Search Results - "Lippolis, R"

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  1. 1

    All trans retinoic acid depresses the content and activity of the mitochondrial ATP synthase in human keratinocytes by Papa, F., Lippolis, R., Sardaro, N., Gnoni, A., Scacco, S.

    “…Proteomic analysis shows that treatment of keratinocytes cultures with all trans retinoic acid (ATRA), under condition in which it inhibits cell growth,…”
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  2. 2

    Periodontal disease and bone pathogenesis: the crosstalk between cytokines and porphyromonas gingivalis by Ballini, A, Cantore, S, Farronato, D, Cirulli, N, Inchingolo, F, Papa, F, Malcangi, G, Inchingolo, A D, Dipalma, G, Sardaro, N, Lippolis, R, Santacroce, L, Coscia, M F, Pettini, F, De Vito, D, Scacco, S

    “…Periodontal disease is the most frequent cause of tooth loss among adults. It is defined as a plaque-induced inflammation of the periodontal tissues that…”
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  3. 3

    Activation of protein phosphatase 2A is responsible for increased content and inactivation of respiratory chain complex i induced by all-trans retinoic acid in human keratinocytes by Papa, F, Sardaro, N, Lippolis, R, Panelli, D, Scacco, S

    “…This study presents the effect of all-trans retinoic acid (ATRA) on cell growth and respiratory chain complex I in human keratinocyte cultures. Keratinocyte…”
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  4. 4

    Proteomic analysis of human nasal mucosa: different expression profile in rhino-pathologic states by GELARDI, M, SICILIANO, R. A, PAPA, F, MAZZEO, M. F, DE NITTO, E, QUARANTA, N, LIPPOLIS, R

    “…Rhinitis comprises several diseases with varying causes and different clinical manifestations and pathological features, but treated as a single clinical…”
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  5. 5

    Overexpression of Upf1p compensates for mitochondrial splicing deficiency independently of its role in mRNA surveillance by de Pinto, B., Lippolis, R., Castaldo, R., Altamura, N.

    Published in Molecular microbiology (01-02-2004)
    “…Summary In yeast the UPF1, UPF2 and UPF3 genes encode three interacting factors involved in translation termination and nonsense‐mediated mRNA decay (NMD)…”
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    Characterization of mitochondrial DNA in primary cardiomyopathies by Bobba, Antonella, Giannattasio, Sergio, Pucci, Angela, Lippolis, Rosa, Camaschella, Clara, Marra, Ersilia

    Published in Clinica chimica acta (29-12-1995)
    “…With the aim of studying the involvement of the mitochondrial genome in the impairment of heart function, mitochondrial DNA was analyzed by modified primer…”
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  11. 11

    Ketone-body metabolism in hyperthyroid rats: reduced activity of D-3-hydroxybutyrate dehydrogenase in both liver and heart and of succinyl-coenzyme A: 3-oxoacid coenzyme A-transferase in heart by Lippolis, R, Altamura, N, Landriscina, C

    Published in Archives of biochemistry and biophysics (01-01-1988)
    “…The specific activity of D-3-hydroxybutyrate dehydrogenase is reduced by about a third in liver and heart mitochondria of hyperthyroid rats. State 3…”
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  12. 12

    Concerning the decreased D-2-hydroxybutyrate dehydrogenase activity in the liver and heart of hyperthyroid rats by Lippolis, R, Morini, P, Conserva, A R, Casalino, E, Landriscina, C

    Published in Molecular and cellular biochemistry (01-01-1990)
    “…Whereas in rat liver mitochondria the hyperthyroid state causes an increase both in fatty acid unsaturation and in the Ea of D-3-hydroxybutyrate dehydrogenase…”
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  13. 13

    Concerning the decreased D-3-hydroxybutyrate dehydrogenase activity in the liver and heart of hyperthyroid rats by Lippolis, R, Morini, P, Conserva, A R, Casalino, E, Landriscina, C

    Published in Molecular and cellular biochemistry (27-03-1990)
    “…Whereas in rat liver mitochondria the hyperthyroid state causes an increase both in fatty acid unsaturation and in the Ea of D-3-hydroxybutyrate dehydrogenase…”
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  14. 14

    Differential action of thyroid hormones on the activity of certain enzymes in rat kidney and brain by Morini, P, Conserva, A R, Lippolis, R, Casalino, E, Landriscina, C

    Published in Biochemical medicine and metabolic biology (01-10-1991)
    “…In rat kidney several mitochondrial and soluble enzyme activities are stimulated by thyroid hormones and the mitochondrial membrane fluidity is also increased…”
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