Page last updated: 2024-08-21

ethylnitrosourea and Liver Steatosis

ethylnitrosourea has been researched along with Liver Steatosis in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's4 (80.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aizawa-Abe, M; Aotani, D; Ebihara, C; Ebihara, K; Hosoda, K; Kusakabe, T; Mashimo, T; Nakao, K; Sakai, T; Serikawa, T; Takizawa, A; Tomita, T; Yamamoto, Y; Yamamoto-Kataoka, S1
Gekakis, N; Lloyd, DJ; Wheeler, MC1
Chen, TH; Chen, YT; Huang, CC; Kao, HJ; Lin, WD; Sabbagha, NG; Tarn, WY; Tsai, FJ; Wu, JY; Yang, CF1
Bezerra, J; Divanovic, S; Hoebe, K; Keddache, M; Lampe, K; Putnam, P; Shanmukhappa, SK; Sheridan, R1
Chen, YH; Chen, YT; Cheng, CF; Huang, CC; Hung, SI; Kao, HJ; Kikuchi, T; Millington, D; Wu, JY1

Other Studies

5 other study(ies) available for ethylnitrosourea and Liver Steatosis

ArticleYear
Generation of leptin-deficient Lepmkyo/Lepmkyo rats and identification of leptin-responsive genes in the liver.
    Physiological genomics, 2013, Sep-03, Volume: 45, Issue:17

    Topics: Animals; Codon, Nonsense; Disease Models, Animal; Ethylnitrosourea; Fatty Liver; Gene Expression; Leptin; Lipid Metabolism; Liver; Male; Mice, Mutant Strains; Mutagenesis; Obesity; Rats, Mutant Strains; Real-Time Polymerase Chain Reaction

2013
A point mutation in Sec61alpha1 leads to diabetes and hepatosteatosis in mice.
    Diabetes, 2010, Volume: 59, Issue:2

    Topics: Amino Acid Substitution; Animals; Diabetes Mellitus; DNA Primers; Ethylnitrosourea; Fatty Liver; Heterozygote; Histidine; Homozygote; Humans; Immunohistochemistry; Islets of Langerhans; Liver; Membrane Proteins; Mice; Mice, Inbred C57BL; Mutagenesis; Pancreas; Phenotype; Point Mutation; Reverse Transcriptase Polymerase Chain Reaction; Risk Factors; SEC Translocation Channels; Tyrosine

2010
Alternative splicing in Acad8 resulting a mitochondrial defect and progressive hepatic steatosis in mice.
    Pediatric research, 2011, Volume: 70, Issue:1

    Topics: Acyl-CoA Dehydrogenase; Alternative Splicing; Amino Acid Metabolism, Inborn Errors; Animals; Base Sequence; Cold Temperature; Disease Models, Animal; Disease Progression; DNA Mutational Analysis; Ethylnitrosourea; Fatty Liver; Gene Expression Regulation, Enzymologic; Genetic Predisposition to Disease; Liver X Receptors; Male; Metabolomics; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Microscopy, Electron, Transmission; Mitochondria, Liver; Mitochondrial Swelling; Molecular Sequence Data; Mutagens; Mutation; Orphan Nuclear Receptors; Oxidoreductases Acting on CH-CH Group Donors; Phenotype; PPAR alpha; PPAR gamma; RNA, Messenger; Thermogenesis; Thermosensing

2011
Lampe1: an ENU-germline mutation causing spontaneous hepatosteatosis identified through targeted exon-enrichment and next-generation sequencing.
    PloS one, 2011, Volume: 6, Issue:7

    Topics: Animals; Ethylnitrosourea; Exons; Fatty Liver; Gene Targeting; Germ-Line Mutation; Humans; Lipid Metabolism; Liver; Liver Neoplasms; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Phenotype; RNA Splice Sites; Sequence Analysis, DNA; Sequence Deletion

2011
ENU mutagenesis identifies mice with cardiac fibrosis and hepatic steatosis caused by a mutation in the mitochondrial trifunctional protein beta-subunit.
    Human molecular genetics, 2006, Dec-15, Volume: 15, Issue:24

    Topics: Adipose Tissue; Animals; Base Sequence; Blotting, Western; Carnitine; Chromosome Mapping; Ethylnitrosourea; Fatty Liver; Female; Fibrosis; Lipid Metabolism Disorders; Male; Mice; Mice, Inbred C57BL; Mitochondrial Trifunctional Protein; Mitochondrial Trifunctional Protein, alpha Subunit; Mitochondrial Trifunctional Protein, beta Subunit; Multienzyme Complexes; Mutagenesis; Myocardium; Point Mutation; Polymerase Chain Reaction; Pregnancy; Tandem Mass Spectrometry

2006