ライフサイエンスコーパス: inner

1 shepherds primary transposase binding to the inner 12DRs (where cleavage does not occur), followed by

2 eformed to MR in-phase was segmented to air, inner air, soft tissue, and continuous bone.

3 al precursor pool began to subdivide into an inner and outer compartment that began to express marker

4 Furthermore, the lipid composition of the inner and outer cotyledons differed from each other, a r

5 hemistry, probing the strong affinity of the inner and outer faces of the gamma-CD for the polyoxomet

6 rtain how differences in tension between the inner and outer leaflets of the membrane contribute to t

7 olipids are trafficked between the bacterial inner and outer membranes through the hydrophilic space

8 e width of the periplasmic space between the inner and outer membranes.

9 drial division requires division of both the inner and outer mitochondrial membranes (IMM and OMM, re

10 Nups is largely restricted to members of the inner and outer NPC rings, but it lacks numerous others

11 erve fiber layer, inner plexiform layer, and inner and outer nuclear layers and within the spindle-sh

12 that small changes in the separation of the inner and outer nuclear membrane are responsible for the

13 -specific differentiation of ASCs within the inner and outer regions of the biphasic scaffolds.

14 rgetics by a tractor mechanism involving the inner and outer root sheaths.

15 functional theory calculations show that the inner and outer structural engineering contributing to t

16 the magnetically disordered regions (in the inner and outer surface of the Fe3O4 shell) and spins lo

17 teomic survey of 1,347 CEPs encompassing 90% inner- and outer-membrane and periplasmic proteins of Es

18 ion by WPC-pectin-maltodextrin along with 5% inner aqueous phase showed a high stability and low rele

19 We test this model on the inner area of Greater London.

20 Considering the ecology and mobility of inner Asian mountain pastoralists, we use 'flow accumula

21 ace of intra-erythrocytic merozoites and the inner aspect of erythrocyte membranes, preventing the ru

22 is immersed in the lipid bilayer, while the inner barrel surface is highly charged.

23 process also contributes to electrons in the inner belt elsewhere.

24 stratification near either the outer or the inner border of the inner plexiform layer.

25 separations associated with cleft formation; inner bud cells remain unaffected.

26 essive formation of a triiron cluster on the inner cage surface of each subunit.

27 ormation of the blastocyst consisting of the inner cell mass (ICM) and trophectoderm (TE).

28 ifferentiate to either trophectoderm (TE) or inner cell mass (ICM), followed by epiblast (EPI) or pri

29 elopment is the segregation of the embryonic inner cell mass and the extra-embryonic trophectoderm.

30 anisms through which FGF signaling regulates inner cell mass lineage restriction and cell commitment

31 omosome inactivation is then reversed in the inner cell mass.

32 meiotic prophase II but is restricted to the inner centromere at metaphase II.

33 show here that direct actin binding, via the inner centromere protein (INCENP), enhances CPC enrichme

34 encompass centromeric regions including the inner centromeric and pericentromeric regions during (pr

35 monocytes sorted with magnetic beads in the inner chamber produced ET-1 when T cells were activated

36 ith the polyanion-binding site located on an inner chamber wall of the enzyme.

37 nded vertical beta-barrel that forms a large inner channel encircled by two concentric rings, one bet

38 A thin 3-sided glass coating on the inner channel walls prevents multi-directional diffusion

39 Others are targeted to the inner chloroplast envelope membrane by undescribed trans

40 eins depends on translocons at the outer and inner chloroplast membrane (TOC and TIC, respectively) c

41 roplast membrane) and TIC (translocon on the inner chloroplast membrane) machineries in the outer and

42 rt at high risk for asthma (n = 560) in four inner cities.

43 Acute care level one trauma center in an inner city of the state of Connecticut, USA.

44 The School Inner-City Asthma Study was a prospective cohort study e

45 Children enrolled in the School Inner-City Asthma Study were followed for 1 academic yea

46 We characterized those inner-city children with and without asthma exacerbation

47 can Americans >/=50 years of age at multiple inner-city community sites in Baltimore, Maryland.

48 years with asthma who were enrolled from 37 inner-city elementary schools in the northeastern United

49 f aged (>60 years) and younger (21-40 years) inner-city patients with asthma.

50 assroom NO2 on lung function and symptoms in inner-city school children with asthma.

51 tes, measured in dust samples collected from inner-city schools.

52 In this study of inner-city students with asthma, exposure to mouse aller

53 by a second encapsulation in its urea-based inner cleft.

54 For those producing inner colonies inside the susceptible range, the parenta

55 (0.8%) consistently produced nonsusceptible inner colonies.

56 All 5 inner colony mutants had reduced growth on minimal mediu

57 he parental strains and their representative inner colony mutants were subjected to MIC testing, whol

58 rate that TFG tethers vesicles harboring the inner COPII coat, which contributes to their clustering

59 utectic in most regions resulting in a sharp inner core boundary, but deviation from the eutectic com

60 The existence of a mushy zone in the Earth's inner core has been suggested, but has remained unproven

61 and the fluorescence of PpIX moieties in the inner core is highly quenched due to strong pi-pi stacki

62 smooth and uniform C-coatings sheathing the inner core metal oxide NPs are made of well-crystallised

63 reactions of meso-arylcorroles, both at the inner core, as well as the peripheral positions of the m

64 The inner-core cells of tumors with radii exceeding 100 mum

65 s led to an uneven PEF effect with the tuber inner cores softening more than the middle regions.

66 MOF (SCU-8) containing channels with a large inner diameter of 2.2 nm and possessing a high surface a

67 Droplets are able to slide through a 4 mm (inner diameter) tube with low sliding angles of less tha

68 suggests that specific residues of the gp120 inner domain layers have coevolved with H375 in order to

69 with a reduction in the number of outer and inner dynein arms.

70 characteristics of DA fibers innervating the inner ear and the hindbrain auditory efferent nucleus in

71 mation of the distinct sensory organs of the inner ear and the non-sensory domains that separate them

72 The aims of this study were to manipulate inner ear connexin expression in vivo using BAAV vectors

73 The vestibular system of the inner ear detects head position using three orthogonally

74 findings highlight a biological link between inner ear dysfunction and behavioral disorders and how s

75 Furthermore, we show that (1) inner ear dysfunction due to the tissue-specific loss of

76 ther hyperactivity or anxiety co-occurs with inner ear dysfunction.

77 Vestibular hair cells in the inner ear encode head movements and mediate the sense of

78 ride cotransporter and is also necessary for inner ear function, causes hyperactivity; (2) vestibular

79 The use of viral vectors for inner ear gene therapy is receiving increased attention

80 annels at the tips of sensory stereocilia of inner ear hair cells are gated by the tension of 'tip li

81 this protein between the frog and the mouse inner ear hair cells.

82 The human inner ear has an intricate spiral shape often compared t

83 oaches to introduce viral particles into the inner ear have been described, presumed physiological ba

84 Mechanoelectrical transduction in the inner ear is a biophysical process underlying the senses

85 BE3 RNPs into both zebrafish embryos and the inner ear of live mice to achieve specific, DNA-free bas

86 iency, we delivered wild-type Ush1c into the inner ear of Ush1c c.216G>A mice using a synthetic adeno

87 Specification of inner ear progenitors is initiated by FGF signalling.

88 rmation of kidney and intestinal microvilli, inner ear stereocilia, immune synapses, endocytic patche

89 cells are specialized sensors located in the inner ear that enable the transduction of sound, motion,

90 mmals owing to the inability of cells in the inner ear to proliferate and replace lost sensory recept

91 tiles shows how minute balance organs in the inner ear transformed at the same time.

92 V2/9 as a novel and atraumatic technique for inner ear transgene delivery in early postnatal mice.

93 Throughout postnatal maturation of the mouse inner ear, cochlear hair cells display at least two type

94 ene deletion/reporter gene activation in the inner ear.

95 (SGNs) are specialzed bipolar neurons in the inner ear.

96 h enlarged endolymphatic compartments of the inner ear.

97 de their hearing sensitivity range and their inner ears are partly undeveloped, which accounts for th

98 Inner ears from two mass strandings of long-finned pilot

99 closer to the fovea and overlapping with the inner edge.

100 ficantly (p < 0.01) higher than those in the inner endodermis.

101 s process requires an ABC transporter in the inner envelope membrane with three subunits, TRIGALACTOS

102 plast membrane) machineries in the outer and inner envelope membranes, respectively.

103 residues in specific protein surfaces of the inner face of the viral matrix and at the Cyclophilin A

104 are identified and explained in terms of the inner flow fields of the ratchet.

105 The presence of ectopic inner foveal layers was negatively correlated with the p

106 thick and associated with continuous ectopic inner foveal layers.

107 In multivariable modeling, the mean inner GCC thickness was associated with advancing age (b

108 neurons originating in the brainstem inhibit inner hair cell spontaneous activity and may further ref

109 cellular mechanism known for HHL is loss of inner hair cell synapses (synaptopathy).

110 hannels and the exocytosis calcium sensor at inner hair cell synapses changes along the mammalian coc

111 TRACT: Just before the onset of hearing, the inner hair cells (IHCs) receive inhibitory efferent inpu

112 e first time, successful transduction of all inner hair cells and the majority of outer hair cells in

113 While hair bundles of inner hair cells are of linear shape, those of outer hai

114 lends support to the recent hypothesis that inner hair cells are stimulated by a net flow, in additi

115 the endogenous release of glutamate from the inner hair cells may increase the strength of efferent i

116 nces in afferent neurons and, in the case of inner hair cells of the cochlea, vulnerability to damage

117 In connexin knock-outs, inner hair cells remained stuck at a prehearing stage of

118 Inner hair cells, auditory synapses and spiral ganglion

119 icted to the cell apical region) in cochlear inner hair cells.

120 cells prevented the functional maturation of inner hair cells.

121 Studies of F103 in the hinge of the inner helix suggest an important role for its bulky side

122 a structure comprising an outer (OM) and an inner (IM) membrane, is essential for life.

123 ius is the atomic (covalent) radius, and the inner is that of the underlying closed-shell orbital.

124 Although a fully assembled inner kinetochore is not required for outer kinetochore

125 ned the subunit topology of COMA, bound with inner kinetochore proteins Nkp1 and Nkp2, from the yeast

126 ndependent role in the proper composition of inner kinetochore proteins.

127 ch in turn regulates proteostasis of certain inner KT components.

128 outer layer of condensed heterochromatin, an inner layer enriched in the histone variant H2AX, and a

129 second observation is the discovery, in the inner layer of the developed turbulent boundary layer, o

130 structs were preferentially expressed in the inner layers of the skin, the root endodermis, the vascu

131 horoid and a thinner retina, particularly in inner layers, after 1 year of follow-up.

132 Surface charges at the inner leaflet of the plasma membrane may contribute to r

133 Several proteins expressed at the inner leaflet of the plasma membrane, including alpha-ac

134 f an endogenous actin cortex attached to the inner leaflet of the plasma membrane.

135 noglycerophospholipids from the outer to the inner leaflet of the plasma membrane.

136 ipid is restricted almost exclusively to the inner leaflet of the plasmalemma.

137 s with a diameter greater than 75 mum and an inner mass are enriched 1.5- and 3.8-fold for pre-organo

138 d the ATP rescue, diminished survival of the inner matrix detached cells, restoring the normal hollow

139 from the nutrition contained in the soluble inner matrix through increases in longevity and fecundit

140 r, and genetic knockdown of TRIP13 in murine inner medullary collecting duct cells in the presence of

141 mbrane protein Large 3 (MmpL3), an essential inner membrane (IM) protein, is implicated in MA transpo

142 translocons on the outer membrane (TOM) and inner membrane (TIM).

143 ysaccharide from the external leaflet of the inner membrane and propels it along a filament that exte

144 ills E. coli by permeabilizing the bacterial inner membrane and subsequently binds the outer membrane

145 This establishes a clear link between inner membrane architecture and functional decline.

146 SLC25A24 encodes a mitochondrial inner membrane ATP-Mg/Pi carrier.

147 drial Ca(2+) uniporter complex (uniplex), an inner membrane Ca(2+) transporter and major pathway of m

148 In the yeast Saccharomyces cerevisiae, this inner membrane complex is composed of 11 protein subunit

149 the envelope-associated needle complex, the inner membrane export apparatus, and a large cytoplasmic

150 ed overexpression of functional PfVIT in the inner membrane of Escherichia coli which, in turn, confe

151 e synthesized at the periplasmic side of the inner membrane of Gram-negative bacteria and are then ex

152 ith COX2 to promote translocation across the inner membrane of the COX2 C-tail that contains the apo-

153 ubtilis, germinant receptors assemble in the inner membrane of the developing spore.

154 bout 50% of mitochondria from old flies, the inner membrane organization breaks down.

155 inner membrane, followed by cleavage by the inner membrane peptidase.

156 and the absence of exogenous substrates upon inner membrane pore formation by alamethicin or Ca(2+)-i

157 gs identify a new route for the targeting of inner membrane proteins in bacteria and highlight the di

158 mplex II (site IIf); (b) pore opening in the inner membrane resulting in rapid efflux of succinate/fu

159 However, increasing the mitochondrial inner membrane surface comprises an alternative mechanis

160 the mitochondrial matrix are targeted to the inner membrane Tim17/23 translocon by their presequences

161 The permeability of the mitochondrial inner membrane to HNO2, but not to NO2(-), combined with

162 reconstituting them in vitro using inverted inner membrane vesicles.

163 hat connects the two membrane proteins CusA (inner membrane) and CusC (outer membrane).

164 exchanges ADP/ATP through the mitochondrial inner membrane, and Ant2 is the predominant isoform expr

165 tribution of bioactives in pomegranate peel, inner membrane, and edible aril portion was investigated

166 in precursor within the lipid bilayer of the inner membrane, followed by cleavage by the inner membra

167 to the four subcompartments: outer membrane, inner membrane, intermembrane space, or matrix.

168 dient via ATP synthase located on the folded inner membrane, known as cristae.

169 a T2SS nanomachines requires the assembly of inner membrane-anchored fibres called pseudopili.

170 Inner membrane-anchored long OPA1 (L-OPA1) undergoes pro

171 ch as dipicolinic acid (DPA) and the spore's inner membrane.

172 bunit on the intermembrane space side of the inner membrane.

173 is in the cytoplasm and secretion across the inner membrane.

174 rochemical gradient (DeltamuH(+)) across the inner membrane.

175 rphological alterations of the mitochondrial inner-membrane (IMM) have not been clearly elucidated.

176 MotA and MotB form an inner-membrane complex that does not conduct protons and

177 with type 1 diabetes exhibited mitochondrial inner-membrane hyperpolarization (MHP).

178 bacterial cytoplasm to the periplasm via an inner-membrane pore complex (TraC and TraG) with homolog

179 on density region, composed of the outer and inner membranes and the cristae cluster, which enclosed

180 lia of approximately 50 x 0.2 mum, devoid of inner membranes embedded in a mucus layer.

181 present an atomic model of a substrate-bound inner mitochondrial membrane AAA+ quality control protea

182 At the onset of this process, the inner mitochondrial membrane becomes depolarized and per

183 nsfer chain, translocates protons across the inner mitochondrial membrane by harnessing the free ener

184 ggers the disorganization of the cristae and inner mitochondrial membrane in several cancer cells and

185 Here, we identify the inner mitochondrial membrane protein, prohibitin 2 (PHB2

186 IRT5 is targeted to protein complexes on the inner mitochondrial membrane via affinity for cardiolipi

187 dylserine to phosphatidylethanolamine in the inner mitochondrial membrane, must undergo an autocataly

188 a carotenoid cleavage enzyme located in the inner mitochondrial membrane.

189 energize precursor translocation across the inner mitochondrial membrane.

190 steps energize precursor passage across the inner mitochondrial membrane.

191 nstitutes a hetero-oligomeric complex on the inner mitochondrial membranes to maintain crista structu

192 Jurassic Jiulongshan Formation of Daohugou, Inner Mongolia, China.

193 ne-rich loop that is predicted to lie at the inner mouth of the channel, which might form a gasket ar

194 RELMbeta, Proteobacteria were present in the inner mucus layer and invaded mucosal tissues.

195 ar wind nebula, as well as structures in the inner nebula including a jet and torus.

196 Then, sheath cells invade the inner notochord and differentiate into vacuolated cells,

197 tion in the retina, efficiently reaching the inner nuclear and outer plexiform, and to a lesser exten

198 uently in Henle's fiber layer (HFL) than the inner nuclear layer (INL) and was highly associated with

199 n cell and inner plexiform layer (GCIPL) and inner nuclear layer (INL) volumes were tested for associ

200 and visual thresholds; total nuclear layer, inner nuclear layer (INL), and outer nuclear layer (ONL)

201 , inner plexiform layer (S6 and N6 sectors), inner nuclear layer (T6 and N6 sectors), and outer plexi

202 egeneration with severe GCL loss, borderline inner nuclear layer thinning, and less prominent photore

203 Microcystoid macular changes in the inner nuclear layer were diagnosed in 52 out of 264 eyes

204 ying cells) have their soma displaced to the inner nuclear layer.

205 ], a family of transmembrane proteins of the inner nuclear membrane (INM) [8, 9], to form the so-call

206 ty is critical for processing lamin A on the inner nuclear membrane and clearing clogged translocons

207 Strikingly, we also find that the inner nuclear membrane protein Sun1 antagonizes Sun2 LIN

208 we find that LINC complexes that contain the inner nuclear membrane protein Sun2 promote focal adhesi

209 ptide 1 (LAP1) is an integral protein of the inner nuclear membrane that has been implicated in stria

210 N and OFF bipolar cell terminals in separate inner (ON) and outer (OFF) sublayers in response to ligh

211 NHANCER (BEN) confines the C-function to the inner petunia floral whorls, in parallel with the microR

212 suppression, but only if the content of the inner phoneme matched the content of the audible phoneme

213 The production of the inner phoneme resulted in electrophysiological suppressi

214 and the potential contribution of comets to inner-planet atmospheres are long-standing problems.

215 The common ganglion cell and inner plexiform layer (GCIPL) and inner nuclear layer (I

216 er-specific arbor specializations within the inner plexiform layer (IPL) that occur consistently at d

217 he segregation of ON and OFF pathways in the inner plexiform layer (IPL), where glutamate is released

218 tivity; (4) restricted lamination within the inner plexiform layer (IPL), which renders J-RGCs respon

219 the ganglion cell layer (I3 and N6 sectors), inner plexiform layer (S6 and N6 sectors), inner nuclear

220 Although the inner plexiform layer appears earlier than the outer ple

221 e that TH cell somata, tapering and varicose inner plexiform layer neurites, and varicose outer plexi

222 different types of amacrine cells across the inner plexiform layer prompts that they should be also i

223 the synaptic layers beginning in stereotyped inner plexiform layer sublaminae.

224 found between CS at 6 cpd and ganglion cell/inner plexiform layer thickness at inferotemporal and in

225 ng was present within the nerve fiber layer, inner plexiform layer, and inner and outer nuclear layer

226 h of this functional diversity arises in the inner plexiform layer, where inhibitory amacrine cells m

227 hat ramify within the outermost layer of the inner plexiform layer.

228 either the outer or the inner border of the inner plexiform layer.

229 some colocalizations of GluR1 and TH in the inner plexiform layer.

230 or example, changes in the ganglion cell and inner plexiform layers, the sites of the retinal ganglio

231 change of -1 dB/year or more (P < 0.01) for inner points or -2 dB/year or more (P < 0.01) for edge p

232 ) aerogels with controlled 3D structures and inner pore architecture are printed using the direct ink

233 e channel is closed by a constriction of the inner pore formed by criss-crossing of the S6 segments a

234 ls is closed by a single constriction of the inner pore formed by the criss-crossing of the cytoplasm

235 -composted biochar that covers the outer and inner (pore) surfaces of biochar particles using high-re

236 he poles and traverse of Jupiter's hazardous inner radiation belts.

237 ed by charge-weighted averaging of outer and inner radii.

238 s trend may be driven by the increase in the inner radius of the obscuring material with incident lum

239 d, we developed an innovative method for the inner-recycling of biomass that could harvest the typica

240 -2 motor KIF17 and thus spatially map to the inner region of the ciliary gating zone.

241 lensing offers an opportunity to resolve the inner regions of galaxies.

242 ration from the retinal vasculature into the inner retina that replenishes the local myeloid cell pop

243 obilization of endogenous microglia from the inner retina to the RPE layer, followed by (2) subsequen

244 d dendritic stratification of neurons in the inner retina.

245 t the relatively impermeable blood-brain and inner retinal barriers) that regulates tissue-fluid home

246 The near transparency of inner retinal cells is advantageous for vision, as light

247 oss-over pathways, indicating dysfunction in inner retinal circuitry.

248 idth (EZW) and outer nuclear layer (ONL) and inner retinal layer (IRL) thickness measurements.

249 The areas of atrophy involved the inner retinal layers and were associated with an absence

250 th LPC had a lower probability of having all inner retinal layers present at the foveal center (odds

251 inal cells, including those in the outer and inner retinal layers.

252 t that, after a chemical lesion that ablates inner retinal neurons, regenerated retinal bipolar neuro

253 nockout animals indicate a contribution from inner retinal photoreceptors.

254 e 3 plexuses, as well as from the all-plexus inner retinal slab.

255 parations were presumably able to access the inner rhamnogalacturonan I dominant coating layers due t

256 ly DBDPE showed inhibition of both outer and inner ring deiodination (O and IRD) of T3 and 3,3'-T2 fo

257 SS needle protein, NAIP2 recognizes the T3SS inner rod protein, and NAIP5 and NAIP6 recognize flagell

258 NAIP isoform is capable of sensing the T3SS inner rod, needle, and flagellin.

259 agen, NF-kappaB activity was observed in the inner root sheath and unilaterally clustered in the HF m

260 t in 6 subjects subtle irregularities at the inner segment ellipsoid band were seen.

261 tochondria cluster at the apical side of the inner segment, directly below the outer segment.

262 scopy showed increased autophagosomes in rod inner segments with HDAC inhibitor (HDACi) treatment, po

263 e ERG are truncated with shortened outer and inner segments.

264 o the current grounding-line position on the inner shelf.

265 zation of more highly charged cations to the inner shell of the ion atmosphere.

266 anostructure with Li2O outer-shell and Li2O2 inner-shell surfaces.

267 Insects are strange "aliens from inner space", with sensory and cognitive worlds wholly d

268 These results demonstrate that inner speech - a purely mental action - is associated wi

269 l study employed a novel design to show that inner speech - the silent production of words in one's m

270 These findings suggest that inner speech may ultimately reflect a special type of ov

271 sults indicated that the bidentate binuclear inner sphere was the most probable type of ligand for ar

272 We show that the formation of an inner-sphere adsorption complex may be a necessary step

273 forms identical adsorption complexes, namely inner-sphere binuclear bidentate.

274 ve iron is directly associated to OC through inner-sphere complexation in coastal sediments, as much

275 etal-rescue experiment provides evidence for inner-sphere divalent metal ion coordination with a nucl

276 at least one catalytic metal ion through an inner-sphere interaction.

277 the resulting loaded complex evolves via an inner-sphere mechanism into a ruthenacyclopropene which

278 econds during which thermodynamically stable inner-sphere Rb(+) slowly transforms to a less stable ou

279 hell scattering contributions, indicating an inner-sphere sorption of Pu on OPA components.

280 Mechanistic studies are consistent with an inner-sphere transfer of the sulfide, which is remarkabl

281 dologies that are believed to proceed via an inner-sphere-type mechanism, with an emphasis on the nat

282 eted type III repeat epitopes cluster on the inner strands of both beta-sheets forming the fibronecti

283 Both the outer and inner stratifying dendrites express postsynaptic density

284 l-based electrocatalyst through an outer and inner structural control to strengthen the electrocataly

285 Herein, a novel strategy involving outer and inner structural engineering is developed for superior w

286 noninvasive technique for investigating the inner structure of objects and organisms.

287 Although the highly acidic inner surface of BPH was in striking contrast to the cav

288 ed hydrophobic and ionizable monomers on the inner surface of solid-state nanopore.

289 metry's strong light-matter interaction, the inner surface provides an excellent on-chip sensing plat

290 cretory functions of glands, which cover its inner surface.

291 Inner tegument protein UL37 is conserved among all three

292 ion factor related to poor concentration and inner tension (r=-0.32; 95% CI=-0.51, -0.08).

293 PAHs in the cuticles and inner tissues were distinguished by sequential extractio

294 ntations of gating zone components along the inner-to-outer axis of the ciliary gating zone.

295 pulse widths, for 21 cell types spanning the inner two layers of the rabbit retina.

296 t TRPV4 may differentially contribute to the inner vs. outer blood-retinal barrier function.

297 sue of the trabecular meshwork together with inner wall endothelium of Schlemm's canal (SC) provide t

298 ed to calculate an air volume sampled by the inner wood layer (cambium) of a tree during a one year g

299 virtually all of the events involved in the inner workings of a cell.

300 rse for pioneering exploration of the veiled inner workings of the Earth.