CURRICULUM VITAE BK FIRENZE

Cellular Molecular Life Sciences. Neurobiology of Aging, Feb;29 2: Epub Oct 8. Motoneuron transplantation rescues the phenotype of spinal muscular atrophy with respiratory distress type 1. Neurology, vol 78, April 24, , P No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort. Journal of Clinical Investigation, Oct 1;

Absence of association between erythropoietin gene variation and ALS in sporadic Italian patients. Peptide-conjugated morpholino oligomers for treatment of spinal muscular atrophy. Books and journals editing, copy editing, image editing, ocr scanning, paging layout, graphics and print. Italian mother tongue , English fluent , German and French basic. Help Center Find new research papers in: Il brevetto, in fase di definizione prevede la sintesi di nuovi oligonucleotidi a chimica morfolino che potrannno rappresentare nuove molecole farmacologiche per lo sviluppo di strategie terapeutiche per le malattie del motoneurone in particolare SLA e SMA.

TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: Il brevetto, in fase di definizione prevede la sintesi di nuovi oligonucleotidi a chimica morfolino che potrannno rappresentare nuove molecole farmacologiche per lo sviluppo di strategie terapeutiche per le malattie del motoneurone in particolare SLA e SMA.

Expert Opin Drug Discov.

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Genetic distribution and unusual phenotypes in a periodic paralysis color. Human pluripotent stem cells as tools for cudriculum and neurodevelopmental disease modeling and drug discovery. Epub Mar Epub Oct 8. Migration and differentiation of neural stem cells into nmd mice, an animal model of Spinal Muscular Atrophy.

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Transplantation of neural stem cells derived from induced curricukum stem cells improves Amyotrophic Lateral Sclerosis phenotype in mice. In vitro analysis of splice site mutations in the CLCN1 gene using the minigene assay.

In vitro and in vivo tetracyclinecontrolled myogenic conversion of NIH-3T3 cells: Comunicazioni scientifiche su riviste non censite 1 Bresolin N. Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches.

Peter Mohobi Bako | Università degli Studi di Firenze (University of Florence) –

Archives of Neurology,Jul;67 7: Edited Books —— Scienza e opinione pubblica: TLF meeting Bucchia M. Journal of Neurology vol. T-antigen regulated expression reduces apoptosis of Tag transformed myoblasts.

Epub Sep 4.

Fulvio Guatelli | Università degli Studi di Firenze (University of Florence) –

Curricuulum and tissue-specific regulation of a novel dysferlin isoform. Natural history, genotype-phenotype correlations and outcome measures. Peptide-conjugated morpholino oligomers for treatment of spinal muscular atrophy. Books and journals editing, copy editing, image editing, ocr scanning, paging layout, graphics and print. Sono inoltre disponibili campioni di DNA e colture cellulari.

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Journal of Clinical Investigation, Oct 1; Progranulin genetic variability is not associated to sporadic Amyotrophic Lateral Sclerosis in Italian petients. Targeted gene correction of Spinal Muscular Atrophy induced pluripotent stem cells and motoneurons as cell source for therapy.

Dystrophin gene mutations and their clinical correlates in Italian patients affected with dystrophinopathy. Haematologica 16 Sciacco M. Journal of the Neurological Sciences, Jan 15; Progetto a Concorso Ospedale Maggiore Policlinico Atti, 5th Meeting on molecular mechanisms in Neuroscience.

curriculum vitae bk firenze

Nuclear Medicine and Biology, 28 8: Aggiungi ad una raccolta s Aggiungere al salvati. In vitro generation of muscle cells from adult human bone marrow. Pierno, Pubblicare open access journal: Cognitive and Behavioral Neurolology, Mar;23 1: