Bassi MT - Search Results

1

Mapping of the murine tbl1 gene reveals a new rearrangement between mouse and human X Chromosomes.

Disteche CM, Dinulos MB, Bassi MT, Elliott RW, Rugarli EI. Disteche CM, et al. Among authors: bassi mt. Mamm Genome. 1998 Dec;9(12):1062-4. doi: 10.1007/s003359900926. Mamm Genome. 1998. PMID: 9880679 No abstract available.

2

A new region of conservation is defined between human and mouse X chromosomes.

Dinulos MB, Bassi MT, Rugarli EI, Chapman V, Ballabio A, Disteche CM. Dinulos MB, et al. Among authors: bassi mt. Genomics. 1996 Jul 1;35(1):244-7. doi: 10.1006/geno.1996.0347. Genomics. 1996. PMID: 8661129

3

Cloning of a human homologue of the Xenopus laevis APX gene from the ocular albinism type 1 critical region.

Schiaffino MV, Bassi MT, Rugarli EI, Renieri A, Galli L, Ballabio A. Schiaffino MV, et al. Among authors: bassi mt. Hum Mol Genet. 1995 Mar;4(3):373-82. doi: 10.1093/hmg/4.3.373. Hum Mol Genet. 1995. PMID: 7795590

4

A gene from the Xp22.3 region shares homology with voltage-gated chloride channels.

van Slegtenhorst MA, Bassi MT, Borsani G, Wapenaar MC, Ferrero GB, de Conciliis L, Rugarli EI, Grillo A, Franco B, Zoghbi HY, Ballabio A. van Slegtenhorst MA, et al. Among authors: bassi mt. Hum Mol Genet. 1994 Apr;3(4):547-52. doi: 10.1093/hmg/3.4.547. Hum Mol Genet. 1994. PMID: 8069296

5

Senataxin modulates neurite growth through fibroblast growth factor 8 signalling.

Vantaggiato C, Bondioni S, Airoldi G, Bozzato A, Borsani G, Rugarli EI, Bresolin N, Clementi E, Bassi MT. Vantaggiato C, et al. Among authors: bassi mt. Brain. 2011 Jun;134(Pt 6):1808-28. doi: 10.1093/brain/awr084. Epub 2011 May 15. Brain. 2011. PMID: 21576111

6

Pleiotropic effects of spastin on neurite growth depending on expression levels.

Riano E, Martignoni M, Mancuso G, Cartelli D, Crippa F, Toldo I, Siciliano G, Di Bella D, Taroni F, Bassi MT, Cappelletti G, Rugarli EI. Riano E, et al. Among authors: bassi mt. J Neurochem. 2009 Mar;108(5):1277-88. doi: 10.1111/j.1471-4159.2009.05875.x. Epub 2009 Jan 29. J Neurochem. 2009. PMID: 19141076 Free article.

7

Characterization and mutation analysis of human LEFTY A and LEFTY B, homologues of murine genes implicated in left-right axis development.

Kosaki K, Bassi MT, Kosaki R, Lewin M, Belmont J, Schauer G, Casey B. Kosaki K, et al. Among authors: bassi mt. Am J Hum Genet. 1999 Mar;64(3):712-21. doi: 10.1086/302289. Am J Hum Genet. 1999. PMID: 10053005 Free PMC article.

8

Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome.

Bassi MT, Schiaffino MV, Renieri A, De Nigris F, Galli L, Bruttini M, Gebbia M, Bergen AA, Lewis RA, Ballabio A. Bassi MT, et al. Nat Genet. 1995 May;10(1):13-9. doi: 10.1038/ng0595-13. Nat Genet. 1995. PMID: 7647783

9

A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22.

Wapenaar MC, Schiaffino MV, Bassi MT, Schaefer L, Chinault AC, Zoghbi HY, Ballabio A. Wapenaar MC, et al. Among authors: bassi mt. Hum Mol Genet. 1994 Jul;3(7):1155-61. doi: 10.1093/hmg/3.7.1155. Hum Mol Genet. 1994. PMID: 7981686

10

A submicroscopic deletion in a patient with isolated X-linked ocular albinism (OA1).

Bassi MT, Bergen AA, Wapenaar MC, Schiaffino MV, van Schooneveld M, Yates JR, Charles SJ, Meitinger T, Ballabio A. Bassi MT, et al. Hum Mol Genet. 1994 Apr;3(4):647-8. doi: 10.1093/hmg/3.4.647. Hum Mol Genet. 1994. PMID: 8069311 No abstract available.

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