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1 nd insulin signalling (IRS2) in subcutaneous abdominal adipose tissue.
2 phase transition (freezing/melting) in human abdominal adipose tissue.
3 age (SSB) intake has been linked to abnormal abdominal adipose tissue.
4 onsumption was not associated with change in abdominal adipose tissue.
5 e intensity may affect the selective loss of abdominal adipose tissue.
6 seline covariates and change in subcutaneous abdominal adipose tissue.
7 sceral (VAT), but not to subcutaneous (SAT), abdominal adipose tissue.
8  in a significant reduction in the amount of abdominal adipose tissue.
9 ng increases IRS2 expression in subcutaneous abdominal adipose tissue.
10 rficial (SSAT), and deep (DSAT) subcutaneous abdominal adipose tissue (all quantified by an in-oppose
11 ed hand vein and veins draining subcutaneous abdominal adipose tissue and forearm muscle, and arterio
12 ast-enhanced ultrasound perfusion imaging of abdominal adipose tissue and skeletal muscle was perform
13 ging-based, semiautomated method to quantify abdominal adipose tissue and thigh muscle volume and hep
14 gh repeatability and accuracy for estimating abdominal adipose tissue and thigh muscle volumes and he
15                                              Abdominal adipose tissue and thigh muscle were segmented
16 tabolic risk, including waist circumference, abdominal adipose tissue, and hepatic fat content.
17 - mice exhibit significantly lower levels of abdominal adipose tissue as compared with the wild-type
18 , ACACA, FATP2, CD36, and G6PC) in liver and abdominal adipose tissues as well as increased IRS1 phos
19                          The distribution of abdominal adipose tissue at birth may give insights into
20 ensitivity to catecholamines in subcutaneous abdominal adipose tissue (AT).
21 bserved for each additional 5 HU decrease in abdominal adipose tissue attenuation.
22 ography/mass spectrometry), and subcutaneous abdominal adipose tissue biopsies.
23 s of GIP in glucose metabolism, subcutaneous abdominal adipose tissue blood flow (ATBF), and lipid me
24 suction decreased the volume of subcutaneous abdominal adipose tissue by 44 percent in the subjects w
25 clude that determining the masses of various abdominal adipose tissue compartments at the L2-L3 inter
26    We assessed the influence of ethnicity on abdominal adipose tissue compartments in Asian neonates
27 opometric values were measured at birth, and abdominal adipose tissue compartments were assessed by M
28 method for determining the masses of various abdominal adipose tissue compartments, we studied the pr
29 ences in the strength of association between abdominal adipose tissue depots and insulin sensitivity
30 eritoneal, retroperitoneal, and subcutaneous abdominal adipose tissue determined on single axial abdo
31 ity to metabolic diseases is associated with abdominal adipose tissue distribution and varies between
32   Insulin sensitivity, body composition, and abdominal adipose tissue distribution were assessed with
33 th controlled direct effects of ethnicity on abdominal adipose tissue; dSAT was significantly greater
34 88.4 to 2418.2; P = .0071), and subcutaneous abdominal adipose tissue (estimated difference 28.4 cm(2
35                        RNA from subcutaneous abdominal adipose tissue from 9 obese subjects was analy
36 of the E3 ubiquitin ligase Pellino3 in human abdominal adipose tissue from obese subjects and in adip
37 iometry and intra-abdominal and subcutaneous abdominal adipose tissue (IAAT and SAAT) by magnetic res
38                         Greater subcutaneous abdominal adipose tissue in obese adults may provide a s
39 an integrative approach to the regulation of abdominal adipose tissue involves feedback from autocrin
40       The accumulation of fat in upper-body (abdominal) adipose tissue is associated with obesity-rel
41                              The net rate of abdominal adipose tissue leptin production (mean 3.2 +/-
42                                              Abdominal adipose tissue leptin production was determine
43 gonists to promote lipolysis in subcutaneous abdominal adipose tissue of obese adolescent girls and w
44 g studies have documented human variation in abdominal adipose tissue patterning.
45 enhanced ultrasound, we investigated whether abdominal adipose tissue perfusion is abnormal in insuli
46 fat (%BF) (r = 0.42, P < 0.01), subcutaneous abdominal adipose tissue (SAAT) (r = 0.40, P < 0.01), to
47 and fifth lumbar vertebrae) and subcutaneous abdominal adipose tissue (SAAT) by using computed tomogr
48            We measured IAAT and subcutaneous abdominal adipose tissue (SAAT) using computed tomograph
49 ivity (S(i)), visceral fat, and subcutaneous abdominal adipose tissue (SAAT) with weight loss in prem
50  Visceral adipose tissue (VAT), subcutaneous abdominal adipose tissue (SAAT), and hepatic fat fractio
51     Visceral adipose tissue and subcutaneous abdominal adipose tissue samples were collected at surgi
52  of measuring both visceral and subcutaneous abdominal adipose tissue (SAT) in association with metab
53  Enlargement of adipocytes from subcutaneous abdominal adipose tissue (SAT), increased intrahepatic l
54  hydrostatic weighing, IAAT and subcutaneous abdominal adipose tissue (SCAAT) by computed tomography,
55 ed molecular responses of human subcutaneous abdominal adipose tissue (SCAT) to 6 weeks of morning fa
56 al)/day for 16 weeks and serial subcutaneous-abdominal-adipose tissue (SCAT) biopsies (weight loss: 2
57 surements for the quantitative assessment of abdominal adipose tissue strongly correlate with clinica
58 sue, including the inability of subcutaneous abdominal adipose tissue to trap and store free fatty ac
59 etary fat interaction on the change in total abdominal adipose tissue, visceral adipose tissue, and S
60   Changes in waist circumference (WC), total abdominal adipose tissue, visceral adipose tissue, and s
61                                              Abdominal adipose tissue volume and intramyocellular lip
62                                              Abdominal adipose tissue volume in cm(3) and attenuation
63 with clinical measurements for assessment of abdominal adipose tissue volumes in healthy (control sub
64 e, waist circumference change, or respective abdominal adipose tissue volumes.
65 o quantify subcutaneous, visceral, and total abdominal adipose tissue volumes.
66                                    Perirenal-abdominal adipose tissue was sampled from ovine fetuses
67 cose homeostasis, and higher body weight and abdominal adipose tissue weight were observed in male of
68 nd quality (attenuation, Hounsfield Unit) of abdominal adipose tissue were measured using computed to
69                     Biopsies of subcutaneous abdominal adipose tissue were obtained before and after

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