Nicola Migone

9q34 loss of heterozygosity in a tuberous sclerosis astrocytoma suggests a growth suppressor-like activity also for the TSC1 gene.

N. Migone, E. Grosso, C. Borrone, 1994, Human molecular genetics.

Selection by two powerful antigens may account for the presence of the major population of human peripheral gamma/delta T cells

A. Lanzavecchia, C. Giachino, P. Matzinger, 1991, The Journal of experimental medicine.

Antigen recognition by human T cell receptor gamma-positive lymphocytes. Specific lysis of allogeneic cells after activation in mixed lymphocyte culture

E. Ciccone, A. Moretta, C. Bottino, 1988, The Journal of experimental medicine.

A novel SH3-containing human gene family preferentially expressed in the central nervous system.

C. Giachino, L. Lanzetti, N. Migone, 1997, Genomics.

Genotype, phenotype and hormonal levels correlation in non-classical congenital adrenal hyperplasia

E. Menegatti, G. Motta, N. Migone, 2011, Journal of endocrinological investigation.

Selection by Two Powerful Antigens May Account for the Presence of the Major Population of Human Peripheral-y / 6 T Cells

A. Lanzavecchia, C. Giachino, P. Matzinger, 2003 .

FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia

B. Castellotti, C. Gellera, L. Orsi, 2005, Neurology.