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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.
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
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.
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.
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.
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
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
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.
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
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.
Molecular-genetics of the hypoalphalipoproteinemias in Italy 1-gen-2003 Bertolini, S.; Pisciotta, L.; Altilia, S.; Calabresi, L.; Franceschini, G.; Calandra, S.
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
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.
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
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
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
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.
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes 1-gen-2005 Pisciotta, Livia; Calabresi, L.; Lupattelli, G.; Siepi, G.; Mannarino, M. R.; Moleri, E.; Bellocchio, A.; Cantafora, A.; Tarugi, P.; Calandra, S.; Bertolini, Stefano
Mostrati risultati da 1 a 20 di 127
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