ライフサイエンスコーパス: wet weight

1 lly relevant concentrations (100-800 pmol/g (wet weight)).

2 variation in energy density (energy per unit wet weight).

3 me period (72 h C(algae)/C(water): 2200 L/kg wet weight).

4 wet weight) and (134)Cs (18.2-356 mBq/kg of wet weight).

5 human muscle as small as approximately 10 mg wet weight.

6 y standards (EQS) for biota are expressed as wet weight.

7 -deoxyuridine labeling index and the uterine wet weight.

8 l of this material is 1168 +/- 278 ng/g worm wet weight.

9 cifically contributed toward maintaining gel wet weight.

10 e total Hg (tHg) concentration of 0.77 mg/kg wet weight.

11 at an average annual rate of -14.9 pg g(-1) wet weight.

12 ish species ranged from 0.021 to 0.568 mug/g wet weight.

13 ts and showing concentrations up to 16 mug/g wet weight.

14 38 (char), and 9.9 +/- 5.9 (trout) ng g(-1) wet weight.

15 and degradates ranged from 0.36 to 8.0 ng/kg wet weight.

16 or congeners ranged from 0.11 to 170.42 ppb, wet weight.

17 roponin C (TNC) molecules, 33.8 mumol per kg wet weight.

18 d amount of collagen normalized to construct wet weight.

19 measured by changes in body weight and ileal wet weight.

20 A, ranging from 0.7 to 4.2 nmol.min(-) (1).g wet weight(-1) (slope = 0.98, r(2) = 0.94).

21 ucose uptake was 0.61+/-0.08 micromol x g of wet weight(-1) x 30 min(-1) (mean+/-SEM).

22 t control levels (0.6+/-0.05 micromol x g of wet weight(-1) x 30 min(-1)), compared with hearts with

23 ificantly lower (0.42+/-0.05 micromol x g of wet weight(-1) x 30 min(-1); P</=0.05).

24 concentrations ranging from 1.5 to 5 nmol.g wet weight-(1).

25 The mean TSC for MIs (59 micromol/g wet weight +/- 10) was 30% higher than that for noninfar

26 lucosyl unit) concentration was 38.1 mmol/kg wet weight+/-14.4.

27 ty, 3,6-bis-(GSyl)TBHQ increased the bladder wet weight 2-fold and caused severe hemorrhaging of the

28 and border zone (for all samples n=60, mean wet weight 2.037+/-0.046 mg).

29 iation for the test, 36 mmol per kilogram of wet weight +/- 2 [range, 34-37 mmol/kg]; for the retest,

30 ights (11.2%, n = 74 retina pairs) than with wet weights (20.5%, n = 93 retina pairs).

31 ielded a total [Na] value of 28.4 mmol/kg of wet weight +/- 3.6 (SD) in normal muscle, consistent wit

32 and was found to be 8.6 mmol per kilogram of wet weight+/-3.1 (range, 3.8-17.6; n=44).

33 infarcted (remote) LV regions (45 micromol/g wet weight +/- 5, P < .001) and that for healthy control

34 elded a total creatine value of 36.2 mmol/kg wet weight +/- 5.0, consistent with prior biopsy data.

35 a decrease (P = < 0.001, both cases) in gel wet weight (53% versus 82%, 100 U/gel; 57%, versus 86%,

36 for tissue adjacent to the MI (50 micromol/g wet weight +/- 6) was intermediate between that for the

37 U/gel) resulted in a slight reduction in gel wet weight (90% versus 96%, P = < 0.001) and depolymeriz

38 th intestinal failure, increasing intestinal wet weight absorption and reducing diarrhea.

39 ng an average loss of 30% in skeletal muscle wet weight and a 50% decrease in myofiber density.

40 ed tumors was reflected by a 29% increase in wet weight and a 58% increase in volume compared with co

41 bining extracellular diffusion analysis with wet weight and dry weight measurements.

42 ation of hypertrophy measured by both muscle wet weight and fiber cross-sectional area occurred in sa

43 ounds (TICs), ranged from 0.05 to 35.03 ng/g wet weight and from 0.03 to 3.32 muM in tuna lipid.

44 fish levels ranged from 0.16 to 138.29 ng/g wet weight and lipid-normalized concentrations from 0.1

45 l content in cells) was normalized to muscle wet weight and protein concentration.

46 as determined by assaying for a reduction in wet weight and proteoglycan content after 3 days of cocu

47 hat proteins constitute 1.24% of the biofilm wet weight and that the compared methods varied in their

48 L/M/S tumor wet weight and volume increased by 1.6- and 2.4-fold, re

49 For both diets, the urogenital wet weights and lymph node wet weights in the 20-mg/kg t

50 concentrations of (137)Cs (234-824 mBq/kg of wet weight) and (134)Cs (18.2-356 mBq/kg of wet weight).

51 s in the variety Kale (13.3 +/- 0.58 mg/100g wet weight) and Cherry plum (1.96 +/- 0.28 mg/100g) for

52 creased from the initial study year (31 ng/g wet weight) and peaked around the late 1990s, followed b

53 arly time points using the myeloperoxidase, %wet weight, and %contraction band necrosis assays; trans

54 otein concentration was normalized to muscle wet weight, and citrate synthase activity (standard meas

55 quired for proteoglycan degradation, loss of wet weight, and macrophage infiltration of cocultured di

56 tivities in mammary gland morphology/uterine wet weight assay in ovariectomized rats.

57 effects of estradiol benzoate in the uterine wet weight assay using immature rats.

58 a pregnancy maintenance assay and a uterine wet weight assay, the two eutomers displayed potent prog

59 0.15 versus 1.5 +/- 0.10 mumol/min per gram wet weight at 1.25 minutes, P < .01).

60 titution showed significantly decreased lung wet weight, bronchoalveolar lavage fluid (BALF) lactate

61 CDD cotreatment inhibited EE-induced uterine wet weight by 37, 23, and 45% at 12, 24, and 72 h, respe

62 e converted to absolute concentrations (g/kg wet weight) by using water as an internal reference.

63 (PFNA) was the dominant PFCA (up to 640 ng/g wet weight) closely followed by the C10 and C11 homologu

64 The mean wet weight concentrations of PCB-153 were ~3-5 times hig

65 rized; when digested with 100 U/gel, the gel wet weight decreased (to 57% of original wet weight vers

66 Kidney wet weight, DNA, and protein all were significantly high

67 The increase in kidney wet weight, DNA, and protein was significantly lower in

68 Wet weights, DNA content, and protein content were quant

69 The water content, defined as (wet weight-dry weight)/wet weight, of a typical isolated

70 nd WT mice after MI (P=NS), whereas the lung wet weight/dry weight ratio was increased in the KO mice

71 Wet weight/dry weight ratios (WW/DW) and histologic scor

72 ed to high CO2 had decreased skeletal muscle wet weight, fiber diameter, and strength.

73 +/- 24 (standard deviation) (n = 8) ng/g of wet weight for noncoastal condors, and simulations predi

74 ors ranged from 1.3, 3.7, 4.0, and 4.4 L/kg (wet weight) for fish muscle, zooplankton, predatory inve

75 rogenesis (higher cell numbers, wet weights, wet weight GAG fractions, and collagen type II levels we

76 sults were obtained by correlation of tissue wet-weight gain with morphological evidence of cell swel

77 uoranthene) were between 3 and 12 mug kg(-1) wet weight in all samples.

78 s (PCr=5.4+/-1.2 versus 9.6+/-1.1 micromol/g wet weight in MI versus control subjects, respectively,

79 ic measurements was 0.11 +/- 0.07 micromol/g wet weight in normal myocardium.

80 the fetal kidney but increased to 17% of the wet weight in the adult kidney.

81 tal protein represented less than 10% of the wet weight in the fetal kidney but increased to 17% of t

82 s, the urogenital wet weights and lymph node wet weights in the 20-mg/kg treatment groups were signif

83 echols were estrogenic and increased uterine wet weights in these neonates.

84 on of tissue TG content (milligrams per gram wet weight) in the control, at-risk, and infarct regions

85 The mean metal concentrations (wet weight) in the examined species ranged from 1.420 to

86 pha mRNA and peptide (1543 +/- 496 pg/g lung wet weight) localized to alveolar macrophages by in situ

87 r protein concentration normalized to muscle wet weight (lowest vs middle tertile; HR = 2.93; P = 0.0

88 orrelated well with observed changes in lung wet weights, lung collagen content, and histological evi

89 d similar oral potency to MPA in the uterine wet weight/mammary gland morphology assay in ovariectomi

90 tration of ascorbate was 1.33 +/- 0.48 mg/gm wet weight (mean +/- SD), estimated to be 14 times its c

91 alleviation -- as measured by MRI and by dry/wet weight measurement of water content -- but did not a

92 a was estimated at 24 hrs using wet - dry) / wet weight method.

93 cycle flux (Vtca = 0.33 +/- 0.09 micromol/g wet weight/min) in liver.

94 from 8.5 ng/kg (norfluoxetine) to 420 ng/kg wet weight (norsertraline).

95 Wet weight of bladder, stomach, intestine, uterus, and a

96 lization were determined and correlated with wet weight of bowel.

97 ortex of diabetic animals as assessed by DNA/wet weight of brain and protein/DNA content.

98 s of EC-SOD (mean +/- SEM 18.8 +/- 3.8 ng/gm wet weight of cartilage).

99 ks of life from 0.313 +/- 0.09 microgram (mg wet weight of slice)-1 (mean +/- S.E.M.) at 1 week to 0.

100 The size and wet weight of the cartilage pellets and glycosaminoglyca

101 100 mg/kg/day) for 14 consecutive days, the wet weight of the prostate was significantly reduced by

102 P F1 (BxT) mice exhibited an increase in the wet weight of the prostate.

103 The wet weight of the testes was obtained.

104 igmaPFASs ranged between 0.66-45 ng per g of wet weight of the whole body.

105 HA content per wet weight of tissue decreased from tip to base of the p

106 imately 20 cal of Gibbs free energy per gram wet weight of tissue).

107 d tumor volume by 35 and 58% (P < 0.05), and wet weight of tumor by 29 and 40% (P < 0.05), respective

108 lume by 44 and 59% (P<0.002 and 0.0001), and wet weight of tumor by 41 and 53% (P<0.05), respectively

109 ets for a total of 63 days, tumor volume and wet weight of tumor were reduced by 53-64% (P < 0.001-0.

110 The wet weights of bovine vitreous gels were compared before

111 There was a trend of a decrease in average wet weights of the urogenital tract and prostate gland i

112 ion and continued for 8 wk; tumor volume and wet weights of tumor were reduced by 39 and 53% (P<0.01

113 Moreover, the average wet-weight of LAP-treated tumors was reduced 46% compare

114 tion limit was <1 ng of muramic acid/100 mg (wet weight) of tissue.

115 content, defined as (wet weight-dry weight)/wet weight, of a typical isolated cerebellum (including

116 se activity when normalized to either muscle wet weight or protein concentration.

117 .07 versus 0.78 +/- 0.12 mumol/ min per gram wet weight [P < .001] for glycogenolysis, respectively,

118 0.04 versus 1.06 +/- 0.06 mumol/min per gram wet weight [P < .01] for glycolysis and 0.15 +/- 0.07 ve

119 1; ATP=3.4+/-1.1 versus 5.5+/-1.3 micromol/g wet weight, P<0.001).

120 PCr (10.3 +/- 2.1 vs 4.3 +/- 2.0 micromol/g wet weight; P <.0001), ATP (6.4 +/- 1.4 vs 3.7 +/- 1.4 m

121 , ATP (6.4 +/- 1.4 vs 3.7 +/- 1.4 micromol/g wet weight; P <.001), and CR (24.7 +/- 6.1 vs 6.3 +/- 3.

122 weight versus LPS+HU: 71.25 +/- 17.75 pg/mg wet weight; P <0.05).

123 e (1.6 +/- 0.6 vs. 3.2 +/- 0.9 micromol/g of wet weight per sec, P <0.0005).

124 Exposure to cadmium increased uterine wet weight, promoted growth and development of the mamma

125 In the jejunum, wet weight, protein mass, and villus height were signifi

126 esulted in a significant reduction in tissue wet weight, proteoglycan content, and cell number and an

127 amples, with concentrations in the mug g(-1) wet weight range.

128 PFASs Log BAFs (wet weight) ranged from 2.6 +/- 0.8 for perfluorohexanes

129 s in lung to body weight ratios, lung dry to wet weight ratios, lung protein to body weight ratios, o

130 were below the 0.5 mg kg(-1) (500 ng g(-1)), wet weight, recommended by the FAO/WHO.

131 Intriguingly, partial brain wet weight recovery was observed in mice treated with th

132 n and of chondroitin sulfate resulted in gel wet weight reduction but not gel destruction.

133 sting in landfill sites (median: 28-280 ng/g wet weight) relative to those from urban industrial and

134 /- 1.05% and 10.12 +/- 3.16% injected dose/g wet weight, respectively).

135 be 1.9+/-0.6, 1.3+/-0.4, and 0.7+/-0.2nmol/g wet weight, respectively, for these tissues.

136 to 3 x 10(6) MAP cell equivalents (CE) g(-1) wet weight soil with the majority of the positive PCR re

137 nd the limit of detection (500-5000 CE g(-1) wet weight soil).

138 regions of infarction (10 [9] SD micromol/g wet weight) than in non-infarcted regions (26 [11] micro

139 inyl esters (approximately 0.5-2 microg/gram wet weight) than the tumor tissues in all seven patients

140 Based on protein yield per gram of cells (wet weight), the OE-SHI strain yields a 100-fold higher

141 ction parameters were derived from ratios of wet weight to dry weight and the forced-oscillation tech

142 Wet weight to dry weight ratios of the lung contralatera

143 The wet-weight to dry-weight ratio and the interstitial spac

144 The wet-weight to dry-weight ratios, histologic changes in l

145 um amylase, histologic grading, and pancreas wet weight-to-body weight ratio.

146 significant differences between the groups: wet weight-to-dry weight ratio (P < 0.001), protein in t

147 tween the amount of virus material and brain wet weight up to day 30 postinfection.

148 ents in the samples, expressed in mug g(-1) (wet weight), varied from <0.01 to 0.20 with an average v

149 gel wet weight decreased (to 57% of original wet weight versus 86% for controls, P = < 0.001) and hya

150 andin E2 (PGE2) (LPS: 159.20 +/- 38.70 pg/mg wet weight versus LPS+HU: 71.25 +/- 17.75 pg/mg wet weig

151 rlands, FBSA concentration was at 80.12 ng/g wet weight (w.w.) and was exceeded only by PFOS.

152 riod, decreasing by 39% from 0.171 mug g(-1) wet weight (w.w.) in 1980 to 0.104 mug g(-1) w.w.

153 ection was 67 nM in buffer and 2.0 mug g(-1) wet weight (w/w) in shellfish sample.

154 The results were expressed as mug/g of wet weight (w/w).

155 In the uterus, the increase in wet weight was accompanied by proliferation of the endom

156 A bioaccumulation factor of 16 L/kg fish wet weight was derived.

157 Cholesterol of 0.07-0.21% wet weight was detected.

158 Lung wet weight was equal to 0.78+/-0.08% of body weight in t

159 histology, and a permanent decrease in brain wet weight was observed after eGFP-CVB3 infection.

160 creased percentage of collagen per construct wet weight was secondary to decreased glycosaminoglycan

161 Following 14 days of DEX treatment, muscle wet weight was significantly decreased in the TS and TA

162 tomyces hyaluronan lyase (30 U/gel), the gel wet weight was the same as that of controls (incubated w

163 an concentration (in millimoles per kilogram wet weight) was 61 +/- 8 (SD) for GM, 69 +/- 10 for WM,

164 itochondrial respiration rates (pmol O2/s/mg wet weight) were 15.05 +/- 3.92 and 11.42 +/- 2.66 for t

165 ly high body burdens of Ag (0.5-3.3 mug Ag/g wet weight) were found in mosquito fish and chironomids

166 nits of C.O. activity (micromol/min/g tissue wet weight) were quantified in cellular compartments (ov

167 , egg SigmaPBDE concentrations (34-2281 ng/g wet weight) were some of the highest reported in birds f

168 he highest concentration found was 865 ng/g (wet weight [wet wt]) in the livers of bottlenose dolphin

169 ffected chondrogenesis (higher cell numbers, wet weights, wet weight GAG fractions, and collagen type

170 contains as much as 150 micro mol citrate/g wet weight, which suggests that salt concentrations may

171 m concentrations ranged from 2.0 to 73.6 ppm wet weight with a mean of 12.8 +/- 2.6 ppm in tissue col

172 l concentrations ranged from 1.7 to 94.6 ppm wet weight with a mean of 15.9 +/- 3.5 ppm and chromium

173 s activity concentrations (103-272 mBq/kg of wet weight) with no detectable (134)Cs activity.

174 fish muscle (e.g. , PFOS: 0.28-2.1 ng g(-1) wet-weight), with little or no differences when comparin

175 lyzed, at concentrations of up to 2950 ng/g (wet weight (wt)) found in the liver of a sea otter from

176 4% of calculated basal metabolic rate (BMR), wet weight (WW) absorption <23 g .

177 getative compartments with up to 97 ng g(-1) wet weight (ww) and 94 ng g(-1) ww in birch leaves and s

178 f CBR values ranged from 2.1 to 16.1 mmol/kg wet weight (ww) within all combinations of chemicals and

179 PFCAs present in the biosolids (0.1-138 ng/g wet weight (ww)) and those produced from 6:2 diPAP degra

180 atorVMS concentrations (median: 178 ng g(-1) wet weight (ww)) compared with those from the urban indu

181 n +/- standard deviation, 1.87 +/- 2.17 ng/g wet weight (ww), range of 0.112-15.3 ng/g ww) were 1-2 o

182 0.005-1.307) and 0.005 (< 0.010-0.143) ng/g wet weight (ww), respectively; beta-HBCD was present in

183 ranged between 187 and 2674 mug/g of sludge wet weight (ww), while sulfonamide concentrations were l

184 oncentrations ranged from 70 to 366 ng g(-1) wet weight (ww).

185 Wet-weight (ww) and organic carbon (OC)-based biota soil

186 Fat (32.3+/-9.8 ng/g wet weight; ww) contained the highest SigmaOP concentrat

187 142-1345 pmol/micromol lipid P; 1-7 microg/g wet weight) yet discovered in a mammalian tissue.