ZOLLO, MASSIMO
ZOLLO, MASSIMO
DIPARTIMENTO DI MEDICINA MOLECOLARE E BIOTECNOLOGIE MEDICHE
Complete mutation scanning of the human SEL 1L gene: a candidate gene for type 1 diabetes.
2001 Larsen, Z. M; Zollo, Massimo
No evidence for SEL1L as a candidate gene for IDDM11-conferred susceptibility.
2001 Pociot, F; Zollo, Massimo
Molecular studies of marsupial X chromosomes reveal limited sequence homology of mammalian X-linked genes
1987 Kaslow, D. C.; 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.
1998 Piccini, M; Zollo, Massimo
Method to express and purify nm23-H2 protein from baculovirus-infected cells.
2003 Garzia, L; Zollo, Massimo
Identification by shotgun sequencing, genomic organization, and functional analysis of a fourth arylsulfatase gene (ARSF) from the Xp22.3 region.
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.
1998 Sperandeo, M. P.; Zollo, Massimo
Sequence and gene content in 52 kb including and centromeric to the G6PD gene in Xq28
1995 Zollo, Massimo
SEL1L, the human homolog of C. elegans sel-1: refined physical mapping, gene structure and identification of polymorphic markers
2000 Biunno, I; Zollo, Massimo
Identification of two paralogous regions mapping to the short and long arms of human chromosome 2 comprising LIS1 pseudogenes
1999 Fogli, A; Zollo, Massimo
Sequencing analysis of forty-eight human image cDNA clones similar to Drosophila mutant protein.
1998 Volorio, S; Zollo, Massimo
Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)
1996 Mastroianni, N; Zollo, Massimo
Evidence for interaction between human PRUNE and nm23-H1 NDPKinase
1999 Reymond, A.; Zollo, Massimo
Molecular heterogeneity of steroid sulfatase deficiency: a multicenter study on 57 unrelated patients, at DNA and protein levels.
1989 Ballabio, Andrea; R., Carrozzo; G., Parenti; A., Gil; Zollo, Massimo; M. G., Persico; E., Gillard; N., Affara; J., Yates; M. A., FERGUSON SMITH
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
1991 Ballabio, A; Zollo, Massimo; R., Carrozzo; A., Caiulo; O., Zuffardi; C. F., Cascioli; D., Viggiano; Strisciuglio, Pietro
Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification.
1990 Ballabio, Andrea; Ranier, J. E.; Chamberlain, J. S.; Zollo, Massimo; Caskey, C. T.
Use of a sensitive fluorescent intercalating dye to detect PCR products of low copy number and high molecular weight.
1993 Ohler, L. D.; Zollo, Massimo; Mansfield, E. S. ROSE E. A.
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.
1991 Ballabio, Andrea; Zollo, Massimo; Carrozzo, R; Caiulo, A; Zuffardi, O; Cascioli, Cf; Viggiano, D; Strisciuglio, Pietro
Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: evidence for an ancestral pseudoautosomal gene?
1987 Fraser, N; Ballabio, Andrea; Zollo, Massimo; Persico, G; Craig, I.
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
1997 Meroni, G; Zollo, Massimo