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tetradecanoylphorbol acetate and Zellweger Syndrome

tetradecanoylphorbol acetate has been researched along with Zellweger Syndrome in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Clark, KJ; Murray, AW1
Gordon, JA; Spector, AA; Warnock, LJ1
Byers, DM; Cook, HW; Logan, HE; Ridgway, ND1

Other Studies

3 other study(ies) available for tetradecanoylphorbol acetate and Zellweger Syndrome

ArticleYear
Evidence that the bradykinin-induced activation of phospholipase D and of the mitogen-activated protein kinase cascade involve different protein kinase C isoforms.
    The Journal of biological chemistry, 1995, Mar-31, Volume: 270, Issue:13

    Topics: Bradykinin; Calcium-Calmodulin-Dependent Protein Kinases; Cells, Cultured; Culture Media, Serum-Free; Enzyme Activation; Epidermal Growth Factor; Fibroblasts; Glyceryl Ethers; Humans; Isoenzymes; Kinetics; Myelin Basic Protein; Phospholipase D; Phosphorylation; Protein Kinase C; Protein Processing, Post-Translational; Skin; Tetradecanoylphorbol Acetate; Zellweger Syndrome

1995
Attenuated prostaglandin formation in peroxisomal-deficient human skin fibroblasts.
    The Journal of clinical investigation, 1993, Volume: 92, Issue:1

    Topics: Arachidonic Acid; Cells, Cultured; Dinoprostone; Fibroblasts; Gene Expression; Humans; Hydrogen Peroxide; In Vitro Techniques; Microbodies; Prostaglandin-Endoperoxide Synthases; Prostaglandins; Refsum Disease; RNA, Messenger; Tetradecanoylphorbol Acetate; Zellweger Syndrome

1993
Phospholipase D activity is altered in X-linked adrenoleukodystrophy heterozygous carriers, but not in hemizygous patients.
    Biochimica et biophysica acta, 1998, Jul-01, Volume: 1407, Issue:1

    Topics: Carrier State; Cells, Cultured; Choline; Enzyme Activation; Female; Fibroblasts; Genetic Linkage; Humans; Intracellular Signaling Peptides and Proteins; Isoenzymes; Male; Membrane Proteins; Monosomy; Myristoylated Alanine-Rich C Kinase Substrate; Oleic Acid; Peroxisomal Disorders; Phosphatidylcholines; Phospholipase D; Protein Kinase C; Proteins; Sex Chromosome Aberrations; Tetradecanoylphorbol Acetate; X Chromosome; Zellweger Syndrome

1998