ライフサイエンスコーパス: hood

1 delivering CO2 nonobstrusively via a plastic hood.

2 half the size of a standard laboratory fume hood.

3 RMR was measured (RMRm) with a ventilated hood.

4 nd with airflow and burner position for each hood.

5 room temperature (20-25 degrees C) in a fume hood.

6 ver deformation which persists through adult-hood.

7 rystallizers, and filters in laboratory fume hoods.

8 halate intakes, corrected for background and hood air exposures.

9 hone 5s), integrated with a custom-made dark hood and base holder assembly.

10 n) was used for colorimetric imaging via the hood and base-holder assembly.

11 The participants either wore a hood and breathed air with phthalate concentrations subs

12 below those in the chamber or did not wear a hood and breathed chamber air.

13 nd time scales derived from the algorithm of Hood and Li, published in 1997.

14 erse polarity of the ectopic flowers seen in Hooded and transgenic kn1 plants results from the transf

15 nal organization for individuals who certify hoods and clean rooms, states in its 2012 certification

16 Pineal gland hoods and eye covers worn 12 hours a day significantly (

17 CE) ranged from <15% to >98%, varying across hoods and with airflow and burner position for each hood

18 Age- and sex-matched pigmented (Lister Hooded) and albino (Wistar) rats were used in this study

19 ation is required to direct PMCs to the oral hood, and suggest that Univin is a relevant ligand for t

20 xpenditure was measured weekly by ventilated hood, and total energy expenditure by doubly labeled wat

21 ng devices such as the Anesthetic Scavenging Hood (ASH), SiBI tube connector and mask stopper.

22 We find that CCR4-NOT facilitates HOOD assembly through its association with the conserved

23 CCR4-NOT also assembles HOODs at retrotransposons and regulated genes containing

24 essor on an intron sequence in the KNOX gene Hooded/Barley Knotted3 (Bkn3) and that AtGRF4, AtGRF5, a

25 esis of atherosclerosis, we applied a likeli-hood-based model selection method to infer gene-disease

26 (1960-70s) demonstrate that the watershed of Hood Canal has received greater atmospheric inputs of th

27 vior of harbor seals (Phoca vitulina) in the Hood Canal region of Washington State with respect to ch

28 The natural rate of recovery in Hood Canal since the 1970s, back to preindustrial metal

29 ric inputs of anthropogenic Pb and Hg to the Hood Canal, Washington.

30 urce of these metals to the watershed of the Hood Canal.

31 ence and violent criminal offending in adult-hood compared with groups with only biological or only s

32 vacuum unit of the IT-SIMS was located in a hood, connected by cables to the externally located elec

33 ve to front burners, presumably because most hoods covered only part of the front burners.

34 k-source vs. wall-source oxygen and a unique hood design.

35 nsory axons from the intact side of the oral hood did not sprout across the midline to the denervated

36 e structures reveals a rotation of the upper hood domain onto the bound ligands by an average of 19.5

37 The catalytic sites are capped with a small hood domain that is unique to the APRTases.

38 for the detection of lesions of the extensor hood, DTML, and palmar plate structures.

39 egrated Peltier element and external heating hood enable the characterization of photopolymerization

40 nges during dilutions and use of common flow hoods for some steps in the preparation of sterile and b

41 motes RNAi-dependent heterochromatin domain (HOOD) formation at EMC-target loci.

42 The Charles H Hood Foundation, the David Rockefeller Center for Latin

43 to stimulation of the right side of the oral hood gradually returned to normal.

44 Open hoods had higher CE than those with grease screen and me

45 The flaps and hood have no structural precedent in the protein databas

46 istar the origin of their mitochondria, Fawn Hooded Hypertensive (FHH) or Wistar rats, respectively.

47 We previously reported that the fawn-hooded hypertensive (FHH) rat is a natural Rab38 knockou

48 me 3, affects the development of CKD in Fawn-Hooded Hypertensive (FHH) rats.

49 r actinomycetemcomitans (Aa)-inoculated Fawn Hooded Hypertensive (FHH), Dahl Salt-Sensitive (DSS), an

50 ackground susceptible to kidney injury (fawn-hooded hypertensive rat [FHH]) were evaluated for BP, pr

51 At advanced stages of FSGS, fawn-hooded hypertensive rat kidneys exhibited distinctly inc

52 and Rf-4 (rat chromosome 14), from the Fawn-hooded hypertensive rat onto the August Copenhagen Irish

53 s to the severity of proteinuria in the Fawn-hooded hypertensive rat.

54 the kidney glomerular function in FHH (fawn-hooded hypertensive) rat.

55 buccal ganglia; in the tentacles of the oral hood; in the sensory end of the rhinophores; and in the

56 Longitudinally, RMR (ventilated hood) increased progressively in 17 subjects in whom glu

57 corded from the striate cortex of Long-Evans hooded intact, monocular visual deprivation (MD) and MD

58 r 12 weeks PC, brief stimulation of the oral hood ipsilateral or contralateral to the crush injury el

59 HRP) to the dorsal part of the anterior oral hood labeled subpopulations of trigeminal components on

60 trasound-induced behavioural response in the hooded Lister and albino Wistar rat.

61 stic startle response (brisk running) in the hooded Lister rat that was followed immediately after ce

62 and caudal periaqueductal grey (PAG) in the hooded Lister rat, while the expression occurred in the

63 produces an escape (defence) response in the hooded Lister rat.

64 Rupture in the sagittal band of the extensor hood mechanism in the two patients was confirmed at surg

65 seful in diagnosing injuries of the extensor hood mechanism.

66 For hoods meeting the sound and fan efficacy criteria for En

67 (DeltaEE%; indirect calorimetry, ventilated hood method) above resting EE in response to non-specifi

68 ated control mice, mice placed in the blower hood, mice treated with a scop patch, and mice treated w

69 pear altered in the barley (Hordeum vulgare) Hooded mutant, in which ectopic expression of the KNOTTE

70 y hvknox3 gene, associated with the dominant Hooded mutant.

71 the expression pattern of hvknox3 in awns of Hooded mutants, suggesting posttranscriptional regulatio

72 (n = 14), transverse fibers of the extensor hood (n = 5), first annular pulley (n = 16), deep transv

73 determined to be arising from underneath the hood of the major papilla.

74 I begin by "lifting the hood" on the conventional tree-like representation of th

75 eye growth in CL conditions, with or without hoods or occluders.

76 At Mount Hood (Oregon, USA), only a small fraction of the total m

77 laps extending in opposite directions; and a hood over the central core formed from the C-terminal su

78 aining accurate measurements in supplemental hood oxygen studies were overcome by using tank-source v

79 Rats (Lister-hooded) pre-treated i.c.v. with either 25 or 100 microg

80 The hood procedure without bleb removal may be preferred for

81 The genetically hypertensive fawn-hooded rat is characterized by the early presence of sys

82 otion, we studied crosses involving the fawn-hooded rat, an animal model of hypertension that develop

83 pothesis, we treated middle-aged male Lister hooded rats (16 months) with amitriptyline until they we

84 to vascular obstruction in patients and fawn-hooded rats (FHRs) with PA hypertension (PAH).

85 tinguish between these possibilities, Lister Hooded rats (n = 8) were trained to navigate from a star

86 combination in Sprague Dawley and Long-Evans hooded rats and FVB mice.

87 ar nucleus was undertaken in male and female hooded rats at four ages across the lifespan.

88 ical acetylcholinesterase (AChE) activity in hooded rats during postnatal development and following b

89 urs and cognitive performance between Lister Hooded rats housed in traditional (single-shelf) cages (

90 ponses of nRt neurons occurred in Long-Evans Hooded rats previously administered U18666A.

91 Long-Evans hooded rats received pressure injections of various comb

92 Adult Long-Evans hooded rats received unilateral naris occlusion or a con

93 Long-Evans hooded rats received unilateral pressure injections of d

94 Male Lister hooded rats were either housed singly (isolation reared)

95 Lister Hooded rats were ovariectomized and implanted with mini-

96 Female Long Evans hooded rats were ovariectomized at middle age (11-12 mon

97 Five-month-old, female Long-Evans hooded rats were randomly assigned to a control or exerc

98 Female hooded rats were tested during proestrus or estrus on th

99 Long-Evans hooded rats were trained to run an alternation pattern i

100 Treatment of male Long Evans Hooded rats with acetaminophen (1 g/kg) resulted in dama

101 d-choice Y maze and a jumping stand in adult hooded rats, and vernier acuity thresholds were establis

102 ine-induced PH and in spontaneous PH in fawn-hooded rats, as well as in chronically hypoxic rats.

103 re pervasive in the primary visual cortex of hooded rats, it is not known whether sex differences occ

104 ent of spatial memory function in Long-Evans hooded rats, we show a persistent neonatal novelty-induc

105 evaluated in non-food-restricted male Lister Hooded rats.

106 of tacrine-induced hepatotoxicity in Lister hooded rats.

107 s of acquired absence epilepsy in Long-Evans Hooded rats.

108 evaluated in four groups of male Long-Evans hooded rats.

109 nce of seven new residential cooking exhaust hoods representing common U.S. designs.

110 rved in hatchery steelhead released into the Hood River in Oregon.

111 of steelhead (Oncorhynchus mykiss) from the Hood River, Oregon, by matching 12 run-years of hatchery

112 nd mice treated with a scop patch and blower hood (scop patch + blower).

113 However, hooded seals currently dominate that niche and may have

114 es the detailed ultrastructure of antennular hooded sensilla and the physiological response propertie

115 These results support the idea that hooded sensilla are bimodal chemo-mechanosensilla and ar

116 morphological characteristics of antennular hooded sensilla are present and have a similar pattern o

117 Hooded sensilla have a porous cuticle and are innervated

118 cal and mechanical stimulation of antennular hooded sensilla.

119 nterspecific and intraspecific homologues of hooded sensilla.

120 Hooded sensillar chemosensory neurons responded to water

121 Furthermore, hooded sensillar homologues are present on most body sur

122 Hooded sensillar mechanosensory neurons were not spontan

123 ther these results support the idea that the hooded sensillum is a singular and biologically importan

124 study we examined setae with features of the hooded sensillum, which is a class of bimodal chemomecha

125 ndant and widely distributed of these is the hooded sensillum.

126 fered for House Wren (Troglodytes aedon) and Hooded Siskin (Spinus magellanicus), but not for Cinereo

127 The airflow rate for this hood surpassed the industry-recommended level of 118 L.s

128 udies of energy metabolism with a ventilated-hood system.

129 used short-term measurements with ventilated-hood systems.

130 sures included resting EE and RQ (ventilated hood technique), body composition (dual-energy X-ray abs

131 cise) on 2 separate days with the ventilated-hood technique.

132 t resting energy expenditure (EE: ventilated hood technique; 6274 +/- 226 vs. 6079 +/- 297 kJ day(1);

133 or oven and front burners--had a large, open hood that covered most of the front burners.

134 The helmet is a transparent hood that covers the entire head of the patient and has

135 or in CL, with or without opaque, removable hoods that covered the top of the head for 12 hours each

136 tant light, with or without opaque removable hoods that covered the top of the head for 12 hours each

137 ivery of a hypoxic gas mixture via a plastic hood; the subjects' oxygen saturation decreased from 98

138 e procedures are performed in a typical fume hood using ordinary laboratory glassware.

139 nth retention of neighbour's song among male hooded warblers, Wilsonia citrina, and there is none for

140 ntal stress was created by placing mice in a hood with a continuous airflow blower.