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F Andreetta

Showing results (1-10 of 19) with videos related to

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Biochemistry International|June 1, 1989
Xanthine oxidase activity: simultaneous HPLC evaluation of the "D" and "O" formsG Cighetti, M Del Puppo, F Andreetta, et al.
Journal of Ultrastructure and Molecular Structure Research|July 1, 1986
Localization and distribution of actin in mammalian sperm headsC Lora-Lamia, L Castellani-Ceresa, F Andreetta, et al.
Journal of Neuroimmunology|June 17, 1998
The expression of co-stimulatory and accessory molecules on cultured human muscle cells is not dependent on stimulus by pro-inflammatory cytokines: relevance for the pathogenesis of inflammatory myopathyP Bernasconi, P Confalonieri, F Andreetta, et al.
Journal of the Neurological Sciences|September 1, 1991
Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathiesF Andreetta, H J Tritschler, E A Schon, et al.
Molecular and Cellular Biology|March 1, 1991
Replication-competent human mitochondrial DNA lacking the heavy-strand promoter regionC T Moraes, F Andreetta, E Bonilla, et al.
The Journal of Clinical Investigation|November 5, 1999
Oral administration of an immunodominant T-cell epitope downregulates Th1/Th2 cytokines and prevents experimental myasthenia gravisF Baggi, F Andreetta, E Caspani, et al.
Journal of Child Neurology|October 12, 2013
Long-term follow-up in infantile-onset lambert-eaton myasthenic syndromeS Portaro, D Parisi, A Polizzi, et al.
The American Journal of Pathology|January 1, 1997
Acetylcholine receptor alpha-subunit isoforms are differentially expressed in thymuses from myasthenic patientsF Andreetta, F Baggi, C Antozzi, et al.
Pediatric Neurology|September 1, 1996
Mitochondrial myopathy simulating spinal muscular atrophyR Pons, F Andreetta, C H Wang, et al.
American Journal of Human Genetics|March 1, 1991
mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseasesC T Moraes, S Shanske, H J Tritschler, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Biochemistry International|June 1, 1989
Xanthine oxidase activity: simultaneous HPLC evaluation of the "D" and "O" formsG Cighetti, M Del Puppo, F Andreetta, et al.
Journal of Ultrastructure and Molecular Structure Research|July 1, 1986
Localization and distribution of actin in mammalian sperm headsC Lora-Lamia, L Castellani-Ceresa, F Andreetta, et al.
Journal of Neuroimmunology|June 17, 1998
The expression of co-stimulatory and accessory molecules on cultured human muscle cells is not dependent on stimulus by pro-inflammatory cytokines: relevance for the pathogenesis of inflammatory myopathyP Bernasconi, P Confalonieri, F Andreetta, et al.
Journal of the Neurological Sciences|September 1, 1991
Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathiesF Andreetta, H J Tritschler, E A Schon, et al.
Molecular and Cellular Biology|March 1, 1991
Replication-competent human mitochondrial DNA lacking the heavy-strand promoter regionC T Moraes, F Andreetta, E Bonilla, et al.
The Journal of Clinical Investigation|November 5, 1999
Oral administration of an immunodominant T-cell epitope downregulates Th1/Th2 cytokines and prevents experimental myasthenia gravisF Baggi, F Andreetta, E Caspani, et al.
Journal of Child Neurology|October 12, 2013
Long-term follow-up in infantile-onset lambert-eaton myasthenic syndromeS Portaro, D Parisi, A Polizzi, et al.
The American Journal of Pathology|January 1, 1997
Acetylcholine receptor alpha-subunit isoforms are differentially expressed in thymuses from myasthenic patientsF Andreetta, F Baggi, C Antozzi, et al.
Pediatric Neurology|September 1, 1996
Mitochondrial myopathy simulating spinal muscular atrophyR Pons, F Andreetta, C H Wang, et al.
American Journal of Human Genetics|March 1, 1991
mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseasesC T Moraes, S Shanske, H J Tritschler, et al.
Pageof 2