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1 circulating, free base form of the drug into subcutaneous fat.
2 earch applications that consider measures of subcutaneous fat.
3 n the liver, intermuscular fat, or abdominal subcutaneous fat.
4 -specific recycling of circulating FFAs into subcutaneous fat.
5 gene in epididymal adipose tissue but not in subcutaneous fat.
6 alysis measurements of glycerol release from subcutaneous fat.
7 gher resistin mRNA levels in human abdominal subcutaneous fat.
8 lipolysis and lipogenesis in human abdominal subcutaneous fat.
9 factor-alpha (by 72%) and leptin (by 60%) in subcutaneous fat.
10 increased cardiometabolic risk compared with subcutaneous fat.
11 49653 in small arteries (n = 44) from human subcutaneous fat.
12 liver, lung, myocardium, skeletal muscle, or subcutaneous fat.
13 ross-sectional area, muscle attenuation, and subcutaneous fat.
14 tion favors more truncal and less peripheral subcutaneous fat.
15 and mouse epididymal fat compared with their subcutaneous fat.
16 h and PTRF mRNA levels was observed in human subcutaneous fat.
17 l bone density, trabecular bone content, and subcutaneous fat.
18 se in visceral (intra-abdominal) compared to subcutaneous fat.
19 he connection between the nervous system and subcutaneous fat.
20 ody mass index, total body fat, or abdominal subcutaneous fat.
21 ge enzymes/proteins in omental and abdominal subcutaneous fat.
22 ations among discrimination and visceral and subcutaneous fat.
23 nsidered important and valid measurements of subcutaneous fat.
24 icantly increased their total, visceral, and subcutaneous fat.
25 , resulting in a higher ratio of visceral to subcutaneous fat (0.15 [0.02] vs 0.07 [0.01], p=0.002).
27 4-387), colostomy (5.07; 2.12-13.0), thicker subcutaneous fat (2.02; 1.33-3.21), and black race (0.35
28 ed weight (-2.9%) and BMI (-2.9%) in men and subcutaneous fat (-3.6% at L2-L3 and -4.7% at L4-L5), we
29 3] vs 1.99 [0.19]%, p=0.03), lower abdominal subcutaneous fat (460 [47] vs 626 [39] cm2, p=0.04), and
31 13.8%) abdominal fat: 1.5 +/- 0.2 kg (13.6%) subcutaneous fat and 0.9 +/- 0.1 kg (16.1%) visceral fat
32 with histologic examination of the skin and subcutaneous fat and evaluation of the skin during reduc
33 reated with antiretroviral agents often lose subcutaneous fat and have metabolic abnormalities, inclu
36 atrophy syndrome is characterized by loss of subcutaneous fat and is associated with increased restin
37 gest that SPARC expression is predominant in subcutaneous fat and its expression and secretion in adi
38 ft-tissue mass with infiltration of adjacent subcutaneous fat and minimal or no extension into the bo
39 d by a layered closure of the ischioanal and subcutaneous fat and skin similar to the control interve
40 re racial differences in the distribution of subcutaneous fat and the length of the limbs relative to
41 were compared with total body fat, abdominal subcutaneous fat, and abdominal visceral fat in univaria
43 the high fat-fed state, enhanced browning of subcutaneous fat, and increased adipose expression of GL
44 ction on DNL, liver fat, visceral fat (VAT), subcutaneous fat, and insulin kinetics in obese Latino a
45 tional QTL influencing heat loss, percentage subcutaneous fat, and percentage heart was found for chr
47 metabolic phenotype and the browning of the subcutaneous fat are impaired by the suppression of type
49 leptin levels were strongly associated with subcutaneous fat area (r = 0.760) but not with intra-abd
50 level of the umbilicus, total, visceral, and subcutaneous fat area (TFA [total fat area], VFA [viscer
53 ciated and predicted more of the variance in subcutaneous fat area than in intra-abdominal fat area.
56 ypertension, even after adjustment for total subcutaneous fat area, abdominal subcutaneous fat area,
57 hypertension even after adjustment for total subcutaneous fat area, abdominal subcutaneous fat area,
58 , when LIS and LIR subjects were matched for subcutaneous fat area, age, and gender, they had similar
59 ression model after adjustment for abdominal subcutaneous fat area, age, sex, 2-h plasma glucose leve
61 t for total subcutaneous fat area, abdominal subcutaneous fat area, body mass index, or waist circumf
63 t for total subcutaneous fat area, abdominal subcutaneous fat area, or waist circumference; however,
64 10-11 years even after adjustment for total subcutaneous fat area, total fat area, BMI, or waist cir
66 c studies and quantification of visceral and subcutaneous fat areas (VFA and SFA) using abdominal com
67 white ethnicity had intra-abdominal fat and subcutaneous fat areas measured as part of the Atheroscl
68 ometric indices with intra-abdominal fat and subcutaneous fat areas measured by magnetic resonance im
71 amined nonadipocyte stromal cells from human subcutaneous fat as a novel source of therapeutic cells.
73 ance (beta=0.08, P<0.05), whereas lower body subcutaneous fat associated with higher cardiac output (
74 2%) and at L4-L5 (men -22.4%, women -17.8%), subcutaneous fat at L2-L3 (men -15.7%, women -11.4%) and
77 us dose of [1-(14)C]oleate followed by timed subcutaneous fat biopsies (abdominal and femoral) and th
78 ]palmitate followed by omental and abdominal subcutaneous fat biopsies to measure direct FFA storage.
85 pose stromal cells from omental fat, but not subcutaneous fat, can generate active cortisol from inac
86 the significantly reduced H-Ras occurred in subcutaneous fat cells, while the reduced PI3K and PCNA
90 absorptiometry), and abdominal visceral and subcutaneous fat (computed tomography) were measured in
91 revented weight gain, decreased visceral and subcutaneous fat content (P < 0.03 and 0.01, respectivel
93 to cortisone) and was higher in omental than subcutaneous fat (cortisone to cortisol, median 57.6 pmo
95 ross tertiles, BMI and percentage of fat and subcutaneous fat decreased, while hepatic fat increased.
96 ed rats did have increased plasma leptin and subcutaneous fat deposition and markedly abnormal glucos
97 correlates with insulin resistance, whereas subcutaneous fat deposition correlates with circulating
101 percentage of total fat tissue but had more subcutaneous-fat deposition than did the uninfected cont
102 ter [P = 0.38] and pterygoid [P = 0.70]) and subcutaneous fat deposits (neck [P = 0.44] and submental
103 hether an imbalance between the visceral and subcutaneous fat depots and a corresponding dysregulatio
110 Gonadal fat develops postnatally, whereas subcutaneous fat develops between embryonic days 14 and
111 m-operated animals, whereas transplants with subcutaneous fat did not affect atherosclerosis despite
114 iety response and have altered abdominal and subcutaneous fat distribution, with Rai1(+/-) female mic
116 ed by glycerol release in microdialysis from subcutaneous fat during a two-step (20 and 120 mU.m(-2).
119 rkedly inhibited beige adipocyte function in subcutaneous fat following cold exposure or beta3-agonis
120 ting lungs, anisotropic skeletal muscle, and subcutaneous fat) forward models were compared with meas
121 of the defatted dry matter and marbling and subcutaneous fat fractions, were assessed on 86 ham samp
122 , from 43.1+/-4.5 kg/m2 to 32.3+/-4.0 kg/m2, subcutaneous fat from 649+/-162 cm2 to 442+/-127 cm2, VA
124 is was altered; Rosi-induced body weight and subcutaneous fat gain and liver lipid accumulation were
125 trate that resident innate lymphoid cells in subcutaneous fat generate and activate beige adipocytes,
126 of visceral fat and relatively low abdominal subcutaneous fat have a phenotype reminiscent of partial
127 composition and energy stores in the form of subcutaneous fat have long-term effects on offspring BP
128 ratio of abdominal visceral fat to abdominal subcutaneous fat improved significantly more in the GHRH
129 direct FFA storage in abdominal and femoral subcutaneous fat in 10 and 11 adults, respectively, duri
130 fat distribution, ie, significant losses of subcutaneous fat in association with metabolic abnormali
135 eater gestational weight gain and accrual of subcutaneous fat in the mother but lower fetal growth co
136 rates were greater in omental than abdominal subcutaneous fat in women (1.2 +/- 0.8 vs. 0.7 +/- 0.4 m
137 asis after RYGB is associated with decreased subcutaneous fat, increased postprandial PYY, GLP-1, and
138 and CD8 T-cell infiltrates in the dermis and subcutaneous fat, increased serum immunoglobulin G2a lev
139 associated with a 1 SD increment in the non-subcutaneous fat index [odds ratio (OR): 1.41; 95% CI: 1
141 each depot separately, we also created a non-subcutaneous fat index with the standard scores of non-s
143 for patients who had histologic evidence of subcutaneous fat involvement in comparison with patients
145 We also found that SirT1 expression in human subcutaneous fat is inversely related to adipose tissue
146 shows that the short TCF7L2 mRNA variant in subcutaneous fat is regulated by weight loss and is asso
147 ascular endothelial cells (EC) from lung and subcutaneous fat is slow, like HDMEC, whereas internaliz
148 fraction occurs at the interface between the subcutaneous fat layer and the glandular parenchyma and
150 s that include profound lymphopenia, loss of subcutaneous fat, lordokyphosis, and severe metabolic de
153 ial Dunnigan lipodystrophy, characterized by subcutaneous fat loss, is frequently caused by an R482W
154 ed waist circumference (11-13 cm), abdominal subcutaneous fat mass (1650-1850 cm(3)), visceral fat ma
155 ing for percent total body fat and abdominal subcutaneous fat mass (partial correlation r = -0.73, P
156 android/gynoid ratio, and preperitoneal and subcutaneous fat mass by physical examinations, dual-ene
158 ing to measure accurately intraabdominal and subcutaneous fat masses in 14 obese [body mass index (BM
160 versus 20.8+/-2.4 kg, P>0.05) and abdominal subcutaneous fat-matched (230.6+/-24.9 versus 261.4+/-34
161 I) for assessment of whole body visceral and subcutaneous fat, maximal aerobic capacity test and musc
162 bcutaneous fat deposition, but not abdominal subcutaneous fat, may be a correlate of coronary atheros
164 increased adipogenesis and/or lipogenesis in subcutaneous fat, mediated by the LPIN1 gene, may preven
166 13, and 13a, decreased after weight loss in subcutaneous fat (n = 46) and liver (n = 11) and was mor
167 rse events were reported in the xenon group: subcutaneous fat necrosis and transient desaturation dur
169 Cs) and whole-fat tissues from the abdominal subcutaneous fat of obese and nonobese subjects, we show
170 6) and liver (n = 11) and was more common in subcutaneous fat of subjects with type 2 diabetes than i
171 mals (P = 0.748) that was not due to reduced subcutaneous fat or LBM, but rather preferential loss of
174 her amount of total body fat (p < 0.001) and subcutaneous fat (p < 0.001) than those without NAFLD.
175 verage, 28% greater total fat and 30% higher subcutaneous fat (P <.001 for both), but 10% less parasp
177 e uptake of meal FAs increased in upper-body subcutaneous fat (P = 0.028) in weight-reduced UOb women
178 cm or greater (P<.001), invasion beyond the subcutaneous fat (P<.003), multiple nerve involvement (P
179 ntly blunted angiogenic growth compared with subcutaneous fat (P<0.001) that was associated with mark
180 significantly elevated in the epididymal and subcutaneous fat pads from ob/ob mice compared with thei
181 ver, spleen, kidneys, bone marrow, skin, and subcutaneous fat pads from these mice showed no abnormal
185 ge, 34.4%-54.9%) and significantly lower for subcutaneous fat (range, 10.3%-12.6%), compared with tha
187 profile, including an increased visceral to subcutaneous fat ratio, insulin resistance, dyslipidemia
188 onoclonal gammopathy, a unique patterning of subcutaneous fat reticulation and hypodense bone marrow
189 factors for metastasis were: invasion beyond subcutaneous fat (RR, 11.21; 95% CI, 3.59-34.97), Breslo
190 , 4.55; 95% CI, 1.41-14.69), invasion beyond subcutaneous fat (RR, 4.49; 95% CI, 2.05-9.82), and peri
191 , 9.64; 95% CI, 1.30-71.52), invasion beyond subcutaneous fat (RR, 7.61; 95% CI, 4.17-13.88), Breslow
193 , as in control subjects, amounts of truncal subcutaneous fat showed a stronger correlation with gluc
195 rmula had greater accretion of visceral than subcutaneous fat, showed increased signs of macrophage i
196 orrelated positively with body-mass index in subcutaneous fat (Spearman correlation=0.51, p=0.006).
197 hydrate intake may have a stronger effect on subcutaneous fat storage than does dietary fat intake.
198 lation; (ii) skinfold thickness, to estimate subcutaneous fat stores necessary to fuel growth and imm
199 ra (T1, 586 msec +/- 73; T2, 49 msec +/- 4), subcutaneous fat (T1, 382 msec +/- 13; T2, 68 msec +/- 4
201 ge of meal FAs in both upper- and lower-body subcutaneous fat than did the LOb and UOb women (P = 0.0
207 Exponential dose increases for increased subcutaneous fat thicknesses can be reduced substantiall
208 y was to quantify the anatomy of the muscle, subcutaneous fat, tibia, fibula and arteries in the lowe
209 no acute effect on WISP1 gene expression in subcutaneous fat tissue in overweight subjects who had u
210 10-fold in epididymal, retroperitoneal, and subcutaneous fat tissue of normal, but not of leptin-rec
216 nitiates adipogenesis after 4 weeks, whereas subcutaneous fat undergoes hypertrophy for a period of u
219 vs. 52,321.87 +/- 5125.05 mm(3), p=0.01) and subcutaneous fat volume (10,599.89 +/- 3683.57 vs. -5224
225 was accurately detected, acceptable if only subcutaneous fat was excluded, or unacceptable if any br
227 -induced visceral adipose formation, whereas subcutaneous fat was reduced similarly in both groups.
228 , visceral adipose tissue, but not abdominal subcutaneous fat, was significantly associated with conc
232 ion, tumor diameter >/=2 cm, invasion beyond subcutaneous fat) were incorporated in the alternative s
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