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Early neonatal death in mice homozygous for a null allele of the insulin receptor gene.

作者信息

Accili D, Drago J, Lee E J, Johnson M D, Cool M H, Salvatore P, Asico L D, José P A, Taylor S I, Westphal H

机构信息

Diabetes Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Nat Genet. 1996 Jan;12(1):106-9. doi: 10.1038/ng0196-106.

DOI:10.1038/ng0196-106
PMID:8528241
Abstract
摘要

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1
Early neonatal death in mice homozygous for a null allele of the insulin receptor gene.胰岛素受体基因无效等位基因纯合子小鼠的早期新生儿死亡。
Nat Genet. 1996 Jan;12(1):106-9. doi: 10.1038/ng0196-106.
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Targeted disruption of the insulin receptor gene in the mouse results in neonatal lethality.小鼠胰岛素受体基因的靶向破坏导致新生期致死。
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Restored insulin-sensitivity in IRS-1-deficient mice treated by adenovirus-mediated gene therapy.通过腺病毒介导的基因疗法治疗的 IRS - 1 缺陷小鼠恢复了胰岛素敏感性。
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Hepatocyte nuclear factor 4alpha (nuclear receptor 2A1) is essential for maintenance of hepatic gene expression and lipid homeostasis.肝细胞核因子4α(核受体2A1)对于维持肝脏基因表达和脂质稳态至关重要。
Mol Cell Biol. 2001 Feb;21(4):1393-403. doi: 10.1128/MCB.21.4.1393-1403.2001.
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Homozygous carnitine palmitoyltransferase 1a (liver isoform) deficiency is lethal in the mouse.纯合子肉碱棕榈酰转移酶1a(肝脏亚型)缺乏在小鼠中是致死性的。
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Mouse embryonic stem cells express receptors of the insulin family of growth factors.小鼠胚胎干细胞表达胰岛素家族生长因子的受体。
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[Insulin and its receptor: lessons learned from the disruption of their gene in mice].[胰岛素及其受体:从小鼠基因敲除研究中获得的经验教训]
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Protein kinase C modulation of insulin receptor substrate-1 tyrosine phosphorylation requires serine 612.蛋白激酶C对胰岛素受体底物-1酪氨酸磷酸化的调节作用需要丝氨酸612。
Biochemistry. 1997 Oct 21;36(42):12939-47. doi: 10.1021/bi971157f.

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