Ballabio A - Search Results

1

Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport.

Ferreirinha F, Quattrini A, Pirozzi M, Valsecchi V, Dina G, Broccoli V, Auricchio A, Piemonte F, Tozzi G, Gaeta L, Casari G, Ballabio A, Rugarli EI. Ferreirinha F, et al. Among authors: ballabio a. J Clin Invest. 2004 Jan;113(2):231-42. doi: 10.1172/JCI20138. J Clin Invest. 2004. PMID: 14722615 Free PMC article.

2

Reelin: a novel extracellular matrix protein involved in brain lamination.

Rugarli EI, Ballabio A. Rugarli EI, et al. Among authors: ballabio a. Bioessays. 1995 Oct;17(10):832-4. doi: 10.1002/bies.950171003. Bioessays. 1995. PMID: 7487964 Review.

3

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. Among authors: ballabio a. Genomics. 1995 May 1;27(1):131-41. doi: 10.1006/geno.1995.1015. Genomics. 1995. PMID: 7665160

4

Different chromosomal localization of the Clcn4 gene in Mus spretus and C57BL/6J mice.

Rugarli EI, Adler DA, Borsani G, Tsuchiya K, Franco B, Hauge X, Disteche C, Chapman V, Ballabio A. Rugarli EI, et al. Among authors: ballabio a. Nat Genet. 1995 Aug;10(4):466-71. doi: 10.1038/ng0895-466. Nat Genet. 1995. PMID: 7670496

5

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: ballabio a. Hum Mol Genet. 1995 Mar;4(3):373-82. doi: 10.1093/hmg/4.3.373. Hum Mol Genet. 1995. PMID: 7795590

6

Kallmann syndrome. From genetics to neurobiology.

Rugarli EI, Ballabio A. Rugarli EI, et al. Among authors: ballabio a. JAMA. 1993 Dec 8;270(22):2713-6. doi: 10.1001/jama.270.22.2713. JAMA. 1993. PMID: 8133589 Review. No abstract available.

7

Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting.

Rugarli EI, Lutz B, Kuratani SC, Wawersik S, Borsani G, Ballabio A, Eichele G. Rugarli EI, et al. Among authors: ballabio a. Nat Genet. 1993 May;4(1):19-26. doi: 10.1038/ng0593-19. Nat Genet. 1993. PMID: 8513320

8

The locus for a novel syndromic form of neuronal intestinal pseudoobstruction maps to Xq28.

Auricchio A, Brancolini V, Casari G, Milla PJ, Smith VV, Devoto M, Ballabio A. Auricchio A, et al. Among authors: ballabio a. Am J Hum Genet. 1996 Apr;58(4):743-8. Am J Hum Genet. 1996. PMID: 8644737 Free PMC article.

9

Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3).

Mastroianni N, De Fusco M, Zollo M, Arrigo G, Zuffardi O, Bettinelli A, Ballabio A, Casari G. Mastroianni N, et al. Among authors: ballabio a. Genomics. 1996 Aug 1;35(3):486-93. doi: 10.1006/geno.1996.0388. Genomics. 1996. PMID: 8812482

10

The Kallmann syndrome gene product expressed in COS cells is cleaved on the cell surface to yield a diffusible component.

Rugarli EI, Ghezzi C, Valsecchi V, Ballabio A. Rugarli EI, et al. Among authors: ballabio a. Hum Mol Genet. 1996 Aug;5(8):1109-15. doi: 10.1093/hmg/5.8.1109. Hum Mol Genet. 1996. PMID: 8842728

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