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Missense Mutations in APOB within the βα1 Domain of Human APOB-100 Result in Impaired Secretion of ApoB and ApoB-containing Lipoproteins in Familial Hypobetalipoproteinemia

机译：在人Apob-100的βα1结构域内的APOB中的畸形突变导致家族性低钾素血症中含有含吸脂蛋白和含孔的脂蛋白的分泌受损

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John R. Burnett; Shumei Zhong; Zhenghui G. Jiang; Amanda J. Hooper; Eric A. Fisher; Roger S. McLeod; Yang Zhao; P. Hugh R. Barrett; Robert A. Hegele; Frank M. van Bockxmeer; Hongyu Zhang; Dennis E. Vance; C. James McKnight; Zemin Yao;
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1. Human resistin stimulates hepatic overproduction of atherogenic ApoB-containing lipoprotein particles by enhancing ApoB stability and impairing intracellular insulin signaling. [J] . Costandi J, Melone M, Zhao A, Circulation research: a journal of the American Heart Association . 2011,第6期

机译：人类抵抗素可通过增强ApoB稳定性并削弱细胞内胰岛素信号传导来刺激肝脏中含有致动脉粥样硬化性ApoB的脂蛋白颗粒的过量生产。
2. Nonsynonymous Mutations within APOB in Human Familial Hypobetalipoproteinemia [J] . Shumei Zhong, Antonia Lucia Magnolo, Meenakshi Sundaram, The Journal of biological chemistry . 2010,第9期

机译：在人类族皮下蛋白蛋白血症中Apob中的非唯一突变
3. Evaluation of clinical diagnosis criteria of familial ligand defective apoB 100 and lipoprotein phenotype comparison between LDL receptor gene mutations affecting ligand-binding domain and the R3500Q mutation of the apoB gene in patients from a South European population [J] . Ejarque I, Real JT, Martinez-Hervas S, Translational research: the journal of laboratory and clinical medicine . 2008,第3期

机译：评价欧洲南部人群患者家族配体缺陷apoB 100的临床诊断标准以及影响配体结合结构域的LDL受体基因突变和apoB基因的R3500Q突变之间脂蛋白表型的比较
4. Iron-Catalyzed Oxidation of ApoB-100 in Low Density Lipoproteins In Vitro Is Selective for Production of Kynurenines From WE Sequences [C] . Charles V. Smith, Hsin-hung Chen, Ching-Yi Chen, ASMS Conference on Mass Spectrometry and Allied Topics . 2007

机译：在体外低密度脂蛋白在低密度脂蛋白中的铁催化氧化是从我们序列中产生鸡舍的产生
5. Homozygous protein C deficiency: identification of a novel missense mutation that causes impaired secretion of the mutant protein C [D] . Yamamoto Koji, Matsushita Tadashi, Sugiura Isamu, 1992

机译：纯合蛋白C缺乏症：鉴定导致突变蛋白C分泌受损的新型错义突变
6. Nonsynonymous Mutations within APOB in Human Familial Hypobetalipoproteinemia [O] . Shumei Zhong, Antonia Lucia Magnolo, Meenakshi Sundaram, 2010

机译：人类家族性低β脂蛋白血症的APOB内的非同义突变
7. Nonsynonymous Mutations within APOB in Human Familial Hypobetalipoproteinemia: EVIDENCE FOR FEEDBACK INHIBITION OF LIPOGENESIS AND POSTENDOPLASMIC RETICULUM DEGRADATION OF APOLIPOPROTEIN B* [O] . Zhong, Shumei, Magnolo, Antonia Lucia, Sundaram, Meenakshi, 2009

机译：人类家族性低β脂蛋白血症APOB内的非同义突变：反馈抑制脂肪生成和内质网后APOLIPO蛋白B降解*

Missense Mutations in APOB within the βα1 Domain of Human APOB-100 Result in Impaired Secretion of ApoB and ApoB-containing Lipoproteins in Familial Hypobetalipoproteinemia

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