethering of G(alpha)(s) to the beta(2)AR causes a confo

77 Tethering of GABARAP to the Golgi by GM130 inhibits auto

78 t that the N-terminal region is important in tethering of GCAP1 to the ROS membranes.

79 We devised an approach for inducible tethering of genes to the inner nuclear membrane (INM),

80 cruits a paranodal complex implicated in the tethering of glial proteins to the axonal membrane and c

81 ex/SAP97 axis plays an important role in the tethering of Glut4 vesicles to the plasma membrane in ad

82 Thus, the tethering of GR to the GnRH distal nGRE, by virtue of a

83 e DNA-binding-independent mechanism involves tethering of GR to the pro-inflammatory transcription fa

84 component of HDL CE selective uptake is the tethering of HDL particles to the cell surface.

85 Moreover, NPM1 was required for efficient tethering of HP1gamma-enriched chromatin to the nucleolu

86 Tethering of LexA-Sir3p adjacent to the telomere is suff

87 tein involved in mitochondrial fusion and in tethering of mitochondria to the endoplasmic reticulum.

88 Together, our results indicate that tethering of MUC5AC-containing domains to the epithelium

89 Further, Cas9-directed tethering of mutant LDB1 to the beta-globin promoter for

90 the Pam18:Pam16 interaction is the physical tethering of Pam18 to the translocon via its interaction

91 We also demonstrate that tethering of peroxisomes to the ER is necessary for pero

92 These findings indicate that tethering of primase to the replisome by pol alpha is cr

93 vivo and suggest that SHP-1 may regulate the tethering of receptors to the cytoskeleton and/or the ex

94 sly studied redox hydrogels results from the tethering of redox centers to the backbone of the cross-

95 usly suggested that this process may involve tethering of ribosomal complexes to the mRNA, in which t

96 vidence of subdiffusion, as would arise from tethering of ribosomes to the DNA.

97 Instead, the tethering of SCF(Dia2) to the replisome progression comp

98 The exocyst complex is required for tethering of secretory vesicles to the apical plasma mem

99 Finally, we demonstrate that tethering of Sir2 is pivotal to the maintenance of heter

100 r chromosome segregation in mitosis requires tethering of spindle microtubules to the kinetochore.

101 Channel formation is further enhanced by tethering of TeNT to the membrane through ganglioside co

102 d constriction of the cell surface through a tethering of the actinomyosin cytoskeleton to the apical

103 Tethering of the arene to the arylsilane provides not on

104 Likely driving forces may include tethering of the C-terminus to the lipid membrane, as we

105 the GTPase Rab8a and the exocyst complex in tethering of the contractile vacuole to the plasma membr

106 hanism entails more than a simple mechanical tethering of the enzyme to the outer face of the inner m

107 t) are ER-anchored proteins that mediate the tethering of the ER to the PM and are thought to mediate

108 LANA is required for tethering of the KSHV episome to the host chromosomes an

109 cessing pathways are identified that require tethering of the metalloproteinase to the cell surface.

110 entally simple steps: (i) it allows for fast tethering of the photoactive core to the unsaturated pen

111 Tethering of the released fluorophore to the cellulose s

112 shment of latent episome maintenance through tethering of the viral genome to the host chromosomes.

113 Tethering of TPP1 to the telomere either via TRF2-TIN2 o

114 Tethering of U1 snRNP to the target pre-mRNA inhibits po

115 overy of vesicles from endosomes, and in the tethering of vesicles to the cytoskeleton.

116 on of E2 with Brd4 is required to ensure the tethering of viral genomes to the host mitotic chromosom

117 ient virus transmission is not simply due to tethering of virus to the cell surface.

118 Tethering of VKD proteins to the carboxylase allows clus

119 Tethering of VKD proteins to the carboxylase via the pro

120 ansferase complexes and is implicated in the tethering of Setd1 complexes to transcriptional start si

121 dependent adhesion by increasing the initial tethering of leukocytes to vascular surfaces and by stre

122 Additionally, artificial tethering of YTHDC1 to XIST rescues XIST-mediated silenc