SPINAL MUSCULAR ATROPHY: MUTATION AND FUNCTIONAL ANALYSIS OF THE SURVIVAL MOTOR NEURON GENE AND ITS PROTEIN PRODUCT
- 3 Anni 1996/1999
 - 154.937€ Totale Fondi
 
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Pubblicazioni Scientifiche
- 2000-01-01 AMINO ACIDS 
Excitatory amino acid stimulation of the survival of rat cerebellar granule cells in culture is associated with an increase in SMN, the spinal muscular atrophy disease gene product
 - 1999-04-01 EUROPEAN JOURNAL OF HUMAN GENETICS 
SMN protein analysis in fibroblast, amniocyte and CVS cultures from spinal muscular atrophy patients and its relevance for diagnosis
 - 2001-02-01 EUROPEAN JOURNAL OF HUMAN GENETICS 
Premature termination mutations in exon 3 of the SMN1 gene are associated with exon skipping and a relatively mild SMA phenotype
 - 1999-12-01 HUMAN MOLECULAR GENETICS 
Detection of the survival motor neuron (SMN) genes by FISH:: further evidence for a role for SMN2 in the modulation of disease severity in SMA patients
 - 1999-04-01 NEUROGENETICS 
The drastic reduction of SMN protein in SMA I spinal cord motor neurons is not due to inefficient transcription