Giglio S - Search Results

1

Identification and characterization of a new human gene encoding a small protein with high homology to the proline-rich region of the SH3BGR gene.

Egeo A, Mazzocco M, Arrigo P, Vidal-Taboada JM, Oliva R, Pirola B, Giglio S, Rasore-Quartino A, Scartezzini P. Egeo A, et al. Among authors: giglio s. Biochem Biophys Res Commun. 1998 Jun 18;247(2):302-6. doi: 10.1006/bbrc.1998.8763. Biochem Biophys Res Commun. 1998. PMID: 9642120

2

Structure and mutation analysis of the glycogen storage disease type 1b gene.

Marcolongo P, Barone V, Priori G, Pirola B, Giglio S, Biasucci G, Zammarchi E, Parenti G, Burchell A, Benedetti A, Sorrentino V. Marcolongo P, et al. Among authors: giglio s. FEBS Lett. 1998 Oct 2;436(2):247-50. doi: 10.1016/s0014-5793(98)01129-6. FEBS Lett. 1998. PMID: 9781688 Free article.

3

Agenesis of the corpus callosum with Probst bundles owing to haploinsufficiency for a gene in an 8 cM region of 6q25.

Pirola B, Bortotto L, Giglio S, Piovan E, Janes A, Guerrini R, Zuffardi O. Pirola B, et al. Among authors: giglio s. J Med Genet. 1998 Dec;35(12):1031-3. doi: 10.1136/jmg.35.12.1031. J Med Genet. 1998. PMID: 9863602 Free PMC article.

4

GCMB, a second human homolog of the fly glide/gcm gene.

Kammerer M, Pirola B, Giglio S, Giangrande A. Kammerer M, et al. Among authors: giglio s. Cytogenet Cell Genet. 1999;84(1-2):43-7. doi: 10.1159/000015210. Cytogenet Cell Genet. 1999. PMID: 10343099

5

Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements.

Giglio S, Pirola B, Arrigo G, Dagrada P, Bardoni B, Bernardi F, Russo G, Argentiero L, Forabosco A, Carrozzo R, Zuffardi O. Giglio S, et al. Eur J Hum Genet. 2000 Jan;8(1):63-70. doi: 10.1038/sj.ejhg.5200394. Eur J Hum Genet. 2000. PMID: 10713889

6

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.

Giglio S, Graw SL, Gimelli G, Pirola B, Varone P, Voullaire L, Lerzo F, Rossi E, Dellavecchia C, Bonaglia MC, Digilio MC, Giannotti A, Marino B, Carrozzo R, Korenberg JR, Danesino C, Sujansky E, Dallapiccola B, Zuffardi O. Giglio S, et al. Circulation. 2000 Jul 25;102(4):432-7. doi: 10.1161/01.cir.102.4.432. Circulation. 2000. PMID: 10908216

7

A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere.

Gianfrancesco F, Esposito T, Montanini L, Ciccodicola A, Mumm S, Mazzarella R, Rao E, Giglio S, Rappold G, Forabosco A. Gianfrancesco F, et al. Among authors: giglio s. Hum Mol Genet. 1998 Mar;7(3):407-14. doi: 10.1093/hmg/7.3.407. Hum Mol Genet. 1998. PMID: 9466997

8

Inverted duplications: how many of them are mosaic?

Pramparo T, Giglio S, Gregato G, de Gregori M, Patricelli MG, Ciccone R, Scappaticci S, Mannino G, Lombardi C, Pirola B, Giorda R, Rocchi M, Zuffardi O. Pramparo T, et al. Among authors: giglio s. Eur J Hum Genet. 2004 Sep;12(9):713-7. doi: 10.1038/sj.ejhg.5201240. Eur J Hum Genet. 2004. PMID: 15266302

9

Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching.

Banfi S, Borsani G, Rossi E, Bernard L, Guffanti A, Rubboli F, Marchitiello A, Giglio S, Coluccia E, Zollo M, Zuffardi O, Ballabio A. Banfi S, et al. Among authors: giglio s. Nat Genet. 1996 Jun;13(2):167-74. doi: 10.1038/ng0696-167. Nat Genet. 1996. PMID: 8640222

10

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: giglio s. Genomics. 1998 Jul 15;51(2):243-50. doi: 10.1006/geno.1998.5348. Genomics. 1998. PMID: 9722947

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