20
results
for author:"D'Angelo M."
in Literature Citations
| Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum. Crimella C., Arnoldi A., Crippa F., Mostacciuolo M.L., Boaretto F., Sironi M., D'Angelo M.G., Manzoni S., Piccinini L., Turconi A.C. et al. J. Med. Genet. 46:345-351(2009) · Mapped (6) |
| Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction. Del Bo R., Moggio M., Rango M., Bonato S., D'Angelo M.G., Ghezzi S., Airoldi G., Bassi M.T., Guglieri M., Napoli L. et al. Neurology 71:1959-1966(2008) · Mapped (6) |
| A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia. Arnoldi A., Tonelli A., Crippa F., Villani G., Pacelli C., Sironi M., Pozzoli U., D'Angelo M.G., Meola G., Martinuzzi A. et al. Hum. Mutat. 29:522-531(2008) · Mapped (4) |
| Autologous transplantation of muscle-derived CD133+ stem cells in Duchenne muscle patients. Torrente Y., Belicchi M., Marchesi C., Dantona G., Cogiamanian F., Pisati F., Gavina M., Giordano R., Tonlorenzi R., Fagiolari G. et al. Cell Transplant 16:563-577(2007) · Mapped (10) |
| Ser58 of mouse p53 is the homologue of human Ser46 and is phosphorylated by HIPK2 in apoptosis. Cecchinelli B., Porrello A., Lazzari C., Gradi A., Bossi G., D'Angelo M., Sacchi A., Soddu S. Cell Death Differ. 13:1994-1997(2006) · Mapped (19) |
| Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia. Crippa F., Panzeri C., Martinuzzi A., Arnoldi A., Redaelli F., Tonelli A., Baschirotto C., Vazza G., Mostacciuolo M.L., Daga A. et al. |
| Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene. Tonelli A., D'Angelo M.G., Salati R., Villa L., Germinasi C., Frattini T., Meola G., Turconi A.C., Bresolin N., Bassi M.T. J. Neurol. Sci. 241:13-17(2006) · Mapped (7) |
| Life at depth: Photobacterium profundum genome sequence and expression analysis. Vezzi A., Campanaro S., D'Angelo M., Simonato F., Vitulo N., Lauro F.M., Cestaro A., Malacrida G., Simionati B., Cannata N. et al. Science 307:1459-1461(2005) · UniProtKB (5,328) |
| Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population. Cagliani R., Fortunato F., Giorda R., Rodolico C., Bonaglia M.C., Sironi M., D'Angelo M.G., Prelle A., Locatelli F., Toscano A. et al. Neuromuscul. Disord. 13:788-795(2003) · UniProtKB (1) |
| MDM4 (MDMX) overexpression enhances stabilization of stress-induced p53 and promotes apoptosis. Mancini F., Gentiletti F., D'Angelo M., Giglio S., Nanni S., D'Angelo C., Farsetti A., Citro G., Sacchi A., Pontecorvi A. et al. J. Biol. Chem. 279:8169-8180(2004) · Mapped (11) |
| Identification, characterization and subcellular localization of TcPDE1, a novel cAMP-specific phosphodiesterase from Trypanosoma cruzi. D'Angelo M.A., Sanguineti S., Reece J.M., Birnbaumer L., Torres H.N., Flawia M.M. Biochem. J. 378:63-72(2004) · UniProtKB (2) |
| The osteopetrotic mutation toothless (tl) is a loss-of-function frameshift mutation in the rat Csf1 gene: evidence of a crucial role for CSF-1 in osteoclastogenesis and endochondral ossification. Van Wesenbeeck L., Odgren P.R., MacKay C.A., D'Angelo M., Safadi F.F., Popoff S.N., Van Hul W., Marks S.C. Jr. Proc. Natl. Acad. Sci. U.S.A. 99:14303-14308(2002) · UniProtKB (2) · Mapped (4) |
| MDMX stability is regulated by p53-induced caspase cleavage in NIH3T3 mouse fibroblasts. Gentiletti F., Mancini F., D'Angelo M., Sacchi A., Pontecorvi A., Jochemsen A.G., Moretti F. Oncogene 21:867-877(2002) · Mapped (42) |
| Sequence and analysis of chromosome 3 of the plant Arabidopsis thaliana. Salanoubat M., Lemcke K., Rieger M., Ansorge W., Unseld M., Fartmann B., Valle G., Bloecker H., Perez-Alonso M., Obermaier B. et al. Nature 408:820-822(2000) · UniProtKB (5,349) |
| Gene disruption and basic phenotypic analysis of nine novel yeast genes from chromosome XIV. Capozzo C., Sartorello F., Dal Pero F., D'Angelo M., Vezzi A., Campanaro S., Valle G. |
| Transplacental injection of somite-derived cells in mdx mouse embryos for the correction of dystrophin deficiency. Torrente Y., D'Angelo M.G., Li Z., Del Bo R., Corti S., Mericskay M., DeLiso A., Fassati A., Paulin D., Comi G.P. et al. Hum. Mol. Genet. 9:1843-1852(2000) · Mapped (7) |
| Extracorporeal circulation as a new experimental pathway for myoblast implantation in mdx mice. Torrente Y., D'Angelo M.G., Del Bo R., DeLiso A., Casati R., Benti R., Corti S., Comi G.P., Gerundini P., Anichini A. et al. Cell Transplant 8:247-258(1999) · Mapped (7) |
| The nucleotide sequence of Saccharomyces cerevisiae chromosome XIV and its evolutionary implications. Philippsen P., Kleine K., Poehlmann R., Duesterhoeft A., Hamberg K., Hegemann J.H., Obermaier B., Urrestarazu L.A., Aert R., Albermann K. et al. Nature 387:93-98(1997) · UniProtKB (1,259) |
| The DNA sequence of cosmid 14-13b from chromosome XIV of Saccharomyces cerevisiae reveals an unusually high number of overlapping open reading frames. de Antoni A., D'Angelo M., Dal Pero F., Sartorello F., Pandolfo D., Pallavicini A., Lanfranchi G., Valle G. Yeast 13:261-266(1997) · UniProtKB (19) |
| TGF beta 1 regulation of collagen metabolism by embryonic palate mesenchymal cells. D'Angelo M., Chen J.M., Ugen K., Greene R.M. J. Exp. Zool. 270:189-201(1994) · Mapped (5) |
