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 romatin fibers with lamin proteins along the nuclear membrane.

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

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

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

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

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

8 6-10 foci that dynamically interact with the nuclear membrane.

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

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

11 ucing variability in the arrival time at the nuclear membrane.

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

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

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

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

16 at links repressive chromatin with the inner nuclear membrane.

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

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

19 amina and particle budding through the inner nuclear membrane.

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

21 mediate lamin filaments that lines the inner nuclear membrane.

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

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

24 erstanding how capsids bud through the inner nuclear membrane.

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

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

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

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

29 lapse the nucleus and drive infolding of the nuclear membrane.

30 embrane, and SUN proteins crossing the inner nuclear membrane.

31 a fatty acylated repair factor at the inner nuclear membrane.

32 uggest that its primary role is at the outer nuclear membrane.

33 ion in the cell: the plasma membrane and the nuclear membrane.

34 y applying a transient tensile stress to the nuclear membrane.

35 lasmic reticulum to a subdomain of the inner nuclear membrane.

36 ned) information to protein complexes in the nuclear membrane.

37 ells) was sufficient to cause rupture of the nuclear membrane.

38 inuclear space surrounded by inner and outer nuclear membranes.

39 ase torsinA on its ability to associate with nuclear membranes.

40 s unclear how this complex is able to engage 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 g the previously reported undulations of the nuclear membranes.

45 sprouting filopodia-like spikes towards the nuclear membranes.

46 ented insights on ER tubules and sheets, and nuclear membranes.

47 S315 is involved in CCTalpha recruitment to nuclear membranes.

48 nucleus that deform it and cause rupture of nuclear membranes.

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

50 ression and chromatin anchoring at the inner nuclear membrane(4).

51 at lamin A/C, but not lamin B2, protects the nuclear membranes against rupture from tensile stress.

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

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

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

55 otein mesh that resides underneath the inner nuclear membrane and consists of lamins and lamina-assoc

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

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

58 lso demonstrate that TMEM43 localizes at the nuclear membrane and interacts with emerin and beta-acti

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

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

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

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

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

64 ids undergo primary envelopment at the inner nuclear membrane and secondary envelopment at organelles

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

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

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

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

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

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

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

72 mposed of KASH proteins traversing the outer nuclear membrane, and SUN proteins crossing the inner nu

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

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

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

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

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

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

79 rane barrier composed of the inner and outer nuclear membranes as well as a ~40-nm wide lumen.

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

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

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

83 [4, 5] that requires A-type lamin, an inner nuclear membrane-associated protein, to accelerated agin

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

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

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

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

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

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

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

91 dictate the neuronal selective phenotype of nuclear membrane budding.

92 t rejoin daughter nuclei are associated with nuclear membrane but devoid of lamin and nuclear pore co

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

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

95 69 in the nucleus and can be tethered to the nuclear membrane by virtue of its interaction with the w

96 Nuclear membranes can form large invaginations inside th

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

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

99 es of NI in NAFLD: inclusions bounded by the nuclear membrane, containing degenerative cell organelle

100 to the protein lamina network and the outer nuclear membrane continuous with the endoplasmic reticul

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

102 The integrity of the nuclear membranes coupled to the selective barrier of nu

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

104 inations incorporating SERCA1 in their outer nuclear membranes demarcate further diverse networks of

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

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

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

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

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

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

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

112 egarding the association of NE proteins with nuclear membranes during the assembly process.

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

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

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

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

117 hesis, suggesting that it is associated with nuclear membrane expansion.

118 ne encompassing the acentrics fuses with the nuclear membrane, facilitating integration of the acentr

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

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

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

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

123 he recruitment of p-PKC-delta and Cap to the nuclear membrane, hence abolishing the phosphorylation o

124 Human nuclear membrane (hNM) invaginations are thought to be c

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

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

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

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

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

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

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

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

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

134 The nucleus is enclosed by the inner nuclear membrane (INM) and the outer nuclear membrane (O

135 NEC deforms the inner nuclear membrane (INM) around the capsid by forming a he

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

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

138 The inner nuclear membrane (INM) is a subdomain of the endoplasmic

139 The inner nuclear membrane (INM) is continuous with the endoplasmi

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

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

142 w that the ESCRT Chm7 and the integral inner nuclear membrane (INM) protein Heh1 are spatially segreg

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

144 riched for subsets of nucleoporins and inner nuclear membrane (INM) proteins, which associate with di

145 the nucleus through interactions with inner nuclear membrane (INM) proteins.

146 The inner nuclear membrane (INM) selectively accumulates proteins

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

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

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

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

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

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

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

154 g the ER-associated formin INF2 at the inner nuclear membrane (INM).

155 oscopy that VAPB also localizes to the inner nuclear membrane (INM).

156 n acetylation-dependent reserve on the inner nuclear membrane (INM).

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

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

159 a physical explanation for the formation of nuclear membrane invaginations.

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

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

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

163 The human nuclear membrane is composed of a double bilayer, the in

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

165 The inner nuclear membrane is functionalized by diverse transmembr

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

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

168 We found that the nuclear membrane lipid extract is composed of a complex

169 allowing to produce milligram quantities of nuclear membrane lipids.

170 Ca(2+) signals are generated by a complex of nuclear membrane-localised ion channels including the DO

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

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

173 re increase, hydroxyl radical production and nuclear membrane modifications on the treatment outcome.

174 entrosome number, primary cilium morphology, nuclear membrane morphology, chromosome segregation, mit

175 nucleus during neuronal migration result in nuclear membrane (NM) ruptures, causing interspersion of

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

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

178 Despite the absence of a nuclear membrane, nucleoid size strongly correlates with

179 acidic pH did not induce these currents, and nuclear membranes obtained from cells expressing rat IP(

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

181 Herpes simplex viruses bud into the nuclear membrane of infected cells.

182 ic chemical signal, the arrival times at the nuclear membrane of proteins that are activated at the c

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

184 Excised patch clamp recordings from nuclear membranes of DT40 cells expressing only TbIP(3)R

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

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

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

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

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

190 e inner nuclear membrane (INM) and the outer nuclear membrane (ONM).

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

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

193 l for timely repair of large ruptures in the nuclear membrane, potentially by facilitating membrane a

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

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

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

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

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

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

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

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

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

203 conditional hepatocyte deletion of the inner nuclear membrane protein lamina-associated polypeptide 1

204 NE integrity, a process involving the inner nuclear membrane protein LEM2 recruiting CHMP7/Cmp7 and

205 detect elevated levels of the integral inner nuclear membrane protein MAN1, an established negative r

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

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

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

209 exposed dynein-binding domains in the outer nuclear membrane protein nesprin-2G, which polarizes the

210 ated the impact of ER stress on ER and inner nuclear membrane protein quality control mechanisms in S

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

212 9 mice that are also deficient for the inner nuclear membrane protein Sun1 show markedly reduced tiss

213 rotein nesprin-2G, which polarizes the inner nuclear membrane protein SUN1.

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

215 e identified S. cerevisiae Mps2 as the outer nuclear membrane protein that connects the LINC complex

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

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

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

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

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

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

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

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

224 terphase, in part through recruitment of the nuclear membrane proteins emerin and Lem-domain-containi

225 investigate the role of fission yeast inner nuclear membrane proteins in determining nuclear size, a

226 ." We surveyed the diffusional mobilities of nuclear membrane proteins to identify proximal effects o

227 peripheral channels, finding that most inner nuclear membrane proteins use only the peripheral channe

228 he homologous architectures of related inner nuclear membrane proteins(7,8), suggest that phase separ

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

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

231 2-emerin-MAN1 (LEM) family of integral inner nuclear membrane proteins, Heh1 and Heh2.

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

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

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

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

236 e intermediate filaments that line the inner nuclear membrane, provide structural support for the nuc

237 Transcriptome compartmentalization by the nuclear membrane provides both stochastic and functional

238 smids to cross both cell plasma membrane and nuclear membrane quickly to promote the transgene expres

239 3 destruction, chromosome decondensation, or nuclear membrane re-assembly.

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

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

242 nuclear envelope barrier would lead to local nuclear membrane remodeling to promote membrane sealing.

243 site of TG synthesis, which is coupled with nuclear membrane remodeling.

244 mbrane proteins in mitosis, also facilitates nuclear membrane repair in interphase, in part through r

245 BAF depletion significantly delayed nuclear membrane repair, with a larger effect on longer

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

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

248 ed DNA-damage response proximal to the inner nuclear membrane, revealing a mechanism of compartmental

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

250 Nuclear membrane rupture allows uncontrolled exchange be

251 Nuclear membrane rupture during interphase occurs in a v

252 whether such deformations are accompanied by nuclear membrane rupture is unknown.

253 Analyses of intracellular delivery and nuclear membrane rupture revealed mechanisms underlying

254 Nuclear membrane rupture scaled with the magnitude of nu

255 Characterization of GFP-BAF accumulation at nuclear membrane rupture sites confirmed BAF is a fast,

256 cal tensile stresses are sufficient to cause nuclear membrane rupture.

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 ear envelope (NE) consists of two concentric nuclear membranes separated by the lumen, an ~40-nm-wide

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

265 hromodomain protein CEC-4 bound to the inner nuclear membrane tethers heterochromatin through H3K9me(

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

267 le barriers, leading to arrival times at the nuclear membrane that are comparable to models in which

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

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

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

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

272 1 (LAP1) is an integral protein of the inner nuclear membrane that has been implicated in striated mu

273 Lamin A is a component of the inner nuclear membrane that, together with epigenetic factors,

274 leus is fundamentally composed by lamina and nuclear membranes that enclose the chromatin, nucleoskel

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

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

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

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

279 s duration are found effective on disrupting nuclear membrane to advance nuclear delivery of plasmid

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

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

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

283 ruit phosphorylated PKC-delta and Cap to the nuclear membrane to phosphorylate lamin A/C, resulting i

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

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

286 tein complexes that fuse the inner and outer nuclear membranes to form channels across the nuclear en

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

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

289 ns in the NE because of the presence of slow nuclear membrane undulations.

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

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

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

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

294 and the mechanical and dynamic properties of nuclear membranes we investigated their lipid compositio

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

296 These F-actin spikes protrude pore-free nuclear membranes, whereas the adjoining stretches of me

297 cruitment of phosphorylated PKC-delta to the nuclear membrane, which further phosphorylates lamin A/C

298 sociation of its alpha-helical M-domain with nuclear membranes, which is negatively regulated by phos

299 otic transmembrane proteins are found on the nuclear membrane, yet how such proteins target and trans

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