ライフサイエンスコーパス: epididymal

1 g-1 was induced in subcutaneous (9-fold) and epididymal (4-fold) fat pads from db/db mice treated for

2 , less hepatosteatatitis, and a reduction in epididymal adipocyte volume.

3 afficking kinetics of GLUT4 and GLUT1 in rat epididymal adipocytes were analyzed by a four-compartmen

4 In rat epididymal adipocytes, practically all of the major gluc

5 o suppress lipolysis from mesenteric but not epididymal adipocytes.

6 ody weight gain, more severe inflammation in epididymal adipose tissue (EAT), and aggravated insulin

7 fat diet (HFD) has major effects on visceral epididymal adipose tissue (eWAT).

8 GLUT4 and adiponectin protein expression in epididymal adipose tissue and increased blood glucose co

9 ced transcription of the adiponectin gene in epididymal adipose tissue but not in subcutaneous fat.

10 IL-6 and IL-10, and CXCL chemokines in white epididymal adipose tissue from both wt and AhRR Tg mice.

11 Epididymal adipose tissue from wild-type mice produced a

12 utophagy and decreased Akt/mTOR signaling in epididymal adipose tissue in wild-type mice.

13 body fat content as well as the quantity of epididymal adipose tissue of male Wistar rats was decrea

14 determine metabolic alterations in blood and epididymal adipose tissue samples that were collected fr

15 ide palmitate in HC- versus CF-fed mice, the epididymal adipose tissue synthesized approximately 1.5-

16 in to stimulate leptin release from isolated epididymal adipose tissue was also enhanced in R6/2 mice

17 ed rates of in vivo triglyceride turnover in epididymal adipose tissue were measured using (2)H(2)O a

18 es of metabolite carbon atoms taken from rat epididymal adipose tissue, goosefish islet cells, Coryne

19 intracellular peptides in gastrocnemius and epididymal adipose tissue, which likely is involved with

20 ectin immunoprecipitated from adipocytes and epididymal adipose tissue.

21 f insulin to stimulate glucose metabolism in epididymal adipose tissue.

22 leptin mRNA at a level comparable to that in epididymal adipose tissue.

23 own-like adipocytes in subcutaneous, but not epididymal, adipose depots.

24 embles in vitro may provide clues on how the epididymal amyloid matrix forms in vivo.

25 nondenatured mouse CRES, a component of the epididymal amyloid matrix, allowing us to examine its as

26 ssed adiposity levels, leptin mRNA levels in epididymal and inguinal white adipose tissue (EWAT and I

27 In epididymal and mesenteric adipose tissue of control rats

28 ue-Dawley rats to either surgical removal of epididymal and perinephric fat pads (VF-; n = 9) or a sh

29 Epididymal and perirenal adipocyte size was increased 20

30 reduction of approximately 60% in weight of epididymal and perirenal depots.

31 plasma leptin levels and a >50% reduction in epididymal and perirenal fat pad size.

32 into BAT resulted in profound reductions in epididymal and retroperitoneal WAT mass, without affecti

33 clamp as well as in adipocytes isolated from epididymal and subcutaneous adipose tissue.

34 ession also is significantly elevated in the epididymal and subcutaneous fat pads from ob/ob mice com

35 fat diet (HFD) upregulated pfn expression in epididymal and subcutaneous white adipose tissue (WAT) b

36 on, by recording CatSper currents from human epididymal and testicular spermatozoa, we show that CatS

37 Inguinal, epididymal, and retroperitoneal fat pads weighed less in

38 significantly smaller in HFpEF than in sham (epididymal AT, 7.59 versus 10.67 mg/g; inguinal AT, 6.34

39 matory cytokines TNF-alpha or osteopontin in epididymal ATMs of obese mice caused significant improve

40 in obese mice selectively silences genes in epididymal ATMs, whereas macrophages within lung, spleen

41 ructural defects were found in two-thirds of epididymal axonemes, with the most common abnormality be

42 a13, and Id2) in murine brown, inguinal, and epididymal (BAT, iWAT, and eWAT) adipose tissues.

43 Our dataset extends on existing knowledge of epididymal biology, and provides a wealth of information

44 Expansion of white adipose tissue-derived epididymal BK(L1/L1) preadipocytes and their differentia

45 Therewith, Trpv6 excision affects epididymal Ca(2+) handling and male fertility to the sam

46 Sperm extracted from the epididymal cauda showed strongly impaired motility chara

47 e employed expression screening of a hamster epididymal cDNA library to obtain the full-length sequen

48 Epididymal clear cells contain abundant V-ATPase in thei

49 Proton secretion by epididymal clear cells is achieved via the proton pumpin

50 In both kidney-intercalated cells and epididymal clear cells, cAMP induces V-ATPase apical mem

51 responding murine genes, indicating that the epididymal cluster is evolutionary conserved.

52 collectively with testosterone to facilitate epididymal coiling by stimulating epithelial proliferati

53 This loss of epididymal coiling did not result from testosterone defi

54 chromocytomas, endolymphatic sac tumors, and epididymal cystadenomas.

55 We previously have shown that the epididymal cystatin CRES (cystatin-related epididymal sp

56 ns indicate that cSrc is essential for cauda epididymal development and suggest an essential role of

57 nter the male reproductive tract to regulate epididymal (downstream) pathways required for sperm matu

58 verexpression triggers male sterility due to epididymal dysfunction caused by epithelial disorganizat

59 lity, we assessed metabolism and measures of epididymal (e)WAT mitochondria and artery function in yo

60 intraperitoneal insulin tolerance tests, and epididymal (eAT) and inguinal subcutaneous AT (iAT) and

61 tiate an immune response if they escaped the epididymal environment.

62 murine subcutaneous (SC) or intra-abdominal epididymal (EP) white adipocytes.

63 These studies support the hypothesis that epididymal epithelial cells are critical to sexual trans

64 ims to determine if accessory sex glands and epididymal epithelial cells are sources of viral persist

65 odeling of the glycocalyx of spermatozoa and epididymal epithelial cells by endogenous sialidases aft

66 Epididymal epithelial cells did not show ZIKV antigen im

67 llent model to study the role of Sertoli and epididymal epithelial cells in the differentiation and m

68 on of miR-29a inhibited the proliferation of epididymal epithelial cells in vitro.

69 bated with EVs collected from stress-treated epididymal epithelial cells produced offspring with alte

70 s also observed in primary cultures of mouse epididymal epithelial cells.

71 functions of the TRPV6(D541A) pore mutant in epididymal epithelial cells.

72 om defects in the functioning of Sertoli and epididymal epithelial cells.

73 rize the sialylation of the apical region of epididymal epithelial cells.

74 ms, CAII and CAIV, are distributed along the epididymal epithelium and appear with the onset of puber

75 ese males show extensive degeneration of the epididymal epithelium in the corpus region, rather than

76 We have shown that Bmp7 expression in epididymal epithelium is developmentally regulated.

77 cSrc is enriched in vesicles released by the epididymal epithelium known as epididymosomes.

78 requirement of different classes of BMPs for epididymal epithelium to survive and have significant im

79 Bmp8atm1 males also show degeneration of the epididymal epithelium, indicating a novel role for BMPs

80 ls in mice disrupts Ca(2+) absorption by the epididymal epithelium, resulting in abnormally high Ca(2

81 s mirrored by a lack of Ca(2+) uptake by the epididymal epithelium.

82 ay originate from sperm, instead of from the epididymal epithelium.

83 In terms of the cluster ancestry, epididymal expression possibly appeared in a PGDS-like l

84 veral strong bands on Western blots of human epididymal extracts from the caput and corpus regions.

85 plete their maturation; however, no specific epididymal factors that mediate this process have so far

86 <0.01) less retroperitoneal, mesenteric, and epididymal fat accumulation, compared to their ob/ob cou

87 ethylation of its promoter in progenitors of epididymal fat compared to Con offspring, which was corr

88 el was lower in human visceral fat and mouse epididymal fat compared with their subcutaneous fat.

89 at 6 mo) and had significantly more (P<0.01) epididymal fat content.

90 leasable and extractable LPL activity in the epididymal fat decreased by 75-80% in the diabetic group

91 lation of Foxa3 have a selective decrease in epididymal fat depot and a cell-autonomous defect to ind

92 tissue (VAT) of lean mice, especially in the epididymal fat depot.

93 that regulates the selective enlargement of epididymal fat depots and suppresses energy expenditure

94 depot could affect vascular disease in mice, epididymal fat depots were transplanted into atheroscler

95 se in the diet, whereas [(3)H]NE turnover in epididymal fat did not respond to either monosaccharide.

96 During HFD feeding, epididymal fat initiates adipogenesis after 4 weeks, whe

97 nce in skeletal muscle, whereas in liver and epididymal fat it was associated with increased expressi

98 Thus, the rapid increase in epididymal fat mass with the cessation of voluntary whee

99 Absolute and relative epididymal fat mass, mean cell volume, and amount of lip

100 NA methylation in the zfp423 promoter in the epididymal fat of OB/Obe offspring, which was correlated

101 in confined well-vascularized sites like the epididymal fat pad (EFP) improved graft outcomes, but on

102 Micro) in the confined and well-vascularized epididymal fat pad (EFP) site, a model of the human omen

103 ouse islets engrafted on the intra-abdominal epididymal fat pad ameliorated streptozotocin-induced hy

104 ia occurred in all mice after removal of the epididymal fat pad bearing the islet graft.

105 This study indicates that the epididymal fat pad maybe a useful islet transplant site

106 eeded scaffolds were then implanted onto the epididymal fat pad of syngeneic mice with streptozotocin

107 The epididymal fat pad was evaluated as a site of islet tran

108 t affected until week 28 (decreased by 14%); epididymal fat pad weight also decreased (25%) at this t

109 yperleptinemia and reduction in food intake, epididymal fat pad weight declined 55% in wild-type but

110 air-fed group, a significant increase in the epididymal fat pad weight, BAT weight, and plasma leptin

111 A significant increase in the epididymal fat pad weight, interscapular brown adipose t

112 ell as lower hepatic triglyceride levels and epididymal fat pad weights than in SHR harboring mutant

113 3) Does short-term elimination of T cells in epididymal fat pad without disturbing the systemic T cel

114 o the devices, which were implanted into the epididymal fat pad(s) of streptozocin diabetic mice.

115 er visceral adipose tissue mass estimated by epididymal fat pad, associated with iron accumulation in

116 w as 50 islets, either intraportal or in the epididymal fat pad, displayed similar glucose tolerance

117 ic mass of syngeneic islets implanted in the epididymal fat pad, followed by a subrenal capsular impl

118 mia and increased homocysteine levels in the epididymal fat pad, which was associated with decreased

119 cally, adiponectin KO mice possessed smaller epididymal fat pads and showed reduced body weight compa

120 To determine the mechanism, epididymal fat pads from normal wild-type (+/+) and obes

121 Acute depletion of T cells from epididymal fat pads improved insulin action in young DIO

122 have greater deposits of s.c. fat and larger epididymal fat pads in comparison with wild-type mice.

123 PPARgamma-regulated genes were higher in the epididymal fat pads of Adipoq-LPL mice than control mice

124 adipocytes from SPARC-null versus wild-type epididymal fat pads were 252 +/- 61 and 161 +/- 33 micro

125 stablish feasibility of fat transplantation, epididymal fat pads were harvested from wild-type C57BL/

126 Incubation of epididymal fat pads with leptin or its i.v. injection in

127 ties, including low fertility, an absence of epididymal fat pads, and a tendency to develop blepharit

128 nd in primary adipocytes isolated from mouse epididymal fat pads, in response to acute activation of

129 ere found to have lower body weight, smaller epididymal fat pads, lower blood levels of nonesterified

130 n messenger RNA (mRNA) and protein levels in epididymal fat pads.

131 that GSK-3 activity increased twofold in the epididymal fat tissue and remained unchanged in muscle a

132 ntrast, GSK-3 activity did not change in the epididymal fat tissue of A/J mice, regardless of the typ

133 th reduced levels of the pP65 protein in the epididymal fat tissue, suggesting less activation of the

134 1 protein levels were significantly lower in epididymal fat tissues from db/db and high fat diet-indu

135 is associated with a prolonged overshoot in epididymal fat triacylglycerol synthesis.

136 The rate of triacylglycerol synthesis in epididymal fat was 4.2-fold greater in SED5 than in WL5,

137 C/EBPalpha protein levels in epididymal fat were 30% greater in SED5 than in WL5.

138 H2O content and wt of epididymal fat were increased by RSG and correlated to i

139 t and GSK3 phosphorylation and activities in epididymal fat were opposite to those of brain after str

140 trophy and interlelukin-6 gene expression in epididymal fat, along with the splenic proinflammatory p

141 quantified by magnetic resonance imaging and epididymal fat-pad weights.

142 showed significantly reduced body weight and epididymal fat.

143 dexamethasone prevented ATM accumulation in epididymal fat.

144 ependent and PPARalpha-independent manner in epididymal fat.

145 neal fat, but was without effect on GLUT4 in epididymal fat.

146 receptor type in islets, liver, kidney, and epididymal fat.

147 a, and an enhanced proinflammatory status of epididymal fat.

148 ce also exhibit adipocyte hypertrophy in the epididymal fat.

149 sion of Egr1 while decreasing ATGL levels in epididymal fat.

150 oliferator-activated receptor (PPAR)gamma in epididymal fat; enzymes of fatty acid oxidation and thei

151 white adipose tissues including inguinal and epididymal fats and also in brown adipose tissue but not

152 Examination of the epididymal fluid and spermatozoa from L68Q mice showed i

153 r these studies suggest that amyloids in the epididymal fluid can be cytotoxic to the maturing sperma

154 The addition of epididymal fluid from L68Q mice to WT spermatozoa result

155 ty compared with WT spermatozoa incubated in epididymal fluid from WT mice.

156 L68Q epididymal fluid that was depleted of cystatin C amyloid

157 Artificial insemination fluid derived from epididymal flush and seminal plasma from the prostate an

158 artificial insemination fluid generated from epididymal flush or seminal plasma from ZIKV infected ma

159 both the maintenance of spermatogenesis and epididymal function and it further suggests that BMP8 an

160 mis, the role of Bmp7 in spermatogenesis and epididymal function cannot be revealed by simply examini

161 gate the role of Bmp7 in spermatogenesis and epididymal function.

162 ting a novel role for BMPs in the control of epididymal function.

163 , we studied the role of RNA interference in epididymal functions.

164 I from sperm results in an inability to bind epididymal glycoconjugates that normally maintain sperm

165 Rat androgen-regulated acidic epididymal glycoprotein (AEG), also known as Protein DE,

166 spermatocytes to Seritoli cells, and acidic epididymal glycoproteins that bind to sperm and have bee

167 aceptive approach frequently associated with epididymal granuloma and sperm autoantibody formation.

168 The mean resistive indexes for the right epididymal head, body, and tail were 0.55, 0.55, and 0.5

169 of mouse adipose cell-size distributions in epididymal, inguinal, retroperitoneal, and mesenteric fa

170 ts in spermatogenesis and in maintaining the epididymal integrity of the caput and caudal regions.

171 sions consisted of scrotal wall liposarcoma, epididymal leiomyosarcoma, and recurrent spindle cell ma

172 Epididymal leptin mRNA measured by Northern blot analysi

173 ervation of a cluster of five genes encoding epididymal lipocalins, differently regulated and regiona

174 Protein DE is secreted into the epididymal lumen and binds to sperm heads during their t

175 CRES, is an integral structure in the mouse epididymal lumen and has proposed functions in sperm mat

176 endogenous transglutaminase activity in the epididymal lumen catalyzed the formation of SDS-resistan

177 The epididymal lumen contains a complex cystatin-rich nonpat

178 ropose that transglutaminase activity in the epididymal lumen may function as a mechanism of extracel

179 ing CRES are a component of the normal mouse epididymal lumen without any apparent cytotoxic effects

180 RES amyloid may also form in vivo within the epididymal lumen.

181 he appearance of numerous round cells in the epididymal lumen.

182 RES has the potential to form amyloid in the epididymal lumen.

183 , but not the viable, spermatozoa within the epididymal lumen.

184 conditions that may approximate those in the epididymal lumen.

185 ility of sperm and a significant increase in epididymal luminal Ca(2+) concentration that is mirrored

186 in abnormally high Ca(2+) concentrations in epididymal luminal fluid and in a dramatic but incomplet

187 he presence of multiple forms of CRES in the epididymal luminal fluid, including SDS-sensitive and SD

188 cessing of mouse fertilin beta occurs during epididymal maturation and involves changes in the cytopl

189 rement for sAC during spermatogenesis and/or epididymal maturation and reveal limitations inherent in

190 of sperm functionality is due to problems in epididymal maturation or to the absence of cSrc in sperm

191 After epididymal maturation, sperm capacitation, which encompa

192 is protein is acquired by sperm later during epididymal maturation.

193 succination of protein is also increased in epididymal, mesenteric, and subcutaneous adipose tissue

194 ng the literature's current understanding of epididymal morphogenesis, we will highlight some of the

195 te in this report that capacitation of cauda epididymal mouse sperm in vitro was accompanied by a tim

196 ion with contralateral testicular atrophy or epididymal obstruction.

197 eptin had no effect on leptin mRNA in either epididymal or retroperitoneal white adipose tissue (WAT)

198 trated into the posterior head domain during epididymal passage.

199 Epididymal, perirenal, and inguinal WAT weighed 139-185%

200 by RT-PCR in the mouse WAT depots examined (epididymal, perirenal, s.c., and mammary gland) and in i

201 ghly expressed in s.c. preadipocytes than in epididymal preadipocytes.

202 ATP release was detected from the mouse epididymal principal cell line (DC2) and increased by ad

203 n human chromosome 20q 12-13.2 called Eppin (Epididymal protease inhibitor) that expresses three mRNA

204 s report we describe the discovery of Eppin (Epididymal protease inhibitor), a gene on human chromoso

205 known genes: two L1 repeat genes and rabbit epididymal protein 52.

206 b and contains nine exons encoding an 1120bp epididymal Protein DE mRNA.

207 el gene Rnase10 encoding a secreted proximal epididymal protein in the mouse results in a binding def

208 nalysis using PSG2 showed that certain sperm/epididymal proteins are undersulfated in Tpst2(-/-) mice

209 A phylogenetic analysis of the new epididymal proteins reveals their spread position in the

210 ke into adipose cells, we incubated isolated epididymal rat adipocytes with the globular domain of re

211 Microsurgical techniques for vasal-epididymal reconstruction and sperm retrieval have been

212 The fold of NGAL is most similar to the epididymal retinoic acid-binding protein, another lipoca

213 increased UCP-2 mRNA by more than 10-fold in epididymal, retroperitoneal, and subcutaneous fat tissue

214 oma, spermatic cord injury or contusion, and epididymal, scrotal, and urethral injuries.

215 Selective overexpression of Human epididymal secretory protein E4 (HE4) points to a role i

216 regulation of CAII and CAIV in the different epididymal sections of the knockout lines.

217 cted lateral mobility in both testicular and epididymal sperm (D < 10(-10) cm(2)/s).

218 ) or ADAM3 (cyritestin) are infertile; cauda epididymal sperm (mature sperm) from these mutant mice c

219 n, as well as percutaneous and microsurgical epididymal sperm aspiration.

220 ugh meiosis and spermiogenesis and generated epididymal sperm at approximately 50% of control levels,

221 e Jackson Laboratory are infertile, have low epididymal sperm concentrations, and produce sperm with

222 Normal epididymal sperm count, spermatozoa morphology, capacita

223 ificant reductions in serum testosterone and epididymal sperm count.

224 Diets that optimized testes mass and epididymal sperm counts (indicators of gamete production

225 e was almost normal, with testis weights and epididymal sperm counts being unaffected.

226 sterile and show reduced sperm motility and epididymal sperm counts.

227 wo types of voltage-gated Ca(2+) channels in epididymal sperm examined prior to capacitation.

228 Mutant epididymal sperm exhibit diminished motility.

229 Mutant epididymal sperm exhibited abnormal morphology, includin

230 Despite their sterility, some epididymal sperm from Tenr mutants have normal morpholog

231 Epididymal sperm from Tnp2-null mice showed an increase

232 gellar waveform analysis show that for mouse epididymal sperm in vitro, the resting flagellar beat fr

233 The addition of S-Ht31 to bovine caudal epididymal sperm inhibits motility in a time- and concen

234 SK3alpha and sperm PP2B are essential during epididymal sperm maturation and during fertilization.

235 Loss of PP2B results in impaired epididymal sperm maturation and motility.

236 iological role of NCOA5 in the regulation of epididymal sperm maturation and suggest that NCOA5 defic

237 suggest an essential role of this kinase in epididymal sperm maturation involving cSrc extracellular

238 During epididymal sperm maturation, the lipid content of the sp

239 ically active calcineurin to function during epididymal sperm maturation.

240 ntal factors that impair spermatogenesis and epididymal sperm maturation.

241 Moreover, epididymal sperm numbers were not affected in FABP9(-/-)

242 rincipal piece in testicular sperm, while in epididymal sperm p109 and p26 were present only in the p

243 Alkaline phosphatase treatment of epididymal sperm proteins demonstrated that p109 was a p

244 d in the tail and acrosomal regions of mouse epididymal sperm, while TSSK2 was found in the equatoria

245 mature flagella on elongating spermatids and epididymal sperm.

246 physiological membrane potentials in corpus epididymal sperm.

247 2 is a key element for stability of ADAM3 in epididymal sperm.

248 9.6% versus 33.2% +/- 7.5% (P = 0.0104) for epididymal sperm.

249 of structural head abnormalities in residual epididymal sperm.

250 ds, but condensation was still incomplete in epididymal sperm.

251 nd cauda epididymis, but on only 6% of caput epididymal sperm.

252 ro" domain of the precursor) were present in epididymal sperm.

253 o-AKAP82 in condensing spermatids but not in epididymal sperm.

254 vels are high in immotile compared to motile epididymal sperm.

255 CRES (cystatin-related epididymal spermatogenic), a member of the cystatin supe

256 e epididymal cystatin CRES (cystatin-related epididymal spermatogenic), cst8, a reproductive-specific

257 n vitro fertilization (IVF) that failed with epididymal spermatozoa alone.

258 etylneuraminic acid residues was detected in epididymal spermatozoa and epithelial cells using combin

259 tigate whether alterations of the sialome of epididymal spermatozoa and surrounding epithelial cells

260 ive form of pig zonadhesin from capacitated, epididymal spermatozoa comprises two covalently associat

261 rain, heart, liver, lung, and muscle, and in epididymal spermatozoa from adult mice.

262 In vitro studies showed that epididymal spermatozoa from L68Q mice were unable to fer

263 nuclear envelope and cytoplasmic droplet of epididymal spermatozoa.

264 of incompletely processed forms remained in epididymal spermatozoa.

265 iece of the flagellum between testicular and epididymal spermatozoa.

266 as localized to the principal piece of mouse epididymal spermatozoa; (2) mouse CABYR has two coding r

267 while the proximal centriole is lost during epididymal stage.

268 e tissues including perivascular, perirenal, epididymal, subcutaneous and brown adipose tissue.

269 3)H]NE turnover in IBAT, but increased it in epididymal, though not retroperitoneal, fat.

270 corticoid receptor protein levels within the epididymal tissue of male breeders.

271 Changes that occur to mammalian sperm upon epididymal transit and maturation render these cells cap

272 osomes (vesicles that fuse with sperm during epididymal transit) carry RNA payloads matching those of

273 During the epididymal transit, polySia carriers were partially inte

274 dual loss of ADAM3 and ADAM6 proteins during epididymal transit.

275 on at multiple levels, enhances lipolysis in epididymal WAT (eWAT) because of the upregulation of gen

276 lerance, reduced insulin signaling in liver, epididymal WAT and heart, and downregulation of oxidativ

277 1 and fatty acid synthase protein levels in epididymal WAT of HFD-fed rats.

278 ght gain (as well as plasma lipid levels and epididymal WAT sizes in HFD-fed rats).

279 sis of intra-abdominal white adipose tissue (epididymal WAT) showed elevated expression of mRNA and p

280 regulated lipolysis and lipogenesis genes in epididymal WAT.

281 t, show no difference in the growth of their epididymal white adipose tissue (epiWAT) but they show e

282 Such Treg activity lost in male epididymal white adipose tissue (eWAT) and female gonada

283 Hepatic lipids extracted from mouse liver, epididymal white adipose tissue (eWAT) and subcutaneous

284 ous nature of these effects, we transplanted epididymal white adipose tissue (eWAT) from wild-type do

285 c mice overexpressing Tnmd develop increased epididymal white adipose tissue (eWAT) mass, and preadip

286 pase (HSL) in cultured adipocytes and in the epididymal white adipose tissue (EWAT) of C57BL/6 mice.

287 ucturally distinct PPARgamma agonists in the epididymal white adipose tissue (EWAT) of db/db mice, 33

288 In epididymal white adipose tissue (eWAT) of PDE3B KO mice

289 hat tissue-resident macrophages from healthy epididymal white adipose tissue (eWAT) tightly associate

290 eek switch protocol caused further increased epididymal white adipose tissue (eWAT) weight, preadipoc

291 increased insulin singling in both liver and epididymal white adipose tissue (eWAT).

292 nd 12.4%, respectively, in the perirenal and epididymal white adipose tissue (PWAT, EWAT) compared to

293 DUSP5, an ERK1/2 phosphatase, was induced in epididymal white adipose tissue (WAT) in response to die

294 thesis leads to inhibition of lipogenesis in epididymal white adipose tissue (WAT), induction of brow

295 naling in liver and visceral adipose tissue (epididymal white adipose tissue [WAT]), reduced WAT infl

296 ch in depot utilisation from subcutaneous to epididymal white adipose tissue was associated with a wo

297 and enhanced MPO expression and activity in epididymal white adipose tissue, with an increase in bod

298 Epididymal white fat cells from cavin-1-null mice were s

299 through multisynaptic pathways to liver and epididymal white fat in mice using pseudorabies virus st

300 ment resulted in a decrease in abdominal and epididymal white fat pad weights, while interscapular br