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991.
992.
Allen D. Hacker Mohammad G. Mustafa Jean J. Ospital Nabil M. Elsayed Si Duk Lee 《Age (Dordrecht, Netherlands)》1986,9(1):1-5
We investigated the relationship of age to rat lung collagen synthesis in response to ozone (O3) exposure. Specific pathogen-free Sprague-Dawley male rats 24, 30, 45, 60, 94, 182 and 365 days old were exposed to either
0.8 ±.05 ppm O3 for 3 days or to 0.8 ± 0.5 ppm O3 for 3 days followed by 4.0 ±.2 ppm O3 for 8 hours and 60 days recovery in air. A matched number of rats from each age group received filtered air and served as
controls. Lung dry weight, protein content, hydroxyproline content, 14C proline incorporation and 14C hydroxyproline formation were determined in control and exposed rat lungs. Rats exposed to 0.8 ppm O3 for 3 days had greater dry weight, protein content, incorporation of 14C proline, and formation of 14C hydroxyproline per lung relative to controls, with the greatest changes occurring in rats older than 60 days. Rats 24 and
94 days old, exposed to 0.8 ppm O3 for 3 days followed by 4.0 ppm O3 for 8 hours and 60 days recovery in air, had greater lung collagen content than controls: 50% and 80%, respectively. These
results suggest that collagen synthesis was increased following O3 exposure and that the degree of change was influenced by age in the rat. Age, therefore, may be an important factor in the
lung’s response to pulmonary injury. 相似文献
993.
994.
“CHARGE‐like presentation,craniosynostosis and mild Mowat–Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases” American Journal of Medical Genetics Part A. 164:2557‐2566, 2014
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Tara L. Wenger Margaret Harr Stefania Ricciardi Elizabeth Bhoj Avni Santani Margaret P. Adam Sarah S. Barnett Rebecca Ganetzky Donna M. McDonald‐McGinn Domenica Battaglia Stefania Bigoni Angelo Selicorni Giovanni Sorge Matteo Della Monica Francesca Mari Elena Andreucci Silvia Romano Guido Cocchi Salvatore Savasta Baris Malbora Giuseppe Marangi Livia Garavelli Marcella Zollino Elaine H. Zackai 《American journal of medical genetics. Part A》2015,167(7):1682-1683
995.
Tyler F. Beck Philippe M. Campeau Shalini N. Jhangiani Tomasz Gambin Alexander H. Li Reem Abo‐Zahrah Valerie K. Jordan Andres Hernandez‐Garcia Wojciech K. Wiszniewski Donna Muzny Richard A. Gibbs Eric Boerwinkle James R. Lupski Brendan Lee Willie Reardon Daryl A. Scott 《American journal of medical genetics. Part A》2015,167(4):831-836
996.
The fetal brain transcriptome and neonatal behavioral phenotype in the Ts1Cje mouse model of Down syndrome
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997.
Marie-Luise Berres Karen Phaik Har Lim Tricia Peters Jeremy Price Hitoshi Takizawa Hélène Salmon Juliana Idoyaga Albert Ruzo Philip J. Lupo M. John Hicks Albert Shih Stephen J. Simko Harshal Abhyankar Rikhia Chakraborty Marylene Leboeuf Monique Beltr?o Sérgio A. Lira Kenneth M. Heym Bj?rn E. Clausen Venetia Bigley Matthew Collin Markus G. Manz Kenneth McClain Miriam Merad Carl E. Allen 《The Journal of experimental medicine》2015,212(2):281
998.
You-Cheol Hwang Tomoshige Hayashi Wilfred Y. Fujimoto Steven E. Kahn Donna L. Leonetti Marguerite J. McNeely Edward J. Boyko 《Diabetes care》2015,38(11):2100-2105
OBJECTIVERecent studies have suggested that HDL cholesterol is inversely associated with the development of type 2 diabetes. However, little is known about the association between different HDL subclasses and the risk for future type 2 diabetes.RESULTSIn univariate analysis, total HDL and HDL2 cholesterol were inversely associated with the incidence of type 2 diabetes, but HDL3 cholesterol was not. In multivariate analysis, total HDL cholesterol (odds ratio per 1-SD increment, 0.72 [95% CI 0.52–0.995], P = 0.047) and HDL2 cholesterol (odds ratio per 1-SD increment, 0.64 [95% CI 0.44–0.93], P = 0.018) were inversely associated with the risk for type 2 diabetes independent of age, sex, BMI, waist circumference, family history of diabetes, lifestyle factors, systolic blood pressure, lipid-lowering medication use, triglyceride level, HOMA-insulin resistance, and 2-h glucose; however, HDL3 cholesterol was not associated with diabetes risk. The association between diabetes risk and total HDL and HDL2 cholesterol became insignificant after adjustment for VAT area.CONCLUSIONSSubjects with higher HDL2 cholesterol were at lower risk for incident type 2 diabetes, but this association was confounded by and not independent of VAT. Higher HDL3 cholesterol was not associated with diabetes risk. 相似文献
999.
1000.
S. A. McDonald S. J. Hutchinson H. A. Innes S. Allen P. Bramley D. Bhattacharyya W. Carman J. F. Dillon R. Fox A. Fraser D. J. Goldberg N. Kennedy P. R. Mills J. Morris A. J. Stanley D. Wilks P. C. Hayes 《Journal of viral hepatitis》2014,21(5):366-376
Primary goals of the Hepatitis C Action Plan for Scotland Phase II (May 2008–March 2011) were to increase, among persons chronically infected with the hepatitis C (HCV) virus, attendance at specialist outpatient clinics and initiation on antiviral therapy. We evaluated progress towards these goals by comparing the odds, across time, of (a) first clinic attendance within 12 months of HCV diagnosis (n = 9747) and (b) initiation on antiviral treatment within 12 months of first attendance (n = 5736). Record linkage between the national HCV diagnosis (1996–2009) and HCV clinical (1996–2010) databases and logistic regression analyses were conducted for both outcomes. For outcome (a), 32% and 45% in the respective pre‐Phase II (before 1 May 2008) and Phase II periods attended a specialist clinic within 12 months of diagnosis; the odds of attendance within 12 months increased over time (OR = 1.05 per year, 95% CI: 1.04–1.07), but was not significantly greater for persons diagnosed with HCV in the Phase II era, compared with the pre‐Phase II era (OR = 1.1, 95% CI: 0.9–1.3), after adjustment for temporal trend. For outcome (b), 13% and 28% were initiated on treatment within 12 months of their first clinic attendance in the pre‐Phase II and Phase II periods, respectively. Higher odds of treatment initiation were associated with first clinic attendance in the Phase II (OR = 1.9, 95% CI: 1.5–2.4), compared with the pre‐Phase II era. Results were consistent with a positive impact of the Hepatitis C Action Plan on the treatment of chronically infected individuals, but further monitoring is required to confirm a sustained effect. 相似文献