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本文引用的文献

1
A zebrafish model of intrahepatic cholangiocarcinoma by dual expression of hepatitis B virus X and hepatitis C virus core protein in liver.在肝脏中同时表达乙型肝炎病毒 X 和丙型肝炎病毒核心蛋白建立肝内胆管癌斑马鱼模型。
Hepatology. 2012 Dec;56(6):2268-76. doi: 10.1002/hep.25914.
2
Sox9b is a key regulator of pancreaticobiliary ductal system development.Sox9b 是胰腺胆管系统发育的关键调节因子。
PLoS Genet. 2012;8(6):e1002754. doi: 10.1371/journal.pgen.1002754. Epub 2012 Jun 14.
3
Highly efficient generation of heritable zebrafish gene mutations using homo- and heterodimeric TALENs.利用同型和异型 TALEN 高效产生可遗传的斑马鱼基因突变。
Nucleic Acids Res. 2012 Sep;40(16):8001-10. doi: 10.1093/nar/gks518. Epub 2012 Jun 7.
4
Improved somatic mutagenesis in zebrafish using transcription activator-like effector nucleases (TALENs).利用转录激活因子样效应物核酸酶(TALENs)提高斑马鱼的体突变率。
PLoS One. 2012;7(5):e37877. doi: 10.1371/journal.pone.0037877. Epub 2012 May 24.
5
The basic helix-loop-helix transcription factor, heart and neural crest derivatives expressed transcript 2, marks hepatic stellate cells in zebrafish: analysis of stellate cell entry into the developing liver.基本螺旋-环-螺旋转录因子,心脏和神经嵴衍生物表达转录本 2,标记斑马鱼中的肝星状细胞:肝星状细胞进入发育中肝脏的分析。
Hepatology. 2012 Nov;56(5):1958-70. doi: 10.1002/hep.25757. Epub 2012 Oct 14.
6
Mutations in vacuolar H+ -ATPase subunits lead to biliary developmental defects in zebrafish.液泡型 H+-ATP 酶亚基突变导致斑马鱼胆道发育缺陷。
Dev Biol. 2012 May 15;365(2):434-44. doi: 10.1016/j.ydbio.2012.03.009. Epub 2012 Mar 16.
7
Review article: the iron overload syndromes.综述文章:铁过载综合征。
Aliment Pharmacol Ther. 2012 Apr;35(8):876-93. doi: 10.1111/j.1365-2036.2012.05051.x. Epub 2012 Mar 4.
8
Intrinsic and extrinsic modifiers of the regulative capacity of the developing liver.发育中肝脏调节能力的内在和外在修饰物。
Mech Dev. 2012 Jan-Feb;128(11-12):525-35. doi: 10.1016/j.mod.2012.01.005. Epub 2012 Jan 31.
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A monocarboxylate transporter required for hepatocyte secretion of ketone bodies during fasting.在禁食期间,肝细胞分泌酮体所需的单羧酸转运蛋白。
Genes Dev. 2012 Feb 1;26(3):282-93. doi: 10.1101/gad.180968.111.
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Fine structure, enzyme histochemistry, and immunohistochemistry of liver in zebrafish.斑马鱼肝脏的精细结构、酶组织化学和免疫组织化学。
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人类肝脏发育和疾病的斑马鱼模型。

Zebrafish models of human liver development and disease.

机构信息

Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

出版信息

Compr Physiol. 2013 Jul;3(3):1213-30. doi: 10.1002/cphy.c120021.

DOI:10.1002/cphy.c120021
PMID:23897685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4784975/
Abstract

The liver performs a large number of essential synthetic and regulatory functions that are acquired during fetal development and persist throughout life. Their disruption underlies a diverse group of heritable and acquired diseases that affect both pediatric and adult patients. Although experimental analyses used to study liver development and disease are typically performed in cell culture models or rodents, the zebrafish is increasingly used to complement discoveries made in these systems. Forward and reverse genetic analyses over the past two decades have shown that the molecular program for liver development is largely conserved between zebrafish and mammals, and that the zebrafish can be used to model heritable human liver disorders. Recent work has demonstrated that zebrafish can also be used to study the mechanistic basis of acquired liver diseases. Here, we provide a comprehensive summary of how the zebrafish has contributed to our understanding of human liver development and disease.

摘要

肝脏具有多种重要的合成和调节功能,这些功能在胎儿发育过程中获得,并贯穿生命始终。其功能紊乱是一组遗传性和获得性疾病的基础,这些疾病影响儿童和成人患者。尽管用于研究肝脏发育和疾病的实验分析通常在细胞培养模型或啮齿动物中进行,但斑马鱼越来越多地被用于补充这些系统中的发现。过去二十年的正向和反向遗传学分析表明,斑马鱼和哺乳动物的肝脏发育的分子程序在很大程度上是保守的,并且可以用斑马鱼来模拟遗传性人类肝脏疾病。最近的工作表明,斑马鱼也可用于研究获得性肝脏疾病的机制基础。在这里,我们全面总结了斑马鱼如何帮助我们理解人类肝脏发育和疾病。