Bassi MT - Search Results

1

Identification and expression of NEU3, a novel human sialidase associated to the plasma membrane.

Monti E, Bassi MT, Papini N, Riboni M, Manzoni M, Venerando B, Croci G, Preti A, Ballabio A, Tettamanti G, Borsani G. Monti E, et al. Among authors: bassi mt. Biochem J. 2000 Jul 1;349(Pt 1):343-51. doi: 10.1042/0264-6021:3490343. Biochem J. 2000. PMID: 10861246 Free PMC article.

2

Cloning of the gene encoding a novel integral membrane protein, mucolipidin-and identification of the two major founder mutations causing mucolipidosis type IV.

Bassi MT, Manzoni M, Monti E, Pizzo MT, Ballabio A, Borsani G. Bassi MT, et al. Am J Hum Genet. 2000 Nov;67(5):1110-20. doi: 10.1016/S0002-9297(07)62941-3. Epub 2000 Sep 29. Am J Hum Genet. 2000. PMID: 11013137 Free PMC article.

3

Molecular cloning and characterization of NEU4, the fourth member of the human sialidase gene family.

Monti E, Bassi MT, Bresciani R, Civini S, Croci GL, Papini N, Riboni M, Zanchetti G, Ballabio A, Preti A, Tettamanti G, Venerando B, Borsani G. Monti E, et al. Among authors: bassi mt. Genomics. 2004 Mar;83(3):445-53. doi: 10.1016/j.ygeno.2003.08.019. Genomics. 2004. PMID: 14962670

4

SLC7A7, encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance.

Borsani G, Bassi MT, Sperandeo MP, De Grandi A, Buoninconti A, Riboni M, Manzoni M, Incerti B, Pepe A, Andria G, Ballabio A, Sebastio G. Borsani G, et al. Among authors: bassi mt. Nat Genet. 1999 Mar;21(3):297-301. doi: 10.1038/6815. Nat Genet. 1999. PMID: 10080183

5

X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeats.

Bassi MT, Ramesar RS, Caciotti B, Winship IM, De Grandi A, Riboni M, Townes PL, Beighton P, Ballabio A, Borsani G. Bassi MT, et al. Am J Hum Genet. 1999 Jun;64(6):1604-16. doi: 10.1086/302408. Am J Hum Genet. 1999. PMID: 10330347 Free PMC article.

6

Identification and characterization of AFG3L2, a novel paraplegin-related gene.

Banfi S, Bassi MT, Andolfi G, Marchitiello A, Zanotta S, Ballabio A, Casari G, Franco B. Banfi S, et al. Among authors: bassi mt. Genomics. 1999 Jul 1;59(1):51-8. doi: 10.1006/geno.1999.5818. Genomics. 1999. PMID: 10395799

7

Identification of a novel homolog of the Drosophila staufen protein in the chromosome 8q13-q21.1 region.

Buchner G, Bassi MT, Andolfi G, Ballabio A, Franco B. Buchner G, et al. Among authors: bassi mt. Genomics. 1999 Nov 15;62(1):113-8. doi: 10.1006/geno.1999.6015. Genomics. 1999. PMID: 10585778

8

SLC7A8, a gene mapping within the lysinuric protein intolerance critical region, encodes a new member of the glycoprotein-associated amino acid transporter family.

Bassi MT, Sperandeo MP, Incerti B, Bulfone A, Pepe A, Surace EM, Gattuso C, De Grandi A, Buoninconti A, Riboni M, Manzoni M, Andria G, Ballabio A, Borsani G, Sebastio G. Bassi MT, et al. Genomics. 1999 Dec 1;62(2):297-303. doi: 10.1006/geno.1999.5978. Genomics. 1999. PMID: 10610726

9

Identification of a new EGF-repeat-containing gene from human Xp22: a candidate for developmental disorders.

Buchner G, Orfanelli U, Quaderi N, Bassi MT, Andolfi G, Ballabio A, Franco B. Buchner G, et al. Among authors: bassi mt. Genomics. 2000 Apr 1;65(1):16-23. doi: 10.1006/geno.2000.6146. Genomics. 2000. PMID: 10777661

10

Identification and characterisation of human xCT that co-expresses, with 4F2 heavy chain, the amino acid transport activity system xc-.

Bassi MT, Gasol E, Manzoni M, Pineda M, Riboni M, Martín R, Zorzano A, Borsani G, Palacín M. Bassi MT, et al. Pflugers Arch. 2001 May;442(2):286-96. doi: 10.1007/s004240100537. Pflugers Arch. 2001. PMID: 11417227

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