Ricerca

RicercaInizia una nuova ricerca
NOTA: è possibile cercare una corrispondenza esatta usando i doppi apici, ad es: "evoluzione della specie". Qualora si cerchi un identificativo, è consigliabile cercarlo in due modi differenti: tra apici con caratteri speciali es: "978-94-6366-274" oppure senza caratteri speciali solo come sequenza numerica: es 978946366274.

cerca in

Risultati 31 - 40 di 677 (tempo di esecuzione: 0.255 secondi).

esporta metadati
- RIS
- EndNote
- BibTeX
- Excel
- CSV
- RefWorks

A novel mutation in the mitochondrial tRNA LeuCUN gene associated with a mitochondrial myopathy with respiratory impairment

2007 R. Virgilio, A. Bordoni, D. Ronchi, F. Saladino, N. Bresolin, M. Sciacco, G.P. Comi

A novel mutation in the ß-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance

2012 R. Romaniello, A. Tonelli, F. Arrigoni, C. Baschirotto, F. Triulzi, N. Bresolin, M. Bassi, R. Borgatti

A Novel Nonsense Mutation in the APTX Gene Associated with Delayed DNA Single-strand Break Removal Fails to Enhance Sensitivity to Different Genotoxic Agents

2011 C. Crimella, O. Cantoni, A. Guidarelli, C. Vantaggiato, A. Martinuzzi, M. Fiorani, C. Azzolini, G. Orso, N. Bresolin, M.T. Bassi

A population genetics study of the familial Mediterranean fever gene : evidence of balancing selection under an overdominance regime

2009 M. Fumagalli, R. Cagliani, U. Pozzoli, S. Riva, G.P. Comi, G. Menozzi, N. Bresolin, M. Sironi

A positively selected APOBEC3H haplotype is associated with natural resistance to HIV-1 infection

2011 R. Cagliani, S. Riva, M. Fumagalli, M. Biasin, S. L. Caputo, F. Mazzotta, L. Piacentini, U. Pozzoli, N. Bresolin, M. Clerici, M. Sironi

A region in the dystrophin gene major hot-spot harbors a cluster of deletion breakpoints and generates double-strand breaks in yeast

2006 M. Sironi, U. Pozzoli, G.P. Comi, S. Riva, A. Bordoni, N. Bresolin, D.K. Nag

A severe pediatric case of congenital Myastenic Syndrome due to a novel mutation in COLQ gene

2013 S. Bonato, D. Piga, S. Pagliarani, R. Del Bo, D. Ronchi, M. Moggio, R. Di Lena, P. Ciscato, C. Agostoni, A. Boccazzi, I.G. Vetrano, D. Spagnoli, N. Bresolin, G.P. Comi

A stop codon mutation in the 5’ of the dystrophin gene associated to a Becker muscular dystrophy phenotype

2008 F. Magri, R. Virgilio, R. Del Bo, F. Fortunato, S. Ghezzi, R. Cagliani, M. Sironi, M.G. D'Angelo, V. Crugnola, M. Moggio, N. Bresolin, G.P. Comi

A Subpopulation of murine bone marrow cells fully differentiates along the myogenic pathway and participates in muscle repair in the mdx dystrophic mouse

2002 S. Corti, S. Strazzer, R. Del Bo, S. Salani, P. Bossolasco, F. Fortunato, F. Locatelli, D. Soligo, M. Moggio, P. Ciscato, A. Prelle, C. Borsotti, N. Bresolin, G. Scarlato, G. Comi

A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis

2012 R. Cagliani, F.R. Guerini, M. Fumagalli, S. Riva, C. Agliardi, D. Galimberti, U. Pozzoli, A. Goris, B. Dubois, C. Fenoglio, D. Forni, S. Sanna, I. Zara, M. Pitzalis, M. Zoledziewska, F. Cucca, F. Marini, G.P. Comi, E. Scarpini, N. Bresolin, M. Clerici, M. Sironi

Titolo	Data di pubblicazione	Autori	Tipo	Abstract
A novel mutation in the mitochondrial tRNA LeuCUN gene associated with a mitochondrial myopathy with respiratory impairment	2007	R. VirgilioA. BordoniD. RonchiF. SaladinoN. BresolinM. SciaccoG.P. Comi + -	Article (author)	-
A novel mutation in the ß-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance	2012	R. RomanielloA. TonelliF. ArrigoniC. BaschirottoF. TriulziN. BresolinM. BassiR. Borgatti + -	Article (author)	-
A Novel Nonsense Mutation in the APTX Gene Associated with Delayed DNA Single-strand Break Removal Fails to Enhance Sensitivity to Different Genotoxic Agents	2011	C. CrimellaO. CantoniA. GuidarelliC. VantaggiatoA. MartinuzziM. FioraniC. AzzoliniG. OrsoN. BresolinM. T. Bassi + -	Article (author)	-
A population genetics study of the familial Mediterranean fever gene : evidence of balancing selection under an overdominance regime	2009	M. FumagalliR. CaglianiU. PozzoliS. RivaG.P. ComiG. MenozziN. BresolinM. Sironi + -	Article (author)	-
A positively selected APOBEC3H haplotype is associated with natural resistance to HIV-1 infection	2011	R. CaglianiS. RivaM. FumagalliM. BiasinS. L. CaputoF. MazzottaL. PiacentiniU. PozzoliN. BresolinM. ClericiM. Sironi + -	Article (author)	-
A region in the dystrophin gene major hot-spot harbors a cluster of deletion breakpoints and generates double-strand breaks in yeast	2006	M. SironiU. PozzoliG.P. ComiS. RivaA. BordoniN. BresolinD. K. Nag + -	Article (author)	-
A severe pediatric case of congenital Myastenic Syndrome due to a novel mutation in COLQ gene	2013	S. BonatoD. PigaS. PagliaraniR. Del BoD. RonchiM. MoggioR. Di LenaP. CiscatoC. AgostoniA. BoccazziI. G. VetranoD. SpagnoliN. BresolinG.P. Comi + -	Article (author)	-
A stop codon mutation in the 5’ of the dystrophin gene associated to a Becker muscular dystrophy phenotype	2008	F. MagriR. VirgilioR. Del BoF. FortunatoS. GhezziR. CaglianiM. SironiM. G. D'AngeloV. CrugnolaM. MoggioN. BresolinG.P. Comi + -	Article (author)	-
A Subpopulation of murine bone marrow cells fully differentiates along the myogenic pathway and participates in muscle repair in the mdx dystrophic mouse	2002	S. CortiS. StrazzerR. Del BoS. SalaniP. BossolascoF. FortunatoF. LocatelliD. SoligoM. MoggioP. CiscatoA. PrelleC. BorsottiN. BresolinG. ScarlatoG. Comi + -	Article (author)	-
A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis	2012	R. CaglianiF. R. GueriniM. FumagalliS. RivaC. AgliardiD. GalimbertiU. PozzoliA. GorisB. DuboisC. FenoglioD. ForniS. SannaI. ZaraM. PitzalisM. ZoledziewskaF. CuccaF. MariniG.P. ComiE. ScarpiniN. BresolinM. ClericiM. Sironi + -	Article (author)	-

Risultati 31 - 40 di 677 (tempo di esecuzione: 0.255 secondi).

↑ Back to top

Legenda icone

file ad accesso aperto
file disponibili sulla rete interna
file disponibili agli utenti autorizzati
file disponibili solo agli amministratori
file sotto embargo
nessun file disponibile

Aggiungere filtri:

Aggiungi

Opzioni

Risultati/pagina

Ordina per

In ordine

Scopri

Accesso al fulltext

no fulltext 378
reserved 165
open 117
partially open 15
internalNetwork 2

IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

A novel mutation in the mitochondrial tRNA LeuCUN gene associated with a mitochondrial myopathy with respiratory impairment

A novel mutation in the ß-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance

A Novel Nonsense Mutation in the APTX Gene Associated with Delayed DNA Single-strand Break Removal Fails to Enhance Sensitivity to Different Genotoxic Agents

A population genetics study of the familial Mediterranean fever gene : evidence of balancing selection under an overdominance regime

A positively selected APOBEC3H haplotype is associated with natural resistance to HIV-1 infection

A region in the dystrophin gene major hot-spot harbors a cluster of deletion breakpoints and generates double-strand breaks in yeast

A severe pediatric case of congenital Myastenic Syndrome due to a novel mutation in COLQ gene

A stop codon mutation in the 5’ of the dystrophin gene associated to a Becker muscular dystrophy phenotype

A Subpopulation of murine bone marrow cells fully differentiates along the myogenic pathway and participates in muscle repair in the mdx dystrophic mouse

A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis

Legenda icone

Aggiungere filtri:

Opzioni

Scopri

Tipologia

Autore

Data di pubblicazione

Editore

Rivista

Settore disciplinare

Keyword

Lingua

Accesso al fulltext

Progetto