Ballabio A - Search Results

1

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

2

Kallmann syndrome due to a translocation resulting in an X/Y fusion gene.

Guioli S, Incerti B, Zanaria E, Bardoni B, Franco B, Taylor K, Ballabio A, Camerino G. Guioli S, et al. Among authors: ballabio a. Nat Genet. 1992 Aug;1(5):337-40. doi: 10.1038/ng0892-337. Nat Genet. 1992. PMID: 1302031

3

Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes.

Incerti B, Guioli S, Pragliola A, Zanaria E, Borsani G, Tonlorenzi R, Bardoni B, Franco B, Wheeler D, Ballabio A, et al. Incerti B, et al. Among authors: ballabio a. Nat Genet. 1992 Dec;2(4):311-4. doi: 10.1038/ng1292-311. Nat Genet. 1992. PMID: 1303285

4

The gene for X-linked Kallmann syndrome: a human neuronal migration defect.

Ballabio A, Camerino G. Ballabio A, et al. Curr Opin Genet Dev. 1992 Jun;2(3):417-21. doi: 10.1016/s0959-437x(05)80152-2. Curr Opin Genet Dev. 1992. PMID: 1504616 Review.

5

Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome.

Ballabio A, Sebastio G, Carrozzo R, Parenti G, Piccirillo A, Persico MG, Andria G. Ballabio A, et al. Hum Genet. 1987 Dec;77(4):338-41. doi: 10.1007/BF00291422. Hum Genet. 1987. PMID: 3480263

6

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.

7

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

8

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

9

Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL gene.

Parenti G, Rizzolo MG, Ghezzi M, Di Maio S, Sperandeo MP, Incerti B, Franco B, Ballabio A, Andria G. Parenti G, et al. Among authors: ballabio a. Am J Med Genet. 1995 Jul 3;57(3):476-8. doi: 10.1002/ajmg.1320570323. Am J Med Genet. 1995. PMID: 7677154

10

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

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