ZOLLO, MASSIMO

ZOLLO, MASSIMO  

DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE  

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dentification and characterization of a novel transcript down-regulated in Dlx1/Dlx2 and up-regulated in Pax6 mutant telencephalon. 1.1 Articolo in rivista 2004 Faedo, A; Quinn, Jc; Stoney, P; Long, Je; Dye, C; Zollo, Massimo; Rubenstein, Jl; Price, Dj; Bulfone, A.
Finishing the euchromatic sequence of the human genome 1.1 Articolo in rivista 2004 F. . S., Collins; Zollo, Massimo
FACL4, a new gene encoding Long-Chain Acyl-CoA Synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation. 1.1 Articolo in rivista 1998 Piccini, M; Vitelli, F; Bruttini, M; Pober, B. R.; Jonsson, J. J.; Villanova, M; Zollo, Massimo; Borsani, G; Ballabio, Andrea; Renieri, A.
A method to direct sequence cosmid LAWRIST16 clones. 1.1 Articolo in rivista 1997 Repetto, M; Ballabio, Andrea; Zollo, Massimo
Identification by shotgun sequencing, genomic organization, and functional analysis of a fourth arylsulphatase gene (ARSF) from the Xp22.3 region. 1.1 Articolo in rivista 1997 Puca, A. A.; Zollo, Massimo; Repetto, M; Andolfi, G; Guffanti, A; Simon, G; Ballabio, Andrea; Franco, Brunella
A mammalian homolog of the Drosophila retinal degeneration B gene: implications for the evolution of phototransduction mechanisms. 1.1 Articolo in rivista 1997 Rubboli, F; Bulfone, A; Bogni, S; Marchitiello, A; Zollo, Massimo; Borsani, G; Ballabio, Andrea; Banfi, S.
Evidence for interaction between human PRUNE and nm23-H1 NDPKinase. 1.1 Articolo in rivista 1999 Reymond, A; Volorio, S; Merla, G; Almaghtheh, M; Zuffardi, O; Bulfone, A; Ballabio, Andrea; Zollo, Massimo
New mutations identified in the ocular albinism type 1 gene. 1.1 Articolo in rivista 2007 Roma, C; Ferrante, P; Guardiola, O; Ballabio, Andrea; Zollo, Massimo
Tagging genes with cassette-exchange sites. 1.1 Articolo in rivista 2005 Cobellis, G.; Nicolaus, G.; Iovino, M.; Romito, A.; Marra, E.; Barbarisi, M.; Sardiello, M.; DI GIORGIO, F. P.; Iovini, N.; Zollo, Massimo; Ballabio, Andrea; Cortese, R.
Telencephalic embryonic subtractive sequences: a unique collection of neurodevelopmental genes. 1.1 Articolo in rivista 2005 Bulfone, A.; Carotenuto, P.; Faedo, A.; Aglio, V.; Garzia, L.; Bello, A. M.; Basile, A.; Andre, A.; Cocchia, M.; Guardiola, O.; Ballabio, Andrea; Rubenstein, J. L.; Zollo, Massimo
The aberrant host response to EBV infection in X-linked Lymphoproliferative disease results from mutations in a novel SH2-domain encoding gene 1.1 Articolo in rivista 1998 Aj, Coffey; Ra, Brooksbank; O., Brandau; T., Oohasai; Gr, Howell; Jm, Bye; Ap, Cahn; J., Durham; P., Heath; P., Wray; R., Pavitt; J., Wilkinson; M., Leversha; E., Huckle; CJ SHAW, Smith; A., Dunham; S., Rhodes; V., Schuster; G., Porta; L., Yin; P., Serafini; B., Sylla; Zollo, Massimo; Franco, Brunella; A., Bolino; M., Seri; A., Lanyi; Jr, Davis; D., Webster; A., Harris; G., Lenoir; G., DE ST BASILE; A., Jones; Bh, Behloradsky; H., Achatz; J., Murken; R., Faessler; J., Sumegi; G., Romeo; M., Vaudin; Mt, Ross; A. MEINDL DR B. E. N. T. L. E., Y.
A new candidate region for the positional cloning of the XLP gene 1.1 Articolo in rivista 1998 A., Bolino; L., Yi; M., Seri; R., Cusano; R., Cinti; A., Coffey; R., Brooksbank; G., Howell; D., Bentley; Jr, Davis; A., Lanyi; D., Huang; M., Stark; M., Creaven; L., Bjrkhaug; F., Heitzmann; J., Lamartine; S., Gaudi; Bs, Sylla; Gm, Lenoir; E., Castagnola; R., Giacchino; G., Porta; Franco, Brunella; Zollo, Massimo; J., Sumegi; G., Romeo
Identification by shotgun sequencing, genomic organization, and functional analysis of a fourth arylsulfatase gene (ARSF) from the Xp22.3 region. 1.1 Articolo in rivista 1997 Puca, A. A.; Zollo, Massimo; M., Repetto; G., Andolfi; A., Guffanti; G., Simon; A. BALLABIO AND B., Franco
The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome. 1.1 Articolo in rivista 1998 Sperandeo, M. P.; Zollo, Massimo
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching. 1.1 Articolo in rivista 1996 Banfi, S; G., Borsani; E., Rossi; L., Bernard; A., Guffanti; F., Rubboli; A., Marchitiello; S., Giglio; E., Coluccia; Zollo, Massimo; O. ZUFFARDI AND A., Ballabio
Sequence of mouse glucose-6-phosphate dehydrogenase cDNA. 1.1 Articolo in rivista 1993 Zollo, Massimo; D'Urso, M; Schlessinger, D; Chen, E. Y.
Method to express and purify nm23-H2 protein from baculovirus-infected cells. 1.1 Articolo in rivista 2003 Garzia, L; Zollo, Massimo
Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiency 1.1 Articolo in rivista 1991 Ballabio, A; Zollo, Massimo; R., Carrozzo; A., Caiulo; O., Zuffardi; C. F., Cascioli; D., Viggiano; Strisciuglio, Pietro
Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels. 1.1 Articolo in rivista 1989 Ballabio, Andrea; R., Carrozzo; G., Parenti; A., Gil; Zollo, Massimo; M. G., Persico; E., Gillard; N., Affara; J., Yates; M. A., FERGUSON SMITH
Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor 1.1 Articolo in rivista 1997 Meroni, G; Zollo, Massimo