A. Egeo

发表

The Dlx5 homeodomain gene is essential for olfactory development and connectivity in the mouse

G. Merlo, G. Levi, S. Mantero, 2003, Molecular and Cellular Neuroscience.

Developmental expression of the SH3BGR gene, mapping to the Down syndrome heart critical region

C. Sandri, S. Schiaffino, P. Scartezzini, 2000, Mechanisms of Development.

TBX3, the gene mutated in ulnar-mammary syndrome, promotes growth of mammary epithelial cells via repression of p19ARF, independently of p53

G. Merlo, I. Zucchi, G. Bertoli, 2007, Cell and Tissue Research.

Novel TBX3 mutation data in families with ulnar-mammary syndrome indicate a genotype-phenotype relationship: mutations that do not disrupt the T-domain are associated with less severe limb defects.

G. Merlo, S. Odent, N. Platonova, 2006, European journal of medical genetics.

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

F. Zara, F. Sotgia, M. Lisanti, 1998, Nature Genetics.

Identification and characterization of a new gene from human chromosome 21 between markers D21S343 and D21S268 encoding a leucine-rich protein.

P. Scartezzini, R. Oliva, J. Vidal-Taboada, 1998, Biochemical and biophysical research communications.

The identification of a novel human homologue of the SH3 binding glutamic acid-rich (SH3BGR) gene establishes a new family of highly conserved small proteins related to Thioredoxin Superfamily.

F. Ghiotto, P. Arrigo, P. Scartezzini, 2002, Gene.

Identification and characterization of a new human gene encoding a small protein with high homology to the proline-rich region of the SH3BGR gene.

P. Arrigo, S. Giglio, P. Scartezzini, 1998, Biochemical and biophysical research communications.

Identification and characterization of a new human cDNA from chromosome 21q22.3 encoding a basic nuclear protein

D. Nižetić, F. Sotgia, P. Arrigo, 1998, Human Genetics.

Cloning a new human gene from chromosome 21q22.3 encoding a glutamic acid-rich protein expressed in heart and skeletal muscle

D. Nižetić, S. Colella, R. Taramelli, 1997, Human Genetics.

High resolution physical mapping and identification of transcribed sequences in the Down syndrome region-2.

E. Fisher, D. Nižetić, N. Katsanis, 1998, Biochemical and biophysical research communications.

Human NRD convertase: a highly conserved metalloendopeptidase expressed at specific sites during development and in adult tissues.

A. Simeone, A. Pizzuti, R. Taramelli, 1998, Genomics.

High-resolution physical map and identification of potentially regulatory sequences of the human SH3BGR located in the Down syndrome chromosomal region.

D. Nižetić, P. Scartezzini, R. Oliva, 1997, Biochemical and biophysical research communications.

A novel human homologue of the SH3BGR gene encodes a small protein similar to Glutaredoxin 1 of Escherichia coli.

R. Ravazzolo, F. Ghiotto, P. Arrigo, 2001, Biochemical and biophysical research communications.