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G Fiorelli

Showing results (201-210 of 252) with videos related to

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Blood|June 5, 2001
Tumor necrosis factor alpha promoter polymorphisms influence the phenotypic expression of hereditary hemochromatosisS Fargion, L Valenti, P Dongiovanni, et al.
Lancet (London, England)|August 17, 1985
Feasibility of prenatal diagnosis of beta-thalassaemia with synthetic DNA probes in two Mediterranean populationsS L Thein, J S Wainscoat, J M Old, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 27, 1998
Aromatase expression and activity in the human leukaemic cell line FLG 29.1G Fiorelli, U Frediani, V Martineti, et al.
Human Mutation|April 11, 2001
Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f-PCT)M D Cappellini, F Martinez di Montemuros, D Tavazzi, et al.
Blood Cells, Molecules & Diseases|February 8, 2002
Acute intermittent porphyria: heterogeneity of mutations in the hydroxymethylbilane synthase gene in ItalyF Martinez di Montemuros, E Di Pierro, G Biolcati, et al.
Biochemical and Biophysical Research Communications|June 30, 1994
Binding and bioeffects of Ipriflavone on a human preosteoclastic cell lineS Benvenuti, M Petilli, U Frediani, et al.
Bone|March 1, 1996
Characterization and function of the receptor for IGF-I in human preosteoclastic cellsG Fiorelli, L Formigli, S Zecchi Orlandini, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1989
Three-month treatment with a long-acting gonadotropin-releasing hormone agonist of patients with benign prostatic hyperplasia: effects on tissue androgen concentration, 5 alpha-reductase activity and androgen receptor contentG Forti, R Salerno, G Moneti, et al.
Human Mutation|May 2, 2000
Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria: report of four novel mutationsF Martinez di Montemuros, E Di Pierro, S Fargion, et al.
Journal of Hepatology|May 1, 1996
Genetic hemochromatosis in Italian patients with porphyria cutanea tarda: possible explanation for iron overloadS Fargion, A L Fracanzani, R Romano, et al.
Pageof 26

Showing results (201-210 of 252) with videos related to

Sort By:
Pageof 26
Blood|June 5, 2001
Tumor necrosis factor alpha promoter polymorphisms influence the phenotypic expression of hereditary hemochromatosisS Fargion, L Valenti, P Dongiovanni, et al.
Lancet (London, England)|August 17, 1985
Feasibility of prenatal diagnosis of beta-thalassaemia with synthetic DNA probes in two Mediterranean populationsS L Thein, J S Wainscoat, J M Old, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 27, 1998
Aromatase expression and activity in the human leukaemic cell line FLG 29.1G Fiorelli, U Frediani, V Martineti, et al.
Human Mutation|April 11, 2001
Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f-PCT)M D Cappellini, F Martinez di Montemuros, D Tavazzi, et al.
Blood Cells, Molecules & Diseases|February 8, 2002
Acute intermittent porphyria: heterogeneity of mutations in the hydroxymethylbilane synthase gene in ItalyF Martinez di Montemuros, E Di Pierro, G Biolcati, et al.
Biochemical and Biophysical Research Communications|June 30, 1994
Binding and bioeffects of Ipriflavone on a human preosteoclastic cell lineS Benvenuti, M Petilli, U Frediani, et al.
Bone|March 1, 1996
Characterization and function of the receptor for IGF-I in human preosteoclastic cellsG Fiorelli, L Formigli, S Zecchi Orlandini, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1989
Three-month treatment with a long-acting gonadotropin-releasing hormone agonist of patients with benign prostatic hyperplasia: effects on tissue androgen concentration, 5 alpha-reductase activity and androgen receptor contentG Forti, R Salerno, G Moneti, et al.
Human Mutation|May 2, 2000
Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria: report of four novel mutationsF Martinez di Montemuros, E Di Pierro, S Fargion, et al.
Journal of Hepatology|May 1, 1996
Genetic hemochromatosis in Italian patients with porphyria cutanea tarda: possible explanation for iron overloadS Fargion, A L Fracanzani, R Romano, et al.
Pageof 26