Andrea Ballabio

发表

Drosophila-related expressed sequences.

G. Borsani, A. Ballabio, S. Banfi, 1997, Human molecular genetics.

Defective intracellular transport and processing of OA1 is a major cause of ocular albinism type 1.

A. Ballabio, M. De Luca, M. Clementi, 2000, Human molecular genetics.

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

E. Rugarli, A. Ballabio, C. Ghezzi, 1996, Human molecular genetics.

Characterization of a human and murine gene (CLCN3) sharing similarities to voltage-gated chloride channels and to a yeast integral membrane protein.

G. Borsani, E. Rugarli, A. Ballabio, 1995, Genomics.

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

G. Borsani, E. Rugarli, A. Ballabio, 1994, Human molecular genetics.

2012 Landes Bioscience. Do not distribute. Guidelines for the use and interpretation of assays for monitoring autophagy

Thomas J. Begley, H. Coller, F. Chisari, 2012 .

Barhl1, a gene belonging to a new subfamily of mammalian homeobox genes, is expressed in migrating neurons of the CNS.

A. Ballabio, V. Broccoli, S. Banfi, 2000, Human molecular genetics.

A 5' regulatory sequence containing two Ets motifs controls the expression of the Wiskott-Aldrich syndrome protein (WASP) gene in human hematopoietic cells.

A. Ballabio, P. Tassone, S. Venuta, 1998, Blood.

A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis.

G. Borsani, A. Ballabio, F. Fougerousse, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Identification of a new EGF-repeat-containing gene from human Xp22: a candidate for developmental disorders.

A. Ballabio, B. Franco, M. Bassi, 2000, Genomics.

A practical guide to orient yourself in the labyrinth of genome databases.

G. Borsani, A. Ballabio, S. Banfi, 1998, Human molecular genetics.