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1 e relationship between metastatic burden and omental adipocyte content.
2                                        Human omental adipocytes display a range of biochemical proper
3              We show here that primary human omental adipocytes promote homing, migration and invasio
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
6                                    Thus, the omental adipose bed represents a highly insulin-resistan
7  This work highlights the critical role that omental adipose inflammatory pathways might play in the
8                                              Omental adipose is a site of prodigious metastasis in bo
9                                              Omental adipose stromal cells (O-ASC) are a multipotent
10 7.5 pmol mg-1 h-1 [82.1-209], p < 0.05) when omental adipose stromal cells were treated with cortisol
11 significantly higher in subcutaneous than in omental adipose tissue (p=0.004).
12                                           An omental adipose tissue biopsy and blood sample were coll
13                            Interestingly, in omental adipose tissue explants, glucose significantly i
14                              Furthermore, in omental adipose tissue explants, insulin and glucose sig
15  mediators (i.e., leukotriene B4 and PGs) in omental adipose tissue from Ob patients.
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
18 the abundance of resistin (RETN) mRNA in the omental adipose tissue of baboons (L0D score 3.8).
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
21 n mRNA (P < 0.05), and protein (P < 0.05) in omental adipose tissue of PCOS women.
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
25                                        Human omental adipose tissue Treg cells also showed high ST2 e
26                                              Omental adipose tissue was obtained from 99 obese patien
27                                              Omental adipose tissue, a biologically active organ secr
28 t exposure of glucocorticoid specifically to omental adipose tissue, suggesting that central obesity
29  four metabolically relevant tissues: liver, omental adipose, subcutaneous adipose, and stomach.
30 ive tissues liver, subcutaneous adipose, and omental adipose.
31  are associated more strongly with increased omental adiposity than with subcutaneous adiposity.
32 ed a bolus of [1-(14)C]palmitate followed by omental and abdominal subcutaneous fat biopsies to measu
33  fatty acid (FA) storage enzymes/proteins in omental and abdominal subcutaneous fat.
34                                              Omental and paravesical tumors were each present in six
35 s, PD specimens had the highest abundance of omental and parietal arteriolar C1q, C3d, terminal compl
36                   Findings were validated in omental and parietal arterioles from independent pediatr
37 tion of mesenteric edema and the presence of omental and retroperitoneal edema.
38 anges occurred in body weight, fat pad mass (omental and retroperitoneal), food intake, serum insulin
39                          Strikingly, in both omental and s.c. WAT from BMI-matched obese humans, expr
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
42                                       Paired omental and subcutaneous adipose tissue samples were obt
43                      Paired samples of human omental and subcutaneous preadipocytes from 12 individua
44                                  Mesenteric, omental, and retroperitoneal edema occur commonly in pat
45 pots studied with a rank order of perirenal, omental, and subcutaneous.
46                                              Omental arteries and plasma were collected from healthy
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
50                                              Omental arteries were evaluated for gene and protein exp
51 ignificantly less methylated in preeclamptic omental arteries, whereas TIMP and COL genes either were
52                            We microdissected omental arterioles from tissue layers not directly expos
53             UA endothelial (UAendo), UA VSM, omental artery endothelium (OA endo), and OA VSM protein
54  antigen-specific serum IgM, identifying the omental B cells as a source of IgM production in the SLP
55                                Peritoneal or omental biopsies obtained from women diagnosed with stag
56  ovaries and fallopian tubes, peritoneal and omental biopsies, and collection of peritoneal washings
57  laparotomy and at least an oophorectomy and omental biopsy) in each group of the study.
58                                   In humans, omental but not subcutaneous IL-6 mRNA expression correl
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
63                                              Omental cyst and omental torsion both are uncommon but i
64              On CECT abdomen the findings of omental cysts and torsion of greater omentum with free f
65                                    Two large omental cysts were found in the pelvic cavity along with
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
69               Conversely, ECMs isolated from omental fat and lung did not redirect testicular cells t
70 at biopsies (abdominal and femoral) and then omental fat biopsy during tubal ligation surgery.
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.
74                     Expression of ST8SIA2 in omental fat of these individuals at baseline was signifi
75        Additionally, paired subcutaneous and omental fat samples were obtained during abdominal surge
76                Concentrations were higher in omental fat than in serum for all POPs.
77 t/activity of FA storage enzymes/proteins in omental fat was dramatically lower in those with more vi
78             The opposite pattern was seen in omental fat with the normal-fat meal and in all depots a
79 dominal wall mass, often involving subjacent omental fat, and may be the only site of recurrent disea
80                   Adipose stromal cells from omental fat, but not subcutaneous fat, can generate acti
81 , and nine (75%) directly involved subjacent omental fat.
82 including elevated glucose levels and excess omental fat.
83 he time representing the delay in collecting omental fat.
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
87 ridement followed by closure using muscle or omental flaps.
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
90  is characterized by numerous peritoneal and omental implants composed of glial tissue.
91 celerating factor composite thymokidneys and omental implants of thymic tissue.
92 orpuscles under the renal capsule and in the omental implants, and with evidence of few host lymphocy
93 itated engraftment of nonvascularized thymic omental implants.
94                                              Omental infusion did not lower systemic free fatty acid
95                                              Omental insulin infusion was extracted at approximately
96 nd 17 miRNAs with differential expression in omental lesions compared to primary tumors.
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
99                                              Omental lipolysis was also pulsatile, with about 10 puls
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
102 sulting in liver necrosis; the remaining two omental lobes (8% liver mass) are left intact.
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
105               Here, we aim to understand how omental metastases differ from primary tumors and how th
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
110 ominant pathway responsible for hematogenous omental metastasis.
111 epletion of ErbB3 in ovarian cancer impaired omental metastasis.
112 tes play distinct and complementary roles in omental metastatic colonization.
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
115                                              Omental milky spots readily concentrate intra-abdominal
116                            Inhibition of the omental neutrophil response exacerbates septic progressi
117 in abdominal subcutaneous (SC) compared with omental (Om) adipocytes.
118                               No patient had omental or retroperitoneal edema alone.
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
121 s lower than that for ovarian (P = .015) and omental (P = .006) sites.
122                               In women, only omental palmitate storage rates were correlated (r = 0.5
123                                              Omental patch closure is appropriate therapy for patient
124                                              Omental patch closure was used in 49 patients and falcif
125 r cells to invade and proliferate into human omental pieces ex vivo and into the omentum of a mouse x
126                                              Omental plasmablasts elicited during Ehrlichia infection
127                            Generation of the omental plasmablasts was route dependent, as they were d
128                                              Omental preadipocytes are therefore more susceptible to
129                                      Primary omental preadipocytes, in which telomeres were longest,
130         The three-tier CRS system applied to omental samples from the validation cohort showed high r
131                                  Adnexal and omental sections were independently scored by three path
132 ct appears to be mediated by the presence of omental stem cells and their secretory products.
133                                 However, the omental stromal cell-derived molecular determinants that
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
137          Four of these baboons also received omental thymic tissue implants.
138 ndings of a cis-eQTL for RETN mRNA in baboon omental tissue and human lymphocytes lends support to th
139                Within the peritoneal cavity, omental tissue is a common site for metastatic disease a
140 ery uncommon however acute presentation with omental torsion and infarction is an unusual entity.
141                             Omental cyst and omental torsion both are uncommon but important causes o
142 ysts in greater omentum leading to secondary omental torsion.
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
145         The second major complication was an omental vessel bleed after a TV cholecystectomy.
146                  In conclusion, increases in omental WAT mitochondrial content between 20 and 40 week
147 pared with cells isolated from mesenteric or omental white fat.
148 in the composite engineered bladders with an omental wrap (56%, 1.58-fold, and 2.79-fold, respectivel
149 tion and implanted either with or without an omental wrap.
150 ulture to precondition grafts and the use of omental wrapping to promote vascularization.

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