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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).
26 3 cm2 vs +3 cm2, respectively; P = .001) and subcutaneous fat (-13 cm2 vs +2 cm2, P = .003).
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
30                              Invasion beyond subcutaneous fat also predicted overall death (HR, 2.1 [
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
34  dwarfism, lordokyphosis, cataracts, loss of subcutaneous fat and impaired wound healing.
35                                Abdominal and subcutaneous fat and increased liver weight account for
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
42  occur in higher numbers in visceral than in subcutaneous fat, and in female versus male mice.
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
46        EBCT-defined CAC scores, visceral and subcutaneous fat, and statin use were assessed in 2001 t
47  metabolic phenotype and the browning of the subcutaneous fat are impaired by the suppression of type
48  (109.5 cm2 vs. 152.9 cm2) but a higher mean subcutaneous fat area (287.8 cm2 vs. 214.6 cm2).
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
51                                          The subcutaneous fat area at each site was calculated by sub
52                                              Subcutaneous fat area can be estimated well by linear me
53 ciated and predicted more of the variance in subcutaneous fat area than in intra-abdominal fat area.
54                                        Total subcutaneous fat area was calculated as the sum of these
55                                        Total subcutaneous fat area was defined as total fat area minu
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
60                                          For subcutaneous fat area, all anthropometric indices were l
61 t for total subcutaneous fat area, abdominal subcutaneous fat area, body mass index, or waist circumf
62       For each 1-cm(2) decrease in abdominal subcutaneous fat area, leptin decreased by 0.044 ng/mL w
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
65 fat area], VFA [visceral fat area], and SFA [subcutaneous fat area], respectively).
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
69                      Intra-abdominal fat and subcutaneous fat areas were quantified by computed tomog
70 und in visceral adipose tissue and abdominal subcutaneous fat areas.
71 amined nonadipocyte stromal cells from human subcutaneous fat as a novel source of therapeutic cells.
72      Abdominal visceral fat (AVF), abdominal subcutaneous fat (ASF), and abdominal total fat (ATF) we
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
75          Body fat was determined by DXA, and subcutaneous fat at triceps, biceps, subscapular, suprai
76 rteriovenous difference across the abdominal subcutaneous fat bed in humans.
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.
79                                              Subcutaneous fat biopsies were obtained from the upper t
80 nd adipose triglyceride lipase expression in subcutaneous fat biopsies.
81 acers were intravenously infused followed by subcutaneous fat biopsies.
82                    Adipocytes collected from subcutaneous fat biopsy samples after normal and restric
83 enes in a subset of subjects who underwent a subcutaneous fat biopsy.
84                                    Abdominal subcutaneous fat, but not visceral fat, area was higher
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
87 gene, PLIN2, expressed only by sebocytes and subcutaneous fat cells.
88 n SR: history of fascial dehiscence, thicker subcutaneous fat, colostomy, and white race.
89 inal fat mass, and increased extra-abdominal subcutaneous fat, compared with wild-type mice.
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
92                                              Subcutaneous fat correlated significantly with mean lept
93 to cortisone) and was higher in omental than subcutaneous fat (cortisone to cortisol, median 57.6 pmo
94                                              Subcutaneous fat declined (-17.2%; P < 0.001), whereas t
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
98                                Excessive non-subcutaneous fat deposition may impair the functions of
99                    The overall burden of non-subcutaneous fat deposition, but not abdominal subcutane
100  BMI and WHR depends on the assumed model of subcutaneous fat deposition.
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
104 ptake into visceral and upper and lower body subcutaneous fat depots in 21 premenopausal women.
105 ed to the phenotype of high visceral and low subcutaneous fat depots in obese adolescents.
106                           Intraabdominal and subcutaneous fat depots were two- to threefold greater i
107         We examined the role of visceral and subcutaneous fat depots, independent of BMI, on the dysl
108         Changes in body weight, visceral and subcutaneous fat depots, oral glucose tolerance, insulin
109 us fat index with the standard scores of non-subcutaneous fat depots.
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
112               Measures of intraabdominal and subcutaneous fat did not predict fasting hyperinsulinemi
113                            APCs derived from subcutaneous fat differentiate well in the presence of c
114 iety response and have altered abdominal and subcutaneous fat distribution, with Rai1(+/-) female mic
115 se in rodents and humans, while expansion of subcutaneous fat does not carry the same risks.
116 ed by glycerol release in microdialysis from subcutaneous fat during a two-step (20 and 120 mU.m(-2).
117          Increased visceral fat, rather than subcutaneous fat, during the onset of obesity is associa
118 lin sensitive, which correlated with massive subcutaneous fat expansion.
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
123  fat gain (rho=-0.42, p=0.004), but not with subcutaneous fat gain (rho=-0.22, p=0.15).
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
131  of MRI to quantify fat content in flesh and subcutaneous fat in fish cutlets was investigated.
132       Discrimination was not associated with subcutaneous fat in minimally (P = 0.95) or fully adjust
133 egulated in human visceral fat compared with subcutaneous fat in obese individuals.
134 ting free fatty acids (FFAs) in visceral and subcutaneous fat in postabsorptive women.
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
140                     The relation between non-subcutaneous fat index and calcified coronary plaque rem
141 each depot separately, we also created a non-subcutaneous fat index with the standard scores of non-s
142                           Transplantation of subcutaneous fat into mice with diet-induced obesity sho
143  for patients who had histologic evidence of subcutaneous fat involvement in comparison with patients
144 ss than 10g lipid per 100g after trimming of subcutaneous fat, irrespective of age.
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
149                      Rates of whole-body and subcutaneous fat lipolysis were assessed by measuring th
150 s that include profound lymphopenia, loss of subcutaneous fat, lordokyphosis, and severe metabolic de
151 te the relation between leptin secretion and subcutaneous fat loss in HIV-infected patients.
152 gnificant reduction in leptin secretion with subcutaneous fat loss in this population.
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
157                                              Subcutaneous fat mass was not associated with any respir
158 ing to measure accurately intraabdominal and subcutaneous fat masses in 14 obese [body mass index (BM
159 to the higher total fat and particularly the subcutaneous fat masses.
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
163 six sites (240 soft-tissue, colonic gas, and subcutaneous fat measurements).
164 increased adipogenesis and/or lipogenesis in subcutaneous fat, mediated by the LPIN1 gene, may preven
165            During cold-induced 'browning' of subcutaneous fat, most 'beige' adipocytes stem from de n
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
168 gth in leukocytes, skeletal muscle, skin and subcutaneous fat of 87 adults (aged 19-77 years).
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
172 ained after further adjustment for abdominal subcutaneous fat (OR: 1.40; 95% CI: 1.00, 1.94).
173  aging including sarcopenia, cataracts, less subcutaneous fat, organ shrinkage, and others.
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
176             In stepwise regression modeling, subcutaneous fat (P <0.0001), but not visceral fat, was
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
182 ncreasing adiposity in the visceral, but not subcutaneous, fat pads of ob/ob mice.
183               Increased visceral rather than subcutaneous fat predicts endothelial dysfunction.
184 otal fat mass (r=0.323, P<0.05) or abdominal subcutaneous fat (r=0.27, P=0.05).
185 ge, 34.4%-54.9%) and significantly lower for subcutaneous fat (range, 10.3%-12.6%), compared with tha
186                 Visceral and the visceral-to-subcutaneous fat ratio increased and insulin sensitivity
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
192 index (Si) and intra-abdominal fat (IAF) and subcutaneous fat (SCF) areas.
193 , as in control subjects, amounts of truncal subcutaneous fat showed a stronger correlation with gluc
194                                    Abdominal subcutaneous fat showed weaker associations with concent
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
200 d to higher triglycerides and more total and subcutaneous fat than darunavir/ritonavir.
201 ge of meal FAs in both upper- and lower-body subcutaneous fat than did the LOb and UOb women (P = 0.0
202 les having more leptin and greater levels of subcutaneous fat than males.
203 al fibrosis with greater preservation of the subcutaneous fat than wild-type mice.
204                            In the dermis and subcutaneous fat, the EVE treated groups showed signific
205                                          For subcutaneous fat, the results were compared with vision
206             The abdominal fat area (AFA) and subcutaneous fat thickness (SFT) were measured using T1-
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
211             WISP1 expression in visceral and subcutaneous fat tissue was associated with markers of i
212 oth-root slices, which were filled with only subcutaneous fat tissue.
213 ly low expression in the gonads, gizzard and subcutaneous fat tissues of chickens.
214            We isolated MSCs from cardiac and subcutaneous fat tissues of mice with LVD 28 days after
215                                    Abdominal subcutaneous fat took up FFAs more avidly than femoral f
216 nitiates adipogenesis after 4 weeks, whereas subcutaneous fat undergoes hypertrophy for a period of u
217 h versus low ratio of visceral to visceral + subcutaneous fat (VAT/[VAT+SAT]).
218                                              Subcutaneous fat, visceral fat, paraspinous musculature,
219 vs. 52,321.87 +/- 5125.05 mm(3), p=0.01) and subcutaneous fat volume (10,599.89 +/- 3683.57 vs. -5224
220                               Arm muscle and subcutaneous fat volumes were measured before and after
221                                              Subcutaneous fat was also significantly related to lepti
222                                              Subcutaneous fat was assessed on the basis of the averag
223                      In contrast, lower body subcutaneous fat was associated with eccentric remodelin
224                      In contrast, lower body subcutaneous fat was associated with higher LV end-diast
225  was accurately detected, acceptable if only subcutaneous fat was excluded, or unacceptable if any br
226                                 Visceral and subcutaneous fat was measured using T(2) (*)-IDEAL.
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
229                                 Visceral and subcutaneous fat were assessed via computed tomography s
230                              Body weight and subcutaneous fat were decreased after RYGB, compared wit
231                          Liver fat, VAT, and subcutaneous fat were determined by magnetic resonance s
232 ion, tumor diameter >/=2 cm, invasion beyond subcutaneous fat) were incorporated in the alternative s

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