ライフサイエンスコーパス: peri-

1 Perilipin (Peri) A is a lipid droplet-associated phosphoprotein tha

2 Perilipin (Peri) A is a phosphoprotein located at the surface of in

3 less attachment of substituents both at the "peri" and the "bay" positions.

4 Perilipin null (peri(-/-)) and wild-type (peri(+/+)) mice consume equal

5 changes associated with the hair loss, i.e., peri-, and intrafollicular inflammatory infiltrates cons

6 t period (<2, 2-12, and >12 months for pre-, peri-, and postmenopause, respectively).

7 s study was to comprehensively examine pre-, peri-, and postoperative characteristics that might pred

8 appropriate setting, with attention to pre-, peri-, and postprocedural detail.

9 Finally, the relationships of pre-, peri-, and postsurgical complications to outcome were in

10 ve skills, behavioral functioning, and pre-, peri-, and postsurgical medical complications.

11 rmore, a multidisciplinary approach of pre-, peri-, and posttransplant modulating of the tumor and/or

12 Pre-, peri-, and posttransplantation clinical events undoubted

13 n how such patients are treated in the pre-, peri-, and posttransplantation settings.

14 n is associated with biphasic recruitment of peri- and contralesional functional fields in the brain.

15 rides, and lipoprotein(a) peaked during late peri- and early postmenopause, while changes in the earl

16 lipoprotein cholesterol also peaked in late peri- and early postmenopause.

17 ormal and dyslexic groups activated the same peri- and extra-sylvian regions of the left hemisphere t

18 esioned monkeys, the m2 receptor was located peri- and extra-synaptically, suggesting that it may be

19 Immunogold labeling revealed peri- and extrasynaptic localization of D2 in postsynapt

20 tic view of and a set of tools for examining peri- and extrasynaptic regulations of pain-afferent tra

21 d to assess the epileptogenic focus, both in peri- and interictal period.

22 ization of angiogenesis and disappearance of peri- and intravascular fibrin.

23 y increased cardiac myocyte apoptosis in the peri- and noninfarct regions and with 50% larger myocard

24 nvestigated the distribution of the regional peri- and paraventricular white matter CBF (WM CBF) in N

25 efficacy of ovarian hormone intervention in peri- and post-menopausal women.

26 -resolution methylomes for early lineages in peri- and postimplantation mouse embryos.

27 This effect of peri- and postmenopausal body size gain was present only

28 cteristics between ages 28 and 32 years, and peri- and postmenopausal fracture risk in a cohort of 87

29 orithms in evaluating typical populations of peri- and postmenopausal women with abnormal vaginal ble

30 Ovarian cancer incidence is highest in peri- and postmenopausal women, and epidemiological stud

31 one loss occurred from all skeletal sites in peri- and postmenopausal women, but premenopausal women

32 n, and with lower estrogens and androgens in peri- and postmenopausal women.

33 apies and bone mineral density (BMD) loss in peri- and postmenopausal women.We systematically searche

34 ained more than 11 kg (24 pounds) during the peri- and postmenopausal years (since age 50 years) had

35 on of retinoid signaling pathways throughout peri- and postnatal development.

36 n the present study we have investigated the peri- and postnatal developmental time course of [Ca2+]i

37 arding MTHFR polymorphisms C677T and A1298C, peri- and postnatal lead measures, and Bayley Mental Dev

38 Initial characterization revealed peri- and postnatal lethal phenotypes in three mutant st

39 ing myocardial infarction, stent thrombosis, peri- and postoperative bleeding and death.

40 ht be at risk for such events may help guide peri- and postoperative care.

41 Prevention, diagnosis, and treatment of peri- and postoperative morbidity are dependent on provi

42 outcome from the time of listing through the peri- and postoperative period.

43 od, its molecular phenotype is confounded by peri- and postoperative proinflammatory events.

44 unction; however, high mortality was seen in peri- and postpartum females by 6 months of age, when se

45 d by inhibition, as a possible substrate for peri- and postpubertal advances in cognitive capacity.

46 in which prefrontal activity changes during peri- and postpubertal cortical maturation is largely un

47 Awareness thereof should have an impact on peri- and posttransplant measures in renal transplant re

48 A total of 42 pre-, peri- and posttransplant variables evaluated in 2982 ped

49 tant to maintain a low hemoglobin S fraction peri- and posttransplantation.

50 The peri(-/-) animals have a greater lean body mass and incr

51 ied show a layer-specific expression in the (peri-)archicortex of the wildtype brain.

52 81 and Cux2 by in situ hybridization in the (peri-)archicortex.

53 to 6.6 mum(2) s(1) and the distribution of D(peri) broadens as growth osmolality increases.

54 In rodents, an early peri-/endovascular type of invasion exerted by trophobla

55 Ultimately a 304-bp(peri) enhancer was identified and shown to be capable of

56 c-ICCs and hilar CCs showed a predominantly (peri-)hilar location, smaller tumor size, and more lymph

57 -1.02 Osm, the mean diffusion coefficient <D(peri)> increases from 3.4 mum(2) s(1) to 6.6 mum(2) s(1)

58 Accordingly, <D(peri)> increases threefold.

59 A periplasmic form of ApbE (ApbE(peri)) lacking the lipoprotein modification allowed an a

60 , this enhanced cross-linking was blunted in Peri-/- MEF adipocytes expressing Peri Adelta1-6.

61 In Peri-/- MEF adipocytes, PKA activation significantly enh

62 mbryonic fibroblasts of perilipin null mice (Peri-/- MEF), we demonstrate by cell fractionation and c

63 Perilipin null (peri(-/-)) and wild-type (peri(+/+)) mice consume equal amounts of food, but the a

64 y (none v any), and menopausal status (pre-, peri-, or postmenopausal).

65 urobehavioral outcome was unrelated to pre-, peri-, or postsurgery complications.

66 Twenty-six healthy amenorrheic (peri- or postmenopausal) women not using hormonal medica

67 ratios = 2.06-4.32), were for women who were peri- or postmenopausal.

68 collagen VIII may therefore be to generate a peri- or subcellular matrix environment that permits or

69 reaction mechanism (Houk) involves a highly peri-, regio-, and stereoselective [6F + 4T] cycloadditi

70 Clinical correlation suggests a peri-/sub-meningothelial source of IGF-liberating protea

71 abeled antibodies correlating morphological (peri-)tumoral characteristics to levels of antibody deli

72 e delivery and histological localization in (peri-)tumoral compartments of antibody-based therapeutic