glycogen and Epistaxis

glycogen has been researched along with Epistaxis* in 2 studies

Other Studies

2 other study(ies) available for glycogen and Epistaxis

ArticleYear
Regulation of energy metabolism in yeast. Inheritance of a pleiotropic mutation causing defects in metabolism of energy reserves, ethanol utilization and formation of cytochrome a.a3.
    Molecular & general genetics : MGG, 1982, Volume: 185, Issue:2

    The recessive, nuclear gene mutation glc1, which causes glycogen deficiency in Saccharomyces cerevisiae, is highly pleiotropic. Studies of the inheritance of glc1 revealed two classes of phenotypic characteristics: I. Traits invariably associated with the mutant gene and II. Traits whose expressions require the presence of glc1 and one or more additional genes. Class I traits include glycogen deficiency and the loss of capacity to accumulate trehalose in nonproliferating conditions. Traits in the second class include a decreased rate of growth on ethanol medium, a deficiency in cytochrome a.a3 and an enhanced accumulation of pigment, probably a metalloporphyrin. Constructed strains containing both glc1 and the constitutive maltose fermentation gene MAL4c can accumulate trehalose but not glycogen during growth on glucose. However, accumulated trehalose is degraded when cells are exposed to nonproliferating conditions. It is proposed that the glc1 mutation affects a regulatory system, probably involving a protein kinase and/or protein phosphatase, which regulates glycogen synthase and trehalase. Independent regulation of trehalose synthesis by a system controlled by MAL4c is indicated.

    Topics: Cytochromes; Epistaxis; Ethanol; Glycogen; Mutation; Saccharomyces cerevisiae; Trehalose

1982
Renal cell carcinoma presenting as epistaxis.
    Journal of surgical oncology, 1980, Volume: 14, Issue:2

    A case of renal cell carcinoma presenting as a nosebleed of three-week duration is described. Light microscopy of a nasal lesion showed a richly vascular tumor, forming glands and uniformly consisting of clear cells. Cytochemically and ultrastructurally, the presence of abundant lipid droplets and glycogen within the neoplastic cells indicated a renal origin. An extended clinical search for a primary kidney tumor was undertaken in view of a negative intravenous tomographic pyelography and renal scan findings. An angiogram finally revealed an intrarenal mass which was proven pathologically as a renal cell carcinoma.

    Topics: Adenocarcinoma; Epistaxis; Glycogen; Humans; Kidney Neoplasms; Lipid Metabolism; Liver Glycogen; Male; Middle Aged; Nose Neoplasms

1980