ライフサイエンスコーパス: messenger ribonucleoprotein

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1 ation, and translational regulation of these messenger ribonucleoproteins.

2 anules (SGs) harbour translationally stalled messenger ribonucleoproteins and play important roles in

3 anslation reaction FMRP interacts with other messenger ribonucleoproteins and pre-exposure of FMRP to

4 RNA hairpin-tagged mRNAs for purification of messenger ribonucleoproteins assembled on transcripts wi

5 erent pre-mRNAs, generating a "splicing" or "messenger ribonucleoprotein code" that determines exon r

6 sults suggest that Tpa1p is a component of a messenger ribonucleoprotein complex bound to the 3' untr

7 e DEAD-box protein Dbp5, promoting localized messenger ribonucleoprotein complex remodeling, and ensu

8 ved cytoplasmic aggregates of nontranslating messenger ribonucleoprotein complexes (mRNPs) implicated

9 ify subsets of mRNAs contained in endogenous messenger ribonucleoprotein complexes (mRNPs) that are c

10 (SGs) are cytoplasmic condensates of stalled messenger ribonucleoprotein complexes (mRNPs) that form

11 sembly, localization, or stability of axonal messenger ribonucleoprotein complexes (mRNPs).

12 e movement of both membranous organelles and messenger ribonucleoprotein complexes by dynein and kine

13 main of NFAR2 was required to associate with messenger ribonucleoprotein complexes containing RNG105/

14 ted by immunoprecipitation of HuR-containing messenger ribonucleoprotein complexes followed by real-t

15 ng small GTPase Rac1 was present in the Fmr1-messenger ribonucleoprotein complexes in vivo.

16 with high affinity, and it is a component of messenger ribonucleoprotein complexes in vivo.

17 ther proteins play a part in the assembly of messenger ribonucleoprotein complexes into transport gra

18 RNA granules are large messenger ribonucleoprotein complexes that regulate tran

19 eta, was not found in the immunoprecipitated messenger ribonucleoprotein complexes.

20 Cul4B licenses the TTP-containing TNF-alpha messenger ribonucleoprotein for loading onto polysomes,

21 that these proteins can also participate in messenger ribonucleoprotein formation in living cells.

22 tein and Actg1 transcript are colocalized in messenger ribonucleoprotein granules responsible for the

23 This messenger ribonucleoprotein has been called the pioneer

24 ut not c-myc and beta-actin mRNAs in vivo by messenger ribonucleoprotein immunoprecipitation analyses

25 ut also results in remodeling of the spliced messenger ribonucleoprotein, influencing various downstr

26 and reduction of Cul4B expression shunts the messenger ribonucleoproteins into the degradative pathwa

27 Stress granules are large messenger ribonucleoprotein (mRNP) aggregates composed o

28 translating polyribosomes as part of a large messenger ribonucleoprotein (mRNP) and modulates the tra

29 In vitro messenger ribonucleoprotein (mRNP) assembly assays demon

30 We provide a model whereby messenger ribonucleoprotein (mRNP) assembly requires Dbp

31 t represent a specific biological program of messenger ribonucleoprotein (mRNP) assembly, but instead

32 ins and how they determine directionality of messenger ribonucleoprotein (mRNP) complex export from t

33 dentified a cytoplasm-restricted beta-globin messenger ribonucleoprotein (mRNP) complex in both cultu

34 selective RNA-binding protein which forms a messenger ribonucleoprotein (mRNP) complex that associat

35 associated with the in vivo configured FMRP messenger ribonucleoprotein (mRNP) complex.

36 or the integrity and function of cytoplasmic messenger ribonucleoprotein (mRNP) complexes called stre

37 To isolate its in vivo targets, messenger ribonucleoprotein (mRNP) complexes containing

38 In vitro reconstitution of messenger ribonucleoprotein (mRNP) complexes demonstrate

39 ed SR proteins remain stably associated with messenger ribonucleoprotein (mRNP) complexes during expo

40 st mRNA export factor Yralp, is recruited to messenger ribonucleoprotein (mRNP) complexes generated b

41 t selectively binds a subset of mRNAs, forms messenger ribonucleoprotein (mRNP) complexes, and associ

42 Cellular mRNAs exist in messenger ribonucleoprotein (mRNP) complexes, which unde

43 nt mechanisms within viral protease-modified messenger ribonucleoprotein (mRNP) complexes.

44 activated C kinase, RACK1, is a component of messenger ribonucleoprotein (mRNP) complexes.

45 A-binding protein, works with other cellular messenger ribonucleoprotein (mRNP) components to ensure

46 fundamental cellular processes by regulating messenger ribonucleoprotein (mRNP) dynamics.

47 By use of messenger ribonucleoprotein (mRNP) immunopurification, w

48 s that recognizes and routes mRNAs through a messenger ribonucleoprotein (mRNP) network.

49 lymerase II (RNAPII), it is assembled into a messenger ribonucleoprotein (mRNP) particle; this is the

50 elicase Xp54 is an integral component of the messenger ribonucleoprotein (mRNP) particles of Xenopus

51 of Xp54, an integral component of the stored messenger ribonucleoprotein (mRNP) particles, can rescue

52 his time a large amount of mRNA is stored as messenger ribonucleoprotein (mRNP) particles.

53 plasmic mRNA export factor docking sites and messenger ribonucleoprotein (mRNP) remodeling machinery

54 nd SmD3 are specific components of the oskar messenger ribonucleoprotein (mRNP), proper localization

55 oocyte maturation and are present in a c-mos messenger ribonucleoprotein (mRNP).

56 eceptor NXF1 (Mex67 in yeast) assembles with messenger ribonucleoproteins (mRNP) in the nucleus and g

57 egulatory factors are mRNA-binding proteins (messenger ribonucleoprotein, mRNP), which control the fa

58 odies (PBs) contain translationally silenced messenger ribonucleoproteins (mRNPs) and serve as extens

59 NA export receptor serving as a link between messenger ribonucleoproteins (mRNPs) and the nuclear por

60 s topoisomerase was a component of cytosolic messenger ribonucleoproteins (mRNPs) and was catalytical

61 d a novel paradigm for how newly synthesized messenger ribonucleoproteins (mRNPs) are matured.

62 At the NPC, messenger ribonucleoproteins (mRNPs) first encounter the

63 ent proteins and image translation of single messenger ribonucleoproteins (mRNPs) in human cells.

64 and proteins that assemble into specialized messenger ribonucleoproteins (mRNPs) localized in the ge

65 Bulk nuclear export of messenger ribonucleoproteins (mRNPs) through nuclear por

66 ctors, the proteasome, and key components of messenger ribonucleoproteins (mRNPs).

67 w that peripherin mRNA-containing particles (messenger ribonucleoproteins [mRNPs]) move mainly along

68 able messenger RNA (mRNA) protein complexes (messenger ribonucleoproteins [mRNPs]).

69 We recently reported that spliceosomes alter messenger ribonucleoprotein particle (mRNP) composition

70 s efficient and ordered assembly of a mature messenger ribonucleoprotein particle (mRNP).

71 show that SLBP is a component of the histone messenger ribonucleoprotein particle (mRNP).

72 t) complex physically couples transcription, messenger ribonucleoprotein particle biogenesis, RNA pro

73 al in sequence, are assembled into different messenger ribonucleoprotein particles (mRNP) in vitro.

74 d may bridge the transition between exported messenger ribonucleoprotein particles (mRNPs) and polyso

75 c transport of two types of cargos, zipcoded messenger ribonucleoprotein particles (mRNPs) and tubula

76 at lead to the formation of export-competent messenger ribonucleoprotein particles (mRNPs) are under

77 p50, the major core protein of messenger ribonucleoprotein particles (mRNPs) in the cyt

78 transcrptionally processed and packaged into messenger ribonucleoprotein particles (mRNPs) in the nuc

79 maternal mRNAs are packaged by protein into messenger ribonucleoprotein particles (mRNPs) that are m

80 mitigated by the ability to form closed-loop messenger ribonucleoprotein particles (mRNPs) via eIF4F-

81 s in mRNA export are the nuclear assembly of messenger ribonucleoprotein particles (mRNPs), the trans

82 ocess, involving the packaging of mRNAs into messenger ribonucleoprotein particles (mRNPs), their tra

83 ated, they are clothed with proteins to form messenger ribonucleoprotein particles (mRNPs), which are

84 rs bind the mRNA in large complexes known as messenger ribonucleoprotein particles (mRNPs).

85 s is preceded by the nuclear assembly of pre-messenger ribonucleoprotein particles (mRNPs).

86 It is a major component of free messenger ribonucleoprotein particles and, at higher con

87 ng machinery, is an important constituent of messenger ribonucleoprotein particles because it partici

88 Following maturation of messenger ribonucleoprotein particles during and after t

89 ins onto mRNA suggests a role for the EJC in messenger ribonucleoprotein remodeling involving interac

90 Here, we characterize the nature of messenger ribonucleoprotein that is targeted for NMD in

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