Sfoglia per Autore
Changes in the expression of cytokeratins and nuclear matrix proteins are correlated with the level of differentiation in human prostate cancer
2000-01-01 Alberti, I; Barboro, P; Barbesino, M; Sanna, P; Pisciotta, Livia; Parodi, Silvio; Nicolo', G; Boccardo, Francesco; Galli, S; Patrone, E; Balbi, C.
Clinical Expression of Familial Hypercholesterolemia in clusters of mutations of LDL-receptor gene causing receptor-defective or receptor-negative phenotype
2000-01-01 Bertolini, Stefano; Cantafora, A; Averna, M; Cortese, C; Motti, C; Martini, S; Pes, G; Postiglione, A; Stefanutti, C; Blotta, I; Pisciotta, Livia; Rolleri, M; Langheim, S; Ghisellini, M; Rabbone, I; Calandra, S.
Changes in the Expression of the Nuclear Matrix Intermediate Filament Complex Proteins are correlated with the Level of Differentiation in Human Prostate Cancer.
2000-01-01 Alberti, I; Barboro, P; Barbesino, M; Sanna, P; Pisciotta, Livia; Nicolò, G; Boccardo, F; Galli, S; Patrone, E; Balbi, C.
Influence of beta(0)-thalassemia on the phenotypic expression of heterozygous familial hypercholesterolemia : a study of patients with familial hypercholesterolemia from Sardinia.
2000-01-01 Deiana, L; Garuti, R; Pes, Gm; Carru, C; Errigo, A; Rolleri, M; Pisciotta, Livia; Masturzo, Paola; Cantafora, A; Calandra, S; Bertolini, Stefano
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease
2001-01-01 Bertolini, Stefano; Pisciotta, Livia; Seri, M; Cusano, R; Cantafora, A; Calabresi, L; Franceschini, G; Ravazzolo, Roberto; Calandra, S.
A “de novo” mutation of the LDL-receptor gene as the cause of familial hypercholesterolemia.
2002-01-01 Pisciotta, Livia; Cantafora, A; DE STEFANO, Francesco; Langheim, S; Calandra, S; Bertolini, Stefano
Investigation into the role of apolipoprotein B gene 8344C/T variant on plasma cholesterol levels by allele-specific PCR amplification
2002-01-01 Cantafora, A.; Bertolini, S.; Blotta, I.; Rivabene, R.; Pisciotta, L.; Langheim, S.; Calandra, S.
Two Italian Kindreds Carrying the Arg136>Ser Mutation of Apo E Gene: Development of Premature and Severe Atherosclerosis in the presence of Epsilon 2 as Second Allele
2003-01-01 Rolleri, M.; Vivona, N.; Emmanuele, G.; Cefalu', A. B.; Pisciotta, Livia; Guido, V.; Noto, D.; Fiore, B.; Barbagallo, C. M.; Notarbartolo, A.; Travali, S.; Bertolini, Stefano; Averna, M. R.
Physical activity modulates effects of some genetic polymorphisms affecting cardiovascular risk in men aged over 40 years.
2003-01-01 Pisciotta, Livia; Cantafora, A; Piana, A; Masturzo, Paola; Cerone, R; Minniti, G; Bellocchio, A; Reggiani, E; Armani, U; Bertolini, Stefano
Evaluation of RNA messangers involved in lipid trafficking of human intestinal cells by RT-PCR with competimer technology and microchip electrophoresis.
2003-01-01 Cantafora, A; Blotta, I; Rivabene, R; Pisciotta, Livia; Bertolini, Stefano
Molecular-genetics of the hypoalphalipoproteinemias in Italy
2003-01-01 Bertolini, S.; Pisciotta, L.; Altilia, S.; Calabresi, L.; Franceschini, G.; Calandra, S.
Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency.
2003-01-01 Pisciotta, Livia; Miccoli, R; Cantafora, A; Calabresi, L; Tarugi, P; Alessandrini, P; Bittolo Bon, G; Franceschini, G; Cortese, C; Calandra, S; Bertolini, Stefano
Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2 +5G>C mutation in ABCA1 gene
2003-01-01 Altilia, S; Pisciotta, Livia; Garuti, R; Tarugi, P.; Cantafora, A.; Calabresi, L; Tagliabue, J; Maccari, S; Bernini, F; Vergani, C; Bertolini, Stefano; Calandra, S.
Le ipercolesterolemie familiari: forme dominanti e recessive (FH, FDB, FH3, FH4, ARH, beta-sitosterolemia, Deficit di 7alpha-idrossilasi).
2004-01-01 Bertolini, S; Pisciotta, Livia
A 33-year-old man with nephrotic syndrome and lecithin-cholesterol acyltransferase (LCAT) deficiency. Description of two new mutations in the LCAT gene
2004-01-01 Frasca', Gm; Soverini, L; Tampieri, E; Franceschini, G; Calabresi, L; Pisciotta, Livia; Preda, P; Vangelista, A; Stefoni, S; Bertolini, Stefano
Beta-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia.
2004-01-01 Calandra, S; Bertolini, Stefano; Pes, Gm; Deiana, L; Tarugi, P; Pisciotta, Livia; Li Volti, S; Li Volti, G; Maccarone, C.
Genetic polymorphisms affecting the phenotypic expression in familial hypercholesterolemia
2004-01-01 Bertolini, Stefano; Pisciotta, Livia; DI SCALA, L; Langheim, S; Bellocchio, A; Masturzo, Paola; Cantafora, A; Martini, S; Averna, M; Pes, G. M.; Stefanutti, C; Calandra, S.
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders.
2004-01-01 Pisciotta, Livia; Hamilton Craig, I; Tarugi, P; Bellocchio, A; Fasano, T; Alessandrini, P; Bon, Gb; Siepi, D; Mannarino, E; Cattin, L; Averna, M; Cefalù, Ab; Cantafora, A; Calandra, S; Bertolini, Stefano
Quantitative polymerase chain reaction and microchip electrophoresis to detect major rearrangements of the low-density lipoprotein receptor gene causing familial hypercholesterolemia.
2004-01-01 Cantafora, A; Blotta, I; Pino, E; Pisciotta, Livia; Calandra, S; Bertolini, Stefano
Denaturing high-performance liquid chromatography (DHPLC) in the detection of mutations of ABCA1 gene in Familial HDL Deficiency.
2005-01-01 Fasano, T; Bocchi, L; Pisciotta, Livia; Bertolini, Stefano; Calandra, S.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Changes in the expression of cytokeratins and nuclear matrix proteins are correlated with the level of differentiation in human prostate cancer | 1-gen-2000 | Alberti, I; Barboro, P; Barbesino, M; Sanna, P; Pisciotta, Livia; Parodi, Silvio; Nicolo', G; Boccardo, Francesco; Galli, S; Patrone, E; Balbi, C. | |
Clinical Expression of Familial Hypercholesterolemia in clusters of mutations of LDL-receptor gene causing receptor-defective or receptor-negative phenotype | 1-gen-2000 | Bertolini, Stefano; Cantafora, A; Averna, M; Cortese, C; Motti, C; Martini, S; Pes, G; Postiglione, A; Stefanutti, C; Blotta, I; Pisciotta, Livia; Rolleri, M; Langheim, S; Ghisellini, M; Rabbone, I; Calandra, S. | |
Changes in the Expression of the Nuclear Matrix Intermediate Filament Complex Proteins are correlated with the Level of Differentiation in Human Prostate Cancer. | 1-gen-2000 | Alberti, I; Barboro, P; Barbesino, M; Sanna, P; Pisciotta, Livia; Nicolò, G; Boccardo, F; Galli, S; Patrone, E; Balbi, C. | |
Influence of beta(0)-thalassemia on the phenotypic expression of heterozygous familial hypercholesterolemia : a study of patients with familial hypercholesterolemia from Sardinia. | 1-gen-2000 | Deiana, L; Garuti, R; Pes, Gm; Carru, C; Errigo, A; Rolleri, M; Pisciotta, Livia; Masturzo, Paola; Cantafora, A; Calandra, S; Bertolini, Stefano | |
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease | 1-gen-2001 | Bertolini, Stefano; Pisciotta, Livia; Seri, M; Cusano, R; Cantafora, A; Calabresi, L; Franceschini, G; Ravazzolo, Roberto; Calandra, S. | |
A “de novo” mutation of the LDL-receptor gene as the cause of familial hypercholesterolemia. | 1-gen-2002 | Pisciotta, Livia; Cantafora, A; DE STEFANO, Francesco; Langheim, S; Calandra, S; Bertolini, Stefano | |
Investigation into the role of apolipoprotein B gene 8344C/T variant on plasma cholesterol levels by allele-specific PCR amplification | 1-gen-2002 | Cantafora, A.; Bertolini, S.; Blotta, I.; Rivabene, R.; Pisciotta, L.; Langheim, S.; Calandra, S. | |
Two Italian Kindreds Carrying the Arg136>Ser Mutation of Apo E Gene: Development of Premature and Severe Atherosclerosis in the presence of Epsilon 2 as Second Allele | 1-gen-2003 | Rolleri, M.; Vivona, N.; Emmanuele, G.; Cefalu', A. B.; Pisciotta, Livia; Guido, V.; Noto, D.; Fiore, B.; Barbagallo, C. M.; Notarbartolo, A.; Travali, S.; Bertolini, Stefano; Averna, M. R. | |
Physical activity modulates effects of some genetic polymorphisms affecting cardiovascular risk in men aged over 40 years. | 1-gen-2003 | Pisciotta, Livia; Cantafora, A; Piana, A; Masturzo, Paola; Cerone, R; Minniti, G; Bellocchio, A; Reggiani, E; Armani, U; Bertolini, Stefano | |
Evaluation of RNA messangers involved in lipid trafficking of human intestinal cells by RT-PCR with competimer technology and microchip electrophoresis. | 1-gen-2003 | Cantafora, A; Blotta, I; Rivabene, R; Pisciotta, Livia; Bertolini, Stefano | |
Molecular-genetics of the hypoalphalipoproteinemias in Italy | 1-gen-2003 | Bertolini, S.; Pisciotta, L.; Altilia, S.; Calabresi, L.; Franceschini, G.; Calandra, S. | |
Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency. | 1-gen-2003 | Pisciotta, Livia; Miccoli, R; Cantafora, A; Calabresi, L; Tarugi, P; Alessandrini, P; Bittolo Bon, G; Franceschini, G; Cortese, C; Calandra, S; Bertolini, Stefano | |
Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2 +5G>C mutation in ABCA1 gene | 1-gen-2003 | Altilia, S; Pisciotta, Livia; Garuti, R; Tarugi, P.; Cantafora, A.; Calabresi, L; Tagliabue, J; Maccari, S; Bernini, F; Vergani, C; Bertolini, Stefano; Calandra, S. | |
Le ipercolesterolemie familiari: forme dominanti e recessive (FH, FDB, FH3, FH4, ARH, beta-sitosterolemia, Deficit di 7alpha-idrossilasi). | 1-gen-2004 | Bertolini, S; Pisciotta, Livia | |
A 33-year-old man with nephrotic syndrome and lecithin-cholesterol acyltransferase (LCAT) deficiency. Description of two new mutations in the LCAT gene | 1-gen-2004 | Frasca', Gm; Soverini, L; Tampieri, E; Franceschini, G; Calabresi, L; Pisciotta, Livia; Preda, P; Vangelista, A; Stefoni, S; Bertolini, Stefano | |
Beta-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia. | 1-gen-2004 | Calandra, S; Bertolini, Stefano; Pes, Gm; Deiana, L; Tarugi, P; Pisciotta, Livia; Li Volti, S; Li Volti, G; Maccarone, C. | |
Genetic polymorphisms affecting the phenotypic expression in familial hypercholesterolemia | 1-gen-2004 | Bertolini, Stefano; Pisciotta, Livia; DI SCALA, L; Langheim, S; Bellocchio, A; Masturzo, Paola; Cantafora, A; Martini, S; Averna, M; Pes, G. M.; Stefanutti, C; Calandra, S. | |
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders. | 1-gen-2004 | Pisciotta, Livia; Hamilton Craig, I; Tarugi, P; Bellocchio, A; Fasano, T; Alessandrini, P; Bon, Gb; Siepi, D; Mannarino, E; Cattin, L; Averna, M; Cefalù, Ab; Cantafora, A; Calandra, S; Bertolini, Stefano | |
Quantitative polymerase chain reaction and microchip electrophoresis to detect major rearrangements of the low-density lipoprotein receptor gene causing familial hypercholesterolemia. | 1-gen-2004 | Cantafora, A; Blotta, I; Pino, E; Pisciotta, Livia; Calandra, S; Bertolini, Stefano | |
Denaturing high-performance liquid chromatography (DHPLC) in the detection of mutations of ABCA1 gene in Familial HDL Deficiency. | 1-gen-2005 | Fasano, T; Bocchi, L; Pisciotta, Livia; Bertolini, Stefano; Calandra, S. |
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