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S Penco

Showing results (21-30 of 52) with videos related to

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Free Radical Biology & Medicine|December 21, 2000
Changes of CYP1A1, GST, and ALDH3 enzymes in hepatoma cell lines undergoing enhanced lipid peroxidationA M Bassi, S Ledda, S Penco, et al.
Neurology|August 3, 1999
A SOD1 gene mutation in a patient with slowly progressing familial ALSS Penco, A Schenone, D Bordo, et al.
Annals of Human Genetics|November 4, 2005
Assessment of the role of genetic polymorphism in venous thrombosis through artificial neural networksS Penco, E Grossi, S Cheng, et al.
Molecular and Cellular Biochemistry|December 11, 2012
Paraoxonase 1 L55M, Q192R and paraoxonase 2 S311C alleles in atherothrombosisL Cozzi, J Campolo, M Parolini, et al.
Farmaco (Societa Chimica Italiana : 1989)|May 1, 1993
Cinnamamide analogs as inhibitors of protein tyrosine kinasesF Buzzetti, M G Brasca, A Crugnola, et al.
Bioorganic & Medicinal Chemistry Letters|February 24, 2001
Novel cytotoxic 7-iminomethyl and 7-aminomethyl derivatives of camptothecinS Dallavalle, A Ferrari, L Merlini, et al.
The EMBO Journal|March 15, 1995
RAR-specific agonist/antagonists which dissociate transactivation and AP1 transrepression inhibit anchorage-independent cell proliferationJ Y Chen, S Penco, J Ostrowski, et al.
Biotechnology and Applied Biochemistry|December 4, 2001
Identification of an import signal for, and the nuclear localization of, human lactoferrinS Penco, S Scarfi, M Giovine, et al.
Journal of Internal Medicine|July 22, 2014
Acquired lecithin:cholesterol acyltransferase deficiency as a major factor in lowering plasma HDL levels in chronic kidney diseaseL Calabresi, S Simonelli, P Conca, et al.
Gene|May 14, 2015
Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucomaF Pasutto, L Mauri, B Popp, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Free Radical Biology & Medicine|December 21, 2000
Changes of CYP1A1, GST, and ALDH3 enzymes in hepatoma cell lines undergoing enhanced lipid peroxidationA M Bassi, S Ledda, S Penco, et al.
Neurology|August 3, 1999
A SOD1 gene mutation in a patient with slowly progressing familial ALSS Penco, A Schenone, D Bordo, et al.
Annals of Human Genetics|November 4, 2005
Assessment of the role of genetic polymorphism in venous thrombosis through artificial neural networksS Penco, E Grossi, S Cheng, et al.
Molecular and Cellular Biochemistry|December 11, 2012
Paraoxonase 1 L55M, Q192R and paraoxonase 2 S311C alleles in atherothrombosisL Cozzi, J Campolo, M Parolini, et al.
Farmaco (Societa Chimica Italiana : 1989)|May 1, 1993
Cinnamamide analogs as inhibitors of protein tyrosine kinasesF Buzzetti, M G Brasca, A Crugnola, et al.
Bioorganic & Medicinal Chemistry Letters|February 24, 2001
Novel cytotoxic 7-iminomethyl and 7-aminomethyl derivatives of camptothecinS Dallavalle, A Ferrari, L Merlini, et al.
The EMBO Journal|March 15, 1995
RAR-specific agonist/antagonists which dissociate transactivation and AP1 transrepression inhibit anchorage-independent cell proliferationJ Y Chen, S Penco, J Ostrowski, et al.
Biotechnology and Applied Biochemistry|December 4, 2001
Identification of an import signal for, and the nuclear localization of, human lactoferrinS Penco, S Scarfi, M Giovine, et al.
Journal of Internal Medicine|July 22, 2014
Acquired lecithin:cholesterol acyltransferase deficiency as a major factor in lowering plasma HDL levels in chronic kidney diseaseL Calabresi, S Simonelli, P Conca, et al.
Gene|May 14, 2015
Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucomaF Pasutto, L Mauri, B Popp, et al.
Pageof 6