Report for Penco S

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References (4)

Title : Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemia - Conca_2012_J.Clin.Lipidol_6_244
Author(s) : Conca P , Pileggi S , Simonelli S , Boer E , Boscutti G , Magnolo L , Tarugi P , Penco S , Franceschini G , Calabresi L , Gomaraschi M
Ref : J Clin Lipidol , 6 :244 , 2012
Abstract : Conca_2012_J.Clin.Lipidol_6_244
ESTHER : Conca_2012_J.Clin.Lipidol_6_244
PubMedSearch : Conca_2012_J.Clin.Lipidol_6_244
PubMedID: 22658148
Gene_locus related to this paper: human-LCAT

Title : No association of DPP6 with amyotrophic lateral sclerosis in an Italian population - Fogh_2011_Neurobiol.Aging_32_966
Author(s) : Fogh I , D'Alfonso S , Gellera C , Ratti A , Cereda C , Penco S , Corrado L , Soraru G , Castellotti B , Tiloca C , Gagliardi S , Cozzi L , Lupton MK , Ticozzi N , Mazzini L , Shaw CE , Al-Chalabi A , Powell J , Silani V
Ref : Neurobiology of Aging , 32 :966 , 2011
Abstract : Fogh_2011_Neurobiol.Aging_32_966
ESTHER : Fogh_2011_Neurobiol.Aging_32_966
PubMedSearch : Fogh_2011_Neurobiol.Aging_32_966
PubMedID: 19525032

Title : New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background - Penco_2008_BMC.Bioinformatics_9_254
Author(s) : Penco S , Buscema M , Patrosso MC , Marocchi A , Grossi E
Ref : BMC Bioinformatics , 9 :254 , 2008
Abstract : Penco_2008_BMC.Bioinformatics_9_254
ESTHER : Penco_2008_BMC.Bioinformatics_9_254
PubMedSearch : Penco_2008_BMC.Bioinformatics_9_254
PubMedID: 18513389

Title : Frequency of butyrylcholinesterase gene mutations in individuals with abnormal inhibition numbers: an Italian-population study - Lando_2003_Pharmacogenet_13_265
Author(s) : Lando G , Mosca A , Bonora R , Azzario F , Penco S , Marocchi A , Panteghini M , Patrosso MC
Ref : Pharmacogenetics , 13 :265 , 2003
Abstract : Lando_2003_Pharmacogenet_13_265
ESTHER : Lando_2003_Pharmacogenet_13_265
PubMedSearch : Lando_2003_Pharmacogenet_13_265
PubMedID: 12724618