P. Mamont

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Potentiating effect of (2-[2-[(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methyl]-phenyl]ethenyl) -phosphonic acid (MDL 74,428), a potent inhibitor of purine nucleoside phosphorylase, on the antiretroviral activities of 2',3'-dideoxyinosine combined with ribavirin in mice.

A. Bernhardt, J. Balzarini, M. Weibel, 1994, Biochemical pharmacology.

A possible role for cathepsins D, E, and B in the processing of beta-amyloid precursor protein in Alzheimer's disease.

C. Guenet, M. Moniatte, A. van Dorsselaer, 1997, European journal of biochemistry.

Analogues of ornithine as inhibitors of ornithine decarboxylase. New deductions concerning the topography of the enzyme's active site.

C. Tardif, C. Danzin, P. Mamont, 1978, Journal of medicinal chemistry.

Assay of α-difluoromethylornithine in body fluids and tissues by automatic amino-acid analysis

J. Fozard, P. Mamont, J. Grove, 1981 .

Initial characterization of a HTC cell variant partially resistant to the anti-proliferative effect of ornithine decarboxylase inhibitors.

C. Tardif, P. Mamont, M. Duchesne, 1978, Experimental cell research.

Anti-proliferative properties of DL-alpha-difluoromethyl ornithine in cultured cells. A consequence of the irreversible inhibition of ornithine decarboxylase.

P. Mamont, M. Duchesne, P. Bey, 1978, Biochemical and biophysical research communications.

Alpha-methyl ornithine, a potent competitive inhibitor of ornithine decarboxylase, blocks proliferation of rat hepatoma cells in culture.

P. McCann, C. Tardif, F. Schuber, 1976, Proceedings of the National Academy of Sciences of the United States of America.

Polyamine oxidase in rat tissues.

N. Seiler, P. Mamont, F. Bolkenius, 1980, Biochimica et biophysica acta.

Fluorinated analogues of spermidine as substrates of spermine synthase.

P. Mamont, J. Wagner, J. Baillon, 1988, European journal of biochemistry.

"Pleiotypic response".

R. Shields, A. Hershko, G. Tomkins, 1971, Nature: New biology.

Antitumor Properties of ( 2 fi , 5 fl )-6-Heptyne-2 , 5-diamine , a New Potent Enzyme-activated Irreversible Inhibitor of Ornithine Decarboxylase , in Rodents JacquesBartholeyns , 1

P. Mamont, 2006 .

Polyamine depletion increases cellular ribonucleotide levels

M. Kanje, S. Oredsson, P. Mamont, 1986, Molecular and Cellular Biochemistry.

Restoration of the polyamine contents in rat hepatoma tissue-culture cells after inhibition of polyamine biosynthesis. Relationship with cell proliferation.

E. Gerner, P. Mamont, 1986, European journal of biochemistry.

Effects of (2R, 5R)-6-heptyne-2,5-diamine, a potent inhibitor of L-ornithine decarboxylase, on rat hepatoma cells cultured in vitro.

A. Bernhardt, P. Mamont, P. Casara, 1984, European journal of biochemistry.

Inhibition of EMT6 tumor growth by interference with polyamine biosynthesis; effects of alpha-difluoromethylornithine, an irreversible inhibitor of ornithine decarboxylase.

A. Sjoerdsma, P. Schechter, J. Koch-weser, 1980, Life sciences.

Biphasic induction of ornithine decarboxylase and putrescine levels in growing HTC cells.

P. McCann, F. Schuber, P. Mamont, 1975, Biochemical and biophysical research communications.

Accumulation of decarboxylated S-adenosyl-L-methionine in mammalian cells as a consequence of the inhibition of putrescine biosynthesis.

C. Danzin, P. Mamont, J. Wagner, 2005, European journal of biochemistry.

Regulation of ornithine decarboxylase by ODC-antizyme in HTC cells.

P. McCann, C. Tardif, P. Mamont, 1977, Biochemical and biophysical research communications.

Pleiotypic control by adenosine 3':5'-cyclic monophosphate: a model for growth control in animal cells.

G. Tomkins, P. Mamont, R. Kram, 1973, Proceedings of the National Academy of Sciences of the United States of America.

The pleiotypic response in mammalian cells: search for an intracellular mediator.

A. Hershko, J. Lust, G. Tomkins, 1972, Biochemical and biophysical research communications.

Regulation of Specific Protein Synthesis in Eucaryotic Cells

R. H. Stellwagen, J. Baxter, G. Tomkins, 1970 .

Comparative antitumor properties in rodents of irreversible inhibitors of L-ornithine decarboxylase, used as such or as prodrugs.

P. Mamont, N. Claverie, 1989, Cancer research.

Reversed-phase ion-pair liquid chromatographic procedure for the simultaneous analysis of S-adenosylmethionine, its metabolites and the natural polyamines.

C. Danzin, P. Mamont, J. Wagner, 1982, Journal of chromatography.

7 – Polyamine Inhibition in Vivo and in Organ Growth and Repair

C. Danzin, P. Mamont, 1987 .

Indirect evidence for a strict negative control of S-adenosyl-L-methionine decarboxylase by spermidine in rat hepatoma cells.

P. Mamont, J. Grove, A. Joder-Ohlenbusch, 1981, The Biochemical journal.

[Quinones in oxidative phosphorylation. II. Acid dimerization of K vitamins].

R. Azerad, P. Cohen, P. Mamont, 1965, Bulletin de la Societe chimique de France.

Marked and prolonged inhibition of mammalian ornithine decarboxylase in vivo by esters of (E)-2-(fluoromethyl)dehydroornithine.

A. Sjoerdsma, C. Danzin, P. Mamont, 1986, Biochemical pharmacology.

Metabolism of N8-monoacetylspermidine in rat hepatoma cells. Investigation of its effect on the activity of L-ornithine decarboxylase.

P. Mamont, M. Siat, A. Joder-Ohlenbusch, 1983, European journal of biochemistry.

Polyamine-mediated regulation of S-adenosylmethionine decarboxylase expression in mammalian cells. Studies using 5'-([(Z)-4-amino-2-butenyl]methylamino)-5'-deoxyadenosine, a suicide inhibitor of the enzyme.

P. Mamont, L. Persson, O. Heby, 1993, European journal of biochemistry.

Effect of alpha-methyl ornithine on ornithine decarboxylase activity of rat hepatoma cells in culture.

P. McCann, C. Tardif, P. Mamont, 1977, Biochemical and biophysical research communications.

Post-translational modification of the protein-synthesis initiation factor eIF-4D by spermidine in rat hepatoma cells.

E. Gerner, A. Bernhardt, P. Mamont, 1986, The Biochemical journal.

Spermidine nuclear acetylation in rat hepatocytes and in logarithmically growing rat hepatoma cells: comparison with histone acetylation.

M. Weibel, P. Mamont, M. Desiderio, 1992, Experimental cell research.

Metabolism of acetyl derivatives of polyamines in cultured polyamine-deficient rat hepatoma cells.

N. Seiler, P. Mamont, B. Knödgen, 1981, Medical biology.

Antitumor properties of (2R,5R)-6-heptyne-2,5-diamine, a new potent enzyme-activated irreversible inhibitor of ornithine decarboxylase, in rodents.

P. Mamont, P. Casara, J. Bartholeyns, 1984, Cancer research.

Inhibition by DL-α-difluoromethylornithine of the pokeweed mitogen-induced immunoglobulin production in cultured human lymphocytes

A. Weryha, P. Mamont, J. Pasquali, 1984 .

Polyamines in Biomedical Research, Joseph M. Gaugas (Ed.). John Wiley and Sons, Berlin - Heidelberg - New-York (1980)

P. Cann, P. Mamont, 1981 .

Inhibition of mammalian spermine synthase by N-alkylated-1,3-diaminopropane derivatives in vitro and in cultured rat hepatoma cells.

P. Mamont, M. Kolb, J. Baillon, 1989, European journal of biochemistry.

Decreased protein-synthetic activity is an early consequence of spermidine depletion in rat hepatoma tissue-culture cells.

N. Seiler, B. Rudkin, P. Mamont, 1984, The Biochemical journal.

Immunosuppressive effects of (2R,5R)-6-heptyne-2,5-diamine an inhibitor of polyamine synthesis: I. Effects on mitogen-induced immunoglobulin production in human cultured lymphocytes.

A. Weryha, P. Mamont, J. Pasquali, 1988, Clinical and experimental immunology.