ライフサイエンスコーパス: nuclear membrane

1 on to the previously identified sites (i.e., nuclear membranes).

2 dditional ESCRT-III proteins to holes in the nuclear membrane.

3 amina and particle budding through the inner nuclear membrane.

4 sprin-1 and KLC-1/2 interaction at the outer nuclear membrane.

5 nd delivered by membrane fusion at the outer nuclear membrane.

6 mediate lamin filaments that lines the inner nuclear membrane.

7 C) and are required for budding at the inner nuclear membrane.

8 ant form of lamin A (termed progerin) to the nuclear membrane.

9 erstanding how capsids bud through the inner nuclear membrane.

10 cell or in trafficking of the capsid to the nuclear membrane.

11 of emerin, an integral protein of the inner nuclear membrane.

12 t grow radially from rafted receptors to the nuclear membrane.

13 ructure and function, primarily at the inner nuclear membrane.

14 an interaction between OGT and PIP(3) at the nuclear membrane.

15 wth, SPB duplication, or distribution in the nuclear membrane.

16 1-UNC-84-domain protein that spans the inner nuclear membrane.

17 elope by fusing with and budding through the nuclear membrane.

18 7 expression results in reduplication of the nuclear membrane.

19 hesion and for chromosome recruitment to the nuclear membrane.

20 fferences in binding affinities in the inner nuclear membrane.

21 ane (INM) and deenveloping them at the outer nuclear membrane.

22 on interactions between chromosomes and the nuclear membrane.

23 rnalized through vesicular structures to the nuclear membrane.

24 ids exit the nucleus by budding at the inner nuclear membrane.

25 (NE) at fusion sites of the inner and outer nuclear membrane.

26 membrane but instead was associated with the nuclear membrane.

27 organized in a punctate pattern on the inner nuclear membrane.

28 d consist of chromatin surrounded by its own nuclear membrane.

29 nuclear migration and localizes to the outer nuclear membrane.

30 6-10 foci that dynamically interact with the nuclear membrane.

31 k lining the nucleoplasmic side of the inner nuclear membrane.

32 erevisiae to the INM as opposed to the outer nuclear membrane.

33 d an SRD-YFP fusion localize with AAL to the nuclear membrane.

34 came a muscle-specific resident of the inner nuclear membrane.

35 d depth until they fused with the flat outer nuclear membrane.

36 eading to its rapid degradation at the inner nuclear membrane.

37 at links repressive chromatin with the inner nuclear membrane.

38 the association of pSmad3 with Imp8 and the nuclear membrane.

39 a cells indicate that SINC targets the inner nuclear membrane.

40 inuclear space surrounded by inner and outer nuclear membranes.

41 evenly spaced bilayers, the inner and outer nuclear membranes.

42 cilitated by microtubules, which pull on the nuclear membranes.

43 h the formation of the NEC and remodeling of nuclear membranes.

44 that diffusion barriers compartmentalize the nuclear membranes.

45 he endoplasmic reticulum and move within the nuclear membranes.

46 lined channel connecting the inner and outer nuclear membranes.

47 s unclear how this complex is able to engage nuclear membranes.

48 narrower spaces between the inner and outer nuclear membranes, (3) reduced numbers of nuclear pores

49 (but not other torsin family members) causes nuclear membrane abnormalities in Tor1a(DeltaE/DeltaE) n

50 To study how properties of the nuclear membrane affect nuclear envelope processes, we a

51 sPom121 lacks the nuclear membrane-anchoring domain and thus does not loca

52 imaged single nuclear pore complexes in the nuclear membrane and aggregates of GFP-conjugated Tau pr

53 critical for processing lamin A on the inner nuclear membrane and clearing clogged translocons on the

54 p63alpha were localized to the cytoplasm and nuclear membrane and co-immunoprecipitated in the same f

55 SUN proteins reside in the inner nuclear membrane and form complexes with KASH proteins o

56 zed to hydrophobic perinuclear features, the nuclear membrane and inside the nucleus within minutes.

57 This led to rapid loss of nuclear membrane and intracellular release of granule pr

58 , Kuduk (Kud), which can reside at the outer nuclear membrane and is required for the development of

59 However, when active transport is across the nuclear membrane and NF-kappaB is additionally actively

60 eases in O(2)(-) (3.5-fold; P<0.01) from the nuclear membrane and nuclear exit of HDAC4 in cardiomyoc

61 or envelopment of nucleocapsids at the inner nuclear membrane and optimal viral DNA synthesis and DNA

62 mooth distribution of pU(L)34/pU(L)31 at the nuclear membrane and precluded the accumulation of virio

63 omplex (NEC), which is anchored to the inner nuclear membrane and provides a scaffold for the assembl

64 or protein expression forms a complex at the nuclear membrane and remodels these membranes to generat

65 mplex consists of KASH proteins in the outer nuclear membrane and SUN proteins in the inner nuclear m

66 s are always attached to a hemisphere of the nuclear membrane and tend to associate in pairs.

67 ibility that protein regulation at the inner nuclear membrane and the nuclear lamina contributes to t

68 e-controlled breakdown and reassembly of the nuclear membrane and the restoration of transcription af

69 cells, TLE1 and NOD2 co-localized around the nuclear membrane and TLE1 inhibited activation of nuclea

70 -type virus recruits protein kinase C to the nuclear membrane and triggers its activation, whereas th

71 FRalpha and PCFT on the plasma membrane and nuclear membrane and within endosomal structures.

72 lthough NOX4 protein immunolocalized to both nuclear membranes and intranuclear inclusions, fluoresce

73 NO(550) crosses cell membranes but not nuclear membranes and is suitable for both intra- and ex

74 ted to interaction with receptors located on nuclear membranes and the nucleoplasm.

75 ristic accumulation of capsids away from the nuclear membrane, and an overall defect in nuclear impor

76 l regulators to ensure that mitotic spindle, nuclear membrane, and nuclear pore assembly occur exclus

77 lized these proteins to the plasma membrane, nuclear membrane, and perinuclear region.

78 ades identify interactions at the tonoplast, nuclear membrane, and pollen tube plasma membrane, empha

79 , traffic from the location of fusion to the nuclear membrane, and undergo the process of uncoating,

80 ted cellular fractions, including cytosolic, nuclear, membrane, and mitochondrial protein extracts.

81 hat may have contributed to the evolution of nuclear membrane architecture.

82 Lipid microdomains localized in the inner nuclear membrane are considered platforms for active chr

83 Lipid microdomains localised in inner nuclear membrane are considered platforms for active chr

84 ges in the separation of the inner and outer nuclear membrane are responsible for the additional fluc

85 The proteins form a complex at the nuclear membrane as judged by live-cell analysis of prot

86 emonstrate for the first time that the inner nuclear membrane Asi proteins function in a degradation

87 uggested by results obtained for luminal and nuclear membrane-associated EGFP-tagged proteins.

88 Finally, nuclear membrane-associated ganglioside GM1 plays a pivo

89 However, the endoplasmic reticulum- and nuclear membrane-associated inverted formin-2 (INF2), a

90 [4, 5] that requires A-type lamin, an inner nuclear membrane-associated protein, to accelerated agin

91 ivity of 5-lipoxygenase mutations that delay nuclear membrane association and disrupt product formati

92 s dependent on the surface area of the outer nuclear membrane available to interact with aster microt

93 Due to betabaculovirus breakdown of the nuclear membrane before occlusion, this function is not

94 their assembly is coordinated with dramatic, nuclear membrane blebbing in oocytes.

95 Our observations support a model where nuclear membrane blebbing is required to increase the tr

96 vides support for the transient existence of nuclear membrane-bound vesicles.

97 , as well as lipin-1, is required for normal nuclear membrane breakdown after zygote formation.

98 oreover, with the divergence of preocclusion nuclear membrane breakdown in betabaculoviruses and memb

99 l contact with genomic DNA from the time the nuclear membrane breaks down in prometaphase until early

100 t restricts GEN1 actions to mitosis when the nuclear membrane breaks down.

101 nuclear lamina, nuclear pore complexes, and nuclear membrane, but it is distinct from nuclear envelo

102 f TAG storage capacity, Pah1 still binds the nuclear membrane, but lipid precursors are redirected to

103 that hindered diffusion of cPKA through the nuclear membrane by a rapid-binding process, but not glo

104 t nuclear envelope processes, we altered the nuclear membrane by deleting the SPO7 gene.

105 69 in the nucleus and can be tethered to the nuclear membrane by virtue of its interaction with the w

106 zygote, in a largely overlapping pattern at nuclear membranes, centrosomes, and spindles.

107 alteration of lamin localization pattern and nuclear membrane change are further supported by in vivo

108 dence that nuclear pore complexes (NPCs) and nuclear membranes coevolved with the endomembrane system

109 ps3 mutants was exacerbated, suggesting that nuclear membrane composition affects spindle pole body f

110 d of proteins within the inner and the outer nuclear membranes, connects the nuclear lamina to the cy

111 ; 2) intracellular mechanics of cellular and nuclear membranes, contractile actin stress fibers, and

112 plex to the nuclear envelope and another for nuclear membrane curvature around capsids.

113 ng intralumenal vesicles fuse with the outer nuclear membrane, delivering the capsids to the cytoplas

114 from the endoplasmic reticulum to the inner nuclear membrane depends on nucleotide hydrolysis.

115 are expressed together, numerous virion-size nuclear membrane-derived vesicles were evident at the nu

116 ane and remodels these membranes to generate nuclear membrane-derived vesicles.

117 and the depolarization of both the cell and nuclear membranes, determined by using FM4-64.

118 sphorylations required for the initiation of nuclear membrane disassembly during mitosis are adapted

119 Stable attachment of progerin to the nuclear membrane disrupts the Ran gradient and results i

120 Because fungal nuclear membranes do not break down during mitosis, simi

121 itro resembles capsid budding into the inner nuclear membrane during HSV-1 infection and nuclear enve

122 Herpes simplex virus 1 (HSV-1) remodels nuclear membranes during virus egress.

123 thought to receive arachidonic acid from the nuclear membrane-embedded 5-LOX-activating protein (FLAP

124 telomere tethering and gene silencing at the nuclear membrane, establishment of sister chromatid cohe

125 at generation and maintenance of NP requires nuclear membrane expansion, actin, and the exocyst compl

126 We propose that nuclear membrane expansion, DNA replication, and exocyst

127 cell diameter, low cell stiffness, and high nuclear membrane fluctuations are highly clonogenic and

128 The coupling of actin cables to the nuclear membrane for nuclear movement via specific membr

129 semble in the nucleoplasm and must reach the nuclear membranes for egress.

130 egress, herpesvirus capsids bud at the inner nuclear membrane forming perinuclear viral particles tha

131 promotes chromosome coalescence, preventing nuclear membranes from enwrapping individual chromosomes

132 These results map the crucial inner/outer nuclear membrane fusion event of NPC assembly downstream

133 Here we mapped inner/outer nuclear membrane fusion in NPC assembly biochemically by

134 teracts directly with Kar5p, suggesting that nuclear membrane fusion is mediated by a protein complex

135 d membrane proteins potentially required for nuclear membrane fusion.

136 embedded in pores formed by inner and outer nuclear membrane fusion.

137 protein, Prm3p, was found to be required for nuclear membrane fusion; disruption of PRM3 caused a str

138 ecture and vital biological functions of the nuclear membranes, how they achieve and maintain such a

139 I components to a virus egress domain on the nuclear membrane.IMPORTANCE The ESCRT system is hijacked

140 luorescein are seen to accumulate around the nuclear membrane in 3T3 cells.

141 topic membrane protein residing in the inner nuclear membrane in association with the nuclear lamina.

142 antibody gave very specific labeling of the nuclear membrane in healthy neurons, with apparent reloc

143 rved that NOX4 and p22(phox) localize to the nuclear membrane in MV4-11 cells expressing FLT3-ITD.

144 und to be accumulated in the vicinity of the nuclear membrane in the cytoplasm.

145 s by budding through the inner and the outer nuclear membranes in a nuclear egress mechanism akin to

146 ed to reside in the endoplasmic reticulum or nuclear membrane) in lysates of infected cells and with

147 a smaller amount of CA than complexes at the nuclear membrane, in the cytoplasm, or in controls.

148 e 1 UL34 that localize properly to the inner nuclear membrane, indicating interaction with UL31, but

149 mitoylation of Rif1 anchored it to the inner nuclear membrane, influencing its role in heterochromati

150 amily of transmembrane proteins of the inner nuclear membrane (INM) [8, 9], to form the so-called LIN

151 veloping DNA-containing capsids at the inner nuclear membrane (INM) and deenveloping them at the oute

152 ly sites at a time that coincides with inner nuclear membrane (INM) and outer nuclear membrane (ONM)

153 ion to uncover new constituents of the inner nuclear membrane (INM) by comparative BioID analysis of

154 membrane proteins are targeted to the inner nuclear membrane (INM) by diffusion within the membrane

155 virus 1 nucleocapsids bud through the inner nuclear membrane (INM) into the perinuclear space to obt

156 tanding the protein composition of the inner nuclear membrane (INM) is fundamental to elucidating its

157 ow proteins specifically enrich at the inner nuclear membrane (INM) is not well understood.

158 Targeting of inner nuclear membrane (INM) proteins is essential for nuclear

159 Sad1/UNC-84 (SUN)-domain proteins are inner nuclear membrane (INM) proteins that are part of bridgin

160 y, such as the conserved SUN family of inner nuclear membrane (INM) proteins, is necessary to elucida

161 that EGFR is then translocated to the inner nuclear membrane (INM) through the INTERNET (integral tr

162 cell surface EGFR is trafficked to the inner nuclear membrane (INM) through the nuclear pore complexe

163 ptor 5 (mGluR5) is concentrated at the inner nuclear membrane (INM) where it mediates Ca(2+) changes

164 Cargo is recruited, enveloped at the inner nuclear membrane (INM), and delivered by membrane fusion

165 eus undergo primary envelopment at the inner nuclear membrane (INM), and then enveloped virus particl

166 otein 1 (SUN1), which localizes to the inner nuclear membrane (INM), are part of the linker of nucleo

167 s were dome-shaped evaginations of the inner nuclear membrane (INM), that grew in diameter and depth

168 ately 100 proteins are targeted to the inner nuclear membrane (INM), where they regulate chromatin an

169 ear pore complex (NPC) en route to the inner nuclear membrane (INM).

170 into genomic areas in proximity to the inner nuclear membrane (INM).

171 ial for targeting both proteins to the inner nuclear membrane (INM).

172 he outer nuclear membrane (ONM) to the inner nuclear membrane (INM).

173 Capsids bud at the inner nuclear membrane into the nuclear envelope lumen.

174 NEC formation, but all abolish remodeling of nuclear membranes into circular structures.

175 evidence that nesprin-2G localization to the nuclear membrane is altered under high-force conditions.

176 lamina is specifically rearranged, the outer nuclear membrane is altered, and the nucleus becomes per

177 iffusion, the probability of AR crossing the nuclear membrane is an important factor in determining t

178 We also see that human torsinA at the inner nuclear membrane is associated with membrane expansion a

179 The nuclear face of the nuclear membrane is enriched with the intermediate filam

180 The Saccharomyces cerevisiae nuclear membrane is part of a complex nuclear envelope e

181 dition, the tethering of the inner and outer nuclear membranes is lost during infection due to a decr

182 lipid-rich subcellular region, possibly the nuclear membrane, is presented.

183 (LINC) complex, composed of outer and inner nuclear membrane Klarsicht, ANC-1, and Syne homology (KA

184 results indicate that VP4 forms pores in the nuclear membrane leading to lysis and virus release.

185 nd revealed only partial colocalization with nuclear membrane markers, probably due to post-mortem ti

186 rafficking of envelope proteins to the inner nuclear membrane, mediated partly through the FP25K prot

187 inB function with torsinA to maintain normal nuclear membrane morphology.

188 accumulate aberrantly in herniations of the nuclear membrane, much as in cells infected with a U(S)3

189 n of CCTalpha is needed for expansion of the nuclear membrane network, but mechanisms for CCTalpha nu

190 called the bouquet, telomeres gather to the nuclear membrane (NM), often near centrosomes.

191 Enveloped virions then fuse with the outer nuclear membrane (NM).

192 Herpesviruses cross nuclear membranes (NMs) in two steps, as follows: (i) ca

193 ther altered the morphology/integrity of the nuclear membrane nor the NPC.

194 ood protein turnover mechanisms at the inner nuclear membrane of higher eukaryotes.

195 nt isoform expressed and is localized in the nuclear membrane of ventricular myocytes.

196 ince it has the capability of binding to the nuclear membranes of HeLa cells.

197 ay occur when active transport is across the nuclear membrane only, or when no species are subject to

198 with inner nuclear membrane (INM) and outer nuclear membrane (ONM) fusion.

199 d1/UNC-84 (SUN) proteins interact with outer nuclear membrane (ONM) Klarsicht/ANC-1/Syne homology (KA

200 nificantly reduced at both the INM and outer nuclear membrane (ONM) of cells infected with a U(L)34 n

201 ng loss, encodes nesprin-4 (NESP4), an outer nuclear membrane (ONM) protein expressed in the hair cel

202 amma-tubulin, depends on Nesprin-1, an outer nuclear membrane (ONM) protein that connects the nucleus

203 eticulum and then transported from the outer nuclear membrane (ONM) to the inner nuclear membrane (IN

204 dergo deenvelopment by fusing with the outer nuclear membrane (ONM).

205 the spindle pole body for insertion into the nuclear membrane or affect spindle pole body duplication

206 earing nucleic acid, derived from either the nuclear membrane or the closely associated rough endopla

207 intracellular particles associated with the nuclear membrane or the nucleus compared to that for con

208 ents interact with many partners such as the nuclear membrane, other chromosomes or nuclear bodies, b

209 s) are preferentially enveloped at the inner nuclear membrane over capsid types lacking DNA.

210 els in the same excised cytoplasmic-side-out nuclear membrane patches exposed alternately to optimal

211 tides in the eukaryotic cell nucleoplasm and nuclear membrane prompted us to study the putative inter

212 In this issue, Ohsaki et al. show that the nuclear membrane, promyelocytic leukemia bodies, and the

213 SUN2 is an inner nuclear membrane protein belonging to the linker of nucl

214 saccharomyces pombe telomere-anchoring inner nuclear membrane protein Bqt4.

215 Here, we report that an inner nuclear membrane protein complex Lem2-Nur1 is essential

216 The TMEM48 protein is a nuclear membrane protein comprising the nuclear pore com

217 ly functional lysine-less mutant of an inner nuclear membrane protein in yeast, Asi2, is polyubiquity

218 n, nuclear fragmentation and cleavage of the nuclear membrane protein lamin A, expression of pro-apop

219 s) torsinA (TA) and its activator, the inner nuclear membrane protein lamina-associated polypeptide 1

220 t BMAL1 is positively modulated by the inner nuclear membrane protein MAN1, which directly binds the

221 associate with pores but not with the inner nuclear membrane protein Mps3.

222 We further demonstrate that the nuclear membrane protein nesprin-2 is a possible linker

223 Strikingly, we also find that the inner nuclear membrane protein Sun1 antagonizes Sun2 LINC comp

224 9 mice that are also deficient for the inner nuclear membrane protein Sun1 show markedly reduced tiss

225 d that LINC complexes that contain the inner nuclear membrane protein Sun2 promote focal adhesion ass

226 ines, prompting us to test whether emerin, a nuclear membrane protein that interacts with lamins and

227 Nesprin 1 is an outer nuclear membrane protein that is thought to link the nuc

228 SUN2 is a nuclear membrane protein that was shown to inhibit HIV i

229 megalovirus (HCMV), this complex consists of nuclear membrane protein UL50, and nucleoplasmic protein

230 ncoding the lamin B receptor (LBR), an inner nuclear membrane protein whose expression is required fo

231 n B receptor (LBR) is a highly unusual inner nuclear membrane protein with multiple functions.

232 Lamin B receptor (LBR) is a bifunctional nuclear membrane protein with N-terminal lamin B and chr

233 Lamin B receptor (LBR), an integral inner nuclear membrane protein, also contains a functional C14

234 is physically associated with another inner nuclear membrane protein, Nur1, and deletion of either l

235 tubule dependent and requires Sun1, an inner nuclear membrane protein.

236 icates that, like plasma membrane integrins, nuclear membrane proteins assemble into actin-dependent

237 arrays of outer (nesprin2G) and inner (SUN2) nuclear membrane proteins assembled on and moved with re

238 Emerin and LEM2 are ubiquitous inner nuclear membrane proteins conserved from humans to Caeno

239 In this study, we show that inner nuclear membrane proteins such as lamin B receptor (LBR)

240 f the LEM (Lap2-Emerin-Man1) family of inner nuclear membrane proteins, and the ESCRT-II/ESCRT-III hy

241 However, Stp1 latency depends on three inner nuclear membrane proteins, Asi1, Asi2, and Asi3.

242 2-emerin-MAN1 (LEM) family of integral inner nuclear membrane proteins, Heh1 and Heh2.

243 ligomerization of the luminal domains of two nuclear membrane proteins, nesprin-2 and SUN2, which int

244 SUN-1 are hypothesized to be outer and inner nuclear membrane proteins, respectively, and to interact

245 (Lap2-emerin-MAN1) family of integral inner nuclear membrane proteins, which binds to an early NPC a

246 eoskeleton that bind LINC complexes and many nuclear membrane proteins.

247 Lap2, emerin, MAN1) family of integral inner nuclear membrane proteins.

248 nisms are distinct and not used by all inner nuclear membrane proteins.

249 ear periphery and interacts with a number of nuclear membrane proteins.

250 3 destruction, chromosome decondensation, or nuclear membrane re-assembly.

251 ticles that subsequently fuse with the outer nuclear membrane, releasing capsids into the cytoplasm.

252 irions that subsequently fuse with the outer nuclear membrane, releasing capsids into the cytosol.

253 SUN proteins residing in the outer and inner nuclear membrane, respectively.

254 with translocation from the cytoplasm to the nuclear membrane, resulting in increased membrane phosph

255 ve that untethering chromatin from the inner nuclear membrane results in highly deformable nuclei in

256 ALA + DFO showed hepatocyte autophagosomes, nuclear membrane ruffling, and porphyrin-containing vacu

257 e nucleus, causing chromatin protrusions and nuclear membrane ruptures at sites with nuclear lamina d

258 Inner nuclear membrane Sad1/UNC-84 (SUN) proteins interact wit

259 ice (Tor1a(DeltaE/DeltaE)) exhibit disrupted nuclear membranes selectively in neurons, mimicking the

260 isolated nucleoplasts stripped of the outer nuclear membrane showed progressive nuclear localization

261 ects, a previously identified determinant of nuclear membrane stability, but did decrease the number

262 generates diacylglycerol from PA, targets a nuclear membrane subdomain that is in contact with growi

263 s (emerin, MAN1, LAP1, and LBR) of the inner nuclear membrane, suggesting that SINC interacts with ho

264 domain of pUL31 mediate interaction but not nuclear membrane targeting.

265 , we find that isolated nuclei lacking inner nuclear membrane tethers are less stiff than wild-type n

266 observed significantly more distant from the nuclear membrane than its nontranslocated counterpart, w

267 clear membrane and SUN proteins in the inner nuclear membrane that bridge the nuclear envelope.

268 rm complexes with KASH proteins of the outer nuclear membrane that connect the nuclear envelope (NE)

269 and more abundant binding sites at the inner nuclear membrane that encircle the NPC.

270 ammalian dynein-binding protein of the outer nuclear membrane that forms a meiotic complex with Sun1.

271 1 (LAP1) is an integral protein of the inner nuclear membrane that has been implicated in striated mu

272 ssemble into a meshwork underneath the inner nuclear membrane, the nuclear lamina.

273 s complex mediates capsid transit across the nuclear membrane, the regulatory components are not clea

274 romatin without prominent margination at the nuclear membrane; they exhibited small punctate nucleoli

275 smic protein UL53, which is recruited to the nuclear membrane through its interaction with UL50.

276 UNC-84 recruits KASH proteins to the outer nuclear membrane to bridge the nuclear envelope (NE), me

277 the cis-Golgi, the centrosome, and the outer nuclear membrane to direct mitotic progression.

278 ape whereby nascent capsids bud at the inner nuclear membrane to form perinuclear virions that subseq

279 ing it bridges the capsid and pU(L)34 in the nuclear membrane to initiate budding.

280 o eventually bind pU(L)34 located within the nuclear membrane to initiate capsid budding.

281 ndent and AA-independent steps that occur on nuclear membranes to control the assembly of the LT synt

282 ric structure that fuses the inner and outer nuclear membranes to form a central channel of ~60 nm in

283 NPCs fuse the inner and outer nuclear membranes to form aqueous translocation channels

284 at mediate the fusion of the outer and inner nuclear membranes to form pores.

285 red for HSV capsids to bud through the inner nuclear membrane, to the vertex-specific complex of HSV

286 ns implicated in endoplasmic reticulum-inner nuclear membrane translocation.

287 ns of RNAs into discrete foci at or near the nuclear membrane triggered by multiple elements; and a n

288 sed of BFRF1 and BFLF2 was visualized at the nuclear membrane using autofluorescent protein fusions.

289 aracterizing calcium release channels in the nuclear membrane, very little is known regarding the pro

290 y biogenesis, repair of the plasma membrane, nuclear membrane vesicle formation, and HIV budding.

291 ather into two to three hyperclusters at the nuclear membrane vicinity.

292 7 cells, we could image invaginations of the nuclear membrane, vimentin fibrils, the mitochondrial ne

293 lamin B2 (LB2), normally associated with the nuclear membrane, was identified as an unexpected major

294 s KASH protein UNC-83 localizes to the outer nuclear membrane where it recruits kinesin-1 to provide

295 Ca(2+) targets 5-LOX to the nuclear membrane, where it co-localizes with the 5-LOX-a

296 ar, of which approximately 60% is located on nuclear membranes, where activation leads to sustained C

297 5-lipoxygenase (5-LO) enzyme translocates to nuclear membranes, where it associates with its scaffold

298 ge proteinaceous channels embedded in double nuclear membranes, which carry out nucleocytoplasmic exc

299 uclear envelope thought to connect the inner nuclear membrane with the underlying nuclear lamina and

300 Mutations in the nuclear membrane zinc metalloprotease ZMPSTE24 lead to d