ライフサイエンスコーパス: be controlled by

1 Variations in the degree of trust are controlled by a confidence factor beta, while the pr

2 rward drive, feedback drive, and prior drive are controlled by a handful of state parameters, which I

3 ormal awake time and that these size changes are controlled by a nuclear mechanism that modulates rib

4 ue patterning and maintenance in Arabidopsis are controlled by a well-established gene network revolv

5 versible colloidal membrane, but it also can be controlled by a dynamic mechanical stimulus using a n

6 e conclude that an entire fusion cascade can be controlled by a GEF.

7 What is interesting the collapse can be controlled by a magnetic field even without long-rang

8 et nodes, suggesting that large networks can be controlled by a relatively small number of inputs as

9 that motility of the receiver strains could be controlled by a sender strain generating a signal gra

10 Efficient MGO and GO detoxification can be controlled by a switch in metal cofactor usage.

11 eous pattern of global vegetation change has been controlled by a combination of multiple forcings, s

12 go a large conformational rearrangement that is controlled by a 'redox switch' centered on an inter-m

13 This developmental process is controlled by a complex regulatory network involving

14 while the propensity to produce distortions is controlled by a conservation factor K.

15 pes in multiple animals, spindle orientation is controlled by a conserved biological machine that med

16 r results show that this monocyte deployment is controlled by a CX3CR1-dependent balance between marg

17 Vascular tone is controlled by a dual mechanism.

18 of the N-methyl D-aspartate receptor (NMDAR) is controlled by a glutamate-binding site and a distinct

19 lso indicate that F. tularensis pathogenesis is controlled by a highly interconnected molecular circu

20 d through an intramolecular interaction that is controlled by a key residue in DENND3, tyrosine 940.

21 The phosphorylation state of Spo0A is controlled by a multi-component phosphorelay.

22 Hyphal formation is controlled by a multilayer regulatory network compose

23 NF-kappaB activation is controlled by a negative feedback regulation through

24 ult low dynamic frictional resistance, which is controlled by a number of physico-chemical lubricatio

25 Circadian locomotor behaviour is controlled by a pacemaker circuit composed of clock-c

26 dle orientational order near the surface and is controlled by a scale-invariant criterion related to

27 ature responsiveness of omega-6 desaturation is controlled by a separate QTL on chromosome 2.

28 A proof-reading by RIG-I and we show that it is controlled by a set of conserved amino acids that cou

29 Selection and export of the effectors is controlled by a set of soluble proteins at the cytoso

30 Subtype specification is controlled by a stochastic decision in R7 and instruc

31 t genus Bacteroides in which gene expression is controlled by a synthetic inducer.

32 show that tankyrase 1 activity at telomeres is controlled by a ubiquitination/deubiquitination cycle

33 Increased yield was controlled by a higher rate of tillering, leading to

34 Removal of ubiquitin chains is controlled by ABRO1/BRCC36 and occurs as cells exit m

35 Immune cell-infiltration is controlled by activated PPARgamma/RXRalpha that inhib

36 Endocycle onset is controlled by activity of the Anaphase Promoting Comp

37 The length of this metallopolymer can be controlled by adding monofunctional subcomponents to

38 te occurs with increasing Ce content and can be controlled by adjusting the PO2 and the heat treatmen

39 spherical and fibrillar nanostructures could be controlled by adjusting the rod-coil block ratios.

40 ycemia in patients with diabetes; this event was controlled by adjusting medication for diabetes.

41 ction-mediated effects on methanogenesis may be controlled by alpha- and beta-diversity.

42 tifunctionality resistance could potentially be controlled by altering soil pH.

43 ways by which this transformation occurs can be controlled by altering the design of individual units

44 species has revealed that behavior and caste are controlled by an interaction between genetic and env

45 Patterns of daily human activity are controlled by an intrinsic circadian clock that prom

46 r a magnetic impurity, whose orientation may be controlled by an external magnetic field, can be used

47 eveloped a codon-optimized L1 transgene that is controlled by an endogenous mouse L1 promoter.

48 (2) The site selectivity of C-H activation is controlled by an N-methoxyamide group rather than a s

49 s key proteins of the endoplasmic reticulum, is controlled by an upstream palmitoyltransferase, ZDHHC

50 Cerebral blood flow (CBF) is controlled by arterial blood pressure, arterial CO2,

51 e demonstrate that protein kinase R activity is controlled by auto-inhibition via an intra-molecular

52 ain-interacting protein) chromatin regulator is controlled by B cell activation and potentiates stead

53 of Cdc5 at the daughter SPB in late anaphase is controlled by Bfa1.

54 This transition is controlled by binding of a novel tetrameric form of t

55 e sexual life cycle of C. reinhardtii, which is controlled by blue and red light at the steps of game

56 Thus, grid cells are controlled by both local geometric boundaries and re

57 m and neuromodulatory responses of breathing are controlled by brainstem neurons in the preBotzinger

58 sts and the interval between their spikelets were controlled by Ca(2+) acting across two nanodomains,

59 Aqueous V concentrations were controlled by Ca3(VO4)2 solubility, which demonstra

60 s pro-inflammatory proteases, whose activity is controlled by calpastatin, their specific inhibitor.

61 n catabolism (glycolysis and TCA cycle), and was controlled by cAMP-Crp.

62 Capsid movement in these viruses is controlled by capsid-associated tegument proteins, ye

63 a well-orchestrated series of contractions, is controlled by cardiac action potentials.

64 stricted to epithelial cells and neurons and is controlled by CD8 T cells.

65 mpo, a learned and quantifiable feature that is controlled by central neural circuitry.

66 tropical peatland carbon storage and fluxes are controlled by changes in climate, sea level, and dra

67 mal MMP13 gene expression in OA chondrocytes is controlled by changes in the DNA methylation status o

68 shown that degree of TAAC polymerization can be controlled by changing gel fiber thickness, which in

69 The roughness of the Al surface is controlled by changing the substrate temperature duri

70 Nucleolar morphology is controlled by chromatin structure, and the high level

71 heir potential upslope (or downslope) shifts were controlled by climate, land-use legacies (past logg

72 Abyssal current variability is controlled by comparable contributions from tides, su

73 nging gel fiber thickness, which in turn can be controlled by concentration.

74 The activity of the alphabeta TCR is controlled by conformational switches.

75 of PKC-2 activity revealed that thermotaxis is controlled by cooperative PKC-2-mediated signaling in

76 arrier-envelope phase (CEP) of HH pulses can be controlled by crystal symmetry.

77 cytosolic and mitochondrial NADPH pools that are controlled by cytosolic NAD(+) kinase levels and rev

78 This process is controlled by cytosolic actin-based constriction mach

79 ntinuously active stem cells, whose activity is controlled by developmental and environmental signals

80 er air-excluded conditions Ca concentrations were controlled by dicalcium silicate dissolution and Ca

81 se results establish that mo-DCs and mo-Macs are controlled by distinct transcription factors and sho

82 unique patterns of effector gene expression, is controlled by distinct combinations of phylogenetical

83 ates of formation of the metallacycloadducts are controlled by distortion energy, analogous to their

84 nding that the magnon chemical potential can be controlled by driving the system's ferromagnetic reso

85 ew the facets of translation elongation that are controlled by EF-P, with a particular focus on the p

86 Ethylene signaling is controlled by EIN2, which is duplicated in L. japonic

87 Therefore, cardiac O2 consumption is controlled by endothelial NO in a paracrine, but not

88 lesions, binding of the nucleotide substrate is controlled by energetics associated with nucleobase d

89 nsory deprivation and activity loss, and can be controlled by enhancing cortical activity.

90 Sporogony is thought to be controlled by environmental conditions and mosquito/p

91 GABA synthesis is controlled by enzymes derived from two glutamic acid

92 ate receptors (NMDARs) and pathological pain are controlled by ephrin-B-induced extracellular phospho

93 the expression of the acetylating gtrC gene is controlled by epigenetic phase variation.

94 an escape response of the primary root that is controlled by ERFVII activity and mediated by auxin s

95 enetic cascades, and that these cascades can be controlled by external signals as well as inter-lipos

96 and electrical characteristics of which can be controlled by external stimuli.

97 e and the female reproductive tissues, which are controlled by extracellular signaling molecules inte

98 bout the degree to which earthquake ruptures are controlled by fault segmentation and should motivate

99 ynthesis in many Bacteria but not in Archaea is controlled by FMN-responsive riboswitches.

100 ls and their entry into the myogenic program is controlled by gene regulatory networks, where paired

101 of the dilated cardiomyopathy phenotype and are controlled by genetic factors.

102 , the gravitropic setpoint angle of rice ARs is controlled by genetic and environmental factors that

103 The diversity and activity of leukocytes is controlled by genetic and environmental influences to

104 acquired nicotine self-administration model is controlled by genetic factors and that the role of so

105 full panoply of mRNAs whose polyadenylation is controlled by GLD4, we performed an unbiased whole ge

106 emonstrate that Southern Ocean-AIS feedbacks were controlled by global atmospheric teleconnections.

107 Available data suggest that most symptoms are controlled by haploinsufficiency of two or more 16p1

108 previously demonstrated that ASS1 silencing is controlled by HIF-1alpha and Arg starvation-reactivat

109 stive and phase-change memory (RRAM and PCM) is controlled by highly localized self-heating effects,

110 very of several host defense proteins to PVs is controlled by IFN-inducible guanylate binding protein

111 e investigated whether VEGF release by HPMCs is controlled by IL-6 in combination with its soluble re

112 iverse cellular functions and are thought to be controlled by independent upstream activation cascade

113 ized by elevated plasma cortisol levels, can be controlled by inhibition of 11beta-hydroxylase (CYP11

114 The position of the nucleus in a cell is controlled by interactions between the linker of nucl

115 hich the lifetime of the drug-target complex is controlled by interactions in the transition state fo

116 ion channel superfamily but their activities are controlled by intracellular cyclic nucleotides inste

117 ransitions between the recognition sites can be controlled by introducing steric "speed bumps" or ele

118 duction, depend on cytoplasmic Ca(2+), which is controlled by ion channels.

119 Ascorbate content in plants is controlled by its synthesis from carbohydrates, recyc

120 pro-resolving circuit, including PCTR1, that is controlled by local neuronal output to regulate tissu

121 Electrode rotation in this new cell design is controlled by magnetically coupling the working elect

122 he energy flow during natural photosynthesis is controlled by maintaining the spatial arrangement of

123 The efficiency of codon translation in vivo is controlled by many factors, including codon context.

124 the extracellular matrices in the human body is controlled by matrix metalloproteinases (MMPs), a fam

125 tional regulation, yet what regulatory steps are controlled by metazoan Nups remains unclear.

126 r spin states of a phosphorus donor that can be controlled by microwave electric fields.

127 clude that enhanced collateral vessel growth is controlled by miRNAs, among which miR-352 is a novel

128 In Leishmania major strain Friedlin, this is controlled by modifications of the stage-specific adh

129 th the photon wavelength, lambda0, which can be controlled by modulating the carrier density of graph

130 genes within DNA damage repair pathways that are controlled by MOF, as correlated with a significant

131 lls in the developing enteric nervous system are controlled by molecules such as the signaling protei

132 Behavioral circadian rhythms are controlled by multioscillator networks comprising fu

133 ses revealed that response to these stresses is controlled by N-end rule regulation of ERFVII functio

134 ng host response that, at some point, has to be controlled by negative regulators to maintain tissue

135 vessels in the central nervous system (CNS) are controlled by neuronal activity.

136 ANCE STATEMENT Rhythmic movements of animals are controlled by neuronal networks that have been conce

137 These cell shape changes are controlled by nonmuscle myosin II (NMII) motor prote

138 er anaerobic conditions, suggesting that Fur is controlled by O2 availability.

139 Transfer of the drugs across FLM was controlled by optimizing the composition and pH of a

140 ( approximately 10-70 km downwind of the OS) are controlled by OS emissions; > 50% of the monthly mea

141 , the cell fusion step in osteoclastogenesis is controlled by phosphatidylserine-regulated activity o

142 Similar to other MAPKs, Smk1 is controlled by phosphorylation of a threonine (T) and

143 Similar to canonically activated MAPKs, Smk1 is controlled by phosphorylation of its activation-loop

144 NLRP3 and demonstrate that NLRP3 activation is controlled by phosphorylation of its pyrin domain (PY

145 ny proteins from the cytosol, a process that is controlled by phosphorylation.

146 ssor of Pol III transcription whose activity is controlled by phosphorylation; in particular, it is i

147 g reproduction, hibernation, and metabolism, are controlled by pituitary hormones released in respons

148 dominated by transpiration, and both fluxes are controlled by plant stomatal conductance.

149 ne signaling, while only AtPMEI11 expression is controlled by PME-related damage-associated molecular

150 complexes in living cells, which appears to be controlled by post-translational acetylation on PFKL.

151 ivation stimulus, and if such modulation can be controlled by post-translational modifications of the

152 nd maintenance of the adipose vascular niche is controlled by PPARgamma acting within APCs.

153 TRPC6 channel activity is controlled by protein expression and stability as wel

154 tral regulator of lipogenesis whose activity is controlled by proteolytic cleavage.

155 vealed that SMX-NO-specific T cell responses are controlled by public TCRs present in all individuals

156 The power of each lens is controlled by pumping a liquid in and out of the lens

157 we show that tumour cell exosomes secretion is controlled by pyruvate kinase type M2 (PKM2), which i

158 tudy we investigated whether MICB expression is controlled by RBPs through its 5'UTR.

159 soluble pollutant, the mobility of which can be controlled by reduction of Cr(VI) to less soluble, en

160 its aggregation and possibly its function(s) are controlled by regulatory mechanisms involving crosst

161 Expression of lamin-A is known to be controlled by retinoic acid receptor (RAR) transcript

162 ction of an actomyosin contractile ring that is controlled by Rho-family small GTPases.

163 This timing is controlled by seed dormancy, which prevents germinati

164 expression of nearly all smooth muscle genes are controlled by serum response factor binding sites in

165 CRL activity is controlled by several proteins or protein complexes,

166 A mRNA's translation rate is controlled by several sequence determinants, includin

167 The phase of few-layer MoTe2 is controlled by simply changing Te atomic flux controll

168 he planetary interior during plate tectonics is controlled by slow convection within the mantle.

169 Cellular movement is controlled by small GTPases, such as RhoA.

170 l precursor molecules is a key parameter and is controlled by so-called cross talk between different

171 Distillation box placement is controlled by so-called schedulers.

172 se oligonucleotides are polymorphic, but may be controlled by solution pH and counter ion species.

173 d approach a limit where their global motion is controlled by solvent friction alone, with ruggedness

174 ic function for these effector kinesins that is controlled by specific Nek kinase signaling modules t

175 triradical forms D(+*)-A-R(-), but its yield is controlled by spin statistics of the uncorrelated A(-

176 l shows that the lability of these bonds can be controlled by steric pressure due to substituents on

177 air humidity affect plant gas exchange that is controlled by stomata, small pores on plant leaves an

178 ity of Piezo mechanically gated ion channels is controlled by stomatin-like protein-3 (STOML3), which

179 CNS and their positioning within the tissue are controlled by stromal cells that construct the barri

180 e concentrations since levels of the steroid were controlled by subcutaneous implants, thus suggestin

181 ase growth, in which phase-boundary movement is controlled by surface reaction or lithium diffusion i

182 e further show that the auxetic behavior can be controlled by tailoring the geometric features of the

183 therefore, reactivity of the MoS2 nanosheets are controlled by the attached functional groups.

184 Therefore, granular layer capillaries are controlled by the balance between vasodilating and v

185 giogenesis and blood-brain barrier integrity are controlled by the canonical Wnt pathway.

186 osynthesis and photosynthetic products which are controlled by the circadian clock feedback to affect

187 , productivity and preservation of mangroves are controlled by the interplay of tectonics, global sea

188 Cell fate decisions are controlled by the interplay of transcription factors

189 l transport behaviours of the nanocomposites are controlled by the magnetic transition of BaFe12O19 n

190 Differentiation and function of TFH cells are controlled by the master gene BCL6, but it is largel

191 t both basal mechanical and neuropathic pain are controlled by the microRNA-183 (miR-183) cluster in

192 tein signaling, whose intensity and duration are controlled by the regulator of G protein signaling (

193 The exchange dynamics are controlled by the relative acidity of the [CpMo(H)(C

194 Levels of OIG-8 expression are controlled by the specific combination of a terminal

195 veal that the dynamics of the allene buildup are controlled by the structural changes, whereas the de

196 he structure and functionalities of the ONPs are controlled by the synthesis of their parent linear b

197 als system wherein the mechanical properties are controlled by the underlying network connectivity.

198 on as translational regulatory elements that are controlled by the viral RNA-binding protein (RBP) NS

199 high-throughput screening of properties that are controlled by the wrapping DNA sequences.

200 ed voltage bias, and their orientation could be controlled by the addition of a single charge to the

201 ctronic properties of the resulting GNRs can be controlled by the annealing temperature, providing GN

202 fraction of submicrometer particles will not be controlled by the composition of the sea surface micr

203 the resulting aggregates are tunable and can be controlled by the concentration of immobilized surfac

204 modulation frequency for generating SSBs can be controlled by the field-like torque and biasing condi

205 DNA, the spread of which in the genome must be controlled by the host, but also as major players in

206 the selectivity of the catalytic systems may be controlled by the nature of the silane, with PhSiH3 f

207 gold and the real electrode surface area can be controlled by the parameters of metal electrodepositi

208 The filament velocities were found to be controlled by the relative number of active HMM per t

209 energy bands form where the new band gap can be controlled by the size and pitch of the quantum dots

210 -of-equilibrium aggregates depend on and can be controlled by the size of the constituent nanoparticl

211 object rapidly and the rate of rotation can be controlled by the source amplitude.

212 that the dynamics of magnetic skyrmions can be controlled by the spin-orbit torque on the nanosecond

213 The kinetics of this reaction can be controlled by the substitution pattern and the solven

214 by the Arrhenius equation and therefore can be controlled by the temperature and lattice mismatch.

215 Messenger RNA function is controlled by the 3' poly(A) tail (PAT) and poly(A)-b

216 (GL) transcription of the constant genes and is controlled by the 3' regulatory region (3'RR) in a st

217 The size of the ring formed is controlled by the alkylammonium cation present.

218 Therefore, the extent of reaction is controlled by the amount of Ox2 added, and the rate o

219 IOP is controlled by the balance between aqueous humor secre

220 We conclude that diastolic [Ca(2+) ]i is controlled by the balance between Ca entry and efflux

221 We report that diastolic [Ca(2+) ]i is controlled by the balance between Ca(2+) entry and Ca

222 ate embryogenesis, dorsal-ventral patterning is controlled by the BMP/Chordin activator/inhibitor sys

223 The block angle at each helical junction is controlled by the change in stripe direction, while t

224 and experiments suggest that starch turnover is controlled by the circadian clock acting as a dynamic

225 genome occupancy of HDAC3 in skeletal muscle is controlled by the circadian clock, these results deli

226 Dynein's activity is controlled by the combinatorial action of several reg

227 se to this nitrosative (NO-triggered) stress is controlled by the Crp/Fnr-type transcriptional regula

228 The amount of coupling is controlled by the degree of asymmetry introduced.

229 C) and antigen-presenting classical DC (cDC) is controlled by the E protein transcription factor TCF4

230 ng of the anion permeation path in this iChS is controlled by the elevator-like movement of the subst

231 s of apicobasal polarization in animal cells is controlled by the evolutionarily conserved Crumbs (CR

232 he morphology of the self-assembled swimmers is controlled by the frequency and amplitude of the magn

233 The stereoselectivity of the process is controlled by the geometry of the double bond of the

234 elopment of the bent-on-both-limbs anticline is controlled by the geometry of the underlying fault-pl

235 gression in mammalian preovulatory follicles is controlled by the granulosa cells around the oocyte.

236 es, and iron mobilization from the liver and is controlled by the hepatic hormone hepcidin.

237 Type I IFN signaling is controlled by the inducible negative regulators suppr

238 mount of Ox2 added, and the rate of reaction is controlled by the injection rate of Ox2 .

239 of the kinases Hippo and LATS via which YAP is controlled by the innate immune pathway.

240 eosome sliding reaches an end point and this is controlled by the Ino80CTD.

241 Entry to and exit from an open burst is controlled by the interaction of ATP with two ATP-bin

242 nt and sensation, since tumbling probability is controlled by the internal state of the organism whic

243 Sleep is controlled by the interplay between sleep homeostasis

244 The activity of the Piezo2-dependent channel is controlled by the intracellular Ca(2+) concentration

245 at the first defect event, signifying yield, is controlled by the intralayer spacing (grain size, d),

246 Cellular iron homeostasis is controlled by the iron regulatory proteins (IRPs) 1 a

247 l, our results indicate that Pfn2 expression is controlled by the IRPs in vivo and that Pfn2 contribu

248 ormation of the Drosophila embryonic termini is controlled by the localized activation of the recepto

249 d the amplitude of the circadian oscillation is controlled by the microbiota through group 3 innate l

250 disassembly rate of preformed Abeta fibrils is controlled by the molecular weight of mPPCs.

251 ERF-VII stability is controlled by the N-end rule pathway, which proposes

252 elanogaster peripheral sensory organ lineage is controlled by the non-neuronally expressed mir-279/99

253 Our studies reveal that pdcA transcription is controlled by the nutrient-regulated transcriptional

254 rtant mechanism to regulate gene expression, is controlled by the opposing action of histone acetyltr

255 at the binding affinity of the incoming dNTP is controlled by the overall hydrophobicity of the nucle

256 Moreover, the mammary clock is controlled by the periductal extracellular matrix in

257 Distinguished site selectivity is controlled by the predominant 1,5-hydrogen atom trans

258 PerR binding to gene promoters is controlled by the presence of iron in the regulatory

259 Thus, PLP activation is controlled by the proximity of the pyridinyl nitrogen

260 release of arsenic by reduction of Fe-oxides is controlled by the reaction rate, arsenic entering the

261 Particle size is controlled by the self-assembly and unique phase tran

262 alytics that the intracellular cargo release is controlled by the sequence of the peptide linker.

263 mbrane proteins to the endoplasmic reticulum is controlled by the signal recognition particle, which

264 The regioselectivity of the diamination is controlled by the solvent and the electronics of the

265 The length of the microwires is controlled by the spacing of the electrodes used for

266 n the network and that the degree of scaling is controlled by the strength of external input.

267 es and observe that the critical temperature is controlled by the total fraction of removed area, ind

268 xidative damage to photosystem II (PSII) and is controlled by the transmembrane pH differences (Delta

269 t, Rpt2, indicating that exocyst degradation is controlled by the ubiquitin-proteasome system.

270 We found that Themis stability is controlled by the ubiquitin-specific protease USP9X,

271 Particle size was controlled by the concentration of the gold source.

272 Progradation was controlled by the local initial environmental condit

273 depends on the extent of aggregation, which was controlled by the solution pH and time.

274 ed Holocene retreat of glaciers in Koge Bugt was controlled by the subglacial topography of the area;

275 The difficulty and viewing duration were controlled by the experimenter.

276 ivity resolution of the SRR dielectric probe were controlled by the geometrical parameters of the SRR

277 w the properties of the different components are controlled by their chemical structures.

278 The bioavailability of heavy metals in soil is controlled by their concentrations and soil propertie

279 In vertebrate cells, the DNA damage response is controlled by three related kinases: ATM, ATR, and DN

280 Their polarization and activation are controlled by transcription factors such as NF-kappa

281 Differential gene activity is controlled by transcription factors but also dependen

282 ian cells and suggest that this activity can be controlled by tRNA levels.

283 t all Golgi cisternae and that this activity is controlled by Tuba and ARHGAP10, two Golgi-associated

284 nder physiologically relevant conditions can be controlled by tuning a single thermodynamic parameter

285 ction of reflected and transmitted atoms can be controlled by tuning the lattice height.

286 l lattice geometry where the frustration can be controlled by tuning the unit cell parameters.

287 ctor, the small fraction of heat transferred is controlled by two dimensionless groupings of physical

288 f the Drosophila sloppy paired 1 (slp1) gene is controlled by two distinct cis-regulatory DNA element

289 Several steps in the ABA-signaling pathway are controlled by ubiquitination involving really intere

290 nd habits (habitual avoidance) are viewed as being controlled by unique circuits that operate noncons

291 currently known about how expression of Eya1 is controlled by upstream regulators.

292 sitol 4-phosphate 5-kinases (PI4P 5-kinases) is controlled by upstream signaling is currently unknown

293 non-Gaussian output mode structures that may be controlled by varying either the input beam power or

294 of reaction under continuous excitation can be controlled by varying the wavelength of light that se

295 c3 activity, at and surrounding invadopodia, is controlled by Vav2 and betaPIX.

296 here antibacterial agents whose activity can be controlled by visible light, while getting into the t

297 ta suggest that FoxM1 abundance and activity are controlled by VprBP and highlight the functional rep

298 by active loop extrusion, whose processivity is controlled by Wapl.

299 Both processes are controlled by Wnt or Norrin (NDP) ligands, Frizzled

300 earch function of XPC in the genomic context is controlled by XPC itself, DDB2, and PARP1.