TGM97000/TI_/Telethon/Italy[Grants and Funding] - Search Results

Year	Number of Results
1997	18
1998	21
1999	26
2024	0

1

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

2

Evidence for interaction between human PRUNE and nm23-H1 NDPKinase.

Reymond A, Volorio S, Merla G, Al-Maghtheh M, Zuffardi O, Bulfone A, Ballabio A, Zollo M. Reymond A, et al. Oncogene. 1999 Dec 2;18(51):7244-52. doi: 10.1038/sj.onc.1203140. Oncogene. 1999. PMID: 10602478

3

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. Genomics. 1999 Nov 15;62(1):113-8. doi: 10.1006/geno.1999.6015. Genomics. 1999. PMID: 10585778

4

Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesity.

Ahmad W, De Fusco M, Faiyaz ul Haque M, Aridon P, Sarno T, Sohail M, ul Haque S, Ahmad M, Ballabio A, Franco B, Casari G. Ahmad W, et al. Eur J Hum Genet. 1999 Oct-Nov;7(7):828-32. doi: 10.1038/sj.ejhg.5200376. Eur J Hum Genet. 1999. PMID: 10573017

5

Expression of a novel human sialidase encoded by the NEU2 gene.

Monti E, Preti A, Nesti C, Ballabio A, Borsani G. Monti E, et al. Glycobiology. 1999 Dec;9(12):1313-21. doi: 10.1093/glycob/9.12.1313. Glycobiology. 1999. PMID: 10561456

6

Sequencing analysis of forty-eight human image cDNA clones similar to Drosophila mutant protein.

Volorio S, Simon G, Repetto M, Cucciardi M, Banfi S, Borsani G, Ballabio A, Zollo M. Volorio S, et al. DNA Seq. 1998;9(5-6):307-15. doi: 10.3109/10425179809008469. DNA Seq. 1998. PMID: 10524757

7

A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis.

Barbieri AM, Lupo G, Bulfone A, Andreazzoli M, Mariani M, Fougerousse F, Consalez GG, Borsani G, Beckmann JS, Barsacchi G, Ballabio A, Banfi S. Barbieri AM, et al. Proc Natl Acad Sci U S A. 1999 Sep 14;96(19):10729-34. doi: 10.1073/pnas.96.19.10729. Proc Natl Acad Sci U S A. 1999. PMID: 10485894 Free PMC article.

8

Expression pattern of the Tbr2 (Eomesodermin) gene during mouse and chick brain development.

Bulfone A, Martinez S, Marigo V, Campanella M, Basile A, Quaderi N, Gattuso C, Rubenstein JL, Ballabio A. Bulfone A, et al. Mech Dev. 1999 Jun;84(1-2):133-8. doi: 10.1016/s0925-4773(99)00053-2. Mech Dev. 1999. PMID: 10473127 Free article.

9

Ocular albinism: evidence for a defect in an intracellular signal transduction system.

Schiaffino MV, d'Addio M, Alloni A, Baschirotto C, Valetti C, Cortese K, Puri C, Bassi MT, Colla C, De Luca M, Tacchetti C, Ballabio A. Schiaffino MV, et al. Nat Genet. 1999 Sep;23(1):108-12. doi: 10.1038/12715. Nat Genet. 1999. PMID: 10471510

10

Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT.

Feliubadaló L, Font M, Purroy J, Rousaud F, Estivill X, Nunes V, Golomb E, Centola M, Aksentijevich I, Kreiss Y, Goldman B, Pras M, Kastner DL, Pras E, Gasparini P, Bisceglia L, Beccia E, Gallucci M, de Sanctis L, Ponzone A, Rizzoni GF, Zelante L, Bassi MT, George AL Jr, Manzoni M, De Grandi A, Riboni M, Endsley JK, Ballabio A, Borsani G, Reig N, Fernández E, Estévez R, Pineda M, Torrents D, Camps M, Lloberas J, Zorzano A, Palacín M; International Cystinuria Consortium. Feliubadaló L, et al. Nat Genet. 1999 Sep;23(1):52-7. doi: 10.1038/12652. Nat Genet. 1999. PMID: 10471498

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