ライフサイエンスコーパス: pant

1 r substrate association with FolT2 than with PanT.

2 rted distinct patterns on the seams of denim pants.

3 Occupancy of the subsite proximal to the Pant-35 region results in significantly greater repressi

4 y the Ybt synthetase A domain, relative to P-pant alone.

5 x formation and represses transcription from Pant and Pmnt promoter variants to varying degrees.

6 transcription from two divergent promoters, Pant and Pmnt, in the immunity I operon of bacteriophage

7 which point cats typically displayed marked panting and vocalization.

8 ase I-mediated biotin-dATP nick translation (PANT) and terminal deoxynucleotidyl transferase-mediated

9 growth, short-term shivering and sweating or panting, and movement between warm and cold sites.

10 PANT- and TUNEL-positive cells appeared in similar numbe

11 r catalytic efficiency for transfer to the P-pant arm of PCP3 by the Ybt synthetase A domain, relativ

12 The suppressive effect of PANt cDNA was mainly due to PA-X, which was expressed by

13 Durations of locomotion (d = 0.54) and panting (d = 0.45) were also higher during fireworks tha

14 nous reconstruction using a retropancreatic "pant" donor-iliac vein graft.

15 Here, we examine the development of pant hoot vocalisations during vocal exchanges in immatu

16 chimpanzee (Pan troglodytes schweinfurthii) 'pant hoot'.

17 which was then integrated into the subject's pant-hoot displays as a percussive tool or 'instrument'.

18 'Pant-hoot displays' are a species-typical, multi-modal c

19 municative behaviour in chimpanzees in which pant-hoot vocalisations are combined with varied behavio

20 tempo, and integrate drumming earlier in the pant-hoot vocalization, typically during the rhythmic bu

21 integrate drumming into their long-distance pant-hoot vocalizations.(6)(,)(7)(,)(8) But whether wild

22 the complex acoustic structure of chimpanzee pant hoots is linked to a range of socially relevant inf

23 Support Vector Machines (SVM) methodology to pant hoots produced by wild male chimpanzees of Budongo

24 ation in rhythm or in its integration within pant-hoots remains unknown.

25 for folate (ECF-FolT2) and pantothenate (ECF-PanT) into proteoliposomes, and assayed for crosstalk du

26 f the two promoters, the-35 proximal site in Pant is the same as the- 10 proximal site in Pmnt.

27 d anti-TNF therapy in Crohn's disease study (PANTS) is a prospective observational UK-wide study.

28 ase I-mediated biotin-dATP nick translation (PANT) labeling.

29 rmia and passive leg heating (water-perfused pant leg).

30 nonasthmatic subjects FVC maneuvers-but not panting maneuvers-produce a fall in NO, suggest that the

31 .6 degrees C), clothing (long-sleeved shirts/pants or T-shirts/shorts), age (teenagers, adults, and s

32 atory role, acting as a chaperone to promote PANT polymerization at low temperatures while preventing

33 ociated N-terminal tetratricopeptide repeat (PANT) polymerization domain and finetuned by the adjacen

34 Abundant PANT-positive cells were also observed in the perihemato

35 Volunteers wearing long-sleeve shirts and pants produced 40% more FAPs relative to those wearing t

36 re of the bound aminoacyl adenylate by the P-pant-SH of the PCP domains, was assayed both by catalyti

37 rocyclopenta[de]quinoline-3-phosphonic acid, PAnt, specifically designed to dynamically interact with

38 wed a stronger effect than the corresponding PANt, suggesting that the unique C-terminal sequences of

39 tly aminoacylates the phosphopantetheinyl (P-pant) thiols on three peptidyl carrier protein (PCP) dom

40 e Ybt system and has similarities to other P-pant transferases such as EntD of Escherichia coli.

41 similarities to known phosphopantetheinyl (P-pant) transferases were found within the pgm locus.

42 t, with resistant varieties like LBG-888 and PANT URD-19 exhibiting thicker leaves, higher trichome d

43 revealed a range of resistance levels, with PANT URD-19 showing the highest resistance (PDI 0.47%) a

44 By characterizing various chimeric PANts, we found that multiple regions of PA, mainly the

45 agment indicated that the N-terminal domain (PANt), which includes the endonuclease active site, is s

46 point source, such as a fossil-fueled power pant, while DAC captures CO(2) from the ambient air.

47 rticotropic hormone, heart rate variability, panting, whining, and body shake all demonstrated signif

48 moregulatory behaviors in budgerigars (e.g., panting, wing venting).

49 Comparison of a crystal structure of ECF-PanT with previously determined structures of ECF-FolT2