ライフサイエンスコーパス: cytoplasmic structure

1 layered, liquid crystal-like, semi-synthetic cytoplasmic structure.

2 al role for this enzyme in the regulation of cytoplasmic structure.

3 ponents of the IFN response into NSs-induced cytoplasmic structures.

4 nding kinase 1 (TBK1) into SFTSV NSs-induced cytoplasmic structures.

5 ic fibroblasts localize survivin to distinct cytoplasmic structures.

6 ers the cell and accumulates in vesicle-like cytoplasmic structures.

7 ive antibodies, which recognized nuclear and cytoplasmic structures.

8 ent protein-LC3 from the nucleus to punctate cytoplasmic structures.

9 ealed that it was localized predominantly to cytoplasmic structures.

10 s human orthologue and localizes to punctate cytoplasmic structures.

11 ss of adhesion molecules, even those with no cytoplasmic structures.

12 and RNase P to the nucleolus and to discrete cytoplasmic structures.

13 the nucleus leaving the fluorescent lipid in cytoplasmic structures.

14 but not CRIK-SK, localizes into corpuscular cytoplasmic structures and elicits recruitment of actin

15 actions seen in PduA crystals persist in the cytoplasmic structures and reveal the profound influence

16 d infected cells, mu NS is found in punctate cytoplasmic structures and sigma 3 is distributed diffus

17 that this polypeptide localizes to punctate cytoplasmic structures and to the centrosome during inte

18 eading frame (ORF), traffics to vacuole-like cytoplasmic structures and was shown recently to be esse

19 I to LC3-II, clustering of LC3 into dot-like cytoplasmic structures, and electron microscopic detecti

20 ukaryotic cells are often polarized in their cytoplasmic structures, and this can be important for th

21 2-kinase, which was present in granule-like cytoplasmic structures, and zona occludens 3.

22 )34 protein also accumulated in pleiomorphic cytoplasmic structures at early times and associated wit

23 riboflavin accumulation in membrane-bounded cytoplasmic structures bearing ATP-dependent ABCG2 trans

24 During retraction, cytoplasmic structure became gradually more uniform thro

25 loping germline cysts are spanned by a large cytoplasmic structure called a fusome, containing alpha-

26 These processes occur at a unique cytoplasmic structure called the assembly complex, which

27 hannels by intracellular cues, mediated by a cytoplasmic structure called the gating ring, is central

28 aternal determinants localised in a distinct cytoplasmic structure called the germ plasm.

29 Cytoplasmic structures called P granules are present in

30 We have previously described TCR-induced cytoplasmic structures called POLKADOTS (punctate and ol

31 significant degradation in cell membrane and cytoplasmic structures, compared to expression of cataly

32 P granules are germ-cell-specific cytoplasmic structures containing RNA and protein, and r

33 Localized alterations in cytoplasmic structure correlated with specific events du

34 in either domain are mutated, suggests these cytoplasmic structures could be functionally coupled thr

35 sight into the role and trafficking of these cytoplasmic structures during virus infection.

36 ized transcriptional program and assembly of cytoplasmic structures for large-scale centriole amplifi

37 nt and are the first to suggest a role for a cytoplasmic structure in the voltage-dependent activatio

38 IG-I signaling components into virus-induced cytoplasmic structures in cells infected with SFTSV.

39 se spots, which are different from all known cytoplasmic structures in D. melanogaster, are evenly el

40 ) from this stereotypic subset strongly bind cytoplasmic structures in HEp-2 cells.

41 Here, we show that BiP localizes in two cytoplasmic structures in infected cells.

42 ession of kAE1 leading to total retention on cytoplasmic structures in polarized epithelial Madin-Dar

43 in producer cells colocalizes with specific cytoplasmic structures, in what are called "A3G complexe

44 Processing bodies (P-bodies) are dynamic cytoplasmic structures involved in mRNA degradation, but

45 nants, which are assembled in electron-dense cytoplasmic structures known as germ or polar granules,

46 05, m06, m07, m09, m10, and m12 localized to cytoplasmic structures near the nucleus, whereas m08 and

47 ing demonstrated that ABA is associated with cytoplasmic structures near, but not within, the endopla

48 We show that Kdm3a localizes to cytoplasmic structures of maturing spermatids affected i

49 The isoform-specific functional role of cytoplasmic structures of two voltage-gated sodium chann

50 P granules are cytoplasmic structures of unknown function that are asso

51 followed by Bcl10 relocalization to punctate cytoplasmic structures, often at sites distant from the

52 stigate the effects of mechanical changes in cytoplasmic structure on intracellular motility, we have

53 nostaining experiments, staining of discrete cytoplasmic structures on the periphery of the endoplasm

54 ap with PDI or ribophorin and may be another cytoplasmic structure or possibly a unique subcompartmen

55 ression plasmid, it concentrated in punctate cytoplasmic structures reminiscent of Us2 localization i

56 t Kdm3a demethylase activity, which affected cytoplasmic structures required to elongate the sperm he

57 nvadolysin protein is predominantly found in cytoplasmic structures resembling invadopodia in fly and

58 an germline, as marked by the spectrosome, a cytoplasmic structure rich in membrane skeletal proteins

59 e transcriptase is bound to a large cellular cytoplasmic structure(s) in a detergent-sensitive comple

60 tributes DDX3X and IKK-alpha to speckle-like cytoplasmic structures shown to be SGs.

61 KK-alpha, which redistribute to speckle-like cytoplasmic structures shown to be stress granules (SGs)

62 Full-length ULK1 localized to cytoplasmic structures, some of which were GFP-LC3-posit

63 Unlike other cytoplasmic structures, such as stress granules and proc

64 localized to the periphery of virus-encoded cytoplasmic structures, termed virus factories (VFs), wh

65 on yeast spindle pole body (SPB) comprises a cytoplasmic structure that is separated from an ill-defi

66 roteins are also components of the fusome, a cytoplasmic structure that spans the cystoblast's progen

67 in areas close to the plasma membrane and in cytoplasmic structures that are heterogeneous in size an

68 Stress granules (SGs) are cytoplasmic structures that are induced in response to e

69 Dap1 localizes to punctate cytoplasmic structures that co-fractionate with endosome

70 which are endoplasmic reticulum (ER)-derived cytoplasmic structures that contain a neutral lipid core

71 Stress granules (SGs) are transient cytoplasmic structures that form when a cell is exposed

72 full-length LARPs were assembled into large cytoplasmic structures that had a strong bias to remain

73 1 are enriched in approximately 1-micrometer cytoplasmic structures that lie very close to the ER.

74 The sequestered p53 localizes to punctate cytoplasmic structures that represent large protein aggr

75 phorin, but was found in as yet unidentified cytoplasmic structures that were juxtaposed to the nucle

76 3(K52R)) mutant exhibited extended, deformed cytoplasmic structures, the phenotype of which was somew

77 d that the accumulation of the pp150 in this cytoplasmic structure was accompanied by at least five o

78 und that some of the SFTS virus NSs-positive cytoplasmic structures were secreted to the extracellula

79 One pool resides in punctate cytoplasmic structures, whereas a significant fraction l

80 These receptors are localized to cytoplasmic structures which are characterized by a vesi

81 s in Drosophila are concentrated in discrete cytoplasmic structures, which we call U bodies, because

82 p53 is preferentially localized to discrete cytoplasmic structures, with no detectable nuclear p53.