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au.\*:("LATTANZI, Giovanna")

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Emerin expression at the early stages of myogenic differentiationLATTANZI, Giovanna; OGNIBENE, Andrea; SQUARZONI, Stefano et al.Differentiation (London). 2000, Vol 66, Num 4-5, pp 208-217, issn 0301-4681Article

Remodelling of the nuclear lamina during human cytomegalovirus infection : role of the viral proteins pUL50 and pUL53CAMOZZI, Daria; PIGNATELLI, Sara; VALVO, Cecilia et al.Journal of general virology. 2008, Vol 89, pp 731-740, issn 0022-1317, 10 p., 3Article

Molecular mechanisms of CD99-induced caspase-independent cell death and cell-cell adhesion in Ewing's sarcoma cells: actin and zyxin as key intracellular mediatorsCERISANO, Vanessa; AALTO, Yan; KNUUTILA, Sakari et al.Oncogene (Basingstoke). 2004, Vol 23, Num 33, pp 5664-5674, issn 0950-9232, 11 p.Article

Novel COL6A1 splicing mutation in a family affected by mild Bethlem myopathyVANEGAS, Olga Camacho; ZHANG, Rui-Zhu; SABATELLI, Patrizia et al.Muscle & nerve. 2002, Vol 25, Num 4, pp 513-519, issn 0148-639XArticle

Troglitazione affects survival of human osteosarcoma cellsLUCARELLI, Enrico; SANGIORGI, Luca; PICCI, Piero et al.International journal of cancer. 2002, Vol 98, Num 3, pp 344-351, issn 0020-7136Article

Nuclear alterations in autosomal-dominant emery-dreifuss muscular dystrophySABATELLI, Patrizia; LATTANZI, Giovanna; OGNIBENE, Andrea et al.Muscle & nerve. 2001, Vol 24, Num 6, pp 826-829, issn 0148-639XArticle

The accumulation of un-repairable DNA damage in laminopathy progeria fibroblasts is caused by ROS generation and is prevented by treatment with N-acetyl cysteineRICHARDS, Shane A; MUTER, Joanne; RITCHIE, Pamela et al.Human molecular genetics (Print). 2011, Vol 20, Num 20, pp 3997-4004, issn 0964-6906, 8 p.Article

LMNA-associated myopathies: The Italian experience in a large cohort of patientsMAGGI, Lorenzo; D'AMICO, Adele; BRENNA, Greta et al.Neurology. 2014, Vol 83, Num 18, pp 1634-1644, issn 0028-3878, 11 p.Article

A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathyARAUJO-VILAR, David; LADO-ABEAL, Joaquin; MARTINEZ-SANCHEZ, Noelia et al.Clinical endocrinology (Oxford. Print). 2008, Vol 69, Num 1, pp 61-68, issn 0300-0664, 8 p.Article

Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotypeLOMBARDI, Francesca; GULLOTTA, Francesca; LATTANZI, Giovanna et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 11, pp 4467-4471, issn 0021-972X, 5 p.Article

Altered pre-lamin A processing is a common mechanism leading to lipodystrophyCAPANNI, Cristina; MATTIOLI, Elisabetta; LATTANZI, Giovanna et al.Human molecular genetics (Print). 2005, Vol 14, Num 11, pp 1489-1502, issn 0964-6906, 14 p.Article

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