ライフサイエンスコーパス: -independent

1 CC expression by Kir4.1-dependent and Kir4.1-independent mechanisms.

2 O(2) affinity, which we attribute to an O(2)-independent antisickling activity, in addition to the O(

3 that mimics both the O(2)-dependent and O(2)-independent antisickling properties of fetal hemoglobin.

4 ns biofilm synergy in a contact and H(2)O(2)-independent manner.

5 ibrosis, our results highlight that the O(2)-independent UQ biosynthetic pathway may represent a targ

6 Thus, the Ca(2+)-independent, Arg-containing NrfA from G. lovleyi represe

7 dies, we characterized its unexpected Mg(2+)-independent binding mode.

8 and subsequent ORAI activation in a Ca(v)1.2-independent and store depletion-independent manner.

9 ve been conflicting reports about the Arp2/3-independent biochemical activities of WAVE1 on actin fil

10 conventional caspase-dependent but caspase 3-independent cell death and that the mechanism of cell de

11 ng chronic filarial infection and that IL-4R-independent/IL-5- and CCR3-dependent pathways are suffic

12 d mitochondrial dysfunction, however, is AAG-independent.

13 ABA-independent SnRK2s act at the posttranscriptional level

14 , SnRK2.6, SnRK2.7, and SnRK2.8, and the ABA-independent subclass 1 protein kinases SnRK2.1, SnRK2.4,

15 A new Abeta-independent hypothesis emerges where the amyloidogenic p

16 3 and ASC into a novel RIPK1 kinase activity-independent cell death complex to drive pyroptosis and a

17 found fully functional RIPK1 kinase activity-independent necroptosis driven by the RIPK3-MLKL pathway

18 However, here we show a kinase activity-independent role for RIPK1 in these processes using a mo

19 at this diversity is the product of activity-independent size fluctuations, which are sufficient to g

20 t forms of synaptic plasticity, yet activity-independent processes might also play some part.

21 Notably, adhesion-dependent and adhesion-independent migration are not mutually exclusive, but ra

22 the IL-33/ST2 pathway in Ag-dependent and Ag-independent asthma-like models.

23 he beta(2)AR exhibits a low level of agonist-independent G protein activation.

24 n mitochondrial function were UCP1- or AKAP1-independent, suggesting compound effects on multiple nod

25 p85beta activates p110 activity and AKT-independent PDK1/SGK3 signaling to promote tumorigenic p

26 Anchorage-independent growth reprogrammes a metabolic network invo

27 al cancer cell proliferation in an anchorage-independent manner.

28 K1 or MSK2, cell proliferation and anchorage-independent cell growth were markedly inhibited.

29 reduced cell growth, migration and anchorage-independent growth of CRC cells.

30 for suppressing cell migration and anchorage-independent growth.

31 of tumor cells on HR signaling for anchorage-independent growth and highlights how the metastatic mic

32 independence and HT resistance in anchorage-independent cells revealed distinct context-dependent me

33 ing acquisition and restoration of anchorage-independent growth in HR(+) tumors.

34 knockdown of which diminished the anchorage-independent growth of ILC cell lines through cell cycle

35 cancer cell lines increased their anchorage-independent growth and inhibited TGFB signaling to a gre

36 Although the TCR-dependent and -independent activation of iNKT cells have been relativel

37 A modest increase in Cas9-dependent and -independent DNA off-target editing, and in transcriptome

38 (+) fluxes by phosphorylation-dependent and -independent events.

39 unoblotting with conformation-dependent and -independent mAbs, which confirmed it to be both pure and

40 and do so via glucocorticoid-dependent and -independent mechanisms, respectively.

41 ins, suggesting that Pol zeta-dependent and -independent roles of Rev7 are relevant to cisplatin resp

42 f POLR3E and elicits promoter-dependent and -independent transcription by Pol III.

43 inal homeostasis through TEAD-dependent and -independent transcription.

44 r antiproliferative activity in the androgen-independent PC3 prostate cancer cell line.

45 Interestingly, angular-independent structural colors, where isotropy in the sca

46 tions have demonstrated a chlamydial antigen-independent immune mechanism for regulating chlamydial p

47 c CD4+ T cell repertoire, suggesting antigen-independent survival of this subset.

48 , via extracellular vesicles in an apoptosis-independent mechanism.

49 ence of an aggressive androgen receptor (AR)-independent neuroendocrine prostate cancer (NEPC) after

50 AR-independent treatment-resistant prostate cancer is a maj

51 pathogen interactions and suggest a new Arf1-independent role for components of the COPI coatomer com

52 winds ~2 turns of the double helix in an ATP-independent fashion.

53 nd Haemophilus influenzae use tripartite ATP-independent periplasmic transporters (TRAPs) to scavenge

54 op formation by Rad51 and Rad54 in an ATPase-independent manner.

55 ell population and is additional to the BAFF-independent effect of B cells on Treg cells.

56 in vivo and in vitro and complemented biotin-independent growth of the M. smegmatis tam deletion muta

57 Finally, we provide insight into BP-independent biological pathways underlying SVD and sugge

58 We report that MCMV RNA contains a cap-independent translation element (CITE) in its 3' untrans

59 ES) to hijack host ribosomes and promote cap-independent translation.

60 activity CBEs while maintaining minimal Cas9-independent off-target editing.

61 -targets present were characteristic of Cas9-independent off-targeting and point to TC motifs as acti

62 induces a low frequency of genome-wide Cas9-independent off-target C*G-to-T*A mutation in mouse embr

63 sufficient to induce necroptosis, a caspase-independent mechanism of host cell death that failed to

64 system, further demonstrating its catalysis-independent nature.

65 Here we have identified a beta-catenin-independent function of BCL9 in a poor-prognosis subtype

66 Cation-independent mannose-6-phosphate receptor, also called in

67 ed by mannose 6-phosphate, suggesting cation-independent, mannose 6-phosphate receptor-mediated endoc

68 /DREB binding factor (CBF)-dependent and CBF-independent cold signaling pathways to tolerate cold.

69 NVS-CECR2-1 also kills cancer cells by CECR2-independent mechanism.

70 d hypoplasia together with diminished T cell-independent (TI) antibody responses.

71 Refractory B cell responses to T cell-independent (TI) carbohydrate antigens (Ags) are critica

72 by both cDCs and Nphs contributes to T cell-independent Ab responses.

73 identification of a cDC-dependent but T cell-independent modality that naturally adjuvants plasma cel

74 B cell differentiation in response to T cell-independent type 2 Ags (TI-2 Ags) has been understudied.

75 own phenotype, demonstrating centralspindlin-independent functions.

76 ts PLK4 from self-assembling into centrosome-independent condensates that serve as ectopic microtubul

77 ambda1 production was also induced in a cGAS-independent and DNA-protein kinase (DNA-PK)-dependent ma

78 tility of serum sphingolipids as cholesterol-independent markers of risk and even future targets for

79 nt decRiPPter (Data-driven Exploratory Class-independent RiPP TrackER), a RiPP genome mining algorith

80 ta show that DNA-PK has RNA-dependent, cNHEJ-independent functions during ribosome biogenesis that re

81 vents to model the amino acids of a cofactor-independent oxygenase.

82 at lacks gC was more sensitive to complement-independent neutralization by a panel of gB monoclonal a

83 findings, we uncovered similar concentration-independent behavior from a control compound, strongly s

84 pesticides were represented by conformation-independent molecular descriptors.

85 Culture-independent 16S rRNA gene analysis revealed that both ba

86 Culture-independent diagnostic techniques that detect pathogens

87 Culture-independent mNGS of blood products afforded rapid and pr

88 ll studied from isolate genomes, but culture-independent metagenomics provide a new window into their

89 opments in methodologies, especially culture-independent approaches, have accelerated and driven this

90 n has been given to hypothesis-free, culture-independent tests that can be performed directly on prim

91 Several powerful culture-independent tools, in particular metagenomics, have subs

92 Against this background, rapid culture-independent diagnostics may allow targeted treatment and

93 e, we apply Hi-C, a high-throughput, culture-independent method, to surveil the bacterial carriage of

94 ctional annotations when compared to culture-independent methods.

95 Cutoff-independent discrimination performance remained low for

96 as been proposed in the past; and (2) a Cx36-independent rod pathway(s) (e.g., direct rod to OFF cone

97 However, possible cell cycle-independent mechanisms behind its oncogenicity remain am

98 6D, and NTRK3L449F), determined via cytokine-independent cellular assays.

99 Data-independent acquisition (DIA) is an attractive alternati

100 Data-independent acquisition modes isolate and concurrently f

101 n-shotgun proteome analysis (DI-SPA) by data-independent acquisition mass spectrometry (DIA-MS), we d

102 Several challenges remain in data-independent acquisition (DIA) data analysis, such as to

103 ection strategies for the processing of data-independent acquisition (DIA) proteomics experiments.

104 mple preparation and rapid, single-run, data-independent mass spectrometry analysis (DIA).

105 of concept, we applied FLEXIQuant-LF to data-independent-acquisition (DIA) data of the anaphase promo

106 Using data-independent acquisition MS analysis, we quantified both

107 n a Ca(v)1.2-independent and store depletion-independent manner.

108 nds that the skyrmion Hall angle is diameter-independent for skyrmions with diameters ranging from 35

109 integration of siRNA sequences into a Dicer-independent RNA stem-loop based on pre-miR-451 microRNA-

110 R-1 modulates both Dicer-dependent and Dicer-independent Argonaute pathways and provide insight into

111 line ones, such as nearly optimal, direction-independent properties and robustness against defects.

112 Ubqln4 engages the J proteins in a J-domain-independent manner, in contrast to the previously report

113 r photoproduct yields are explained by donor-independent, fast charge recombination with rates of ~0.

114 , which could cause salicylic acid- and EDS5-independent mutant phenotypes.

115 comprises representations that are effector-independent.

116 zation, the behavioral signature of effector-independent representations, to address this crucial gap

117 nt NSCLC models with EGFR-dependent and EGFR-independent resistance mechanisms, IACS-13909, administe

118 gregates that appear to interfere with ESCRT-independent NE sealing.

119 of PI3K suppresses PRR11-mediated, estrogen-independent growth.

120 es that flu-produced (1)O(2) triggers an EX1-independent signaling pathway and proves that SAFE1 supp

121 derived metabolite, and identify an excision-independent mechanism.

122 hese results advance our understanding of FA-independent ICL repair and establish a role for the RecQ

123 8-FADD (FADDosome) complex and reveal a FADD-independent inflammatory role of caspase-8 that involves

124 itions can be converted into potent FcgammaR-independent agonists with remarkable antitumor activity

125 pair through the electrostatic Coulomb force-independent of its electronic band gap.

126 nculin association, our data show that force-independent relief of autoinhibition is sufficient to me

127 affect Treg suppressive function via a FOXP3-independent mechanism, thus sustaining the clinical impr

128 consequence of both fuel-dependent and fuel-independent mechanisms; they undergo slower decompositio

129 ty-six (ETS) fusion-dependent and ETS fusion-independent cancer cell lines revealed improved ETS fusi

130 ncer cell lines revealed improved ETS fusion-independent/dependent selectivity indices for select 2'-

131 disease status and used the G-SCI (Genotype-independent Signal Correlation and Imbalance) test(1) to

132 chanism by which E449K activates Int for gp3-independent attL x attR recombination.

133 Recent data have revealed glutathione/GPX4-independent axes for suppressing ferroptosis, and insigh

134 These findings reveal a GTPase-independent role for Rac1 in mediating a PI3K-independen

135 In addition, Hh-independent GLI2 accumulation at the PC tip in cells fro

136 ese findings identify FTO as a potential HIF-independent therapeutic target for the treatment of VHL-

137 inib targeted both Hippo-dependent and Hippo-independent regulation of YAP1, ablating rhabdomyosarcom

138 ld domain and the hairpin, exhibited hormone-independent interactions with PhMAX2A and PhD53A, respec

139 and represents a novel mechanism for hormone-independent pathogenesis of endometrial adenocarcinoma.

140 In contrast, BMSC induced hormone-independent growth of breast cancer and prostate cancer

141 se data characterize the pleiotropic hormone-independent mechanisms underlying acquisition and restor

142 t is essential for both the prenatal hormone-independent as well as the pubertal hormone-dependent br

143 1(+)CD16/32(+) hematopoietic-stem-cell (HSC)-independent erythro-myeloid progenitors (EMPs) present i

144 our data indicate that CHP-1 plays an HSP90-independent function in controlling EGFR trafficking thr

145 cognition, ATP converts MutS to a hydrolysis-independent, diffusive mobile clamp that no longer recog

146 Zika virus through a type I interferon (IFN)-independent mechanism.

147 l cell death that is in part mediated by IFN-independent activities of STING.

148 agonists 4-OI and DMF induce a distinct IFN-independent antiviral program that is broadly effective

149 FN-dependent activities while preserving IFN-independent activities of STING.

150 t STING controls HSV-1 infection through IFN-independent activities.

151 hat mammalian STING possesses widespread IFN-independent activities that are important for restrictin

152 e neoantigens are well studied; however, IgE-independent reactions are less well understood.

153 The excellent immunotherapy-independent outcomes of autoantibody-positive patients w

154 Here, we describe an inflammasome-independent pathway of IL-1beta production that was trig

155 r in inflammasome-dependent and inflammasome-independent manners.

156 both inflammation-dependent and inflammation-independent functions, such as NF-kappaB-mediated cell s

157 In addition, 9/10 became insulin-independent versus 15/30 (P = 0.03).

158 ient cells leading to an increase in insulin-independent glucose transporter levels, enhanced cellula

159 imaging (FLIM) is a quantitative, intensity-independent microscopical method for measurement of dive

160 onical gp130 signaling, SarA function is JAK-independent but requires GSK-3, a key regulator of metab

161 G16L1 by a nuclear factor kappaB (NF-kappaB)-independent pathway.

162 rf2 function: a tonic effect through a Keap1-independent mechanism under basal conditions and an indu

163 omoting effects of CDK6 are, in part, kinase-independent in Ph+ ALL.

164 netic ablation phenotypes, suggesting kinase-independent functions for ERK5.

165 l regulation of tankyrase serves as a ligand-independent developmental mechanism for post-translation

166 1 in the PI3K signaling cascades in a ligand-independent fashion.

167 mulate bICP0 E promoter activity in a ligand-independent manner in mouse neuroblastoma cells (Neuro-2

168 , resembling the ligand-dependent and ligand-independent states.

169 f the embryo, is dispensable for both ligand-independent signaling pathway activation and ligand-resp

170 However, ligand-independent transcriptional activation occurring during

171 es that CXCR4 exhibits some degree of ligand-independent activity, a relevant feature for drug develo

172 erface do not affect the stability of ligand-independent EGFR oligomers.

173 results underscore the importance of ligand-independent TNFR1 dimerization in NF-kappaB signaling.

174 tion requirement, resulting in robust ligand-independent induction of proinflammatory genes and oncog

175 tions in the ligand-dependent and the ligand-independent states.

176 cture and physiological role of these ligand-independent oligomers remain unclear.

177 High ECM stiffness leads to ligand-independent phosphorylation of ephrin receptor EPHA2, wh

178 owing APC mutations, resulting in Wnt ligand-independent stabilization and nuclear accumulation of be

179 Therefore, femoral dP/dtmax is not a load-independent marker of left ventricular contractility and

180 ere we report the first high-precision, mass-independent Ru isotope compositions for Eoarchaean ultra

181 The mass-independent minor oxygen isotope compositions (Delta'(17

182 A unique, versatile, and material-independent approach to manipulate contactlessly and mer

183 We employ a heterologous media-independent induction system to express the yeast HO end

184 for multiple membrane modeling and membrane-independent cellular processes.

185 results suggest that a loss of NOD-LNSC MHC-independent suppressive mechanisms may contribute to dia

186 is promoted by oocyte-specific, microtubule-independent enrichment of the antiparallel microtubule c

187 atural model system for studying microtubule-independent cytoskeletal phenotypes.

188 that pestiviruses, although capable of miRNA-independent replication, took advantage of miRNAs as ess

189 S phase entry is mitogen-independent in the daughter G1 phase, but remains sensit

190 Modality-independent V1 LPZ responses only in the task condition

191 ordinated brain activity to extract modality-independent meaning from the input.

192 e modality-specific activation from modality-independent activation.

193 a direct quantification of sensory modality-independent brain activity, revealing fast activation of

194 Coupled with model-independent reconstruction algorithms based on rigorous

195 tination results in DNA2-dependent but MRE11-independent nucleolytic degradation of nascent DNA at st

196 ontrast, MPs activate translation in an mTOR-independent manner due, at least in part, to proteasomal

197 racellular HIV through the induction of MTOR-independent autophagy.

198 mined the HIV-inhibitory effects of the MTOR-independent inducer of autophagy, trehalose.

199 However, our knowledge about Munc13-independent contributions of RIM to active zone function

200 ant defense response in addition to COI1/MYC-independent functions in plant growth and development, s

201 ing lies near the phagocytic cup in a myosin-independent fashion.

202 of cathepsin B, Tnf and Bid in a neutrophil-independent manner.

203 with either BRJ+ or BRJ-, indicating nitrate-independent effects of BRJ.

204 ll as water to control for potential nitrate-independent effects.

205 onstrate that both NLRP3-dependent and NLRP3-independent inflammasome activation mechanisms induce CN

206 n CNV occurs via NLRP3 or also through NLRP3-independent mechanisms, and (3) whether complement activ

207 ition (with negative or neutral results), NO-independent soluble guanylate cyclase (sGC) activation,

208 Also, the non-independent testing of even fewer signaler-recipient dya

209 illator model of aromaticity), NICS (nucleus-independent chemical shift), ACID (anisotropy of the ind

210 In this sense, nucleus-independent chemical shift (NICS) and anisotropy of the

211 esonance scans using a reproducible operator-independent fully automatic open-source end-to-end pipel

212 faces are aligned to a view- and orientation-independent face template encoded in a face-centered ref

213 Our newly discovered bifunctional oxygen-independent pathway, widespread in bacteria, salvages at

214 p53-independent roles of the Mdm proteins are emerging, and

215 here is less information available about p53-independent roles of MDMX or the MDM2-MDMX complex.

216 lpha interaction may account for certain p53-independent functions of MDMX.

217 Therefore, understanding the p53-independent mechanisms of the netrin-UNC5B axis, such as

218 of immature viral particle assembly in a p6-independent manner.

219 ng protein-1 (FUNDC1), an effector of Parkin-independent mitophagy, also participates in cellular pla

220 exo-HAV, infectivity of HAV particles is pH-independent and requires HAVCR1 or another as yet uniden

221 NHE module but not by those including the pH-independent CaV and BK module or proportionate mixed sce

222 volves slowly and involves a phosphorylation-independent proteolytic pathway.

223 phyB-independent growth restriction of the jazD mutant was ti

224 ndependent role for Rac1 in mediating a PI3K-independent MET-to-mTOR pathway and suggest alternative

225 s been deleted (CRISPR-Cas9) to identify PKA-independent responses to vasopressin.

226 We propose that this plaque-independent inflammatory reaction originates from neuron

227 TBtools is platform-independent software that can be run under all operating

228 port asymmetric modification, while the PolI-independent pSC101 origin does not.

229 yglutamine-expanded (mHTT) and polyglutamine-independent HTT specific immunoassays for validation in

230 in a Tir-dependent but actin polymerisation-independent manner, which was enhanced by priming with i

231 erpene (-)-jiadifenolide on action potential-independent inhibitory currents at GABAergic synapses, u

232 events were consistent with action-potential-independent spontaneous glutamate release, suggesting pl

233 s; p = 0.005) and remained stable in preload-independent ones (mean change = 49.2 mm Hg.s; p = 0.114)

234 s (r = 0.618; p = 0.032), but not in preload-independent ones.

235 with HSF1 protein at a noncanonical, proline-independent SH3 interaction motif.

236 cells, which was accompanied by proteasomal-independent losses of the viral genome and integrase enz

237 eefold accumulation, suggesting a proteasome-independent mechanism.

238 In contrast, proteasome-independent non-proteolytic polyubiquitin chains regulat

239 the action of beta-catenin in a largely PYGO-independent manner.

240 e that osmotolerance is conferred through Q8-independent protection of respiration, not by altering p

241 nogenic DNA damage taking advantage of Rad51-independent single-strand annealing (SSA) assays in the

242 structured RNAs such as vault RNAs is RanGTP-independent.

243 ) and Donachie's hypothesis of a growth-rate-independent initiation mass(4).

244 Materials and Methods A heart rate-independent, free-breathing 3D T2 mapping technique at 3

245 Additional pathways for RecA-independent recombination, possibly mediated by helicase

246 makes a major enzymatic contribution to RecA-independent recombination.

247 naloxone promote neurogenesis in a receptor-independent manner at least during the early stage.

248 nts (EPSCs) are followed by GABA(A) receptor-independent outward currents, reflecting the hyperpolari

249 s result was consistent with increased renin-independent aldosterone production and hypertension.

250 d pressure category had a continuum of renin-independent aldosterone production, where greater severi

251 histone H3.1 and the predominant replication-independent deposition of histone H3.3.

252 ity in proteoliposomes, which is respiration-independent.

253 also reveal ribosome-dependent and ribosome-independent mRNA-surveillance pathways.

254 ost-assembly host species richness, richness-independent host phylogenetic diversity, and colonizatio

255 gen-activated protein kinase-dependent Ripk1-independent IL-1 and tumor necrosis factor production, a

256 DM as in the original model, there is an RNA-independent maintenance phase involving CMTs followed by

257 then based on a combination of RdDM and RNA-independent mechanisms involving DNA methyltransferase M

258 ope, and reference electrodes provide sample-independent reference potentials over a wide range of el

259 with a decreased likelihood of schizophrenia-independent of intelligence-and, hence, may be entangled

260 The evolution of semi-independent modules is hypothesized to underlie the func

261 roups, indicating the existence of a sensory-independent knowledge coding system in both groups.

262 tructural complexity in mt tRNAs by sequence-independent induced-fit adaption to the cognate mitochon

263 Binding is sequence-independent with residues N13, R16, R17 and Q41 interact

264 episodes, children had short-lived, sequence-independent increases in average whole-protein seroreact

265 c force microscopy data support the sequence-independent nature of the Hfq-DNA interaction and a role

266 a high-throughput assay for assessing sgRNA-independent off-target effects of CBEs in rice protoplas

267 use genome-wide off-target changes via sgRNA-independent DNA deamination.

268 Drosophila to form sleep-dependent and sleep-independent memory.

269 of DNA damage response genes is largely SOG1-independent in fbl17 In addition, through analyses of ro

270 RNA is determined to be universal and spacer-independent for enhancing the sensitivity and specificit

271 These species-independent A(3)AR-selective nucleosides are low efficac

272 pendent tensor force to a predominantly spin-independent scalar force.

273 ing to demonstrate that NuMA plays a spindle-independent role in forming a single, round nucleus.

274 Overall, this work establishes the spindle-independent function of NuMA in choreographing proper ch

275 Here, we show that Stattic exerts many STAT3-independent effects on cancer cells, calling for reasses

276 ple fMRI paradigms, suggesting a brain-state-independent neural phenotype underlying individual genet

277 The sTF-independent activity of FVIIa-VY(T) was partly mediated

278 ly relevant tissue actions of TRPV4, stretch-independent responses, and underlying mechanisms are unk

279 QR4 in breast tumors was found to be subtype-independent and correlated with increased ceramidase act

280 des a single nonribosomal peptide synthetase-independent siderophore (NIS) synthetase.

281 MPH-220 provides a potential nervous-system-independent option to treat spasticity and muscle stiffn

282 cient mice, suggesting that it maintains a T-independent response.

283 nses to immunizations with T-dependent and T-independent (Type 1) Ags, but Ab responses to a multival

284 1) Ags, but Ab responses to a multivalent T-independent (Type 2) Ag were impaired, a surprise findin

285 ndent antigens, the conjugates also retain T-independent properties, leading to detrimental effects o

286 measure could be employed as a robust, task-independent index of interpersonal behaviour.

287 Fast, robust and technology-independent computational methods are needed for supervi

288 spacing, small Stokes shift, and temperature-independent PL linewidth and PL lifetime (between room t

289 ment, TfR1 was endocytosed in an AP2- and Tf-independent pathway and trafficked to the lysosome for d

290 Furthermore, Th1-independent roles for Tbet were suggested by significant

291 and TLR2 ligand stimulation but not for TLR-independent stimuli.

292 xpression was significantly reduced by a TOR-independent pathway.

293 s was found to be dependent on transcription-independent functions of IRF3 and also on Bax, a pro-apo

294 3) (+)) or, alternatively, a proton transfer-independent nucleophilic ferric peroxo anion (compound 0

295 s to light through an arrestin-translocation-independent mechanism.

296 d with gene expression, as well as cell-type-independent principles of chromatin organization.

297 on, 2) stimulate uncoupling protein 1 (UCP1)-independent respiration in subcutaneous white fat, 3) ch

298 The proposed water-independent nature of tissue Na(+) could induce local pa

299 ese results suggest that LSG may have weight-independent effects on metabolic disease and should be c

300 rom the previous Wnt-dependent view to a Wnt-independent one and unveil a previously unappreciated HI

301 inhibit HIV-1 gene expression through a ZAP-independent mechanism.