ライフサイエンスコーパス: mitotic apparatus

1 otting the presence of galectin-8 within the mitotic apparatus.

2 logous to motor proteins associated with the mitotic apparatus.

3 osomes being dependent on a fully functional mitotic apparatus.

4 as an integral biophysical component of the mitotic apparatus.

5 otubules and the midzone microtubules of the mitotic apparatus.

6 the microtubular cytoskeleton, including the mitotic apparatus.

7 -based forces to asymmetrically position the mitotic apparatus.

8 gate their chromosomes without a conspicuous mitotic apparatus.

9 ell extracts and colocalized with MTs in the mitotic apparatus.

10 in the localization of cyclin B1 mRNA to the mitotic apparatus.

11 esult from changes in the orientation of the mitotic apparatus.

12 eld acts directly on the microtubules of the mitotic apparatus.

13 er because it unbalances the elements of the mitotic apparatus.

14 nd may function as components of a bacterial mitotic apparatus.

15 By maintaining SAC proteins near the mitotic apparatus, An-Mlp1 may help monitor mitotic prog

16 hat cyclin D1 can induce deregulation of the mitotic apparatus and aneuploidy, effects that could con

17 l forces are essential for building a robust mitotic apparatus and correcting inappropriate chromosom

18 lation is important for the integrity of the mitotic apparatus and for cell division.

19 s mRNA results in a morphologically abnormal mitotic apparatus and inhibited cell division.

20 specifically localized to the midzone of the mitotic apparatus and phragmoplast.

21 nd DNA, nuclear matrix protein NuMA (Nuclear mitotic apparatus), and splicing factors Sm and SC35 per

22 ation of a survivin-caspase-9 complex on the mitotic apparatus, and caspase-9-dependent apoptosis of

23 the cyclin-dependent kinase p34(cdc2) on the mitotic apparatus, and is phosphorylated on Thr(34) by p

24 hanisms that link cell-cycle controls to the mitotic apparatus are poorly understood.

25 shown previously that many components of the mitotic apparatus are present and functional in GNU embr

26 A 62-kDa (p62) mitotic apparatus-associated protein is important for th

27 A (Nu-clear protein that associates with the Mitotic Apparatus) at the polar ends of the mammalian mi

28 has been delivered to the cortex, the entire mitotic apparatus can be removed without affecting cell

29 Microtubules of the mitotic apparatus determine the position at which the cy

30 sion cells but much stronger staining of the mitotic apparatus during division.

31 to the centrosome during interphase and the mitotic apparatus during mitosis.

32 3T3 cells, while it becomes localized to the mitotic apparatus during mitosis.

33 Associating with the mitotic apparatus, EB1 may play a physiologic role conne

34 PV E2C is critical for localization with the mitotic apparatus, enabling the HPV DNA to sustain persi

35 A as it replicates and lack a eukaryote-like mitotic apparatus for segregating chromosomes.

36 ganized, pronuclear migration fails, and the mitotic apparatus forms at the posterior, orients incorr

37 lear theca, and the exclusion of the nuclear mitotic apparatus from the decondensing sperm nuclear ap

38 cell death pathways, insulator function, and mitotic apparatus function.

39 pression at mitosis and association with the mitotic apparatus have been of interest to cell biologis

40 We show that an elastic membrane around the mitotic apparatus helps to focus MT minus ends and provi

41 erentially localize to key structures of the mitotic apparatus in a cell cycle-dependent manner.

42 The discovery of a mitotic apparatus in bacteria has led to significant rec

43 ll elongation, suggesting the existence of a mitotic apparatus in bacteria.

44 uclear matrix, centrosomes, and parts of the mitotic apparatus in dividing cells.

45 GEF-H1 localized to the mitotic apparatus in HeLa cells, particularly at the tip

46 for activation of the Pins(TPR)-Mud (nuclear mitotic apparatus in mammals) spindle orientation pathwa

47 ell as spearheaded integrative models of the mitotic apparatus in particular and regulation of the mi

48 critical for this protein to localize on the mitotic apparatus in somatic cells.

49 Sea urchin EMAP localizes to the mitotic apparatus in vivo and modifies the assembly dyna

50 f CDK1, a single focus of the phosphonuclear mitotic apparatus is observed, but it is not focused in

51 In animal cells, microtubules (MTs) of the mitotic apparatus (MA) communicate with the cell cortex

52 Astral microtubules (MTs) emanating from the mitotic apparatus (MA) during anaphase are required for

53 physically manipulated the proximity of the mitotic apparatus (MA) to the cell cortex in combination

54 osis and its transcripts are associated with mitotic apparatus (MA).

55 cleavage of the CD cell entails a symmetric mitotic apparatus moving and anisotropically growing rig

56 le-mediated transport of Galphai/LGN/nuclear mitotic apparatus (NuMA) complex from cell cortex to spi

57 und to contain autoantibodies to the nuclear mitotic apparatus (NuMA) protein and to several novel nu

58 ss of mitotic function allele of the nuclear mitotic apparatus (NuMA) protein in mice and cultured pr

59 The large nuclear mitotic apparatus (NuMA) protein is an essential player

60 -asparagine repeat protein (LGN) and nuclear mitotic apparatus (NuMA) protein, two essential factors

61 form specifically interacts with the nuclear mitotic apparatus (NuMA) protein.

62 of Drosophila Partner of Inscuteable/nuclear mitotic apparatus (NuMA) ternary complex.

63 Nuclear mitotic apparatus (NuMA), a long microtubule-binding pro

64 ical protein complex, including LGN, nuclear mitotic apparatus (NuMA), and dynein/dynactin, plays a k

65 ins)/LGN, Mushroom Body Defect (Mud)/Nuclear Mitotic Apparatus (NuMa), Galphai, and Dynein, which int

66 Type 1 nuclear mitotic apparatus (NuMA-1) antibodies were identified in

67 gene encodes a kinase that localizes to the mitotic apparatus of a dividing cell.

68 ation-induced translation are present on the mitotic apparatus of animal pole blastomeres in embryos.

69 he centrosome, which contributes both to the mitotic apparatus of the nucleus and to the cilia struct

70 hase and anaphase, suggesting defects in the mitotic apparatus or kinetochore.

71 set of genes identified, we showed that the mitotic apparatus organizing protein DLGAP5 (HURP/DLG7)

72 ic flagellum (undulipodium in her usage) and mitotic apparatus originated from an endosymbiotic, spir

73 on in the Drosophila blastoderm with how the mitotic apparatus positions the cleavage furrow for stan

74 t pattern cortical Galphai, LGN, and nuclear mitotic apparatus protein (NuMA) [3, 7-18].

75 Here, we report that the nuclear mitotic apparatus protein (NuMA) and LANA can associate

76 during mitosis after perturbation of nuclear mitotic apparatus protein (NuMA) and the human homologue

77 soform(s) associate with tubulin and Nuclear Mitotic Apparatus protein (NuMA) in intact HeLa cells in

78 etric distribution of the LGN target nuclear mitotic apparatus protein (NuMa) in Lp/Lp cortical proge

79 Nuclear mitotic apparatus protein (NuMA) is indispensable for th

80 The Nuclear Mitotic Apparatus protein (NuMA) is recruited from inter

81 A carboxyl-terminal region of the nuclear-mitotic apparatus protein (NuMA), a nuclear protein requ

82 rate an interaction between 4.1N and nuclear mitotic apparatus protein (NuMA), a nuclear protein requ

83 2), the LGN- and microtubule-binding nuclear mitotic apparatus protein (NuMA), and Galphai regulate a

84 itotic-spindle organization proteins Nuclear Mitotic Apparatus protein (NuMA), dynein, and dynactin.

85 ect cortical localization of LGN and nuclear-mitotic apparatus protein (NuMA), proteins that generate

86 s of the microtubule binding site of nuclear mitotic apparatus protein (NuMA), which is implicated in

87 hed protein (LGN) and the capture of nuclear mitotic apparatus protein (NuMA)-positive astral microtu

88 (Mud), the Drosophila counterpart of nuclear mitotic apparatus protein (NuMA).

89 ith centrosomes and interaction with nuclear mitotic apparatus protein (NuMA).

90 nes, including the gene encoding the nuclear mitotic apparatus protein (NuMA).

91 te tankyrase partners, including the nuclear/mitotic apparatus protein (NuMA).

92 e show that HPV16 E7 associates with nuclear mitotic apparatus protein 1 (NuMA) and that NuMA binding

93 ed differential proteomics and found nuclear mitotic apparatus protein 1 (NuMA1) is downregulated in

94 umor recognition protein (NKTR), and nuclear mitotic apparatus protein 1 (NUMA1).

95 tionarily conserved ternary complex (nuclear mitotic apparatus protein [NuMA]-LGN-Galpha in human cel

96 nus ends and the localization of the nuclear mitotic apparatus protein at spindle poles when injected

97 instruct the accumulation of LGN and nuclear mitotic apparatus protein at the lateral cortex to ensur

98 damage via a process mediated by the nuclear mitotic apparatus protein NuMA (also known as NUMA1).

99 to the centrosomal protein CEP170 and to the mitotic apparatus protein NuMA, and both CEP170 and NuMA

100 nucleoprotein particle, lamin B, the nuclear mitotic apparatus protein NuMA, DNA topoisomerases I and

101 ntigens (e.g., alpha-fodrin, La, and nuclear mitotic apparatus protein) and tissue-restricted autoant

102 ive spindles have mislocalized NuMA (nuclear mitotic apparatus protein), a 4.1R binding partner essen

103 N (GSPM2), NuMA (microtubule binding nuclear mitotic apparatus protein), and dynein at the metaphase

104 We found that NUMA (nuclear mitotic apparatus protein)-mediated clustering of microt

105 The nuclear mitotic apparatus protein, NuMA, is involved in major ce

106 Nuclear mitotic apparatus protein-retinoic acid receptor alpha (

107 aragine repeat protein (LGN) and the nuclear mitotic apparatus protein.

108 the recently reported role of NuMA (nuclear mitotic apparatus) protein in promoting transcription an

109 kinetochore-microtubule interactions in the mitotic apparatus (see [1] [2] [3] [4] for reviews).

110 or targets of the autoimmune response in the mitotic apparatus, since most of the selected sera (base

111 Whereas microtubules of the mitotic apparatus specify the division site in animal ce

112 ut mitosis, Plk3 appeared to be localized to mitotic apparatus such as spindle poles and mitotic spin

113 The mitotic apparatus then orients so as to cleave the embry

114 periments suggest that the competence of the mitotic apparatus to initiate cytokinesis is not depende

115 le disengagement and targeting NuMA (nuclear mitotic apparatus) to spindle poles.

116 as begun, after which it associates with the mitotic apparatus until the cyclins are degraded in anap

117 Shrinking the mitotic apparatus with colchicine revealed pRLC suppress