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1 pelvic floor muscle activation and voluntary gluteal activation, but not during voluntary finger acti
2 d to percentage body fat (P<0.0001), whereas gluteal adipocyte size was related to visceral fat area
3 solated subcutaneous abdominal, femoral, and gluteal adipocytes was measured by direct microscopy or
4 ardiometabolic diseases, whereas lower-body (gluteal and femoral) fat may be protective.
5 is from the primary tumor in the tail to the gluteal and iliac lymph nodes (maximum nodal weight decr
6 ests that deranged energy storage in femoral-gluteal and other peripheral sites is important; the mol
7                                      SUVs in gluteal and quadriceps areas were 0.56+/-0.09 and 0.64+/
8                      18F-FDG PET/CT scans of gluteal and quadriceps muscle area were obtained with ar
9 gluteal and quadriceps muscles, and WSCV for gluteal and quadriceps muscles was 2.2% and 3.6%, respec
10 .96) and 0.96 (0.82-0.99), respectively, for gluteal and quadriceps muscles, and WSCV for gluteal and
11                  Arteries were obtained from gluteal biopsies and resected lung tissue and studied wi
12 eries (250 to 350 microm) were obtained from gluteal biopsies from volunteers and New Zealand White r
13 se tissue uptake (abdominal subcutaneous and gluteal biopsy samples) in 13 upper-body obese (UOb) men
14                                              Gluteal fat aspirates were obtained from 291 postmenopau
15 rnal diameter 201+/-26 microm) isolated from gluteal fat biopsies were cannulated and perfused in cha
16 lind, placebo-controlled trial, subcutaneous gluteal fat biopsies were taken from 16 hypercholesterol
17 tivity of resistance arteries (isolated from gluteal fat biopsies) were evaluated in A and BD.
18 t includes preferential lipolysis in femoral-gluteal fat depots is presented.
19 etermined bilaterally in supraclavicular and gluteal fat depots.
20                     Stimulating the inferior gluteal motor nerve (0.1 ms pulse, 100 Hz for 500 ms) ev
21 n volume and mass of the moderately affected gluteal muscle but not of the severely affected psoas mu
22 SP-1 modestly inhibited inflammation only in gluteal muscle of male mice.
23 la system and a surface coil placed over the gluteal muscle region.
24 liver, lung, adrenal gland, retroperitoneum, gluteal muscle, inguinal mass, and subcutaneous tissues
25 d downward to mid-thigh and upward under the gluteal muscles almost to the top of the iliac crest.
26 s such as previously unknown co-existence of gluteal muscles hypoplasia.
27 ement was found in hamstring, paraspinal and gluteal muscles on MRI, which correlated well with reduc
28 nergistically during voluntary activation of gluteal muscles, but not during voluntary activation of
29 me with incidental hypoplasia of ipsilateral gluteal muscles.
30 s were hamstrings followed by paraspinal and gluteal muscles.
31 f the posterior cutaneous nerve and inferior gluteal nerve, and found that the cholera toxin B subuni
32  kg; both P = 0.001), including less femoral-gluteal SAT, more VAT (African American: 0.7 kg, P < 0.0
33 ic area which was later proven to be a large gluteal sebaceous cyst.
34 anging from 0 to 2 minimum erythema dose, on gluteal skin, with or without sunscreen, 48 h prior to s
35            Paired transcriptomic analysis of gluteal subcutaneous adipose tissue (GSAT) and abdominal
36 (mg meal fat/g adipose lipid) was greater in gluteal than in abdominal fat (P = 0.022) in LOb women,
37 wer (P < 0.0001) in supraclavicular BAT than gluteal WAT in all pediatric subjects.

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