Borsani G - Search Results

1

FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation.

Piccini M, Vitelli F, Bruttini M, Pober BR, Jonsson JJ, Villanova M, Zollo M, Borsani G, Ballabio A, Renieri A. Piccini M, et al. Among authors: borsani g. Genomics. 1998 Feb 1;47(3):350-8. doi: 10.1006/geno.1997.5104. Genomics. 1998. PMID: 9480748 Free article.

2

The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome.

Sperandeo MP, Borsani G, Incerti B, Zollo M, Rossi E, Zuffardi O, Castaldo P, Taglialatela M, Andria G, Sebastio G. Sperandeo MP, et al. Among authors: borsani g. Genomics. 1998 Apr 15;49(2):230-6. doi: 10.1006/geno.1998.5252. Genomics. 1998. PMID: 9598310

3

Cloning and characterization of NEU2, a human gene homologous to rodent soluble sialidases.

Monti E, Preti A, Rossi E, Ballabio A, Borsani G. Monti E, et al. Among authors: borsani g. Genomics. 1999 Apr 1;57(1):137-43. doi: 10.1006/geno.1999.5749. Genomics. 1999. PMID: 10191093

4

Characterization of a human and murine gene (CLCN3) sharing similarities to voltage-gated chloride channels and to a yeast integral membrane protein.

Borsani G, Rugarli EI, Taglialatela M, Wong C, Ballabio A. Borsani G, et al. Genomics. 1995 May 1;27(1):131-41. doi: 10.1006/geno.1995.1015. Genomics. 1995. PMID: 7665160

5

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. Among authors: borsani g. Genomics. 1999 Dec 1;62(2):297-303. doi: 10.1006/geno.1999.5978. Genomics. 1999. PMID: 10610726

6

Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil alpha-helical domains.

de Conciliis L, Marchitiello A, Wapenaar MC, Borsani G, Giglio S, Mariani M, Consalez GG, Zuffardi O, Franco B, Ballabio A, Banfi S. de Conciliis L, et al. Among authors: borsani g. Genomics. 1998 Jul 15;51(2):243-50. doi: 10.1006/geno.1998.5348. Genomics. 1998. PMID: 9722947

7

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: borsani g. Genomics. 2004 Mar;83(3):445-53. doi: 10.1016/j.ygeno.2003.08.019. Genomics. 2004. PMID: 14962670

8

Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8.

Mills KA, Mathews KD, Scherpbier-Heddema T, Buetow KH, Baldini A, Ballabio A, Borsani G. Mills KA, et al. Among authors: borsani g. Genomics. 1996 Sep 1;36(2):374-6. doi: 10.1006/geno.1996.0480. Genomics. 1996. PMID: 8812471 No abstract available.

9

Drosophila-related expressed sequences.

Banfi S, Borsani G, Bulfone A, Ballabio A. Banfi S, et al. Among authors: borsani g. Hum Mol Genet. 1997;6(10):1745-53. doi: 10.1093/hmg/6.10.1745. Hum Mol Genet. 1997. PMID: 9300667 Review.

10

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. Among authors: borsani g. Am J Hum Genet. 1999 Jun;64(6):1604-16. doi: 10.1086/302408. Am J Hum Genet. 1999. PMID: 10330347 Free PMC article.

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