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4 d that endogenous oils from subcutaneous and omental adipocytes, and from healthy and unhealthy obese
5 hat LBSQ adipocytes, in contrast to UBSQ and omental adipocytes, store more FFA in women with greater
7 This work highlights the critical role that omental adipose inflammatory pathways might play in the
10 7.5 pmol mg-1 h-1 [82.1-209], p < 0.05) when omental adipose stromal cells were treated with cortisol
16 and adiponectin (ADIPOQ) mRNA expression in omental adipose tissue in adult, pedigreed baboons (Papi
17 port, for the first time, elevated serum and omental adipose tissue levels of vaspin in overweight PC
19 enes were significantly downregulated in the omental adipose tissue of obese individuals with extreme
20 ng circulating vaspin, from subcutaneous and omental adipose tissue of PCOS women and matched control
22 -1 mRNA (P < 0.01) and protein (P < 0.05) in omental adipose tissue of women with PCOS (P < 0.01).
23 entin-1, including circulating omentin-1, in omental adipose tissue of women with PCOS and matched co
24 ion, likely because of the resistance of the omental adipose tissue to insulin suppression and the co
28 t exposure of glucocorticoid specifically to omental adipose tissue, suggesting that central obesity
32 ed a bolus of [1-(14)C]palmitate followed by omental and abdominal subcutaneous fat biopsies to measu
35 s, PD specimens had the highest abundance of omental and parietal arteriolar C1q, C3d, terminal compl
38 anges occurred in body weight, fat pad mass (omental and retroperitoneal), food intake, serum insulin
40 r cells preferentially lodge and grow within omental and splenoportal fat, which contain milky spots,
41 soforms (1 and 2) of 11 beta-HSD in cultured omental and subcutaneous adipose stromal cells from 16 p
47 ssayed the differences in DNA methylation in omental arteries from normal pregnant and preeclamptic w
48 ine and bradykinin) in small resistance-size omental arteries obtained during surgery from women with
49 se expression was significantly increased in omental arteries of preeclamptic women and in VSMCs co-c
51 ignificantly less methylated in preeclamptic omental arteries, whereas TIMP and COL genes either were
54 antigen-specific serum IgM, identifying the omental B cells as a source of IgM production in the SLP
56 ovaries and fallopian tubes, peritoneal and omental biopsies, and collection of peritoneal washings
59 Three marker lesions-primary ovarian mass, omental cake, and peritoneal deposit-were outlined by a
60 baseline ADCs among primary ovarian cancer, omental cake, and peritoneal deposits indicate that diff
61 tic indices were more than twofold higher in omental cells (serum-free medium: P < 0.05; TNF-alpha: P
62 nd CCAAT/enhancer-binding protein alpha than omental cells, as in primary preadipocytes, while hTERT
66 stantially greater in preadipocytes from the omental depot than in those from the subcutaneous depot,
67 11c-expressing B cells nearly eliminated the omental Ehrlichia-specific plasmablasts and reduced anti
68 cent to the abdominal wall without overlying omental fat and central displacement of colon and were f
71 s, with separate models run for each medium (omental fat in the operative cohort, serum in both cohor
72 se findings provide evidence for the role of omental fat in the pathogenesis, and potentially, the pr
73 ed significantly (P < 0.001) more weight and omental fat mass compared with OLETF-EX and LETO-SED.
77 t/activity of FA storage enzymes/proteins in omental fat was dramatically lower in those with more vi
79 dominal wall mass, often involving subjacent omental fat, and may be the only site of recurrent disea
84 led that STAT4 overexpression induced normal omental fibroblasts and adipose- and bone marrow-derived
85 one patient, and bilateral pectoralis and an omental flap in one patient who required additional cove
86 2000, the authors successfully harvested 135 omental flaps (64 pedicled, 71 free transfer) for recons
88 s, intermediate in mesenteric, and lowest in omental hTERT-expressing strains, as in primary preadipo
89 ngle abdominal subcutaneous, mesenteric, and omental human preadipocytes by stably expressing human t
92 orpuscles under the renal capsule and in the omental implants, and with evidence of few host lymphocy
97 iRNAs, miR-146a and miR-150, up-regulated in omental lesions, stimulate survival and increase drug to
98 s with significantly increased expression in omental lesions, with concomitant decreased expression o
100 that local infusion of insulin did suppress omental lipolysis, but only at extremely high insulin co
101 liver regenerative response in the residual omental liver lobes (weight, protein content, incorporat
103 , we evaluated the tumor stroma of 108 human omental metastases and determined that fibronectin was c
104 ding protein 4 (FABP4, also known as aP2) in omental metastases as compared to primary ovarian tumors
106 s of primary EOC tumors and their respective omental metastases from 9 patients using miRNA Taqman qP
107 home to and proliferate in the omentum, yet omental metastases typically represent the largest tumor
108 primary ovarian carcinoma tumors, secondary omental metastases, and ascites cells isolated from sero
109 o model the net accumulation of experimental omental metastases, we show that MKK4-expressing implant
113 the mouse genetic background does not alter omental milky spot number and size, nor does it affect o
114 anatomically associated with lymph nodes and omental milky spots have site-specific properties that e
119 ic edema occurred alone in 26 (38%) and with omental or retroperitoneal edema in 40 (58%) of the 69 p
120 Biocompatibility was demonstrated by either omental or subcutaneous xenotransplantation of liver sca
125 r cells to invade and proliferate into human omental pieces ex vivo and into the omentum of a mouse x
134 scle tumorlets diffusely stud peritoneal and omental surfaces in females, predominantly of reproducti
135 ated palmitate storage rates were greater in omental than abdominal subcutaneous fat in women (1.2 +/
136 han cortisol to cortisone) and was higher in omental than subcutaneous fat (cortisone to cortisol, me
138 ndings of a cis-eQTL for RETN mRNA in baboon omental tissue and human lymphocytes lends support to th
140 ery uncommon however acute presentation with omental torsion and infarction is an unusual entity.
143 ur observations suggest that cancer cells in omental tumors express key miRNAs differently than prima
144 rived from neighbouring stromal cells in the omental tumour microenvironment, and that inhibiting the
148 in the composite engineered bladders with an omental wrap (56%, 1.58-fold, and 2.79-fold, respectivel
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