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21篇 您的检索式:作者名="Harly"
    题名 作者 年代 出处 被引量
1Neuroticism, extraver sion,life events and depression: the cardiff depression study 显示文摘Farmer A Redman K Harlis T 2002Br J Psychiatry2002,181,:1
2Telomeres shorten during aging of human fibroblasts显示文摘Harly CB Futcher AB Greider CW 0,,:1
3Control of IPM synchronous generator for maximum wind power generation considering magnetic saturation显示文摘QIAO W QU L HARLY R G 2009IEEETrans on Industry Applications2009,45,3:1
4Sex, drug and HIV : Does methadone maintenance reduce drug use and risky sexual ,ehavior显示文摘harlie ML Harry SS Dale DC 2000J Behav Med2000,23,6:1
5Telomere loss:mitotic clock or genetic time bomb显示文摘 1991Mutat Res1991,256,:1
6Telomeres shorten during aging of human fibroblasts显示文摘Harly CB Greider CW Futcher AB 0,,:1
7The NS3 protein of bluetongue virus exhibits vi- roporin-like properties显示文摘Han Z Harly RN 2004J Biol Chem2004,279,43:1
8Up-regulation of cytolytic functions of human V82-~/T lymphocytes through engagement of ILT2 expressed by tumor target cells 显示文摘Harly C Peyrat MA Netzer S 2011Blood2011,117,:1
9Chronic intermittent hypoxia activates nuclear factor-κB in cardiovascular tissues in vivo显示文摘Harly Greenberg Xiaobing Ye David Wilson Aung K. Htoo Todd Hendersen Shu Fang Liu 2006Biochemical and Biophysical Research Communications2006,,2:1
10Transmitter deficits in Alzheimer's disease显示文摘Harly J Adolfsson K Alafuzoff I 1985Neurochem Intl1985,7,:1
11Up-regulation of cyto- lyric functions of human Vδ2-γ tlymphoeytes through engage- ment of ILT2 expressed by tumor target cells 显示文摘Harly C Peyrat MA Netzer S 2011Blood2011,117,10:1
12Chronic intermittent hypoxia activates nuclear factor-κB in cardiovascular tissues in vivo显示文摘Harly Greenberg Xiaobing Ye David Wilson Aung K. Htoo Todd Hendersen Shu Fang Liu 2006Biochemical and Biophysical Research Communications2006,,2:1
13Up-regulation of cytolytic functions of human Vδ2-γ T lymphocytes through engagement of ILT2 expressed by tumor target cells显示文摘Harly C Peyrat MA Netzer S 0,,10:1
14The telomere hypothesis of cellular aging显示文摘C B Harly H Viziri C Counter 1992Exp Gerontol1992,27,:1
15Up-regulation of cytolytic functions of human Vδ2-γT lymphocytes through engagement of ILT2expressed by tumor target cells显示文摘Harly C Peyrat M A Netzer S 2011Blood2011,117,10:1
16Enterocutaneous fistula aretreatments improving显示文摘Draus JM Huss SA Harly NJ 2006surgery2006,140,4:1
17Neurotieism, extra- version, life events and depression: the cardiff depression study 显示文摘Farmer A Redman K Harlis T 2002Br J Psychiatry2002,181,:1
18A comparison between com-mercial kits and conventional methods for enumeration of salivary mutans streptococci and lactobacilli显示文摘Davenport ES Day S Harlie JM 1992Community Dent Health1992,9,3:1
19Telomerase shorten during aging of fibroblasts 显示文摘Harly CB Futcher AB Greider CW 1990Nature1990,345,6724:1
20Latent, sex-specific metabolic health effects in CD-1 mouse offspring exposed to PFOA or HFPO-DA (GenX) during gestation显示文摘Background:Perfluorooctanoic acid(PFOA)is an environmental contaminant associated with adverse metabolic outcomes in developmentally exposed human populations and mouse models.Hexafluoropropylene oxide-dimer acid(HFPO-DA,commonly called GenX)has replaced PFOA in many industrial applications in the U.S.and Europe and has been measured in global water systems from<1 to 9350 ng/L HFPO-DA.Health effects data for GenX are lacking.Objective:Determine the effects of gestational exposure to GenX on offspring weight gain trajectory,adult metabolic health,liver pathology and key adipose gene pathways in male and female CD-1 mice.Methods:Daily oral doses of GenX(0.2,1.0,2.0 mg/kg),PFOA(0.1,1.0 mg/kg),or vehicle control were administered to pregnant mice(gestation days 1.5-17.5).Offspring were fed a high-or low-fat diet(HFD or LFD)at weaning until necropsy at 6 or 18 weeks,and metabolic endpoints were measured over time.PFOA and GenX serum and urine concentrations,weight gain,serum lipid parameters,body mass composition,glucose tolerance,white adipose tissue gene expression,and liver histopathology were evaluated.Results:Prenatal exposure to GenX led to its accumulation in the serum and urine of 5-day old pups(P=0.007,P<0.001),which was undetectable by weaning.By 18 weeks of age,male mice fed LFD in the 2.0 mg/kg GenX group displayed increased weight gain(P<0.05),fat mass(P=0.016),hepatocellular microvesicular fatty change(P=0.015),and insulin sensitivity(P=0.014)in comparison to control males fed LFD.Female mice fed HFD had a significant increase in hepatocyte single cell necrosis in 1.0 mg/kg GenX group(P=0.022)and 1.0 mg/kg PFOA group(P=0.003)compared to control HFD females.Both sexes were affected by gestational GenX exposure;however,the observed phenotype varied between sex with males displaying more characteristics of metabolic disease and females exhibiting liver damage in response to the gestational exposure.Conclusions:Prenatal exposure to 1 mg/kg GenX and 1 mg/kg PFOA induces adverse metabolic outcomes in adult mice that are diet-and sex-dependent.GenX also accumulated in pup serum,suggesting that placental and potentially lactational transfer are important exposure routes for GenX.Harlie A.Cope Bevin E.Blake Charlotte Love James McCord Susan A.Elmore Janice B.Harvey Vesna A.Chappell Suzanne E.Fenton 2021Emerging Contaminants2021,7,1:1
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