ライフサイエンスコーパス: increased weight

1 ggesting that there is no healthy pattern of increased weight.

2 ine also increased hypoglycemia and modestly increased weight.

3 e with increased expenditure associated with increased weight.

4 d from malalignment and the excess load from increased weight.

5 the vehicle or MS1 conditions significantly increased weight (9-20 g) and produced smaller reduction

6 1-null mice grow longer than wild type, with increased weight and adiposity, when restricted in vitam

7 Endometrial cancer is associated with increased weight and body size, diabetes, and other cond

8 vided to women living with HIV significantly increased weight and CD4+ T cells and such interventions

9 vided to women living with HIV significantly increased weight and CD4+ T cells, and such intervention

10 el of inflammation, Nbs1(B/B) animals showed increased weight and ear thickness.

11 may increase dieting, a risk factor for both increased weight and eating disorders in adolescents.

12 and pediatric isolates were associated with increased weight and gestational age of newborns (P </=

13 osure to reduced rations was associated with increased weight and greater indexes of fat deposition a

14 Iron treatment significantly increased weight and hemoglobin nadirs and provided enha

15 tica pathogenesis, mice lacking Gal-1 showed increased weight and survival, lower bacterial load, and

16 f protein from animal-source foods generally increased weight and weight-for-length in children, but

17 hort-term adverse events-acne, night sweats, increased weight, and altered mood and libido-are recogn

18 e, which results in flies with larger cells, increased weight, and decreased life span compared to wi

19 Anemia, older age, increased weight, and dyspnea as a warning symptom were

20 g the atypical subtype, such as hyperphagia, increased weight, and leaden paralysis.

21 cerebellar Purkinje neurons reduced ataxia, increased weight, and prolonged life, but it did not pre

22 ies also support the notion that fatigue and increased weight are linked to higher osteoarthritis pai

23 Hand OA was significantly associated with increased weight at ages 26 years, 43 years, and 53 year

24 Although higher dietary energy intake increased weight, body fat, and menstrual frequency, bon

25 pplementation in term infants/young children increased weight by <=0.14 kg.

26 Accordingly, SI compared to DS increased weight by 89 g (95% CI 27, 150; p = 0.005) whe

27 dia [e.g., redox flow batteries (RFBs)], the increased weight can be better distributed for improved

28 he single mutants had higher oil content and increased weight compared to those of the wild type, wit

29 ce between regular and highly palatable food increased weight compared with access to regular food on

30 , and/or lifestyle behaviors account for the increased weight, fat mass, and central adiposity experi

31 exposed to GDM in utero, infants exposed had increased weight, FM, and percent body fat at birth.

32 Both iron and DHA/EPA significantly increased weight-for-age z scores.

33 pothalamic satiation signaling, hyperphagia, increased weight gain and adiposity, and enhanced lipoge

34 leptin signaling (Leprdb/db mice), including increased weight gain and adiposity, hyperphagia, cold i

35 We found that ovariectomy increased weight gain and adiposity.

36 p neurons improved metabolic efficiency, and increased weight gain and adiposity.

37 ictive feeding practices are associated with increased weight gain and higher weight status, and pres

38 Low circulating adropin predicts increased weight gain and metabolic dysregulation during

39 ition of GDF-15 with ponsegromab resulted in increased weight gain and overall activity level and red

40 hat these Npc1(+/-) mice were susceptible to increased weight gain characterized by increased whole b

41 hers and F1 daughters of HFD-fed fathers had increased weight gain compared to controls.

42 90-4.621) were associated with significantly increased weight gain compared to TDF-only use.

43 glucose intolerance, insulin resistance, and increased weight gain during, but not prior to, pregnanc

44 imuli, with MC3R knockout mice demonstrating increased weight gain following anabolic challenges and

45 Lastly, we showed that while PD consumption increased weight gain in both young and aged rats, this

46 HFD resulted in 9.7% and 14.7% increased weight gain in male and female F0 respectively

47 icate that maternal ACEs are associated with increased weight gain in male infants during the first t

48 fat in black adults and was associated with increased weight gain in Nigerian women.

49 Asthma leads to increased weight gain in nonpregnant populations, but st

50 ght gain (diet-induced obese [DIO] rats) had increased weight gain in response to consuming saccharin

51 that daily insulin injections significantly increased weight gain in the transgenic lines expressing

52 ut inducing adverse side effects such as the increased weight gain induced by TZDs.

53 The increased weight gain of SMRT(mRID1) mice on a high-fat

54 intermediate metabolizers could explain the increased weight gain on dolutegravir compared with efav

55 ng, whereas group-housed female mice display increased weight gain on high-fat diet, reduced behavior

56 GH administration increased weight gain only in hypoxic animals (p < .001)

57 ted protein 2 antibodies was associated with increased weight gain with either intensive or conventio

58 These data support the hypothesis that increased weight gain with intensive therapy might be ex

59 , we report that reduced BRD7 levels lead to increased weight gain with little effect on glucose meta

60 hort day hamsters were also characterized by increased weight gain, and heavier adrenal glands (p < 0

61 nd cardiovascular disease-related mortality, increased weight gain, and high risk for severe hypoglyc

62 IL-18R(-/-) mice display increased weight gain, ectopic lipid deposition, inflamm

63 rdination and cognitive function but exhibit increased weight gain, elevated white adipose tissue dep

64 Unexpectedly, CD40(-/-) mice exhibited increased weight gain, impaired insulin secretion, augme

65 Although not exhibiting increased weight gain, male CD40(-/-) mice in DIO displa

66 Chronic HFD/SW feeding led to significantly increased weight gain, serum and liver lipid levels, liv

67 g insulin concentrations are associated with increased weight gain, whereas insulin resistance seems

68 igh-fat diet feeding, despite no evidence of increased weight gain.

69 ed glucose tolerance only secondary to their increased weight gain.

70 e of deceased donor LT from pediatric donors increased (weighted HR, 1.201.311.42; P < 0.001), and ac

71 essive gestational weight gain may result in increased weight in children; however, studies have not

72 ld have an important role in the response to increased weight in people.

73 43% of the patients), diarrhea (in 39%), and increased weight (in 26%).

74 order of magnitude variation in body weight; increased weight is supported solely through disproporti

75 Pioglitazone increased weight less among patients at higher risk but

76 ggest that, despite a known association with increased weight, long-term sulfonylurea therapy may red

77 ctive protein concentrations correlated with increased weight loss (r = 0.24, P < 0.001).

78 MC4R (I251L), a rare variant associated with increased weight loss after RYGB and increased basal act

79 ulted in more severe disease, as measured by increased weight loss and airway resistance, as compared

80 We found increased weight loss and decreased survival, increased

81 istering DSS to IL-17R(-/-) mice resulted in increased weight loss and more severe intestinal inflamm

82 en in mice infected with M. tuberculosis and increased weight loss and mortality in mice infected wit

83 tudy, we found that STING-deficient mice had increased weight loss and roughly 10-fold-increased syst

84 ore susceptible to endotoxemia, evidenced by increased weight loss and serum TNF-alpha, IL-6, and IL-

85 and intestinal-secreted IgA correlated with increased weight loss at the end of DSS administration.

86 za infection, iron deficient mice experience increased weight loss but mount antigen specific T cells

87 es, fully blocked CR-induced hypothermia and increased weight loss during CR independent of calorie i

88 eight gain following anabolic challenges and increased weight loss following anorexic challenges (i.e

89 a significantly reduced survival percentage, increased weight loss, and a more-rapid increase in bact

90 se characterized by delayed viral clearance, increased weight loss, and immunopathology.

91 monstrated a reduced UPR in colonic tissues, increased weight loss, and less effective clearance of b

92 These effects lead to increased weight loss, but do not require p75NTR during

93 ctivated RSV-vaccinated children, as well as increased weight loss, clinical illness, and enhanced pa

94 zed with vacvG results in the development of increased weight loss, clinical illness, and Penh simila

95 CI increased weight loss, diarrhea, inappetence and letharg

96 sodium (DSS)-induced colitis, manifested by increased weight loss, macrophage infiltration, and infl

97 s in exacerbated disease severity, including increased weight loss, morbidity, and enhanced airway re

98 espiratory pathology, higher virus loads and increased weight loss.

99 BS >/=40 was associated with increased weight loss.

100 vation 2 weeks following surgery experienced increased weight loss.CONCLUSIONThe anatomical and/or me

101 Reduced amount of ovarian fluid and increased weight of the ovarian sac indicate disturbance

102 on in lateral central beta power reflects an increased weighting of peripheral sensory information im

103 The placentas showed a trend to increased weight (OT1DM 690 + or - 19 g; control 641 + o

104 frequencies, below 1 Hz, was associated with increased weighting over parietal channels, which was no

105 ermediate variables and may not be caused by increased weight per se.

106 effectively decreased soil bulk density and increased weight percentage of water-stable aggregate an

107 stature, black race, age 55 years or older, increased weight, rapid pulse, and smoking history (< or

108 ses of FFM potentially being associated with increased weight regain and appetite.

109 Female TDP-43(Q331K) knock-in mice displayed increased weight relative to wild-type and increased foo

110 , arthralgia, arthritis, increased appetite, increased weight, restlessness, tendon disorder, and pot

111 rs, greater maternal BMI was associated with increased weight SDS (p < 0.001), BMI SDS (p = 0.005), a

112 Carbohydrate overfeeding increased weight (+/-SEM) by 2% (1.8 +/- 0.3 kg; P < 0.0

113 verse events in both safety populations were increased weight (seven [10%] of 68 patients in the NTRK

114 -fast blood glucose normally associated with increased weight, suggesting a role for resistin in medi

115 Rats gradually increased weight support.

116 ethoxy-4-iodophenyl-2-aminopropane), further increased weight-supported stepping in transplant rats.

117 rease of energy intake needed to sustain the increased weight (the maintenance energy gap) has amount

118 were present in the aged subjects, including increased weight, triglycerides, lactate dehydrogenase (

119 ice with equal mean body weights (42 and 58% increased weight versus lean mice).

120 ce estimates using Gray's k-sample P values, increased weight was ascribed to the earlier data becaus

121 mr1(-/y)), but not female Fmr1(-/-), exhibit increased weight when compared to wild-type controls, si