ライフサイエンスコーパス: biogenesis

1 RPLP1/2 in multi-pass transmembrane protein biogenesis.

2 s a key role in outer membrane protein (OMP) biogenesis.

3 of bacteria recently implicated in ribosome biogenesis.

4 ecruitment to the nucleolus and 60S ribosome biogenesis.

5 in mitochondrial iron-sulfur (Fe-S) cluster biogenesis.

6 nship between TORC1 inactivation and vacuole biogenesis.

7 levance of each of these steps of telomerase biogenesis.

8 es of previously unknown function in surface biogenesis.

9 a broader role in polytopic membrane protein biogenesis.

10 s pattern primarily associated with ribosome biogenesis.

11 otein ESCRT complex participating in exosome biogenesis.

12 during the autocatalytic process of cofactor biogenesis.

13 n part, through inhibition of let-7 microRNA biogenesis.

14 related compounds, and based on their common biogenesis.

15 c mechanisms that regulate membrane flux and biogenesis.

16 RNA is preserved due to its role in ribosome biogenesis.

17 l platform for the completion of overall MRC biogenesis.

18 rwood as a new model for the study of lignin biogenesis.

19 te transitions between these two modes of PG biogenesis.

20 nges seen across indicators of mitochondrial biogenesis.

21 ike AC9, ERK7 is required for apical complex biogenesis.

22 ur results lead to a mechanistic model of LB biogenesis.

23 iption, which is a critical step in ribosome biogenesis.

24 ols nicotinic acetylcholine receptor (nAChR) biogenesis.

25 ates TFEB, the master regulator of lysosomal biogenesis.

26 ed role of staphylococcal lipoproteins in EV biogenesis.

27 cket collar (FPC), which is essential for FP biogenesis.

28 h is generally linked to defects in ribosome biogenesis.

29 stent with a phenotype of perturbed ribosome biogenesis.

30 on allowing for stringent control of peptide biogenesis.

31 vide a source of lipids during autophagosome biogenesis.

32 ing an unexpected RILP role in autophagosome biogenesis.

33 ic activity that is essential for apicoplast biogenesis.

34 ts precursor and is thus required for signal biogenesis.

35 irst dual inhibitor of AChE and microRNA-15b biogenesis.

36 was required to abrogate its function in 60S biogenesis.

37 oporin essential for interphase nuclear pore biogenesis.

38 R-18a, and miR-20a, thereby inhibiting their biogenesis.

39 n of ribosomal DNA (rDNA) genes and ribosome biogenesis.

40 fission-fusion, mitophagy, and mitochondrial biogenesis.

41 of its target genes, and impaired complex I biogenesis.

42 f genes involved in translation and ribosome biogenesis.

43 ption is generated by aberrant cell envelope biogenesis.

44 y PHY-mediated signalling and proper plastid biogenesis.

45 round centriolar MTs and promoting centriole biogenesis.

46 oter-proximal RNA polymerase II during piRNA biogenesis.

47 ane fusion during nuclear pore complex (NPC) biogenesis.

48 known about the regulation of apical complex biogenesis.

49 f platelet size in flow-accelerated platelet biogenesis.

50 bile heme in the regulation of mitochondrial biogenesis.

51 e, suggesting GPI7 is required for cell wall biogenesis.

52 I (Pol I) is the first key step of ribosome biogenesis.

53 le assembly, primarily dedicated to ribosome biogenesis.

54 that colocalizes genes involved in ribosome biogenesis.

55 oss of HSCB results in impaired Fe-S cluster biogenesis, a defect in RBC hemoglobinization, and the d

56 nt of new antibiotics that disrupt cell wall biogenesis, a process essential to the survival of bacte

57 hanolamine (PE), a critical step in membrane biogenesis and a potential target for development of ant

58 posttranslational modifications for peptide biogenesis and activity are largely unknown.

59 r EB (TFEB), a master regulator of lysosomal biogenesis and autophagy(4,5), is phosphorylated by mTOR

60 aster transcriptional regulator of lysosomal biogenesis and autophagy-is activated during the lysosom

61 olism and catabolism by regulating lysosomal biogenesis and autophagy.

62 r EB (TFEB), a master regulator of lysosomal biogenesis and autophagy.

63 und that labile heme regulates mitochondrial biogenesis and cell growth.

64 thway that plays a major role in controlling biogenesis and cell size.

65 We further determined rates of RNA biogenesis and decay to uncover RNA regulatory strategie

66 However, the biogenesis and downstream biological effects of EVs rele

67 on levels of genes involved in mitochondrial biogenesis and dynamics in the prelimbic mPFC.

68 aveolin-1 (Cav1) centrally regulates exosome biogenesis and exosomal protein cargo sorting through th

69 induce adaptations related to mitochondrial biogenesis and fat oxidation.

70 unctions as a master controller of lysosomal biogenesis and function during lysosomal stress, control

71 Light-mediated induction of lysosomal biogenesis and function is impaired in the RPE from miR-

72 ranscription, nucleotide synthesis, ribosome biogenesis and function, as well as lipid metabolism.

73 tional regulators of postnatal mitochondrial biogenesis and function, serve a role in the broader car

74 Here, we review the latest findings on the biogenesis and functions of EVs from Gram-positive bacte

75 he fundamental mechanisms underpinning cilia biogenesis and functions remain only partly understood.

76 s; in turn, the nucleus fine-tunes lysosomal biogenesis and functions through transcriptional control

77 ed by mutations in the mitochondrial cristae biogenesis and fusion protein optic atrophy 1 (Opa1), re

78 P2, and RAB7 proteins required for lysosomal biogenesis and fusion.

79 While ribosome biogenesis and global protein synthesis were unaffected

80 alyses revealed an increase of mitochondrial biogenesis and global translational rate in Lmna (LCS/LC

81 for decades, and our understanding of their biogenesis and host cell interaction is incomplete.

82 ered, to what extent ABS involves in circRNA biogenesis and how it is regulated in different human ti

83 the spationumerical regulation of flagellar biogenesis and implies that flagellar assembly transcrip

84 with the host protein TBC1D5 during vacuole biogenesis and intracellular replication.

85 opose that SEIP-1 may maternally regulate LD biogenesis and lipid homeostasis to orchestrate the form

86 nd in human macrophages it induced foam cell biogenesis and M1 polarization.

87 tein 1 (Drp1) is necessary for mitochondrial biogenesis and maintenance of healthy mitochondria.

88 CLPP has essential roles in chloroplast biogenesis and maintenance, but the significance of the

89 show that shear stress favours mitochondrial biogenesis and metabolic reprogramming to ensure energy

90 Mitochondria undergo dynamic fusion/fission, biogenesis and mitophagy in response to stimuli or stres

91 cium homeostasis, lipid metabolism, membrane biogenesis and organelle remodelling.

92 S) facilitates the initial steps of ribosome biogenesis and other functions.

93 layers and mechanisms involved in peroxisome biogenesis and peroxisome degradation, very few studies

94 anscriptional programs that promote ribosome biogenesis and protein synthesis in cells stimulated to

95 of RNA structure and regulation of ribosome biogenesis and protein synthesis.

96 ith the need for nascent D1 during both PSII biogenesis and PSII repair in plant chloroplasts.

97 eceptor from ILC precursors interrupted ILC3 biogenesis and rendered newborn mice susceptible to pneu

98 ly of the 90S/SSU processome during ribosome biogenesis and repress nucleolar stress.

99 LP integrates the processes of autophagosome biogenesis and retrograde transport to control autophagi

100 y can rescue the defect in notochord vacuole biogenesis and scoliosis in dstyk mutants.

101 es have described mechanisms responsible for biogenesis and secretion of SGs, but how SGs mature rema

102 (1)/S(2) subunits, which is processed during biogenesis and sets this virus apart from SARS-CoV and S

103 he EGRESS complex as key players in lysosome biogenesis and shed light on the molecular etiology of B

104 smRNAs play a central role in modulating JA biogenesis and signaling during hemibiotrophic fungal in

105 dolysosomal trafficking is essential for WPB biogenesis and sought to identify BLOC-2-interacting pro

106 recently that the mechanisms underlying the biogenesis and specificity of m(6)A modification in cell

107 subcomponents and proteins implicated in the biogenesis and stability of the apical complex and, in t

108 s associated with mRNA translation, ribosome biogenesis and stress signaling.

109 Nucleoli, the sites of ribosome biogenesis and the largest structures in human nuclei, f

110 ing that vitamin B12 regulates mitochondrial biogenesis and then affects mitochondrial fission via ch

111 or 5' tRNA fragment control of noncoding RNA biogenesis and, consequently, global chromatin organizat

112 underscore the role of vesicles in thylakoid biogenesis and/or maintenance.

113 ), but not endurance capacity, mitochondrial biogenesis, and fiber type transformation.

114 as key proteins involved in their identity, biogenesis, and fusion.

115 TP53 contributed to miR-30e-3p biogenesis, and MDM2 was identified among its target gen

116 It is critical in cell division, centriole biogenesis, and neuronal morphogenesis.

117 l catabolic genes, impairment of chloroplast biogenesis, and reduction of carotenoid synthesis in lea

118 ER localization signal during active protein biogenesis, and that alpha(1D)-AR N-terminal glycosylati

119 r RP-mRNAs, enhancing RP synthesis, ribosome biogenesis, and the overall protein synthesis in migrato

120 critical genomic features regulating circRNA biogenesis are still lacking.

121 e biosynthesis and iron-sulfur cluster (ISC) biogenesis are two major mammalian metabolic pathways th

122 iesterase 5 inhibitor, induced mitochondrial biogenesis as measured by increased uncoupled oxygen con

123 light-responsive miR-211 controls lysosomal biogenesis at the beginning of light-dark transitions in

124 lay a role with select SEIPIN isoforms in LD biogenesis at the ER, and additional experimental eviden

125 logical course of autophagy in neurons, from biogenesis at the synapse to degradation in the soma.

126 rol efflux and the rate-limiting step of HDL biogenesis both in vitro and in vivo.

127 clear protein that is not required for piRNA biogenesis but is essential for piRNA-directed TE de nov

128 DEPS-1 is not required for piRNA biogenesis but piRNA-dependent silencing: deps-1 mutants

129 the absence of complex III blocks complex I biogenesis by preventing the incorporation of the NADH m

130 r degradation and thereby controls centriole biogenesis by restraining HsSAS-6 recruitment to the mot

131 gosomal pathway and the control of lysosomal biogenesis by TFEB, thus ensuring coordinated activation

132 f essential genes involved in outer membrane biogenesis can also trigger T6SS activation in P. aerugi

133 t with a role in multi-pass membrane protein biogenesis, cells lacking different accessory components

134 ile proteins that play critical roles in the biogenesis, cellular localization and transport of RNA.

135 lational programs, and the impaired ribosome biogenesis checkpoint (IRBC) provide a foundation for th

136 nscription factors involved in mitochondrial biogenesis compared to HC.

137 BACKGROUNDDICER1 is the only miRNA biogenesis component associated with an inherited tumor

138 plex are two critical steps in autophagosome biogenesis, connected by WIPI2.

139 Impairment of muscle biogenesis contributes to the progression of Duchenne mu

140 , autophagosome closure, multivesicular body biogenesis, cytokinesis, and other cell processes.

141 the same RP gene can drive similar ribosome biogenesis defects yet still have markedly different dow

142 RNA helicases play various roles in ribosome biogenesis depending on the ribosome assembly pathway an

143 Chloroplast biogenesis describes the transition of non-photosyntheti

144 nance (dyskeratosis congenita), and ribosome biogenesis (Diamond-Blackfan anemia, Shwachman-Diamond s

145 d to change at the RNA level (e.g., ribosome biogenesis) did not do so at the protein level, and vice

146 stages of protein biosynthesis and ribosome biogenesis during both stages of hibernation that sugges

147 localization as a key regulator of ribosome biogenesis during cell migration and demonstrate a role

148 y, which accounts for the intricacy of miRNA biogenesis during de-etiolation.

149 enotype, suggesting that CstK fine-tunes CCV biogenesis during the infection.

150 nds have been reported, the details of their biogenesis, especially the mechanisms for assembly of di

151 At night retinas undergo a mitochondrial biogenesis event, corresponding to an increase in the nu

152 Membrane protein biogenesis faces the challenge of chaperoning hydrophobi

153 fy apum23-4, a mutant allele of the ribosome biogenesis factor (RBF) gene ARABIDOPSIS PUMILIO23 (APUM

154 The ribosome biogenesis factor Las1 is an essential endoribonuclease

155 , where multiple ribosome-associated protein biogenesis factors (RPBs) direct nascent proteins to dis

156 ranscripts and messenger RNAs encoding piRNA biogenesis factors.

157 proteins with demonstrated roles as ribosome biogenesis factors; knockdown of GLTSCR2 impairs maturat

158 e regulatory components that control lipid A biogenesis, focusing on the rate-limiting step performed

159 ires the induction of autophagy and lysosome biogenesis for the efficient recycling of macromolecules

160 of the mechanisms involved in autophagosome biogenesis has increased substantially during the last 2

161 external cues by stimulating beige adipocyte biogenesis; however, the developmental origin and pathwa

162 echanisms of rcDNA deproteination and cccDNA biogenesis.IMPORTANCE The covalently closed circular DNA

163 we recast mechanisms controlling peroxisome biogenesis in a framework that integrates inference from

164 romotes autophagy and lysosomal function and biogenesis in a TFEB-dependent manner.

165 trimental effect of hypoxia on mitochondrial-biogenesis in activated mouse CD8(+) T cells.

166 sembly intermediates (AIs) of complex I (CI) biogenesis in Drosophila will enable the characterizatio

167 rther affirm the involvement of Fe-S cluster biogenesis in erythropoiesis and hematopoiesis and defin

168 r contributions toward understanding betaOMP biogenesis in Gram-negative bacteria and in mitochondria

169 cation method for the dissection of ribosome biogenesis in human cells.

170 with epigenetic regulation of mitochondrial biogenesis in human placenta in a fetal sex-dependent ma

171 organelle heterogeneity on splicing particle biogenesis in mammalian cells.

172 compartments and is involved in the lysosome biogenesis in mammalian cells.

173 us Bccip loss was insufficient to impair 60S biogenesis in mouse embryo fibroblasts, but a profound r

174 s draw new parallels between snRNA and piRNA biogenesis in nematodes and provide evidence of a role f

175 cyte homeostasis in osteoarthritis, ribosome biogenesis in osteoarthritis is unexplored.

176 We found that TOR regulates ribosome biogenesis in plants at multiple levels, but through mec

177 that it has an essential role in basal body biogenesis in T. brucei Further investigation of the fun

178 during folding in vivo Current models of OMP biogenesis in the cellular environment are still in flux

179 depends on nutrient status stimulating mtDNA biogenesis in the developing germline.

180 Membrane protein biogenesis in the endoplasmic reticulum (ER) is complex

181 We report that 10 uM DOX blocks apicoplast biogenesis in the first cycle and is rescued by isopente

182 explains the strong acceleration of platelet biogenesis in the presence of an external flow, which we

183 show differences in hybrid and WT RsRubisco biogenesis in tobacco correlated with assembly in Escher

184 alysis describing the regulation of phasiRNA biogenesis in wheat and barley anthers.

185 ulating muscle stem cells involved in muscle biogenesis, in addition to affecting signalling pathways

186 enomic feature annotation related to circRNA biogenesis, including length of introns flanking circula

187 n that regulates rRNA synthesis and ribosome biogenesis, interacts with CSA and CSB.

188 el intermediate with BAM/SAM in route to its biogenesis into the membrane.

189 for biological processes such as amino acid biogenesis, iron-sulfur cluster formation, and redox hom

190 S-layer biogenesis is a complex multi-step process, disruption o

191 Ribosome biogenesis is a fundamental process required for cell pr

192 with one another to affect accurate protein biogenesis is an emerging question.

193 Mitoribosome biogenesis is an expensive metabolic process that is ess

194 sised that successful initiation of phasiRNA biogenesis is conservatively maintained, while phasiRNA

195 Ribosome biogenesis is crucial for cellular metabolism and has im

196 Protein biogenesis is essential in all cells and initiates when

197 ndicating that the role of CL in iron-sulfur biogenesis is highly conserved.

198 g of the bacterial factors that regulate LPS biogenesis is incomplete.

199 Dicer-mediated miRNA biogenesis is required for embryonic brain development a

200 Let-7 biogenesis is tightly regulated by several RNA-binding p

201 How RLBs relate to SGs and their mode of biogenesis is unknown.

202 pite having only negligible effects when NPC biogenesis is unperturbed.

203 ity with other ER functions, such as protein biogenesis, is unclear.

204 identified to participate in outer-membrane biogenesis: LPS transport via the Lpt machine, and phosp

205 ipts encoding protein synthesis and ribosome biogenesis machinery and regulated by the mTOR pathway.

206 n, an essential component of the iron-sulfur biogenesis machinery, in mitochondria from TAZ-KO mouse

207 1), but not with other proteins of the miRNA biogenesis machinery.

208 n of the translation initiation and ribosome biogenesis machinery.

209 We also found increased mitochondrial biogenesis, mitochondrial fusion and synaptic activity a

210 that has been suggested to regulate collagen biogenesis, muscle development, ciliogenesis, and variou

211 ensitivity and protein synthesis to the tRNA biogenesis mutants, but not to the mutant reducing amino

212 hion compared to other chaperones in the OMP biogenesis network.

213 eal a key role of DSTYK in notochord vacuole biogenesis, notochord morphogenesis and spine developmen

214 cs drives a significant increase in ribosome biogenesis, nucleolar expansion and cell growth in a man

215 o recruit proteins to ER subdomains where LD biogenesis occurs.

216 epresents a decisive cytoplasmic step in the biogenesis of 40S ribosomal subunits.

217 However, molecular insights into the biogenesis of a functional cilia gate remain elusive.

218 luster, which suggests a role for CBs in the biogenesis of animal miRNAs.

219 hosphoryl lipid A, MPLA) displayed increased biogenesis of bacterial outer membrane vesicles (OMVs).

220 ucial role of EphB1/Cav-1 interaction in the biogenesis of caveolae and in coordinating the signaling

221 We show here that the biogenesis of CLEL6 and CLEL9 peptides in Arabidopsis th

222 to its role in differentially regulating the biogenesis of distinct client protein classes.

223 Here, we review recent insights into the biogenesis of eRNAs and the mechanisms underlying their

224 The biogenesis of exosomes involves their origin in endosome

225 The unique biogenesis of exosomes, their ubiquitous production by a

226 ecies (ROS) and inflict cellular damage, the biogenesis of Fe-S clusters is highly regulated.

227 bation of cellular machinery involved in the biogenesis of intralumenal vesicles at endosomes (the so

228 ells ensure this asymmetry by regulating the biogenesis of lipid A, the conserved and essential ancho

229 Because biogenesis of lysosomal related organelle-2 (BLOC-2) fun

230 he Drosophila CLP1 orthologue, cbc, promotes biogenesis of mature tRNAs and circularized tRNA introns

231 function for ER-mitochondria contacts in the biogenesis of MDCs.

232 The biogenesis of mitochondria requires the import of hundre

233 Genetic deletion of XPO5 compromises the biogenesis of most miRNAs and leads to severe defects du

234 al skeleton segmentation due to dysregulated biogenesis of notochord vacuoles and notochord function.

235 of the first two steps are also required for biogenesis of numerous essential cytosolic and nuclear F

236 ther subunit of the PAT complex show reduced biogenesis of numerous multi-spanning membrane proteins.

237 Notably, factors in the ER required for the biogenesis of peroxisomes also impact the formation of l

238 Biogenesis of plastid ribosomes is facilitated by auxili

239 elated organelle-2 (BLOC-2) functions in the biogenesis of platelet dense granules and melanosomes, w

240 a subset of nuclear genes with roles in the biogenesis of respiratory complex I and the mitoribosome

241 The ability of metformin to affect the biogenesis of selected microRNAs (miRNAs) was recently s

242 an RNA endonuclease that is crucial for the biogenesis of small nuclear RNAs and enhancer RNAs.

243 w BBS-causative mutations interfere with the biogenesis of the BBSome.

244 ct the spatiotemporal events involved in the biogenesis of the LBs at the genetic, molecular, biochem

245 diate in the radical S-adenosyl-L-methionine biogenesis of the M-cluster.

246 s expression and provides a platform for the biogenesis of the nascent transcripts emanating from the

247 We review up-to-date knowledge on the biogenesis of the RNA m(6)A modification, including the

248 The biogenesis of these disks is initiated at the OS base, b

249 ained a substantial amount of attention, the biogenesis of these extracellular RNA fragments remains

250 therefore, it is essential to understand the biogenesis of this class of membrane proteins.

251 The proteins that initiate the biogenesis of this structure are largely unknown.

252 n induced by gene inactivations of lysosomal biogenesis or acidification factors causes vitamin B12 d

253 ic pattern by a second mutation in lysosomal biogenesis or acidification.

254 infertility but does not affect either piRNA biogenesis or the localization of MIWI2 to the nucleus.

255 Besides providing insights into OMP biogenesis, our work describes a novel, streamlined meth

256 Fe-2S clusters from the chloroplastic 2Fe-2S biogenesis pathway to different cytosolic and chloroplas

257 ly of SGs and the canonical dsRNA-induced SG biogenesis pathway, because RLBs did not require protein

258 r EB (TFEB), a master regulator of lysosomal biogenesis, plays an essential role in the lysosomal exo

259 y to tRF-GG, and are required for Cajal body biogenesis, positioning these proteins as strong candida

260 -small size and intricate post-translational biogenesis preclude the use of simple genetic tagging in

261 but essential role in the regulation of LPS biogenesis, presents a new structural basis for the sele

262 mTORC1 mediates ribosome biogenesis, protein translation, and autophagy, whereas

263 e training period, suggesting that ribosomal biogenesis regulates the dose-response relationship betw

264 function: an endosomal compartment and a DCV biogenesis-related compartment.

265 d general and domain-specific effects on sEV biogenesis/release.

266 er nematodes; however, many aspects of their biogenesis remain unclear.

267 LB biogenesis remains mysterious but requires surfactant pr

268 n, our current understanding of tetrapyrrole biogenesis represents a remarkable biochemical milestone

269 piRNA precursors underlie the distinct piRNA biogenesis requirements at uORFs and UDRs.

270 MDC biogenesis requires the ER-mitochondria encounter struct

271 Chloroplast biogenesis requires the import of thousands of nuclear-e

272 Ribosome biogenesis (RiBi) is one of the most complex and energy

273 gnificant functions associated with ribosome biogenesis, rRNA processing, ribosome binding, GTP bindi

274 Exercise training-mediated mitochondrial biogenesis, running endurance, and beneficial glycemic e

275 Biogenesis, secretion, and uptake of immune cell-derived

276 chemotherapy or radiation therapy, ribosome biogenesis stress, and possibly inflammation may increas

277 to DRE2, a key protein of the cytosolic Fe-S biogenesis system, and propose that the availability of

278 S proteins, as well as to the cytosolic Fe-S biogenesis system, and that uncoupling this process trig

279 The miRNA pathway has three segments-biogenesis, targeting and downstream regulatory effector

280 uncover various genes involved in EV subtype biogenesis that play a regulatory role in RNA transfer.

281 entifies mechanisms of V-ATPase assembly and biogenesis that rely on the integrated roles of ATP6AP1,

282 cNHEJ-independent functions during ribosome biogenesis that require the kinase activity of DNA-PKcs

283 onse (UPR(mt)), autophagy, and mitochondrial biogenesis, thereby rescuing the mitochondrial phenotype

284 Pharmacological restoration of lysosomal biogenesis through Ezrin inhibition rescued the miR-211(

285 down inhibits notochord vacuole and lysosome biogenesis through mTORC1-dependent repression of TFEB n

286 wing centriole initiates and times centriole biogenesis to ensure that centrioles grow at the right t

287 By gating the transition from 30S biogenesis to translation initiation, RbfA and IF3 maint

288 le of this therapeutic target, including its biogenesis, trafficking to and from the plasma membrane,

289 G protein-coupled receptor (GPCR) biogenesis, trafficking, and function are regulated by p

290 lation, mRNA processing and export, ribosome biogenesis, translation initiation, and protein processi

291 NO66 suppression of ribosomal biogenesis via demethylase activity is the mechanism beh

292 rons, Leu negatively regulates autophagosome biogenesis via its metabolite, acetyl-coenzyme A (AcCoA)

293 alpha, the master regulator of mitochondrial biogenesis, we searched for compounds that induce this p

294 n central and energy metabolism and ribosome biogenesis were dysregulated more in physiologically rel

295 ER-PB contact and PB biogenesis were modulated by altering PB composition, ER

296 nscription factors involved in mitochondrial biogenesis were quantified by real-time qPCR.

297 of genes involved in autophagy and lysosomal biogenesis, were examined in the context of C. burnetii

298 ular processes, such as splicing or ribosome biogenesis, where they remodel large RNA-protein complex

299 Ribosome biogenesis, which takes place mainly in the nucleolus, i

300 olecular mechanisms underlying autophagosome biogenesis, with a specific emphasis on membrane modelin