ライフサイエンスコーパス: contribute

1 enetic background, clone, and passage number contribute.

2 hane (CH4 ) emissions from tropical wetlands contribute 60%-80% of global natural wetland CH4 emissio

3 Organic aerosol contributes a significant fraction of PM in the United S

4 Macroalgae contribute approximately 15% of the primary productivity

5 tion of alternatively activated macrophages, contributed by deregulation of the miR-155 target gene t

6 Divergent synaptic connections did not contribute directly to the vast majority of synchronized

7 he microglia-mediated innate immune response contributes directly to the development of Alzheimer's d

8 This phenomenon may be a major contributing factor in treatment failure in patients wit

9 Contributing factors appear to be exaggerated polycythem

10 methylation at specific genomic locations as contributing factors to both non-familial and familial N

11 explanation for EgWRI1 as an important gene contributing hybrid vigor in lipid biosynthesis in oil p

12 fied, the (1)H NMR chemometrics approach may contribute in the choice of the temperature and time to

13 All contributing mechanisms are evolutionarily conserved off

14 s suggest that shared genetic susceptibility contributes modestly to MDD and AD comorbidity.

15 death responsible for more YLLs overall also contributed more significantly to geographical inequalit

16 on and soma-targeting inhibition (the latter contributes non-dipole-like features to Ve responses).

17 escendants of Sfrp5-expressing cells at E7.5 contribute not only to the SV but also to the LV, atria

18 rocessing enables the dense VG3-AC plexus to contribute precise object motion signals to diverse targ

19 sed during a mouse M. tuberculosis infection contribute significantly to its T cell response.

20 a few binding sites near the collision point contribute significantly to the binding energy.

21 DMATS enzymes thus contribute significantly to the biological and pharmacol

22 aling pathway is active during infection and contributes significantly to GAS pathogenesis at multipl

23 tes it from other members of this family and contributes significantly to its biological activity.

24 We conclude that the PCP pathway contributes significantly to the motility and hence the

25 icroarrays, and we expect such approaches to contribute substantially to the understanding of importa

26 Collectively, these mutations contribute to 10% of probands.

27 geneity of midbrain dopaminergic neurons and contribute to a better understanding of this functionall

28 ight than the Amadori rearrangement product, contribute to a large extent to the multitude of interme

29 These efforts will contribute to a more complete understanding of global ca

30 Proteins from leaves can contribute to a more complete use of resources and help

31 identify future research directions that can contribute to a more comprehensive understanding of symb

32 very little is known about how zDHHC enzymes contribute to acyl chain heterogeneity.

33 f interstrand cross-links in genomic DNA may contribute to aging, neurodegeneration, and cancer.

34 of mitochondrial reactive oxygen species and contribute to alcohol-induced hepatocyte injury.

35 airway smooth muscle/mast cell interactions contribute to asthma severity by transiently increasing

36 ed with slowed nerve conduction, which could contribute to behavioral deficits in AS, including motor

37 that extrinsic factors, such as water depth, contribute to behavioural sexual segregation.

38 Our results contribute to better interpreting the off-target efficac

39 l as the Reelin-mediated generation of L1-80 contribute to brain development at early developmental s

40 onomous changes in both neurons and glia may contribute to C9orf72-mediated disease, as has been show

41 estin-GFP(high) perivascular population, and contribute to cartilage repair.

42 veals that His175, Arg186, Thr276 and Tyr278 contribute to CdiA-CTYkris activity, suggesting that the

43 identify GC-regulated "effector" genes that contribute to cell death, as well as genes that affect t

44 r fluctuations in archaeal cell cycle events contribute to cell size variability and control.

45 papillomavirus type 16 (HPV16) oncoproteins contribute to cellular transformation in vitro.

46 of the PAF1 transcription elongation complex contribute to Chd1 recruitment to highly transcribed gen

47 ring neuroinflammation, yet, how these cells contribute to CNS antigen drainage is still unknown.

48 ents a founder allele that may significantly contribute to deafblindness in this population.

49 tions and their relationships, and how these contribute to development of AP in mice and rats.

50 a tool to harness creative thinking that can contribute to development of new research tools and appr

51 in protein levels that arise due to diabetes contribute to different VSMC behavior and thus vascular

52 malignancy, suggesting that these mutations contribute to disease initiation.

53 anding of how mutations in genes such as GRN contribute to disease pathogenesis and neurodegeneration

54 ectious, and the potential exists for HK2 to contribute to disease.

55 in contrast to Tet2 loss, Aid loss does not contribute to enhanced HSC self-renewal or cooperate wit

56 ganization and Polycomb group (PcG) proteins contribute to epigenetically inheritable phenotypic vari

57 the molecular basis for how these mutations contribute to epileptic encephalopathies, we compared th

58 ting tips and identification of factors that contribute to experimental variability.

59 Animal feces contribute to fecal contamination, and fecal indicator b

60 nderstanding how biophysical characteristics contribute to function.

61 tems in DS model mice, that such defects may contribute to functional impairment in DS, and that thes

62 O accumulation in denitrification, which may contribute to further design strategies to control green

63 e for optimal analysis and which potentially contribute to gaps in sequence coverage of proteins.

64 evidence that reductions in Reln expression contribute to GCp proliferative defects and cerebellar h

65 Hyperglycemia and dyslipidemia contribute to glucolipotoxicity that leads to type 2 dia

66 rent declines with postnatal age, PIEZO2 may contribute to hair cell development, but it does not und

67 tand the relative importance of factors that contribute to heat generation and accumulation.

68 BRCA mutations have also been identified and contribute to hereditary breast cancer syndromes.

69 ly unappreciated mitotic defects that likely contribute to HPV-mediated cancer progression.

70 sults suggest a general mechanism that could contribute to immune-mediated diseases.

71 th an elevated thromboxane A2 production may contribute to impaired functional dilator and hyperaemic

72 rds for conducting systematic reviews, would contribute to improved patient care and inform future re

73 The revised RPA has the potential to contribute to improving the accurate assessment of progn

74 multiple pleiotropic loci with small effects contribute to increased disease risk.

75 vidence that intensive coal combustion could contribute to increased light-absorptivity of ambient Br

76 neutrophil activation and NET formation may contribute to inflammatory manifestations observed in pa

77 These properties may contribute to inhibition of distinct NMDAR subpopulation

78 , adversely regulate myocyte metabolism, and contribute to insulin resistance via paracrine effects.

79 Innate immune responses triggered by cGAMP contribute to limiting the spread of DENV to adjacent un

80 NADPH oxidases contribute to LPS-induced reactive oxygen species (ROS)

81 these species instead of Norway spruce will contribute to maintaining a high level of productivity a

82 Not only do individual risk factors contribute to many different disorders but most disorder

83 in, and carboxyl-terminal tail identity both contribute to MLO activity during PT reception.

84 strate that structural regions unique to NS1 contribute to modulation of host responses, including in

85 B cells contribute to multiple aspects of autoimmune disorders a

86 orsal root ganglion (DRG) neurons, which may contribute to nerve injury-induced neuropathic pain.

87 Defective mitophagy is thought to contribute to normal aging and to various neurodegenerat

88 new modes of control and could realistically contribute to operational control in the next 5 years.

89 ed antimicrobial properties, neutrophils can contribute to optimal host protection by limiting the ex

90 minal complement complex (TCC) that together contribute to organ failure and death.

91 dent reflexes in the lower urinary tract and contribute to our understanding of the pathophysiology o

92 naturants, forming a robust layer that would contribute to overall spore resistance.

93 Purpose Deleterious germline mutations contribute to pancreatic cancer susceptibility and are w

94 uency hearing, suggesting that gap junctions contribute to passive cochlear mechanics and energy dist

95 vation of the integrated stress response may contribute to pathogenesis in a subset of neurodegenerat

96 iviruses and primate immune systems that may contribute to pathogenesis.

97 ta support this standard practice, which may contribute to perioperative fluid overloading.

98 aller genetic variants but may substantially contribute to phenotypic diversity and evolution.

99 Comutated, myeloid tumor-suppressor genes contribute to phenotypic variability, phenotypic shifts,

100 ulation, transport activity, and interaction contribute to PIN functional specificity.

101 anced mGluR1 function, a mechanism likely to contribute to PN dysfunction and loss in SCA2.

102 the risk factors and movement patterns that contribute to poliovirus transmission across Pakistan wo

103 ion and interactions among demographic rates contribute to population growth rate (lambda) is key to

104 ration and angiogenesis, which may, in turn, contribute to positive PET/CT and CT performances.

105 Whereas some contribute to progressive cognitive deterioration, other

106 idence has emerged that MPO-derived oxidants contribute to propagation of inflammatory diseases.

107 D4 effector and effector memory T cells that contribute to protection.

108 ndicate that non-neutralizing antibodies can contribute to protection.

109 exclusion of molecules needed for growth may contribute to regeneration decline.

110 eurons innervate subcortical structures that contribute to reward-seeking behaviours, such as the ven

111 gest that upregulation and release of miR-21 contribute to sensory neuron-macrophage communication af

112 unication among intermingled PC subsets that contribute to separate brain networks remains unclear.

113 c signal after a stimulus train and does not contribute to short-term plasticity, but induces a stead

114 city may thus facilitate sperm migration and contribute to successful fertilization.

115 Biosensors will contribute to the 4th revolution in agriculture by incor

116 [(+)RNA] viruses and cellular membranes that contribute to the biogenesis of virus-induced membrane o

117 ion between RNA polymerase and ribosomes may contribute to the coupling of transcription to translati

118 le vongole or carciofi alla romana showed to contribute to the daily nutritional recommendations resp

119 axotomy, strongly suggest that A1 astrocytes contribute to the death of neurons and oligodendrocytes

120 tanding of how thermally activated processes contribute to the denaturation of adsorbed proteins.

121 y in beta-cell number in infants with CF may contribute to the development of glucose intolerance in

122 gammadelta T cells might contribute to the development of hypertension in humans.

123 ge influence each other over development and contribute to the development of the concept of number.

124 vel of expression of restriction factors may contribute to the differential susceptibility of CD4(+)

125 atory disease and that sulfatide in APCs may contribute to the endogenous pathway of iNKT cell activa

126 ate normal cell fates during development and contribute to the epigenetic plasticity that underlies m

127 ent sRNAs can be acted upon by selection and contribute to the evolution of phenotypic diversity.

128 he disordered vanadium oxide nanosheets will contribute to the exploration of disordered structures f

129 ms supporting face and voice processing both contribute to the extraction of important information fo

130 dew-water evaporation has shown potential to contribute to the gas-phase HONO levels during the morni

131 his myeloid-derived IL-1beta did not vitally contribute to the generation and plasticity of Th17 cell

132 Fluke secreted and tegumental proteins contribute to the generation of a tumorigenic environmen

133 ys a key role in attention orienting and may contribute to the hypervigilance that is a common sympto

134 knowledge of the T cell response may further contribute to the identification of robust correlates of

135 TCR sequence that modulate functionality and contribute to the increased antiviral capacity of HIV-sp

136 needed to address whether similar mechanisms contribute to the increased risk for calcium oxalate sto

137 Thus, cAMP-independent signals contribute to the induction of hyphal responses.

138 ue produce high levels of CCL-2 and IL-8 and contribute to the inflammatory process promoting the rec

139 How cortical circuits are altered and contribute to the intense sensation associated with allo

140 etostriction, the low field anomaly does not contribute to the magnetic susceptibility.

141 not known whether endogenous IL-4 and IL-13 contribute to the maintenance of peripheral tolerance an

142 nulation by PgLPS1690 and PgLPS1435/1449 may contribute to the modulation of disease progression.

143 Surface functional groups contribute to the overall electron flux of pyrogenic car

144 ive in maintaining IgG populations, FcRn can contribute to the pathogenesis of autoimmune disorders w

145 Abnormal methylation pattern could contribute to the pathogenesis of cancer either by silen

146 inherited (ie, case) genetic factors likely contribute to the pathogenesis of congenital heart defec

147 ssion of IL-19 by intestinal macrophages may contribute to the pathogenesis of inflammatory bowel dis

148 roinflammation in the adult hypothalamus may contribute to the pathogenesis of obesity.

149 find evidence that malaria parasitemia does contribute to the pathogenesis of retinopathy-negative C

150 natural killer T and Treg cells that likely contribute to the patients' immunodeficiency and autoimm

151 alpha-synuclein (alpha-syn) is suggested to contribute to the progression of neuropathology in Parki

152 sustained benefit and that Ly6C(low) MPs may contribute to the progressive fibrosis and dysfunction o

153 Yet, the presence of defectors who do not contribute to the public good but do reward themselves (

154 nscription, suggesting that other activators contribute to the regulation of CCC1 transcription.

155 in both basal and LPS-induced activation and contribute to the sexually dimorphic effects of morphine

156 ate that periaqueductal gray (PAG) microglia contribute to the sexually dimorphic effects of morphine

157 eukemogenesis of MLL-Af4 myeloid cells could contribute to the strong B-cell ALL association of MLL-A

158 differences in cochlear delay systematically contribute to the total travel time by comparing for ind

159 ic control of CRF levels in the amygdala may contribute to the transition from moderate to compulsive

160 daytime, suggesting that human occupants may contribute to their abundance either through direct emis

161 pacity of subtypes A and C may paradoxically contribute to their more efficient spread in sub-Saharan

162 Such differences may ultimately contribute to their unique behavioral profiles and poten

163 dial medulla (RVM) are thought to critically contribute to this process; however, the neural circuits

164 hondria and mitochondrial fission and fusion contribute to this rejuvenation, but local protein synth

165 to test whether DAT and SERT N and C termini contribute to transporter substrate and inhibitor affini

166 ffects on protein folding homeostasis likely contribute to UPR activation, but deletion of the unfold

167 ration, and that polymorphism rs11185644 may contribute to variation in 25(OH)D dose-response in heal

168 polymorphisms in the CYP2R1 and GC gene may contribute to variation in baseline serum 25(OH)D concen

169 uggest that disruption of this process could contribute to various deficits associated with alcohol d

170 In endothelial cells, this phenomenon might contribute to vascular disease.

171 sites of arterial injury and that platelets contribute to venous thrombosis has prompted trials comp

172 nregulation of HLA-E by high-risk HPV E7 may contribute to virus-induced immune evasion during HPV pe

173 order operations, such sensory anomalies can contribute to widespread dysfunctions, presenting an add

174 need to understand how brain reward networks contribute to youth depression.

175 emiology is the size of the population which contributed to a given wastewater sample.

176 discuss how basic developmental studies have contributed to and are needed to advance clinical goals.

177 and international partners is likely to have contributed to findings that children were killed in inc

178 ectly involved in IL-8 production and likely contributed to neutrophilic asthma.

179 pted vaccines and circulating strains likely contributed to reduced vaccine effectiveness during the

180 ne networks that, in addition to Crh, likely contributed to the augmented care-induced phenotype, inc

181 This genomic change probably contributed to the high evolutionary rate of the outbrea

182 tumor necrosis factor-alpha (TNFalpha) that contributed to the increased tumor resistance to BRAF in

183 (OAV) and the number of double bonds mostly contributed to the modulation of habituation.

184 and endoplasmic reticulum stress, could have contributed to the neutral trial results in RELAX.

185 and furthermore that young repeats have also contributed to the p300-bound regulatory landscape follo

186 Before and after RYGB, high oxalate intake contributed to the severity of hyperoxaluria.

187 o abrogate the G2 cell cycle checkpoint both contributed to the synergistic induction of apoptosis an

188 soluble CD137 produced by regulatory T cells contributed to their autoimmune-suppressive function in

189 our data suggest that the heptad repeat LIZ contributed to TM-TM association and is important for F

190 This work contributes to a better understanding of the roles of di

191 Enterohepatic recirculation most probably contributes to a concentration-time profile after oral a

192 ticity, raising the question of whether this contributes to adaptive evolution.

193 understanding of how defective FA signaling contributes to aging and cancer at the energy metabolism

194 etabolism, favor bile acid accumulation that contributes to AhR-mediated hepatotoxicity.

195 These findings establish that PXR signaling contributes to ALD development and suggest that PXR anta

196 Bacteriuria contributes to antibiotic overuse through treatment of a

197 nd 3-linked arabinose oligosaccharides, that contributes to around a 50% reduction in arabinosylation

198 Therefore, TLR7 contributes to atherogenesis in Apoe (-/-) mice by regul

199 Cathepsin B (CtsB) contributes to atherosclerosis and cancer progression by

200 yelinating disorder multiple sclerosis (MS), contributes to axonal dysfunction and neurodegeneration.

201 bacteria from aminoglycoside antibiotics and contributes to biofilm architecture through ionic intera

202 otassium channel subunit Kv1.1 substantially contributes to both the excitability and short-term plas

203 e mechanism by which CTCF haploinsufficiency contributes to cancer development is not well understood

204 Chromosomal instability (CIN) contributes to cancer evolution, intratumor heterogeneit

205 Hypertension affects nearly 1 of 3 women and contributes to cardiovascular disease, the leading cause

206 l (NES) at the N terminus (AAs 176-192) that contributes to CASZ1 nuclear-cytoplasmic shuttling in a

207 role in constraining HIV-1 transmission and contributes to defining subsequent AIDS pathogenesis.

208 ealed that the arthropod HSP70-like molecule contributes to differential fibrinogenolysis during tick

209 s in a given somatic cell lineage that later contributes to differentiation of gametes, and the secon

210 ar mechanisms by which dysfunction of TDP-43 contributes to disease pathogenesis and progression rema

211 RSV binding to CX3CR1 contributes to disease pathogenesis; therefore, we inves

212 the biological responses during droughts and contributes to elucidate the molecular mechanisms involv

213 The basolateral amygdala (BLA) contributes to emotion-related behaviors that differ bet

214 Ca(2+) -mediated activation of SK channels, contributes to exacerbated MNC activity in HF rats.

215 n-containing ETS transcription factor, which contributes to goblet cell hyperplasia.

216 Consequently, ClpG largely contributes to heat tolerance of P. aeruginosa primarily

217 Adipose-derived lactate likely contributes to high endogenous glucose production in sea

218 The repressive status of chromatin largely contributes to HIV latency.

219 n the developing kidney that in adult kidney contributes to homeostasis, predominantly of the collect

220 nesis indicate that phosphorylation of Cdc55 contributes to Igo/ENSA dissociation.

221 Inappropriate expression of MMP9 also contributes to impaired re-epithelialization.

222 The extent to which ischemia contributes to ischemia/reperfusion injury has not been

223 ity by depletion of CD4 Th cells most likely contributes to loss of immune control of LTBI in HIV-inf

224 lation of lung microvascular homeostasis and contributes to lung pathology in ARDS.

225 demonstrate that elevated Ctnnd1 expression contributes to maintenance of murine B-ALL cells with co

226 ashion that promotes survival and ultimately contributes to metastatic outgrowth.

227 rtality provides evidence that GBS infection contributes to NE.

228 creased Rac1 activity caused by OGD/ischemia contributes to neuronal death in hippocampal neurons via

229 ease of toxic blood molecules into the brain contributes to neuronal injury during stroke and other c

230 Thus, this study contributes to our understanding of protein function wit

231 X15 enhances AR transcriptional activity and contributes to PCa progression through Siah2.

232 In vivo, EspL cysteine protease activity contributes to persistent colonization of mice by the EP

233 Here, we investigated whether PLK2 contributes to podocyte dysfunction, a characteristic ch

234 line breast cancer treatment, which probably contributes to poorer overall and breast cancer-specific

235 Toll-like receptor (TLR) activation contributes to premalignant hematologic conditions, such

236 form of the motility regulator protein Mena, contributes to prometastatic phenotypes.

237 ect of pedalism suggests that, if right pSTS contributes to recognizing of conspecifics, it does so b

238 This article contributes to reliability and uncertainty discourses in

239 ion between IP3 and ryanodine receptors that contributes to sex differences in hyperalgesic priming.S

240 rce generated by a tissue-level myosin cable contributes to SG invagination.

241 ardiac precursor differentiation resumes and contributes to SHF-derived regions and the dorsal closur

242 osus (SLE); however, it is unclear how Ox40L contributes to SLE pathogenesis.

243 Rhg4 is a major genetic locus that contributes to soybean cyst nematode (SCN) resistance in

244 inflammatory responses in the joint but also contributes to subsequent clearance of Brucella and reso

245 cells, as in tumor keratinocytes themselves, contributes to suppression of BCC carcinogenesis.

246 otor neurons, but astrocyte dysfunction also contributes to the disease in mouse models.

247 The mitotic kinase Plk1 contributes to the DNA damage response (DDR) by targetin

248 of L-type Ca(2+) channels, whose alteration contributes to the dramatic disease Timothy Syndrome.

249 es while a shift to Th1 or Treg cells mainly contributes to the efficacy of SIT by helping B cells to

250 hey conclude that each complex independently contributes to the expression of all genes transcribed b

251 ally polymorphic site at Nef position 9 that contributes to the MHC-B downregulation function in HIV-

252 ion represents another distinct process that contributes to the molecular basis of graphene cytotoxic

253 lso indicate that dysregulation of microglia contributes to the pathogenesis of neurodegenerative and

254 Disruption of neuronal morphology contributes to the pathology of neurodegenerative disord

255 Significantly, this deficit contributes to the pathophysiology of FXS as the GABABR

256 pathology, suggesting glial tau transmission contributes to the progression of tauopathies.

257 vels in the lateral hypothalamus and that HS contributes to the regulation of cocaine seeking and tak

258 MEK is activated by HSR and contributes to the regulation of proteome stability.

259 e complex regulation may exist, which likely contributes to the specificity of signal-response coupli

260 A-like recruits the corepressor TOPLESS that contributes to the suppressive function of NaJAZi on flo

261 difference in aromaticity between the rings contributes to the thermodynamic balance of the metal li

262 ence of HSC to nutrient sensing through RagA contributes to their molecular resilience to nutritional

263 immune response controls parasite burden and contributes to tissue damage, and what mechanisms underl

264 rexpression of anti-apoptotic BCL-2 proteins contributes to tumor development and resistance to thera

265 tumorigenic glioma stem cells (GSCs), which contributes to tumor initiation and treatment resistance

266 However, how this altered metabolism contributes to tumour metastasis remains elusive.

267 ropose that defective intercellular adhesion contributes to uncontrolled cSCC growth by preventing in

268 paminergic neurons, the dysfunction of which contributes to various neurological and psychiatric dise

269 This suggests that Piezo2 is capable of contributing to a larger range of mechano-activated curr

270 ocytes resulted in skewed T cell repertoire, contributing to a reduction in the frequency of self-rea

271 ive TH17 responses may be disadvantageous by contributing to autoimmune responses associated with ant

272 fects in filaggrin expression and processing contributing to barrier disruption and AD, and therefore

273 IL-7R-STAT signaling in T cell progenitors, contributing to both the quantitative and qualitative na

274 RATIONALE: Mechanisms contributing to chronic lung disease after preterm birth

275 a consequence of brain aging in later life, contributing to cognitive and memory decline, is unknown

276 NAs in the cells are among the major factors contributing to differential RNAi efficiency reported am

277 gulates growth factor-driven PI3K signaling, contributing to extension of lifespan, cardioprotection,

278 Aging promotes inflammation, a process contributing to fibrosis and decline in organ function.

279 rment of endogenous NPY release, potentially contributing to heightened anxiety.

280 ene product interactions during development, contributing to improved understanding of the genetic et

281 cur at optimal atrioventricular delay (AVD), contributing to its hemodynamic superiority, and evaluat

282 d only modestly to such approaches, possibly contributing to local or distant recurrence.

283 Individual factors contributing to mental health in transgender persons inc

284 eriphery can remotely affect brain function, contributing to neurodegenerative processes and cognitiv

285 atory variants when determining risk factors contributing to neurodevelopmental and neuropsychiatric

286 ity, invasion of PDAC cells-all collectively contributing to PDAC progression.

287 altered DNA methylation may be a second hit contributing to penetrance.

288 model for elucidating epigenetic mechanisms contributing to pulmonary carcinogenesis and highlight A

289 INAVA recruited 14-3-3tau, thereby contributing to recruitment of a signaling complex that

290 ving our understanding of disease mechanisms contributing to risk and resilience.

291 ale-specific prostate cancer but also likely contributing to sex differences in the health and diseas

292 , miR156-SPLs were critical regulatory nodes contributing to the diversity of double flower forms.

293 rogenitor cells that are capable of not only contributing to the hair and supporting cells but also t

294 (3) the rise in the practice of oral sex is contributing to the increased prevalence of C. trachomat

295 n of the bacterial repair pathway perhaps by contributing to the RecA homology search before ternary

296 study, we report three regulatory mechanisms contributing to the specificity of ATXR5/6.

297 ars' atmospheric gas has been lost to space, contributing to the transition in climate from an early,

298 of FOXP3/EZH2-enforced T cell gene networks contributing to the underlying intestinal inflammation.

299 as been one of the more critical innovations contributing to their extraordinary diversity.

300 ared to observation-based average k), likely contributing to underestimation of positive feedbacks of