About: DNA excision in liver by an albumin-Cre transgene occurs progressively with age

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description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 2000 (uk) im Februar 2000 veröffentlichter wissenschaftlicher Artikel (de) wüsseschaftlicher Artikel, wo im Hornig 2000 veröffentlicht worden isch (gsw) article scientifique publié en février 2000 (fr)
publication date	wds:Q61203358-4B9F5EBB-7532-4B65-AD4F-3F526ABFEF5F wds:Q61203358-A98A3619-C992-4F24-9888-C2791CCBAAB4
publication date	2000-02-01 00:00:00Z (xsd:dateTime)
rdfs:label	DNA excision in liver by an albumin-Cre transgene occurs progressively with age (en) DNA excision in liver by an albumin-Cre transgene occurs progressively with age (nl)
skos:prefLabel	DNA excision in liver by an albumin-Cre transgene occurs progressively with age (en) DNA excision in liver by an albumin-Cre transgene occurs progressively with age (nl)
name	DNA excision in liver by an albumin-Cre transgene occurs progressively with age (en) DNA excision in liver by an albumin-Cre transgene occurs progressively with age (nl)
author	wds:Q61203358-1BA04278-AA8C-4A94-9D8A-12EECB1ACC89 wds:Q61203358-27602919-F0D0-42C9-81C8-C73FCF471D3D
author	Mark Magnuson Catherine Postic
title	wds:Q61203358-74D73E54-30A2-4BDA-A7C2-D8BACFF89D0E
title	DNA excision in liver by an albumin-Cre transgene occurs progressively with age (en)
page(s)	wds:Q61203358-4E780128-9270-42A6-8001-69F25C2B7F88
page(s)	149-150
instance of	wds:Q61203358-7CDEBB8E-671F-4322-8A34-D6C762F74309
instance of	scholarly article
PubMed ID	wds:Q61203358-FC51FC8F-C51D-4E4F-A01F-7795E5675A74
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10686614
PubMed ID	10686614
published in	wds:Q61203358-2BCD2DFB-017D-4D62-A6F0-0F4A97E4C5FC
published in	Genesis
issue	wds:Q61203358-9911F6C3-72CB-49EE-A2B6-EB5D9FAE191B
volume	wds:Q61203358-9ED4C1A5-6834-4FD1-AF75-A8DD54C205F0
issue	2
volume	26
DOI	wds:Q61203358-12B37DD9-6562-4FCF-8CC6-FAD40F2A0C1F
DOI	http://dx.doi.org/10.1002/(SICI)1526-968X(200002)26:2%3C149::AID-GENE16%3E3.0.CO;2-V
DOI	10.1002/(SICI)1526-968X(200002)26:2<149::AID-GENE16>3.0.CO;2-V
is owl:sameAs of	DNA excision in liver by an albumin-Cre transgene occurs progressively with age
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q61203358
is cites work of	Beta-catenin regulates vitamin C biosynthesis and cell survival in murine liver Hypoxia-inducible factor-2 (HIF-2) regulates hepatic erythropoietin in vivo Irs1 and Irs2 signaling is essential for hepatic glucose homeostasis and systemic growth The Irs1 branch of the insulin signaling cascade plays a dominant role in hepatic nutrient homeostasis Loss of insulin signaling in hepatocytes leads to severe insulin resistance and progressive hepatic dysfunction The NF-κB subunit RelA/p65 is dispensable for successful liver regeneration after partial hepatectomy in mice Cre activity in fetal albCre mouse hepatocytes: Utility for developmental studies Loss of c-Met disrupts gene expression program required for G2/M progression during liver regeneration in mice Liver-specific inactivation of Notch2, but not Notch1, compromises intrahepatic bile duct development in mice. Selective ablation of retinoid X receptor alpha in hepatocytes impairs their lifespan and regenerative capacity Hepatic suppression of Foxo1 and Foxo3 causes hypoglycemia and hyperlipidemia in mice Hepatocyte-specific Pten deficiency results in steatohepatitis and hepatocellular carcinomas Foxm1b transcription factor is essential for development of hepatocellular carcinomas and is negatively regulated by the p19ARF tumor suppressor Essential metabolic, anti-inflammatory, and anti-tumorigenic functions of miR-122 in liver. Liver-specific deletion of negative regulator Pten results in fatty liver and insulin hypersensitivity [corrected] MicroRNAs control hepatocyte proliferation during liver regeneration Hepatocyte growth factor/c-met signaling pathway is required for efficient liver regeneration and repair Conditional beta-catenin loss in mice promotes chemical hepatocarcinogenesis: role of oxidative stress and platelet-derived growth factor receptor alpha/phosphoinositide 3-kinase signaling. Notch signaling regulates bile duct morphogenesis in mice IKKβ Is Required for Prevention of Apoptosis Mediated by Cell-Bound but Not by Circulating TNFα Fate tracing of mature hepatocytes in mouse liver homeostasis and regeneration A novel prognostic subtype of human hepatocellular carcinoma derived from hepatic progenitor cells. YAP Inhibition Restores Hepatocyte Differentiation in Advanced HCC, Leading to Tumor Regression Lack of protein S in mice causes embryonic lethal coagulopathy and vascular dysgenesis Genetic modelling of the PTEN/AKT pathway in cancer research The roles of PTEN in development, physiology and tumorigenesis in mouse models: a tissue-by-tissue survey Stress-induced Apoptosis Associated with Null Mutation of ADAR1 RNA Editing Deaminase Gene Matricellular protein CCN1 promotes regression of liver fibrosis through induction of cellular senescence in hepatic myofibroblasts. The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore A screen in mice uncovers repression of lipoprotein lipase by microRNA-29a as a mechanism for lipid distribution away from the liver. Activated Nrf2 impairs liver regeneration in mice by activation of genes involved in cell-cycle control and apoptosis. The p85alpha regulatory subunit of phosphoinositide 3-kinase potentiates c-Jun N-terminal kinase-mediated insulin resistance Liver-specific loss of beta-catenin blocks glutamine synthesis pathway activity and cytochrome p450 expression in mice Akt stimulates hepatic SREBP1c and lipogenesis through parallel mTORC1-dependent and independent pathways Identification of Akt-independent regulation of hepatic lipogenesis by mammalian target of rapamycin (mTOR) complex 2 Notch signaling regulates formation of the three-dimensional architecture of intrahepatic bile ducts in mice. In vivo evidence that furin from hepatocytes inactivates PCSK9 MicroRNA-194 is a target of transcription factor 1 (Tcf1, HNF1α) in adult liver and controls expression of frizzled-6. MicroRNA-21 is a potential link between non-alcoholic fatty liver disease and hepatocellular carcinoma via modulation of the HBP1-p53-Srebp1c pathway Nf2/Merlin controls progenitor homeostasis and tumorigenesis in the liver Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice. Fbxw7 regulates lipid metabolism and cell fate decisions in the mouse liver Largen: a molecular regulator of mammalian cell size control Hippo signaling is a potent in vivo growth and tumor suppressor pathway in the mammalian liver Mammalian Mst1 and Mst2 kinases play essential roles in organ size control and tumor suppression NF2/Merlin mediates contact-dependent inhibition of EGFR mobility and internalization via cortical actomyosin Precise let-7 expression levels balance organ regeneration against tumor suppression Deletion of Gab1 in the liver leads to enhanced glucose tolerance and improved hepatic insulin action Dyskerin ablation in mouse liver inhibits rRNA processing and cell division Cholesteryl ester transfer protein expression partially attenuates the adverse effects of SR-BI receptor deficiency on cholesterol metabolism and atherosclerosis Efficient temporally controlled targeted somatic mutagenesis in hepatocytes of the mouse Regulation of notch1 signaling by nrf2: implications for tissue regeneration Liver heparan sulfate proteoglycans mediate clearance of triglyceride-rich lipoproteins independently of LDL receptor family members Mouse model of intrahepatic cholangiocarcinoma validates FIG-ROS as a potent fusion oncogene and therapeutic target Hepatic HIF-2 regulates erythropoietic responses to hypoxia in renal anemia. Glucokinase links Krüppel-like factor 6 to the regulation of hepatic insulin sensitivity in nonalcoholic fatty liver disease The class IA phosphatidylinositol 3-kinase p110-beta subunit is a positive regulator of autophagy Knockout of myeloid cell leukemia-1 induces liver damage and increases apoptosis susceptibility of murine hepatocytes. Liver-specific ablation of integrin-linked kinase in mice results in abnormal histology, enhanced cell proliferation, and hepatomegaly Mosaic analysis of insulin receptor function

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