ライフサイエンスコーパス: adipose

1 pting the balance between somatic growth and adipose accumulation.

2 These data suggest that sialidases promote adipose and liver inflammation in response to a high-fat

3 In the current study, adipose and liver metabolic responses were measured in t

4 ndependently of anorexia, leading to reduced adipose and muscle mass and function in tumor-bearing mi

5 macrophages, neutrophils also accumulate in adipose and muscle tissues during high-fat diets and con

6 Autologous adipose and muscle-derived stem cells seem to be the int

7 er autophagy plays a role in alcohol-induced adipose atrophy and how altered adipocyte autophagy cont

8 nectin and were resistant to alcohol-induced adipose atrophy and liver injury.

9 ine + citrulline, +29%; P=2.8x10(-169)), and adipose browning (12,13-dihydroxy-9Z-octadecenoic acid +

10 L-10 regulates basic processes of neural and adipose cells and how it promotes CD8 T cell activation,

11 hat affect the differentiation of muscle and adipose cells(3).

12 r SNS-resident macrophages in modulating SNS-adipose crosstalk.

13 gh its varied secretome that targets distant adipose depots, skeletal muscle, and the nervous system.

14 g on a soft matrix (soft priming) will delay adipose-derived stem cell (ASC) transition to a pro-fibr

15 oring TM function and normalizing IOP, human adipose-derived stem cells (ADSCs) were induced to diffe

16 Adipose-derived stem cells (ASCs) can be chemically diff

17 Human adipose-derived stem cells (ASCs) have potential to impr

18 eta (TGF-beta) mediated tenogenesis in human adipose-derived stem cells (hASCs).

19 se of the scaffolds was assessed using human adipose-derived stem cells.

20 Glucose uptake in muscle and adipose did not show similar effects, suggesting that im

21 and disease and highlights emerging roles of adipose FABP (A-FABP) and epidermal FABP (E-FABP) in the

22 iated variants within the FAM13A locus alter adipose FAM13A expression, which in turn, regulates adip

23 e accumulation of the additives in liver and adipose fat of 91 to 120,000 times the rate from the nat

24 ts, and in situ immunofluorescence of murine adipose fat pads.

25 Recent studies demonstrate that adipose fatty acid binding protein (FABP4) promotes obes

26 R agonist mirabegron, which stimulates beige adipose formation in subcutaneous white adipose tissue (

27 ssue (eg, liver, brain), whereas others (ie, adipose, heart) have considerable transcriptomic overlap

28 he main known features of lipoedema, such as adipose hypertrophy, dysfunction of blood and lymphatic

29 tochondrial oxidants as a unifying driver of adipose insulin resistance, serving as a signal of nutri

30 s to mechanistically link nutrient excess to adipose insulin resistance.

31 We further validated the functions of 3 new adipose IR genes by overexpression-based phenotypic resc

32 Physiologically, FGF6/9 expression in adipose is upregulated by exercise and cold in mice, and

33 s multiple mouse tissues (e.g., heart, brown adipose, kidney, liver).

34 air follicles were shorter, not reaching the adipose layer.

35 uced interferon-gamma expression and induced adipose leptin expression via increased miR181b-5p and m

36 t adipogenesis, and deleting Pdgfra in adult adipose lineage did not affect WAT homeostasis.

37 and the deletion of Pdgfra in developmental adipose lineage disrupted white adipose tissue (WAT) for

38 Using in vivo adipose lineage tracking and deletion mouse models, we f

39 uch a scenario could progressively attenuate adipose mass and function, giving rise to "lipodystrophy

40 However, consistent with normal adipose mass in GPAT3-null mice, GPAT3 inhibition did no

41 dipose tissue (BMAT) comprises >10% of total adipose mass, yet unlike white or brown adipose tissues

42 Visceral adipose NLRP3 was required for deficits in long-term pot

43 Here, we report that inducible deletion of adipose OGT causes a rapid visceral fat loss by specific

44 Moreover, adipose OGT overexpression inhibits lipolysis and promot

45 ing performance and upregulated muscular and adipose Pgc-1alpha transcript levels, whereas exercise a

46 agonist, it inhibits the effect of BMP2/4 on adipose precursor cell commitment/differentiation.

47 Adipose-resident leukocytes have non-traditional immunol

48 we first outline the established reciprocal adipose-SNS relationship comprising the neuroendocrine l

49 matrix production and lipid accumulation in adipose stem cells and/or adipocytes as observed in vivo

50 n mice, the serous surface of the mesenteric adipose streaks contains lymphocyte-rich organoids compr

51 on with epithelial structures and within the adipose stroma, and are important for mammary gland deve

52 regarding the effects of macrophages on the adipose stroma.

53 lar and molecular features that comprise the adipose thermogenic milieu.

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

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

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

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

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

59 Adipose tissue (AT) inflammation contributes to systemic

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

103 1-expressing cell clusters in inguinal white adipose tissue after chronic cold exposure.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

123 Adipose tissue biopsies were collected from 13 adult fem

124 In adipose tissue biopsies, changes in fibrosis were evalua

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

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

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

128 AA measured by adipose tissue compartment volumes-abdominal superficial

129 Adipose tissue contains beta3-adrenergic receptors (beta

130 Human adipose tissue contains higher numbers of cells of this

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

132 Adipocytes and adipose tissue derived cells have been investigated for

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

134 Sex differences in adipose tissue distribution and function are associated

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

152 ss remain insufficiently understood owing to adipose tissue heterogeneity.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 BACKGROUNDBeige adipose tissue is associated with improved glucose homeo

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

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

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

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

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

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

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

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

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

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

182 nergy expenditure via sympathetic control of adipose tissue lipolysis.

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

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

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

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

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

188 Adipose tissue metabolic dysfunction, including fibrosis

189 The adipose tissue microenvironment drives specific metaboli

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

191 Adipose tissue mitochondrial dysfunction is emerging as

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

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

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

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

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

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

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

199 White adipose tissue plays an important role in physiological

200 Adipose tissue plays important roles in health and disea

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

219 Serum and SUBQ adipose tissue vitamin D3 concentrations increased propo

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

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

222 avir were associated with larger pericardial adipose tissue volume.

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

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

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

226 ifferences in associations with subcutaneous adipose tissue were identified.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

262 dimorphism, and the mechanical compliance of adipose tissue.

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

264 er unsaturated fatty acid incorporation into adipose tissue.

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

266 erioles supplying skeletal muscle, heart and adipose tissue.

267 creased thermogenic gene expression in brown adipose tissue.

268 normal myelopoiesis, osteopenia, and reduced adipose tissue.

269 olic disease on the mechanical properties of adipose tissue.

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

271 tal workflow for validating gene transfer to adipose tissue.

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

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

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

275 solated from human peripheral blood vs human adipose tissue.

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

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

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

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

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

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

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

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

284 Adipose tissues dynamically remodel their cellular compo

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

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

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

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

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

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

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

292 ) initiates thermogenesis in brown and beige adipose tissues.

293 r understanding of cellular heterogeneity in adipose tissues.

294 pathway, with a discriminative flux between adipose tissues.

295 ient, which in breast, ranges from primarily adipose to fibroglandular tissue.

296 ipocytes by multiple mechanisms, hydrolyzing adipose triglyceride and generating excess NEFAs.

297 Silencing adipose triglyceride lipase (ATGL) in human pseudoislets

298 es, notably proline dehydrogenase (POX), and adipose triglyceride lipase (ATGL), as well as markedly

299 enesis by increasing the activity of hepatic adipose triglyceride lipase, intrahepatic lipolysis, hep

300 egulation of miR-203-3p limits glycolysis in adipose under conditions of metabolic stress.