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11篇 您的检索式:作者名="Keito"
    题名 作者 年代 出处 被引量
1Adsorption isotherms of pigments of from alkali-refined vegetable oils with clay minerals显示文摘Keito Boki Moriaki Kubo Naohito Kawasaki 1992JAOCS1992,69,4:1
2Bleaching of alkali-refined vegetable oils with clay minerals显示文摘Keito Boki Moriaki Kubo Tetsuyuki Wada Takamichi Tamura 1992Journal of the American Oil Chemists Society1992,,3:1
3A red fuorescent protein,DsRed2,as a visual reporter for transient Expression and stable transformation in soybean显示文摘Keito N Y 2006Plant Cell Rep2006,1,:1
4Bleaching of alkalirefined vegetable oil with clay minerals显示文摘KEITO B MORIAKI K TETSUYUKI W 1992JAOCS1992,69,:1
5Assessment of the importanceof a-amylase inhibitor-2 in bruchid resistance of wild commonbean显示文摘Keito N Masayoshi T Shigeru U 2007Theoretical and Applied Genetics2007,114,4:1
6Assessment of the Importance of α-amylase Inhibitor-2 in Bruchid Resistance of Wild Common Bean显示文摘Keito Nishizawa Masayoshi Teraishi Shigeru Utsumi 2007Theoretical and Applied Genetics2007,114,4:1
7Irno-catalyzed cross-coupling of primary and secondary alkyl halides with aryl Grignard reagents显示文摘Masaharu N Keito M Shingo I 2004J Am Chem Soc2004,126,12:1
8Anti- hypertensive activity of genetically modified soybean seeds accu- mulating novokinin显示文摘Yuko Yamada Keito Nishizawa Megumi Yokoo 2008Peptides2008,29,3:1
9Bleaching of Alkali-Refined Vegetable Oils With Clay Minerals显示文摘Keito B Moriaki K Tetsuyuki W etal 1992JAOCS1992,69,:1
10A vacuolar sorting deter- minant of soybean 13-conglycinin 13 subunit resides in a C-terminal sequence显示文摘KEITO N NOBUYUKI M RYOHEI S 2004Plant Science2004,,167:1
11Mechanistic studies of PEG-asparaginase-induced liver injury and hepatic steatosis in mice显示文摘PEGylated-L-asparaginase(PEG-ASNase)is a chemotherapeutic agent used to treat pediatric acute lymphoblastic leukemia(ALL).Its use is avoided in adults due to its high risk of liver injury including hepatic steatosis,with obesity and older age considered risk factors of the injury.Our study aims to elucidate the mechanism of PEG-ASNase-induced liver injury.Mice received 1500 U/kg of PEG-ASNase and were sacrificed 1,3,5,and 7 days after drug administration.Liver triglycerides were quantified,and plasma bilirubin,ALT,AST,and non-esterified fatty acids(NEFA)were measured.The mRNA and protein levels of genes involved in hepatic fatty acid synthesis,β-oxidation,very low-density lipoprotein(VLDL)secretion,and white adipose tissue(WAT)lipolysis were determined.Mice developed hepatic steatosis after PEG-ASNase,which associated with increases in bilirubin,ALT,and AST.The hepatic genes Ppara,Lcad/Mcad,Hadhb,Apob100,and Mttp were upregulated,and Srebp-1 c and Fas were downregulated after PEG-ASNase.Increased plasma NEFA,WAT loss,and adipose tissue lipolysis were also observed after PEG-ASNase.Furthermore,we found that PEG-ASNase-induced liver injury was exacerbated in obese and aged mice,consistent with clinical studies of ASNase-induced liver injury.Our data suggest that PEG-ASNase-induced liver injury is due to drug-induced lipolysis and lipid redistribution to the liver.Gundala Venkata Naveen Kumar Keito Hoshitsuki Sanjay Rathod Manda J.Ramsey Lauren Kokai Erin E.Kershaw Wen Xie Christian A.Fernandez 2021Acta Pharmaceutica Sinica B2021,11,12:0
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