Andolfi G - Search Results

1

Identification of SCML2, a second human gene homologous to the Drosophila sex comb on midleg (Scm): A new gene cluster on Xp22.

Montini E, Buchner G, Spalluto C, Andolfi G, Caruso A, den Dunnen JT, Trump D, Rocchi M, Ballabio A, Franco B. Montini E, et al. Among authors: andolfi g. Genomics. 1999 May 15;58(1):65-72. doi: 10.1006/geno.1999.5755. Genomics. 1999. PMID: 10331946

2

Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region.

Meroni G, Franco B, Archidiacono N, Messali S, Andolfi G, Rocchi M, Ballabio A. Meroni G, et al. Among authors: andolfi g. Hum Mol Genet. 1996 Apr;5(4):423-31. doi: 10.1093/hmg/5.4.423. Hum Mol Genet. 1996. PMID: 8845834

3

Identification by shotgun sequencing, genomic organization, and functional analysis of a fourth arylsulfatase gene (ARSF) from the Xp22.3 region.

Puca AA, Zollo M, Repetto M, Andolfi G, Guffanti A, Simon G, Ballabio A, Franco B. Puca AA, et al. Among authors: andolfi g. Genomics. 1997 Jun 1;42(2):192-9. doi: 10.1006/geno.1997.4716. Genomics. 1997. PMID: 9192838

4

A novel human serine-threonine phosphatase related to the Drosophila retinal degeneration C (rdgC) gene is selectively expressed in sensory neurons of neural crest origin.

Montini E, Rugarli EI, Van de Vosse E, Andolfi G, Mariani M, Puca AA, Consalez GG, den Dunnen JT, Ballabio A, Franco B. Montini E, et al. Among authors: andolfi g. Hum Mol Genet. 1997 Jul;6(7):1137-45. doi: 10.1093/hmg/6.7.1137. Hum Mol Genet. 1997. PMID: 9215685

5

Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region.

Montini E, Andolfi G, Caruso A, Buchner G, Walpole SM, Mariani M, Consalez G, Trump D, Ballabio A, Franco B. Montini E, et al. Among authors: andolfi g. Genomics. 1998 Aug 1;51(3):427-33. doi: 10.1006/geno.1998.5391. Genomics. 1998. PMID: 9721213

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: andolfi g. Genomics. 1999 Jul 1;59(1):51-8. doi: 10.1006/geno.1999.5818. Genomics. 1999. PMID: 10395799

7

MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development.

Buchner G, Montini E, Andolfi G, Quaderi N, Cainarca S, Messali S, Bassi MT, Ballabio A, Meroni G, Franco B. Buchner G, et al. Among authors: andolfi g. Hum Mol Genet. 1999 Aug;8(8):1397-407. doi: 10.1093/hmg/8.8.1397. Hum Mol Genet. 1999. PMID: 10400986

8

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

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: andolfi g. Genomics. 2000 Apr 1;65(1):16-23. doi: 10.1006/geno.2000.6146. Genomics. 2000. PMID: 10777661

10

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22.

Quaderi NA, Schweiger S, Gaudenz K, Franco B, Rugarli EI, Berger W, Feldman GJ, Volta M, Andolfi G, Gilgenkrantz S, Marion RW, Hennekam RC, Opitz JM, Muenke M, Ropers HH, Ballabio A. Quaderi NA, et al. Among authors: andolfi g. Nat Genet. 1997 Nov;17(3):285-91. doi: 10.1038/ng1197-285. Nat Genet. 1997. PMID: 9354791 Free article.

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