Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Silvia Capra"'
Autor:
Daniela Pletto, Silvia Capra, Adele Finardi, Francesca Colciaghi, Paola Nobili, Giorgio Stefano Battaglia, Denise Locatelli, Cinzia Cagnoli
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0199105 (2018)
Spinal Muscular Atrophy (SMA) is a severe autosomal recessive disease characterized by selective motor neuron degeneration, caused by disruptions of the Survival of Motor Neuron 1 (Smn1) gene. The main product of SMN1 is the full-length SMN protein (
Externí odkaz:
https://doaj.org/article/da9d6add2f674cbe9eeca9ceb75941bc
Autor:
Paolo d'Errico, Marina Boido, Antonio Piras, Valeria Valsecchi, Elena De Amicis, Denise Locatelli, Silvia Capra, Francesco Vagni, Alessandro Vercelli, Giorgio Battaglia
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e82654 (2013)
Loss of the survival motor neuron gene (SMN1) is responsible for spinal muscular atrophy (SMA), the most common inherited cause of infant mortality. Even though the SMA phenotype is traditionally considered as related to spinal motor neuron loss, it
Externí odkaz:
https://doaj.org/article/faebacf483944dcd9bb330b83995b183
Autor:
Francesca Colciaghi, Denise Locatelli, Daniela Rita Pletto, Adele Finardi, Giorgio Battaglia, Paola Nobili, Cinzia Cagnoli, Silvia Capra
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0199105 (2018)
Spinal Muscular Atrophy (SMA) is a severe autosomal recessive disease characterized by selective motor neuron degeneration, caused by disruptions of the Survival of Motor Neuron 1 (Smn1) gene. The main product of SMN1 is the full-length SMN protein (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20f0efe92f64631da925f92c866a0987
http://europepmc.org/articles/PMC6001960?pdf=render
http://europepmc.org/articles/PMC6001960?pdf=render
Autor:
Denise Locatelli, Veronica Setola, Mineko Terao, Giorgio Battaglia, Enrico Garattini, Francesca Colciaghi, Silvia Capra, Adele Finardi, Paolo d'Errico
Publikováno v:
Journal of Neurochemistry. 121:465-474
The axonal survival of motor neuron (a-SMN) protein is a truncated isoform of SMN1, the spinal muscular atrophy (SMA) disease gene. a-SMN is selectively localized in axons and endowed with remarkable axonogenic properties. At present, the role of a-S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91834df60a31fbd3a3539124175166ad
https://doi.org/10.1111/j.1471-4159.2012.07689.x
https://doi.org/10.1111/j.1471-4159.2012.07689.x
Autor:
Giorgio Battaglia, Marina Boido, Antonio Piras, Francesco Vagni, Denise Locatelli, Paolo d'Errico, Elena De Amicis, Valeria Valsecchi, Silvia Capra, Alessandro Vercelli
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 12, p e82654 (2013)
PLoS ONE, Vol 8, Iss 12, p e82654 (2013)
Loss of the survival motor neuron gene (SMN1) is responsible for spinal muscular atrophy (SMA), the most common inherited cause of infant mortality. Even though the SMA phenotype is traditionally considered as related to spinal motor neuron loss, it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43634f90887817a7b63affdfb9f1ad70
http://europepmc.org/articles/PMC3855775
http://europepmc.org/articles/PMC3855775
Autor:
Paolo d'Errico, Denise Locatelli, Enrico Garattini, Maddalena Fratelli, Maria Monica Barzago, Silvia Capra, Adriana Zanetti, Giorgio Battaglia, Mami Kurosaki, Monica Lupi, Mineko Terao, Andrea Uggetti
Publikováno v:
The Journal of Biological Chemistry
Background: Axonal SMN is a truncated product of the spinal muscular atrophy (SMA) disease gene SMN1. Results: Forced expression of axonal SMN in motoneuron-like NSC34 cells modulates growth, axonogenesis, and motility. Conclusion: Axonal SMN induces
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0db29a839b5b27f78e40c83d0f00a321
https://pubmed.ncbi.nlm.nih.gov/22669976
https://pubmed.ncbi.nlm.nih.gov/22669976
Publikováno v:
Viruses, Vol 7, Iss 10, Pp 5388-5409 (2015)
The origin and evolution of viruses is a subject of ongoing debate. In this study, we provide a full account of the evolutionary relationships between proteins of significant sequence and structural similarity found in viruses that belong to differen
Externí odkaz:
https://doaj.org/article/cfb7543030244c16aa2f49fda4499e3a