ライフサイエンスコーパス: adipose tissue

1 l tissues (e.g., heart, skeletal muscle, and adipose tissue).

2 sm in the liver, heart, skeletal muscle, and adipose tissue.

3 er unsaturated fatty acid incorporation into adipose tissue.

4 ntly higher mRNA expression of CysC in white adipose tissue.

5 erioles supplying skeletal muscle, heart and adipose tissue.

6 creased thermogenic gene expression in brown adipose tissue.

7 normal myelopoiesis, osteopenia, and reduced adipose tissue.

8 olic disease on the mechanical properties of adipose tissue.

9 sion of uncoupling protein 1 (UCP1) in brown adipose tissue.

10 tal workflow for validating gene transfer to adipose tissue.

11 lic tissues including the liver, muscle, and adipose tissue.

12 fication of triglycerides in ex vivo porcine adipose tissue.

13 een human DM and non-diabetic (NDM) visceral adipose tissue.

14 innervation of subcutaneous white and brown adipose tissue.

15 rmined visceral (VAT) and subcutaneous (SAT) adipose tissue.

16 se to thermogenic adipocytes in subcutaneous adipose tissue.

17 gy expenditure and 18FDG-PET uptake in brown adipose tissue.

18 (TGs) compared to other tissues, except for adipose tissue.

19 solated from human peripheral blood vs human adipose tissue.

20 dimorphism, and the mechanical compliance of adipose tissue.

21 ) initiates thermogenesis in brown and beige adipose tissues.

22 r understanding of cellular heterogeneity in adipose tissues.

23 pathway, with a discriminative flux between adipose tissues.

24 detailed lipid metabolic maps of the 2 major adipose tissues.

25 ed diet index, percentage change in visceral adipose tissue: -4.9%, 95% CI: -8.6%, -2.0%).

26 This makes adipose tissue a reservoir for SARS-CoV-2 viruses and th

27 grate from the bone marrow to populate white adipose tissue, a process that accelerates during weight

28 high risk if they have an excess of visceral adipose tissue-a condition often accompanied by accumula

29 circulating T cells, but not in perivascular adipose tissue adipocytes.

30 1-expressing cell clusters in inguinal white adipose tissue after chronic cold exposure.

31 investigated associations between abdominal adipose tissue, alterations in kynurenine pathway of try

32 s, such as taxanes, have a high affinity for adipose tissue and a resulting higher volume of distribu

33 Inguinal subcutaneous white adipose tissue and dWAT in REDD1 knockouts were expanded

34 locomotor activity, alterations in visceral adipose tissue and hepatic development, and persistent d

35 ipose tissue inflammation, thereby improving adipose tissue and hepatic insulin sensitivity.

36 e the association between sums of muscle and adipose tissue and hospital length of stay (LOS), number

37 sity MAIT cells promote inflammation in both adipose tissue and ileum, leading to insulin resistance

38 This review focuses on inflammation in adipose tissue and its potential role in insulin resista

39 (HFD)-induced inflammation and steatosis of adipose tissue and liver are associated with a variety o

40 Transcriptional activation in both adipose tissue and liver as well as serum levels were st

41 In this context, adipose tissue and liver inflammation have been particul

42 lumes of visceral and subcutaneous abdominal adipose tissue and liver signal intensity (LSI), a measu

43 a distinct transcriptome that contributes to adipose tissue and metabolic dysfunction in obesity.

44 gr1 in Myf5(+) precursor cells impairs brown adipose tissue and muscle development.

45 r vitamin D repletion could correct aberrant adipose tissue and muscle metabolism in a mouse model of

46 Hence, excessive amounts of visceral adipose tissue and of ectopic fat largely define the car

47 obesity, macrophages infiltrate the visceral adipose tissue and promote inflammation that contributes

48 oupling protein 1 (Ucp1) expression in white adipose tissue and protects mice from developing obesity

49 challenges associated with gene transfer to adipose tissue and report on innovations that improve ef

50 eliorated expression of thermogenic genes in adipose tissue and skeletal muscle in CKD mice.

51 muscle of terminal arterioles in the heart, adipose tissue and skeletal muscle.

52 rmogenic activity of human compared to mouse adipose tissue and suggests that targeting this pathway

53 our growth through crosstalk between muscle, adipose tissue and tumour.

54 lipid networks in visceral and subcutaneous adipose tissues and suggests an integrative pathway, wit

55 ition affect the physiological activities of adipose tissues and their dysfunctions, which lead to se

56 l fat mass at DXA, visceral and subcutaneous adipose tissue, and liver and pancreatic fat at MRI.

57 e significantly lower in iBAT, gonadal white adipose tissue, and livers of ppHF dams.

58 -cost technology for reducing and contouring adipose tissue, and present ECLL as a potential new appl

59 increased elastic modulus, is enhanced in DM adipose tissue, and suggest that measures of tissue mech

60 enome of hMSCs derived from the bone marrow, adipose tissue, and umbilical cord blood without alterin

61 aining increases overall miRNA expression in adipose tissue, and up-regulation of miR-203-3p limits g

62 use proinflammatory macrophages recruited to adipose tissue are central to the metabolic complication

63 r axis might provide new insights into brown adipose tissue as a stress-responsive endocrine organ an

64 to variability in the amount of subcutaneous adipose tissue as the amount of visceral fat was indepen

65 st body weight gain and induction of UCP1 in adipose tissues associated with dietary protein restrict

66 sically activated M1-like phenotype in obese adipose tissue (AT) and may contribute to AT inflammatio

67 e a majority of the resident immune cells in adipose tissue (AT) and regulate both tissue homeostasis

68 h chronic low-grade inflammation of visceral adipose tissue (AT) characterized by an increasing numbe

69 llular studies RSPO3 may limit gluteofemoral adipose tissue (AT) expansion by suppressing adipogenesi

70 ng protein-4 (RBP4) is elevated in serum and adipose tissue (AT) in obesity-induced insulin resistanc

71 Adipose tissue (AT) inflammation contributes to systemic

72 in insulin sensitivity due to dysfunction of adipose tissue (AT) is one of the earliest pathogenic ev

73 linemic-euglycemic clamping with concomitant adipose tissue (AT) microdialysis and an in-depth analys

74 Adipose tissue (AT) plays a central role in both metabol

75 ocyte fraction, but not the total undigested adipose tissue (ATs), from obese patients has decreased

76 ranscript is highly enriched in mature brown adipose tissue (BAT) and is further induced by cold and

77 Brown adipose tissue (BAT) contains mitochondria-enriched ther

78 nctionally competent, energy-consuming brown adipose tissue (BAT) in adult humans, much effort has be

79 tudies have explored the role of human brown adipose tissue (BAT) in energy expenditure.

80 Brown adipose tissue (BAT) is an important tissue for thermoge

81 Brown adipose tissue (BAT) is highly metabolically active tiss

82 Brown adipose tissue (BAT) is the primary non-shivering thermo

83 assess the repeatability of activated brown adipose tissue (BAT) radiomic features.

84 lating AKG induces muscle hypertrophy, brown adipose tissue (BAT) thermogenesis, and white adipose ti

85 Importantly, direct exposure of brown adipose tissue (BAT) to light in living mice significant

86 anisms that regulate the adaptation of brown adipose tissue (BAT), a key organ for non-shivering ther

87 express Opn5 regulate thermogenesis in brown adipose tissue (BAT).

88 urons as a critical component of a SNS/brown adipose tissue (BAT)/thermogenesis axis.

89 tin slowly increases SNA to muscle and brown adipose tissue, because it induces the expression of its

90 ifferences in primary tumour and peritumoral adipose tissue between obese patients and those at a nor

91 Adipose tissue biopsies were collected from 13 adult fem

92 In adipose tissue biopsies, changes in fibrosis were evalua

93 or each SD increment in LA concentrations in adipose tissue/blood compartments were 0.91 (95% CI: 0.8

94 Bone marrow adipose tissue (BMAT) comprises >10% of total adipose ma

95 ated expression of key molecules involved in adipose tissue browning and ameliorated expression of th

96 ealed increased hydroxyproline content in DM adipose tissue, but no difference in Sirius Red staining

97 ministration reverses these abnormalities in adipose tissue, but the underlying mechanism remains to

98 diverticulitis, PNLIP leaking into visceral adipose tissue can cause excessive visceral adipose tiss

99 btbd2 accumulate p85alpha in white and brown adipose tissues, causing insulin resistance, moderate ra

100 onment in which adventitial and perivascular adipose tissue cells initiate and regulate important vas

101 AA measured by adipose tissue compartment volumes-abdominal superficial

102 Brown and beige adipose tissues contain thermogenic fat cells that can b

103 Adipose tissue contains beta3-adrenergic receptors (beta

104 Human adipose tissue contains higher numbers of cells of this

105 In adipose tissue, creatine controls thermogenic respiratio

106 Muscle and adipose tissue cross-sectional area at the fifth, eighth

107 Adipocytes and adipose tissue derived cells have been investigated for

108 e, we assessed the chondrogenic potential of adipose tissue derived human MSCs (hMSCs) mixed with ate

109 neuroendocrine loop facilitated primarily by adipose tissue-derived leptin and SNS-derived noradrenal

110 Betatrophin is a liver and adipose tissue-derived protein which has recently been l

111 estigated to determine their contribution to adipose tissue development and function.

112 th a significant increase in intra-abdominal adipose tissue DFA uptake from 0.15 (0.04-0.31] before t

113 Sex differences in adipose tissue distribution and function are associated

114 s characterized by excessive accumulation of adipose tissue due to chronic energy imbalance.

115 tic triglyceride lipase (PNLIP) increased in adipose tissue during pancreatitis and entered adipocyte

116 Adipose tissues dynamically remodel their cellular compo

117 Hypoxia appears to be a key factor in adipose tissue dysfunction affecting not only adipocytes

118 tail how prolonged metabolic stress leads to adipose tissue dysfunction, inflammation, and adipokine

119 the beiging of SC WAT by mirabegron reduces adipose tissue dysfunction, which enhances muscle oxidat

120 Epicardial adipose tissue (EAT) is associated with cardiovascular r

121 inical studies have reported that epicardial adipose tissue (EpAT) accumulation associates with the p

122 Treg activity lost in male epididymal white adipose tissue (eWAT) and female gonadal gWAT.

123 Lipoedema is associated with widespread adipose tissue expansion, particularly in the proximal e

124 s critical for adipocyte differentiation and adipose tissue expansion.

125 Similar to findings in adipose tissue, expression of proinflammatory cytokines

126 y due to digestion/modification of the dense adipose tissue extracellular matrix by MMP14, thereby re

127 d), fed with a high fat diet which increases adipose tissue favouring overweight and obesity, and hou

128 tter resolve disease-specific differences in adipose tissue fibrosis compared with histologic measure

129 acids (FFAs), which were transported to the adipose tissue for storage and triggered greater insulin

130 sed to preferentially target skin-associated adipose tissue for therapeutic purposes.

131 Here we use thermogenic adipose tissue from mice as a model system to show that

132 alters genome-wide gene transcription in the adipose tissue from mother polar bears and their cubs, h

133 elial function in vivo, and the relevance to adipose tissue function and obesity.

134 However, the modulatory role of ECs in adipose tissue function is not fully understood.

135 In addition, adipose tissue functions as a signalling hub that regula

136 Increasing thermogenic brown and beige adipose tissue futile cycling may be an important strate

137 wet weight and were associated with altered adipose tissue gene expression in both mothers and cubs.

138 From as little as 2 g of intact human adipose tissue, greater than 10(4) eosinophils were puri

139 Acute pancreatitis-associated adipose tissue had ongoing lipolysis in the absence of a

140 , and the central nervous system, its use in adipose tissue has been limited.

141 vation of IIS components specifically in the adipose tissue has been shown before to improve metaboli

142 Mice with autophagy deficiency in adipose tissue have impaired adipogenesis.

143 Dissecting white adipose tissue heterogeneity revealed that the MCT1 is e

144 ss remain insufficiently understood owing to adipose tissue heterogeneity.

145 c diseases and, more recently, in regulating adipose tissue homeostasis.

146 minal adipose tissue (SAAT), intra-abdominal adipose tissue (IAAT), and liver fat were measured by MR

147 ration and assessed the role of peribrachial adipose tissue in determining brachial arterial distensi

148 ver, hurdles exist in activating thermogenic adipose tissue in humans.

149 nic, low-grade inflammation originating from adipose tissue in obese subjects is widely recognized to

150 metabolic intermediates are altered in brown adipose tissue in response to cold exposure.

151 a better understanding on the involvement of adipose tissue in wound healing, and may help to uncover

152 was applied for quantification of skatole in adipose tissue (in-situ).

153 was applied for quantification of skatole in adipose tissue (in-situ).

154 s the accumulation of T cells and B cells in adipose tissue-including plasma cells that express immun

155 which GDF15 elicits a lipolytic response in adipose tissue independently of anorexia, leading to red

156 Infiltrating adipose tissue (inFAT) is a newly recognized proarrhythm

157 ckout [KO]) mice worsened obesity-associated adipose tissue inflammation and dysfunction, as assessed

158 activation in the context of obesity-induced adipose tissue inflammation and insulin resistance.

159 phage proinflammatory polarization, promotes adipose tissue inflammation and lipolysis, increases lip

160 We found increased peritumoral adipose tissue inflammation in obese patients relative t

161 in mice reduced high-fat diet (HFD)-induced adipose tissue inflammation, thereby improving adipose t

162 e in a sex-hormone-dependent manner to limit adipose tissue inflammation.

163 ion of Hif1alpha on cDCs results in enhanced adipose-tissue inflammation and atherosclerotic plaque f

164 ols will soon allow a more detailed study of adipose tissue innervation in metabolic function, yet, t

165 way, control vascularization and function of adipose tissues, insulin sensitivity, and whole-body met

166 proaches to preserve mitochondrial function, adipose tissue integrity, and beta-cell mass during obes

167 seases, a reliable automated segmentation of adipose tissue into subcutaneous and visceral adipose ti

168 NThese data support a key pathogenic role of adipose tissue IR to increase glycerol and FFA availabil

169 Thermogenic adipose tissue is a metabolic sink for excess fuel and i

170 ns in energy storage and energy expenditure, adipose tissue is also a dynamic endocrine organ that se

171 Increased pericardial adipose tissue is associated with higher risk of cardiov

172 BACKGROUNDBeige adipose tissue is associated with improved glucose homeo

173 this, progressive reduction of subcutaneous adipose tissue is commonly observed.

174 Insulin action in adipose tissue is crucial for whole-body glucose homeost

175 This is largely because adipose tissue is distributed throughout the body in dis

176 dipose tissue into subcutaneous and visceral adipose tissue is required.

177 of lymphocytes to the omental and mesenteric adipose tissues is partly mediated by L-selectin.

178 ight loss with specific losses of muscle and adipose tissue, is driven by reduced food intake, increa

179 including the pancreas, skeletal muscle, and adipose tissue, its functions are poorly characterized.

180 postganglionic inputs to the inguinal white adipose tissue (iWAT) is limited.

181 ached caveolae were found in brown and white adipose tissue lacking EHD2, and increased caveolar mobi

182 expression of MMP14 in the established obese adipose tissue leads to enlarged adipocytes and increase

183 food consumption and fat mass, and increased adipose tissue leptin mRNA expression in HFD-treated rec

184 med by the impaired food restriction-induced adipose tissue lipid mobilization in CT-1 null mice.

185 enocyte Pvf1 signaling inhibits expansion of adipose tissue lipid stores as the process reaches compl

186 adipose tissue can cause excessive visceral adipose tissue lipolysis independently of adipocyte-auto

187 nergy expenditure via sympathetic control of adipose tissue lipolysis.

188 ling reduces body weight while also inducing adipose tissue lipolysis.

189 everal traits (body mass index, subcutaneous adipose tissue, low-density lipoproteins and total chole

190 Asxl2DeltaLysM mice resisted HFD-induced adipose tissue macrophage infiltration and inflammatory

191 er, the metabolic programs that characterize adipose tissue macrophages (ATM) in obesity are poorly d

192 t drives specific metabolic reprogramming of adipose tissue macrophages, contributing to the inductio

193 potential of GPAT inhibitors to rescue white adipose tissue mass in CGL2.

194 ls of chimerism showed a significantly lower adipose tissue mass than animals with high levels of chi

195 The difference in adipose tissue mass was attributed to variability in the

196 sulin challenge, decreased thermogenic brown adipose tissue mass, and exaggerated hepatic endocannabi

197 ated diversity of microbes in the mesenteric adipose tissue (MAT) surrounding the GI tract.

198 nt of glucose uptake and catabolism in white adipose tissue may be a key contributor to the antidiabe

199 t might be beneficial include a reduction in adipose tissue-mediated inflammation and pro-inflammator

200 nergy expenditure in obesity, however, brown adipose tissue metabolic activity is lower with obesity.

201 Adipose tissue metabolic dysfunction, including fibrosis

202 The adipose tissue microenvironment drives specific metaboli

203 en the clear cell RCC tumour and peritumoral adipose tissue microenvironment might have clinical rele

204 Adipose tissue mitochondrial dysfunction is emerging as

205 within metabolically active tissues, such as adipose tissue, muscle, liver, and pancreas.

206 White adipose tissue of HF/HC-fed ALR-deficient mice developed

207 White adipose tissue of HFD-fed Asxl2DeltaLysM mice also exhib

208 obic exercise training up-regulates DICER in adipose tissue of mice and humans.

209 e catabolism in primary adipocytes and white adipose tissue of nitrate-treated rats.

210 y of dual positive gammaH2AX & p16 nuclei in adipose tissue of OSA patients receiving statin, aspirin

211 ptional response and gene networks active in adipose tissue of rhesus macaques following FGF21-induce

212 We found that the LDs in adipose tissues of Adipo-Drp1(flx/flx) mice exhibited mo

213 cant phenotype in the subcutaneous and brown adipose tissues of KO mice, with greater vascularity and

214 dietary surveys and/or LA concentrations in adipose tissue or blood compartments) with mortality fro

215 , IL-1R(-/-) mice have more severe liver and adipose tissue pathology during acute infection, consist

216 id (CA) on metabolic risk factors, liver and adipose tissue pathology, brain function, structure (by

217 Visceral adipose tissue plays a critical role in numerous disease

218 White adipose tissue plays an important role in physiological

219 Adipose tissue plays important roles in health and disea

220 optogenetics stimulation in the subcutaneous adipose tissue potently activates Ca(2+) cycling fat the

221 hat the severe osteopenia and the changes in adipose tissue present in these mice were mediated by in

222 r injury and dysfunction of the perivascular adipose tissue promote expansion of the vasa vasorum, ac

223 Adipose tissue provides a defense against starvation and

224 ith increased DFA storage in intra-abdominal adipose tissues (r = -0.79, P = 0.05) and reduced DFA sp

225 of Saa3 in plasma after injection of LPS was adipose tissue rather than liver.

226 Ablation of IL-17RC specifically in adipose tissue reduces expression of TGFbeta1 in adipocy

227 Body contouring achieved via subcutaneous adipose tissue reduction has notably advanced over the p

228 f the healthy plant-based diet with visceral adipose tissue remained statistically significant (per 1

229 ation of HIF-1alpha in ATM of obese visceral adipose tissue resulted in induction of IL-1beta and gen

230 The omentum is a visceral adipose tissue rich in fat-associated lymphoid clusters

231 The omentum, an adipose tissue rich in fat-associated lymphoid clusters

232 Subcutaneous abdominal adipose tissue (SAAT), intra-abdominal adipose tissue (I

233 Paired visceral and subcutaneous adipose tissue samples were obtained from 17 overweight

234 increased FAM13A expression in subcutaneous adipose tissue (SAT) and an insulin resistance-related p

235 nterior and posterior abdominal subcutaneous adipose tissue (SAT) depths of 1.6 and 2.0 cm, respectiv

236 e of excessive dietary fat into subcutaneous adipose tissue (SAT) prevents ectopic lipid deposition-i

237 in levels were higher in liver, subcutaneous adipose tissue (SAT), and visceral adipose tissue (VAT)

238 eige adipose formation in subcutaneous white adipose tissue (SC WAT), would induce other beneficial c

239 ned in biopsies of subcutaneous and visceral adipose tissue (SCAT and VAT, respectively) from 14 noni

240 ng multielectrode arrays showed that cardiac adipose tissue-secreted factors slowed conduction veloci

241 Fast (range, 5-7 seconds) and reliable adipose tissue segmentation can be performed with high D

242 Automated adipose tissue segmentation is feasible in 3D whole-body

243 Adipose tissue serves as the body's primary energy stora

244 r adipogenesis-related genes in subcutaneous adipose tissue sex differences in the genetic and enviro

245 sis in major metabolic organs, including the adipose tissue, skeletal muscle, and liver by 9 weeks po

246 the metabolic subsequences, we generated an adipose tissue-specific DRP1 knockout model (Adipo-Drp1(

247 We generated a doxycycline-inducible adipose tissue-specific MMP14 overexpression model to st

248 s and visceral regions may shed new light on adipose tissue-specific roles in systemic metabolic pert

249 me metabolites were found in both plasma and adipose tissue, such as the bile acid derivative deoxych

250 pression and proteomic analysis of liver and adipose tissue suggested that a major source of Saa3 in

251 amounts of beige cells in subcutaneous white adipose tissue (sWAT) and increased thermogenic gene exp

252 onic leptin treatment of ob/ob mice restores adipose tissue sympathetic innervation, which in turn is

253 ly compacted leaf-like part connected to the adipose tissue that can also efficiently bind B cells an

254 nced cold-induced browning of inguinal white adipose tissue that is linked to induction of MC2R, a re

255 ow that males accumulate more macrophages in adipose tissues that are also more inflammatory.

256 ces in the metabolic infrastructure of the 2 adipose tissues that may have functional and nutritional

257 Although Sik2 is highly expressed in brown adipose tissue, the male and female Sik2(S587A) mice tha

258 verexpressing MMP14 in the early-stage obese adipose tissue, the transgenic mice showed a healthier m

259 nergic receptor (beta-AR) potently stimulate adipose tissue thermogenesis and increase whole-body ene

260 Nonshivering thermogenesis occurs in brown adipose tissue to generate heat in response to cold ambi

261 The ability of adipose tissue to undergo energy expenditure through hea

262 investigated sex differences in subcutaneous adipose tissue transcriptional regulation using omic-sca

263 ) is transcriptionally up-regulated in brown adipose tissue upon exposure to the cold and suppresses

264 g molecules for regulating glucose uptake in adipose tissues upon insulin stimulation, and this regul

265 IV-related microbiota signature and visceral adipose tissue (VAT) area (P for interaction = .01).

266 cutaneous adipose tissue (SAT), and visceral adipose tissue (VAT) in morbidly obese subjects undergoi

267 In particular, visceral adipose tissue (VAT) is critical for the regulation of s

268 degree of unsaturation was lower in visceral adipose tissue (VAT) phospholipids, indicating lower uns

269 masome protein cryopyrin (NLRP3) in visceral adipose tissue (VAT) promotes release of the proinflamma

270 e Treg cell clone isolated from the visceral adipose tissue (VAT), and identified surrogate agonist p

271 he plasticity of sympathetic architecture of adipose tissue via a top-down neural pathway that is cru

272 Serum and SUBQ adipose tissue vitamin D3 concentrations increased propo

273 PET-CT scans quantified brown adipose tissue volume and activity, and we conducted in

274 pendently associated with larger pericardial adipose tissue volume and to explore possible HIV-specif

275 avir were associated with larger pericardial adipose tissue volume.

276 al [CI], 10-23; P < .001) larger pericardial adipose tissue volume.

277 % CI, -6 to -25; P = .002) lower pericardial adipose tissue volume.

278 d to regional differences in associations to adipose tissue volumes in upper versus lower body, and d

279 deep subcutaneous (dSAT), and internal (IAT) adipose tissue-was quantified from MRI images.

280 normalized postnatal growth, decreased white adipose tissue (WAT) and hepatic fat, improved glucose a

281 evelopmental adipose lineage disrupted white adipose tissue (WAT) formation.

282 Recently, browning of white adipose tissue (WAT) has gained attention as a therapeut

283 id-burning pathways in the fat-storing white adipose tissue (WAT) is a promising strategy to improve

284 dipose tissue (BAT) thermogenesis, and white adipose tissue (WAT) lipolysis in vivo.

285 recruitment of beige adipocytes in the white adipose tissue (WAT) of mice and humans, a process that

286 amming; however, the effect of IUGR on white adipose tissue (WAT) progenitors is unknown.

287 Aifm2 in BAT and subcutaneous white adipose tissue (WAT) promotes oxygen consumption, uncoup

288 sity fosters low-grade inflammation in white adipose tissue (WAT) that may contribute to the insulin

289 in the adaptive metabolic response of white adipose tissue (WAT) to cold exposure (CE) in mice, expl

290 uces chronic low-grade inflammation in white adipose tissue (WAT).

291 otal adipose mass, yet unlike white or brown adipose tissues (WAT or BAT) its metabolic functions rem

292 ogenase onto the MB-SPCE surface; samples of adipose tissue were analysed using the biosensors in con

293 ifferences in associations with subcutaneous adipose tissue were identified.

294 oedema is an oestrogen-dependent disorder of adipose tissue, which is triggered by a dysfunction of c

295 ondrial metabolism in both fly and mammalian adipose tissue, which likely contributes to the health-

296 at vary by BMI in the tumour and peritumoral adipose tissue, which might contribute to the apparent s

297 allowing controlled substrate utilization in adipose tissue, which, in turn, supports skeletal muscle

298 eutrality promotes the infiltration of white adipose tissue with mast cells that are highly enriched

299 Given the unique association of visceral adipose tissue with obesity-related metabolic diseases,

300 s to novel roles for FST, PEPD, and PDGFC in adipose tissue, with consequences for cardiometabolic di