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1 rogresses, and mutant FUS accumulates at the rough endoplasmic reticulum.
2  is involved in collagen biosynthesis in the rough endoplasmic reticulum.
3 brane, and the relative paucity of stacks of rough endoplasmic reticulum.
4 trated an association of QM protein with the rough endoplasmic reticulum.
5 co-fractionated primarily with polysomes and rough endoplasmic reticulum.
6 inds and remodels the luminal leaflet of the rough endoplasmic reticulum.
7 -terminal helix resulted in proliferation of rough endoplasmic reticulum.
8 e that the HN and F proteins interact in the rough endoplasmic reticulum.
9 e still associated with the membranes of the rough endoplasmic reticulum.
10 iated vesicles and adjacent cisternae of the rough endoplasmic reticulum.
11 ed somatic staining for GluR1, mainly in the rough endoplasmic reticulum.
12 ites in nascent proteins in the lumen of the rough endoplasmic reticulum.
13  colocalized with calnexin, a marker for the rough endoplasmic reticulum.
14 vesicular bodies, and an increased amount of rough endoplasmic reticulum.
15 id to the integrity of the polyribosomes and rough endoplasmic reticulum.
16 e nuclear membrane or the closely associated rough endoplasmic reticulum.
17 uld function as a disulfide isomerase in the rough endoplasmic reticulum.
18 ate-limiting step in collagen folding in the rough endoplasmic reticulum.
19 s and their phagosomes are remodelled by the rough endoplasmic reticulum.
20 e IX collagen (Col9), and matrillin-3 in the rough endoplasmic reticulum.
21 d lysosomal markers and are remodeled by the rough endoplasmic reticulum.
22 ssage from the base of the microvilli to the rough endoplasmic reticulum.
23 fter their co-translational insertion in the rough endoplasmic reticulum.
24 he failure of the LCP to be remodeled by the rough endoplasmic reticulum.
25 ession results in association of p6 with the rough endoplasmic reticulum.
26 to be major constituents of the lumen of the rough endoplasmic reticulum.
27 uggested localization of this protein in the rough endoplasmic reticulum.
28 in body formation at specific regions of the rough endoplasmic reticulum.
29 there were structures with the appearance of rough endoplasmic reticulum.
30  found associated with polyribosomes and the rough endoplasmic reticulum.
31 himera, with retention of the protein in the rough endoplasmic reticulum.
32 l-lysosomal pathway and is surrounded by the rough endoplasmic reticulum.
33 mplex and in the ground plasm but not in the rough endoplasmic reticulum.
34 ying peroxisomes, abundant mitochondria, and rough endoplasmic reticulum.
35                     A paradoxical absence of rough endoplasmic reticulum above and Golgi zones below
36 ion, we show that free GPIs: 1) can exit the rough endoplasmic reticulum and are present on the surfa
37 synthase is associated with membranes of the rough endoplasmic reticulum and catalyzes mannosyl trans
38 a new cell type packed with highly organized rough endoplasmic reticulum and containing deposits of C
39 showed that somatic GRIP was associated with rough endoplasmic reticulum and Golgi apparatus.
40 ng in neuronal perikarya was associated with rough endoplasmic reticulum and Golgi apparatus; in dend
41 hose in NTScom by virtue of better-developed rough endoplasmic reticulum and Golgi, and less convolut
42 ich, by electron microscopy, are enriched in rough endoplasmic reticulum and Golgi, supporting high a
43 he endothelium, as evidenced by expansion of rough endoplasmic reticulum and increased ribosomal anti
44 tensive cytoskeletal network surrounding the rough endoplasmic reticulum and increased synthesis of c
45 trastructurally, NS cells displayed abundant rough endoplasmic reticulum and many cellular processes
46  The biosynthesis of collagens occurs in the rough endoplasmic reticulum and requires a large numbers
47 ible for the degradation of the probe in the rough endoplasmic reticulum and the intramembrane cleava
48 egion contained myofilaments, ribosomes, and rough endoplasmic reticulum and were larger than tarsal
49 nules with paracrystalline contents, dilated rough endoplasmic reticulum, and electron-lucent granula
50 bundant cytoplasm containing large masses of rough endoplasmic reticulum, and exhibited distinctive d
51 ss of the retinol stores, an increase in the rough endoplasmic reticulum, and increases in extracellu
52 thin membrane-bound vesicles associated with rough endoplasmic reticulum, and L. pneumophila dot/icm
53          Collagen biosynthesis occurs in the rough endoplasmic reticulum, and many molecular chaperon
54 ocyte-like cells, prominent mitochondria and rough endoplasmic reticulum, and some have lysosomes and
55 DNA library for the screen was prepared from rough endoplasmic reticulum-bound mRNA and is therefore
56 h in ribosomes, particularly near or between rough endoplasmic reticulum cisternae.
57 s, which form an ordered matrix within large rough endoplasmic reticulum cisternae.
58 ar amyloid fibrils in close proximity to the rough endoplasmic reticulum, coated vesicles, and electr
59 on of chromaffin vesicles and an increase in rough endoplasmic reticulum compared with wild-type mice
60  from epiphyseal cartilage exhibited dilated rough endoplasmic reticulum containing linear lamellae o
61 ignals for insertion into the bilayer of the rough endoplasmic reticulum during de novo synthesis.
62 mmunogold particles were associated with the rough endoplasmic reticulum (ER) and cytoplasm.
63 ymogenic cells (ZCs) involves an increase in rough endoplasmic reticulum (ER) and formation of many l
64 the major storage protein synthesized by the rough endoplasmic reticulum (ER) and stored in specializ
65 me association and Ago2 interaction steps on rough endoplasmic reticulum (ER) before the miRNA-mediat
66                  They are synthesized on the rough endoplasmic reticulum (ER) in a sequential manner
67  synthesized on the cytosolic leaflet of the rough endoplasmic reticulum (ER), and functions as a man
68 es with abundant Golgi complexes and dilated rough endoplasmic reticulum (ER).
69  that overexpressed DeltaCT and proliferated rough endoplasmic reticulum exhibited severalfold higher
70           Immunoprecipitated OST-48 from rat rough endoplasmic reticulum fractions exhibited both AGE
71 nce was found for phosphorylation of apoB in rough endoplasmic reticulum fractions.
72 ressed Rab14 were localized to biosynthetic (rough endoplasmic reticulum, Golgi, and trans-Golgi netw
73 ed numerous organelles, including smooth and rough endoplasmic reticulum, Golgi, mitochondria, peroxi
74 tion assay and Brefeldin A disruption of the rough endoplasmic reticulum-Golgi-trans-Golgi network.
75 -associated vesicles was also increased, and rough endoplasmic reticulum had fewer ribosomes.
76 icroscopy analysis displayed swelling in the rough endoplasmic reticulum in CFKO-2a embryonic cardiom
77 nsmission electron microscopy showed dilated rough endoplasmic reticulum in iHeps from all individual
78 or VZV glycoprotein, gE, was retained in the rough endoplasmic reticulum in the absence of gI.
79              These interactions occur in the rough endoplasmic reticulum in the presence of various c
80             In cartilage, both patients have rough endoplasmic reticulum inclusions in chondrocytes.
81                  Within cytotrophoblast, the rough endoplasmic reticulum incorporated the most [3H]ga
82 that prevent degradation of the probe in the rough endoplasmic reticulum increase the amount of the a
83                             Furthermore, the rough endoplasmic reticulum is implicated as the possibl
84  analysis of resting cells demonstrated that rough endoplasmic reticulum is more abundant in MZB cell
85 eptides during N-linked glycosylation in the rough endoplasmic reticulum lumen.
86 myosin, a discontinuous basal lamina, sparse rough endoplasmic reticulum, many mitochondria and a wel
87 rotein complex that directs ribosomes to the rough endoplasmic reticulum membrane by binding to targe
88 by PrP antibodies that faithfully recognized rough endoplasmic reticulum membranes and amyloid fibril
89 vealed labeling at the cytosolic side of the rough endoplasmic reticulum membranes, in the nucleus, o
90 -zein proteins on cisternal and protein body rough endoplasmic reticulum membranes.
91     Mutant matrilin-3 is retained within the rough endoplasmic reticulum of chondrocytes and is assoc
92 tructural basis for retention of COMP in the rough endoplasmic reticulum of differentiated PSACH and
93 form accretions called protein bodies in the rough endoplasmic reticulum of maize endosperm cells.
94 n, as well as retroviruses that populate the rough endoplasmic reticulum of neuroblastoma cells, were
95 monstrated localization of E1 protein in the rough endoplasmic reticulum of RNA-transfected IHH.
96 c defects are associated with defects in the rough endoplasmic reticulum of the major secretory cells
97                Cell compartments packed with rough endoplasmic reticulum or Golgi vesicles (acinar ce
98 ed fusiform cell shape, abundant cytoplasmic rough endoplasmic reticulum/polyribosomes, and accumulat
99 se activities that are characteristic of the rough endoplasmic reticulum (RER) (mannose) or the Golgi
100 (CYPB; encoded by PPIB), which reside in the rough endoplasmic reticulum (RER) and can form a complex
101 etabolic demand by active expansion of their rough endoplasmic reticulum (rER) and increased synthesi
102  trophoblast synthesized protein in both its rough endoplasmic reticulum (RER) and its ground plasm w
103  identified numerous paired cisternae of the rough endoplasmic reticulum (RER) and other ultrastructu
104  event between pocket-like structures of the rough endoplasmic reticulum (rER) and the plasma membran
105 ynthesized as a transmembrane protein of the rough endoplasmic reticulum (RER) and then buds into the
106 y assays, which reconstitute the movement of rough endoplasmic reticulum (RER) and vesicles present i
107 rent strain in their capacity to recruit the rough endoplasmic reticulum (RER) around the phagosome.
108 llular replication, and the role of the host rough endoplasmic reticulum (rER) at the recently descri
109 rmal complex that is accumulated in expanded rough endoplasmic reticulum (rER) cisternae, a hallmark
110                  Proteins synthesized by the rough endoplasmic reticulum (RER) co-translationally cro
111 MP and the mutant protein is retained in the rough endoplasmic reticulum (rER) of chondrocytes and ma
112 midal neurons on the outer nuclear membrane, rough endoplasmic reticulum (rER), and ribosomes.
113 ar matrix proteins are biosynthesized in the rough endoplasmic reticulum (rER), and the triple-helica
114 otein response (UPR) as evidenced by dilated rough endoplasmic reticulum (RER), and upregulation of U
115 A generally resulted in fragmentation of the rough endoplasmic reticulum (RER).
116 CoV spike (S) glycoprotein does not encode a rough endoplasmic reticulum (rER)/Golgi retention signal
117    Of the three DnaJ homologues in the yeast rough endoplasmic reticulum (RER; Scj1p, Sec63p, and Jem
118                                          The rough endoplasmic reticulum-resident FK-506-binding prot
119                                          The rough endoplasmic reticulum-resident protein complex con
120 in translocation complex (translocon) in the rough endoplasmic reticulum (rough ER) membrane.
121  oligosaccharyltransferase complex, enriched rough endoplasmic reticulum, smooth endoplasmic reticulu
122 ight and sets of three parallel cisternae of rough endoplasmic reticulum spanning between clustered m
123 ys, was assessed when identical fractions of rough endoplasmic reticulum-specific membrane proteins w
124 not contain alphaA, alphaB fractionates with rough endoplasmic reticulum, suggesting that alphaA has
125 distant hosts, the bacterium multiplies in a rough endoplasmic reticulum-surrounded phagosome that is
126 ucture of the host cell, on the formation of rough endoplasmic reticulum-surrounded replicative phago
127 ytoplasm and a less well-organized system of rough endoplasmic reticulum than their counterparts in o
128 ysplasia (EDM1) patients display an enlarged rough endoplasmic reticulum that accumulates extracellul
129 nositol trisphosphate receptors are found in rough endoplasmic reticulum that closely invests apical
130 oposed that Hsp47 and FKBP65 interact in the rough endoplasmic reticulum, there is neither clear evid
131 re cotranslationally translocated across the rough endoplasmic reticulum through a proteinaceous chan
132 ated transit times of 21 +/- 15 min from the rough endoplasmic reticulum to Golgi apparatus and 111 +
133 ly synthesized proteins across the mammalian rough endoplasmic reticulum (translocation) is supported
134                            Enlarged lamellar rough endoplasmic reticulum vesicles were shown to conta
135 /-cells, DMVs were not detected; rather, the rough endoplasmic reticulum was dramatically swollen.
136 ls associated with postsynaptic cisterns and rough endoplasmic reticulum) were smaller and the number
137 ate that alphaB predominantly sediments with rough endoplasmic reticulum, whereas alphaA fractionates
138 ollen mitochondria and a lack of distinctive rough endoplasmic reticulum which are typically associat
139 mes, the number of vacuoles, and the average rough endoplasmic reticulum width, were observed with TE
140  coupled with a significant expansion of the rough endoplasmic reticulum (without endoplasmic reticul

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