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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 n by suppressing adipogenesis and increasing gluteal adipocyte susceptibility to apoptosis.
4 ciated with reduced lower-body fat, enlarged gluteal adipocytes and insulin resistance.
5 solated subcutaneous abdominal, femoral, and gluteal adipocytes was measured by direct microscopy or
6  studies in immortalized human abdominal and gluteal adipocytes.
7  increased centripetal and/or reduced femoro-gluteal adiposity, is causally associated with and bette
8 rticipants with >=3 years of experience with gluteal administration during the ATLAS-2M study.
9 ive adaptations in mitochondrial function in gluteal and abdominal SAT depots.
10 ardiometabolic diseases, whereas lower-body (gluteal and femoral) fat may be protective.
11 is from the primary tumor in the tail to the gluteal and iliac lymph nodes (maximum nodal weight decr
12 ests that deranged energy storage in femoral-gluteal and other peripheral sites is important; the mol
13 rging tunnels develop in axillary, inguinal, gluteal and perianal body sites.
14                                      SUVs in gluteal and quadriceps areas were 0.56+/-0.09 and 0.64+/
15                      18F-FDG PET/CT scans of gluteal and quadriceps muscle area were obtained with ar
16 gluteal and quadriceps muscles, and WSCV for gluteal and quadriceps muscles was 2.2% and 3.6%, respec
17 .96) and 0.96 (0.82-0.99), respectively, for gluteal and quadriceps muscles, and WSCV for gluteal and
18 ponses elicited by RSPO3 in abdominal versus gluteal APs in vitro are associated with differential ch
19 tracts develop in the axillae, inguinal, and gluteal areas, typically during or after puberty.
20 d arterial vessels were as follows: inferior gluteal artery (2), superficial external pudendal artery
21 erior gluteal artery perforator, or inferior gluteal artery perforator flap; or both neoadjuvant and
22 reconstruction; a latissimus dorsi, superior gluteal artery perforator, or inferior gluteal artery pe
23                  Arteries were obtained from gluteal biopsies and resected lung tissue and studied wi
24 eries (250 to 350 microm) were obtained from gluteal biopsies from volunteers and New Zealand White r
25 se tissue uptake (abdominal subcutaneous and gluteal biopsy samples) in 13 upper-body obese (UOb) men
26 in de novo lipogenesis in both abdominal and gluteal depots, compared with obese girls with the favor
27                                              Gluteal fat aspirates were obtained from 291 postmenopau
28 rnal diameter 201+/-26 microm) isolated from gluteal fat biopsies were cannulated and perfused in cha
29 lind, placebo-controlled trial, subcutaneous gluteal fat biopsies were taken from 16 hypercholesterol
30 tivity of resistance arteries (isolated from gluteal fat biopsies) were evaluated in A and BD.
31 t includes preferential lipolysis in femoral-gluteal fat depots is presented.
32 etermined bilaterally in supraclavicular and gluteal fat depots.
33 ous adipose tissue mass, particularly in the gluteal-femoral area.
34  and cells in the subcutaneous abdominal and gluteal/femoral adipose tissue (SAT) of weight-stable ob
35 sed differences in mitochondrial function in gluteal (gSAT) and abdominal subcutaneous adipose tissue
36 , participants received a 3 mL intramuscular gluteal injection (long-acting injectable cabotegravir 6
37 igh injection (day 1-week 16), and return to gluteal injection (week 16-week 24).
38 tion parameters were statistically higher vs gluteal injections (paired comparison).
39 e (CAB + RPV) administered via intramuscular gluteal injections is the first complete long-acting reg
40              Overall, 30% preferred thigh vs gluteal injections.
41                     Stimulating the inferior gluteal motor nerve (0.1 ms pulse, 100 Hz for 500 ms) ev
42 n volume and mass of the moderately affected gluteal muscle but not of the severely affected psoas mu
43 SP-1 modestly inhibited inflammation only in gluteal muscle of male mice.
44 la system and a surface coil placed over the gluteal muscle region.
45 liver, lung, adrenal gland, retroperitoneum, gluteal muscle, inguinal mass, and subcutaneous tissues
46 ocal relapses and ratio of tumor SUV(max) to gluteal-muscle SUV(mean) for nonlocal prostate cancer le
47 d downward to mid-thigh and upward under the gluteal muscles almost to the top of the iliac crest.
48 s such as previously unknown co-existence of gluteal muscles hypoplasia.
49 ement was found in hamstring, paraspinal and gluteal muscles on MRI, which correlated well with reduc
50 nergistically during voluntary activation of gluteal muscles, but not during voluntary activation of
51 me with incidental hypoplasia of ipsilateral gluteal muscles.
52 s were hamstrings followed by paraspinal and gluteal muscles.
53 f the posterior cutaneous nerve and inferior gluteal nerve, and found that the cholera toxin B subuni
54 cipants; hematospermia, one participant; and gluteal pain, two participants).
55 d of mature adipocytes in both abdominal and gluteal SAT may contribute to metabolic impairment and t
56  kg; both P = 0.001), including less femoral-gluteal SAT, more VAT (African American: 0.7 kg, P < 0.0
57 ic area which was later proven to be a large gluteal sebaceous cyst.
58 s were dissected with or without PVAT from a gluteal skin biopsy from 11 women with treated HIV (WWH)
59 anging from 0 to 2 minimum erythema dose, on gluteal skin, with or without sunscreen, 48 h prior to s
60            Paired transcriptomic analysis of gluteal subcutaneous adipose tissue (GSAT) and abdominal
61  participant experienced an activity-related gluteal tear, with no other adverse events recorded.
62  lateral elbow epicondyles, patellar tendon, gluteal tendons and the Achilles tendon.
63 (mg meal fat/g adipose lipid) was greater in gluteal than in abdominal fat (P = 0.022) in LOb women,
64 one event in a repositioning of the anterior gluteals that maximizes control of pelvic drop during up
65 wer (P < 0.0001) in supraclavicular BAT than gluteal WAT in all pediatric subjects.
66          Exposure of cultured adipocytes and gluteal white adipose tissue (WAT) to cool temperatures