ライフサイエンスコーパス: contribute to

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

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

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

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

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

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

7 ly affect the cells in which they appear and contribute to a variety of diseases, including cardiovas

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

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

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

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

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

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

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

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

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

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

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

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

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

21 Bacteriuria contributes to antibiotic overuse through treatment of a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 RATIONALE: Mechanisms contributing to chronic lung disease after preterm birth

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

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

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

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

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

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

54 muscle cells and adventitial fibroblasts may contribute to development of TAAD and proliferative occl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

75 nderstanding how biophysical characteristics contribute to function.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

91 tion (SV) influences genome organization and contributes to human disease.

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

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

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

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

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

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

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

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

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

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

102 These properties may contribute to inhibition of distinct NMDAR subpopulation

103 y suggest that adaptive immune responses can contribute to innate IEL activation during mucosal infla

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

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

106 elieved to be multiple subtypes of CD, which contributes to its observed clinical heterogeneity.

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

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

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

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

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

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

113 how inflammation-mediated CD11d upregulation contributes to macrophage retention at inflammatory site

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

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

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

117 Individual factors contributing to mental health in transgender persons inc

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

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

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

121 pensate for the muscle hyperexcitability and contribute to motor impersistence.SIGNIFICANCE STATEMENT

122 B cells contribute to multiple aspects of autoimmune disorders a

123 rtality provides evidence that GBS infection contributes to NE.

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

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

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

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

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

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

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

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

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

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

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

135 This review examines recent work that has contributed to our understanding of LOS-deficiency and c

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

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

138 , in particular by plants, and its emissions contribute to ozone destruction in the stratosphere.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

158 Whereas some contribute to progressive cognitive deterioration, other

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

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

161 sponses to the more conserved fusion protein contribute to protection against heterologous CDV strain

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

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

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

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

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

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

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

169 This article contributes to reliability and uncertainty discourses in

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

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

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

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

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

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

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

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

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

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

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

181 We unexpectedly found that Co neurons contribute to striatal-like projection neurons in the ce

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

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

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

185 -) APC and CD4(+) T cells in the aortic wall contribute to T cells re-activation and pro-atherogenic

186 sion protein to tumor-specific enhancers and contributes to target gene activation.

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

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

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

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

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

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

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

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

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

196 ng of distant frontal cortical areas and can contribute to the development of tools for potentially n

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

198 ivity disorder can elucidate mechanisms that contribute to the disorder, which affects 7% of childre

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

232 onstrate that two distinct chemical entities contribute to the temporal evolution and spectral shape

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

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

235 or LMM lesions underwent staged surgery and contributed to the analysis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

260 ational study on the epidemiology of SJS/TEN contributes to the understanding of this still underinve

261 volving these strains localized a Chr 10 QTL contributing to the difference.

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

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

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

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

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

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

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

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

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

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

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

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

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

275 maintenance in cancer cells and whether this contributes to therapy resistance.

276 he main constituents of planetary bodies can contribute to this debate.

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

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

279 t a decline in the autophagy-lysosome system contributes to this as evidenced by a derangement in key

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

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

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

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

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

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

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

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

288 AMD and their impact on visual function may contribute to understanding AMD pathogenesis.

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

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

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

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

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

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

295 mediated vasoconstriction, two abnormalities contributing to vascular dysfunction.

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

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

298 unclear whether (and how) lymphangiogenesis contributes to visceral metastasis.

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

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