Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Carmen Vitiello"'
Autor:
Ida Luisa Rotundo, Stefania Faraso, Elvira De Leonibus, Gerardo Nigro, Carmen Vitiello, Alessio Lancioni, Daniele Di Napoli, Sigismondo Castaldo, Vincenzo Russo, Fabio Russo, Giulio Piluso, Alberto Auricchio, Vincenzo Nigro
Publikováno v:
PLoS ONE, Vol 6, Iss 9, p e24729 (2011)
We have previously demonstrated that gene therapy can rescue the phenotype and extend lifespan in the delta-sarcoglycan deficient cardiomyopathic hamster. In patients with similar genetic defects, steroids have been largely used to slow down disease
Externí odkaz:
https://doaj.org/article/485dd427309145caaa4e304473e3957c
Autor:
Carmen Vitiello, Stefania Faraso, Nicolina Cristina Sorrentino, Giovanni Di Salvo, Edoardo Nusco, Gerardo Nigro, Luisa Cutillo, Raffaele Calabrò, Alberto Auricchio, Vincenzo Nigro
Publikováno v:
PLoS ONE, Vol 4, Iss 3, p e5051 (2009)
The BIO14.6 hamster is an excellent animal model for inherited cardiomyopathy, because of its lethal and well-documented course, due to a spontaneous deletion of delta-sarcoglycan gene promoter and first exon. The muscle disease is progressive and av
Externí odkaz:
https://doaj.org/article/f5f738dbdf494d37b616f5ea359c589b
Autor:
Carmen Vitiello, Vincenzo Nigro, Maria Nolano, S. Aurino, Chiara Fiorillo, Stefania Faraso, Vincenzo Provitera, Lucio Santoro
Publikováno v:
Muscle & Nerve. 41:392-398
Clinical trials for muscular dystrophy molecular treatment require multiple sampling of skeletal muscle to monitor protein rescue. This practice is invasive and could raise ethical problems. A less invasive tool to obtain sequential muscle sampling i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a48bf2795644be02b4382bc673a327c
https://doi.org/10.1002/mus.21506
https://doi.org/10.1002/mus.21506
Autor:
Raffaela Pero, Francesca Lembo, Monica Fedele, Lorenzo Chiariotti, Alfredo Fusco, Carmen Vitiello, Emiliano A. Palmieri, Carmelo B. Bruni
Publikováno v:
Journal of Biological Chemistry. 277:3280-3285
PATZ is a transcriptional repressor affecting the basal activity of different promoters, whereas RNF4 is a transcriptional activator. The association of PATZ with RNF4 switches the activation to repression of selected basal promoters. Because RNF4 in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd921c95f764d5164fb74f6896edfabc
https://doi.org/10.1074/jbc.m109491200
https://doi.org/10.1074/jbc.m109491200
Autor:
Kazunori Takano, Carmen Vitiello, Paolo Kunderfranco, Gerald Coulis, Serena Camerini, Ju Chen, Marie Louise Bang, Jianlin Zhang, Pradeep K. Luther, Daniel L. Yamamoto, Marco Crescenzi, Alessandra Castaldi, Takeshi Endo, Richard L. Lieber, Fabio Piaser, Peter J. Eggenhuizen, Maria Carmela Filomena, David S. Gokhin
Publikováno v:
Journal of cell science. 126(Pt 23)
Nemaline myopathy (NM) is a congenital myopathy with an estimated incidence of 1∶50,000 live births. It is caused by mutations in thin filament components, including nebulin, which accounts for about 50% of the cases. The identification of NM cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f576cbfceb9dd50dadbe4c6faffe37e7
https://pubmed.ncbi.nlm.nih.gov/24046450
https://pubmed.ncbi.nlm.nih.gov/24046450
Autor:
Fabio Russo, Alessio Lancioni, Elvira De Leonibus, Vincenzo Nigro, Gerardo Nigro, Ida Luisa Rotundo, Vincenzo Russo, S. Castaldo, Giulio Piluso, Carmen Vitiello, Daniele Di Napoli, Stefania Faraso, Alberto Auricchio
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 9, p e24729 (2011)
PLoS ONE; Vol 6
PLoS ONE, Vol 6, Iss 9, p e24729 (2011)
PLoS ONE; Vol 6
We have previously demonstrated that gene therapy can rescue the phenotype and extend lifespan in the delta-sarcoglycan deficient cardiomyopathic hamster. In patients with similar genetic defects, steroids have been largely used to slow down disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ecdbb6c4616a376a18971bc9cd321b0
http://europepmc.org/articles/PMC3170375
http://europepmc.org/articles/PMC3170375
Autor:
Lucio, Santoro, Maria, Nolano, Stefania, Faraso, Chiara, Fiorillo, Carmen, Vitiello, Vincenzo, Provitera, Stefania, Aurino, Vincenzo, Nigro
Publikováno v:
Musclenerve. 41(3)
Clinical trials for muscular dystrophy molecular treatment require multiple sampling of skeletal muscle to monitor protein rescue. This practice is invasive and could raise ethical problems. A less invasive tool to obtain sequential muscle sampling i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::14256989d7081dbfd8fba2b860b8240b
https://pubmed.ncbi.nlm.nih.gov/20162678
https://pubmed.ncbi.nlm.nih.gov/20162678
Publikováno v:
American journal of medical genetics. Part A. (1)
Oculodentodigital dysplasia (ODDD) is a rare autosomal dominant pleiotropic disorder, caused by mutations in the Connexin 43 gene (GJA1) [Paznekas et al. (2003): Am J Hum Genet 72:408-418], which is localized to human chromosome 6q22-q23. Here, we de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::777ff3b8547239e42fd06705167dfdd0
https://pubmed.ncbi.nlm.nih.gov/15637728
https://pubmed.ncbi.nlm.nih.gov/15637728
Autor:
Carmelo B. Bruni, Raffaela Pero, Lorenzo Chiariotti, Rodolfo Iuliano, Francesca Lembo, Tiziana Angrisano, Carmen Vitiello
We have identified a human gene encoding a novel MBD2-interacting protein (MBDin) that contains an N-terminal GTP-binding site, a putative nuclear export signal (NES), and a C-terminal acidic region. MBDin cDNA was isolated through a two-hybrid inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2bf094a618c8f0256d34f8848b65f6f
http://hdl.handle.net/11588/131556
http://hdl.handle.net/11588/131556
Autor:
Carmen Vitiello, Maria Nolano, Stefania Faraso, S. Aurino, Vincenzo Nigro, Vincenzo Provitera, Chiara Fiorillo, Lucia Santoro
Publikováno v:
Neuromuscular Disorders. 19:604
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cb4d87692e7a4b6305e8fdf3825d1e0
https://doi.org/10.1016/j.nmd.2009.06.192
https://doi.org/10.1016/j.nmd.2009.06.192