ライフサイエンスコーパス: cisternal

1 ed perspective, we propose a model, based on cisternal adhesion and cisternal maturation as the two c

2 stacking might have occurred using only weak cisternal adhesive processes because of the differential

3 binding protein domains that are attached to cisternal adhesive proteins allows mitochondria to invad

4 When isolated from the cisternal and protein body ER, the PDI protein resolves

5 ha-zein and the 27-kD gamma-zein proteins on cisternal and protein body rough endoplasmic reticulum m

6 The endoplasmic reticulum (ER) contains both cisternal and reticular elements in one contiguous struc

7 rain compression was calculated by using the cisternal angle (the angle formed at the intersection of

8 Cisternal angle is an objective measure of midbrain comp

9 The presence of a cisternal angle less than 25 degrees (indicating severe

10 dure midbrain compression, as indicated by a cisternal angle of less than 25 degrees , which was sign

11 The cisternal angle was measured in 100 control subjects wit

12 xon signed rank test was used to compare the cisternal angles ipsilateral and contralateral to the tu

13 l change in response to depletion of nuclear cisternal Ca2+ levels.

14 disease, in which surgical implantation of a cisternal catheter allowed bacterial instillation and ce

15 D-reared subjects demonstrated elevations of cisternal cerebrospinal fluid (CSF) corticotropin-releas

16 er a 4-year period after obtaining blood and cisternal cerebrospinal fluid (CSF) samples from 49 free

17 zyme to be present throughout the subsurface cisternal complex (SSC), especially near the innermost l

18 obility within ER membranes, indicating that cisternal connectivity was not disrupted.

19 aily temporal pattern of hypocretin-1 in the cisternal CSF of the squirrel monkey, a New World primat

20 er 2 h, 36.9+/-4.6% 125I-T4 was recovered in cisternal CSF.

21 ally from the stack and are continuous with "cisternal" domains that maintain normal thickness and al

22 the Golgi complex into juxtanuclear, stacked cisternal elements.

23 han the rest of the endocytic pathway, early cisternal endosomes, spherical late endosomes, late endo

24 ins in the endocytic pathway up to the early cisternal endosomes.

25 pha-globulin RNAs are not distributed to the cisternal ER as expected for a PSV-localized protein, bu

26 Mis-targeting of alpha-globulin RNAs to the cisternal ER dramatically alters the spatial arrangement

27 increase of PDI in fl2 occurs mainly in the cisternal ER fraction, whereas the most dramatic increas

28 rter RNA redirects its localization from the cisternal ER to the protein body ER.

29 reticulum (ER), the protein body ER and the cisternal ER, in developing rice seeds.

30 protein body endoplasmic reticulum (ER) and cisternal ER.

31 , however, redirects RNA localization to the cisternal ER.

32 ), whereas glutelin RNAs are targeted to the cisternal ER.

33 A splicing and cytosolic localization to the cisternal-ER.

34 h is required for proper RNA localization to cisternal-ER.

35 e, these GM130 and GRASP65-dependent lateral cisternal-fusion reactions are necessary to achieve unif

36 ac1 cycles between endoplasmic reticulum and cisternal Golgi compartments.

37 hysiological role of the extensively studied cisternal Golgi rab protein, rab6, is modulation of Golg

38 Furthermore, cisternal hematoma volume correlated with HO-1 activity

39 t pups at postnatal day (P)2-3 with an intra-cisternal injection of 5,7-dihydroxytryptamine (5,7-DHT;

40 gue-Dawley rats had hydrocephalus induced by cisternal kaolin injection.

41 ed in regard to route of administration (ie, cisternal, lumbar, ventricular).

42 We measured ALLO content in four cisternal-lumbar fractions of cerebrospinal fluid (CSF)

43 The cisternal lumen averaged 18 nm so that the cisternal vol

44 lasma membrane, and the average width of the cisternal lumen were recorded.

45 Following nocodazole removal, all cisternal markers accumulated at the same rate in a juxt

46 ose a model, based on cisternal adhesion and cisternal maturation as the two core principles, illustr

47 rough the secretory pathway, suggesting that cisternal maturation can account for the kinetics of sec

48 According to the cisternal maturation hypothesis, endoplasmic reticulum (

49 veal that COPI tubular transport complements cisternal maturation in explaining how anterograde Golgi

50 Our findings suggest that cisternal maturation involves a COPI-dependent pathway t

51 In our analysis cisternal maturation is a robust consequence of vesicle

52 The rate of cisternal maturation matches the rate of protein transpo

53 The results support the cisternal maturation mechanism.

54 This motif precisely matches the cisternal maturation model of the Golgi, which was devel

55 e through bi-directional vesicles, while the cisternal maturation model postulates that transient cis

56 The cisternal maturation model predicts that each cisterna i

57 The cisternal maturation model proposes that secretory prote

58 late Golgi cisternae is consistent with the cisternal maturation model.

59 given to endoplasmic reticulum (ER)-derived, cisternal maturation models of Golgi assembly while in m

60 or COPI-independent intra-Golgi transport by cisternal maturation with a shift in mechanism to antero

61 in the same cisterna, whereas, according to cisternal maturation, Golgi residents recycle from dista

62 secretion of certain proteins and for Golgi cisternal maturation.

63 by the movement of Golgi cisternae, known as cisternal maturation.

64 Cisternal membrane fusion requires two AAA ATPases, p97

65 thought to multiply span the subrhabdomeric cisternal membrane.

66 perature shift, exaggerated stacks of curved cisternal membranes (aberrant endosome) also accumulated

67 ms that (i) facilitate the fusion/fission of cisternal membranes and control the directionality and s

68 The Golgi apparatus is comprised of stacked cisternal membranes forming subcompartments specialized

69 Direct fusion of ER/Golgi intermediates with cisternal membranes of the Golgi stack was not observed

70 these spherical particles were wrapped with cisternal membranes, analogous to intracellular and extr

71 und in vesicles that could be separated from cisternal membranes.

72 Golgi ribbon from one side to the other via cisternal openings.

73 Kv2.1 clustering on the AIS are sites where cisternal organelles, specialized intracellular calcium

74 maintained their juxtanuclear localization, cisternal organization and are competent for the anterog

75 ickness, membrane structure, cargo staining, cisternal origin, and spatial distribution.

76 f beta-endorphin, we conducted a ventricular-cisternal perfusion with artificial cerebrospinal fluid

77 subject of intense debate, with two models, cisternal progression and intercisternal exchange, emerg

78 vations on protein transport cannot rule out cisternal progression as contributing significantly to t

79 ith addressing this question in yeast, where cisternal progression has been extensively studied.

80 However, there is very limited evidence that cisternal progression is regulated, and no evidence for

81 mbrane cargoes and directly demonstrated the cisternal progression of cargoes from the cis- to the tr

82 in the rapid transport of aggregates without cisternal progression on this time scale.

83 nges in Ypt1 and Ypt31 activity affect Golgi cisternal progression, early-to-transitional and transit

84 prevailing view of intra-Golgi transport is cisternal progression, which has a key prediction--that

85 ae via retrograde carriers in synchrony with cisternal progression.

86 GTPases regulate two separate steps of Golgi cisternal progression.

87 n sorting compartment of the cell-occurs via cisternal progression/maturation and that Ypt/Rab GTPase

88 Accumulation of cisternal proteins in scattered Golgi elements was not b

89 ospinal fluid (CSF) samples were obtained by cisternal puncture.

90 ab6a', and rab33b, the most commonly studied cisternal rab proteins.

91 We conclude that Golgi cisternal rabs, and in particular rab6a, are regulators

92 The ER in rtn1Delta cells is predominantly cisternal rather than reticular, yet the net surface are

93 p97-mediated cisternal regrowth is p115-independent, but we now demon

94 NSF-mediated cisternal regrowth requires a vesicle tethering protein,

95 reconstructs these events has revealed that cisternal regrowth requires interplay between soluble fa

96 emplate for postmitotic Golgi reassembly and cisternal remodeling.

97 ible fragmentation through unstacking of the cisternal ribbon and disassembly into radially dispersed

98 sent in the Golgi apparatus was localized to cisternal rims and peri-Golgi vesicles exclusively.

99 Toxoplasma Rab6 was localized to cisternal rims of the late Golgi and trans-Golgi network

100 bles accurate identification of the proximal cisternal segment of the trochlear nerve and its neurova

101 3D CISS MR imaging depicted the proximal cisternal segment of the trochlear nerve in the transver

102 ly rearing was associated with elevations of cisternal somatostatin and of serotonin and dopamine met

103 Large extracellular cisternal spaces were visible between overlapping AG cel

104 SP65 is required in assays that reconstitute cisternal stacking and vesicle tethering.

105 esive energy gluing cisternae dictates Golgi cisternal stacking, irrespective of which molecules medi

106 vesicle transport, cisternae formation, and cisternal stacking.

107 organelles with improved ribbon linking and cisternal stacking.

108 lar H+-ATPase is associated with this cupped cisternal structure, indicating that it corresponds to t

109 bbon is to create synaptic vesicles from the cisternal structures that are abundant at the base of ha

110 The large cisternal structures were attached to the ribbon by fila

111 rge and numerous unanticipated intercellular cisternal structures, defines the magnitude of stratum c

112 nstrate a profound structural disruption and cisternal swelling of the Golgi apparatus (GA) in the co

113 Similarly structured cisternal synapses mediate cholinergic inhibition of coc

114 ne the ultrastructure of genetically altered cisternal synapses.

115 C (cisternal) synapses with a near membrane postsynaptic ci

116 human disease was established using a blind cisternal tap technique to inoculate 4 x 10(3)-1 x 10(6)

117 to commence by laying down and compacting a cisternal tongue against the inside of the axolemma.

118 he CNS following intracerebroventricular and cisternal transplantation in neonatal mice.

119 NAc from the medial to trans-Golgi via inter-cisternal tubules.

120 ading to a loss of Golgi membrane tethering, cisternal unlinking, and Golgi breakdown.

121 of GRASP65 oligomerization and causes Golgi cisternal unstacking.

122 During in vivo ventriculo-cisternal (V-C) perfusion in the anesthetized rabbit (me

123 e cisternal lumen averaged 18 nm so that the cisternal volume was approximately 30% larger than that

124 e those of wild-type littermates except that cisternal volumes were significantly larger.