ライフサイエンスコーパス: perirenal

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1 Perirenal-abdominal adipose tissue was sampled from ovin

2 Epididymal and perirenal adipocyte size was increased 20% in alphaERKO

3 -beta, -gamma; and GR in female but not male perirenal adipose tissue and in male but not female live

4 c responsiveness becomes desensitized in the perirenal adipose tissue of IUGR fetuses and lambs by me

5 Perirenal adipose tissue was collected from IUGR and con

6 xpressed in fetal liver, skeletal muscle and perirenal adipose tissue.

7 ytes derived from subcutaneous and visceral (perirenal) adipose depots.

8 ly communicated with each other and with the perirenal and anterior and posterior pararenal spaces of

9 vel by 11.4% and 12.4%, respectively, in the perirenal and epididymal white adipose tissue (PWAT, EWA

10 Epididymal, perirenal, and inguinal WAT weighed 139-185% more in alp

11 ots were examined (epididymal, subcutaneous, perirenal, and interscapular).

12 of interest (ROIs), automated elliptical and perirenal background ROIs and no background correction a

13 Medial perirenal contrast extravasation was seen in all 10 pati

14 653 for 5 days, preadipocytes from the human perirenal depot accumulated lipid, and a proportion of c

15 human pre-adipocytes, particularly from the perirenal depot, showed a marked increase in UCP-1 expre

16 pproximately 60% in weight of epididymal and perirenal depots.

17 d in adipose tissues including perivascular, perirenal, epididymal, subcutaneous and brown adipose ti

18 ed (P<0.05) subcutaneous, intramuscular, and perirenal fat deposition, and induced hyperglycemia, hyp

19 chow diet from weaning, exhibited increased perirenal fat pad mass relative to body weight and adipo

20 evels and a >50% reduction in epididymal and perirenal fat pad size.

21 BMI, perirenal fat thickness, pancreatic duct width on comput

22 nal amplitudes of the thermal ablation zone, perirenal fat, and normal renal cortex on the MR images.

23 d at the highest levels in testes, aorta and perirenal fat.

24 lem with the interpretation of the images of perirenal haematoma is their ability to change in time.

25 the renal parenchyma, who were suspected of perirenal haematoma, underwent a CE-US examination after

26 gnificant, difference in the echogenicity of perirenal haematomas compared to the routine examination

27 s to assess the echogenicity and the size of perirenal haematomas in patients after kidney transplant

28 Apart from two small self-limited perirenal hematomas, no intra- or postprocedural complic

29 sion from urinothorax and late effusion from perirenal lymphocele years after kidney transplantation.

30 Immunohistochemical analysis of perigonadal, perirenal, mesenteric, and subcutaneous adipose tissue r

31 from all depots studied with a rank order of perirenal, omental, and subcutaneous.

32 associated with the lateral, elliptical and perirenal ROIs were not significantly different from zer

33 n the mouse WAT depots examined (epididymal, perirenal, s.c., and mammary gland) and in interscapular

34 ight anterior pararenal space (n = 8), right perirenal space (n = 7), right posterior pararenal space

35 ach kidney, no apparent fascia separates the perirenal space from the central retroperitoneum.

36 Air extended posteriorly into the right perirenal space in seven (88%) of eight patients followi

37 assessment of the size of haematomas in the perirenal space that appeared during early post-operativ

38 thway to the free spread of disease from the perirenal space to the central retroperitoneum or from t

39 right anterior pararenal space and the right perirenal space.

40 m or from the central retroperitoneum to the perirenal space.

41 scular, and extraperitoneal regions, and the perirenal space.

42 = 37), and neoplasia (n = 21) involving the perirenal spaces or the central retroperitoneum.

43 tion, perfusion index, regional cerebral and perirenal tissue oxygenation, heart rate, transcutaneous

44 sectioned from proximal to distal including perirenal tissues and examined after paraffin embedding,

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