AAAAAA

   
Results: 1-8 |
Results: 8
TSC1 and TSC2 deletions differ in size, preference for recombinatorial sequences, and location within the gene
Authors: Longa, L Saluto, A Brusco, A Polidoro, S Padovan, S Allavena, A Carbonara, C Grosso, E Migone, N
Citation: L. Longa et al., TSC1 and TSC2 deletions differ in size, preference for recombinatorial sequences, and location within the gene, HUM GENET, 108(2), 2001, pp. 156-166
Treatment of the pulmonary involvement in the patient with tuberous sclerosis complex
Authors: Roccatello, D Obert, R Sena, GM Longa, L Rossi, D Grosso, E Cavallo, R Sena, LM Giachino, O Migone, N
Citation: D. Roccatello et al., Treatment of the pulmonary involvement in the patient with tuberous sclerosis complex, CONTR NEPHR, 136, 2001, pp. 292-298
Molecular genetic analysis of von Hippel-Lindau disease by denaturing high-performance liquid chromatography
Authors: Menegatti, E Ferrone, M Gallone, S Mameli, M Grosso, E Migone, N
Citation: E. Menegatti et al., Molecular genetic analysis of von Hippel-Lindau disease by denaturing high-performance liquid chromatography, CONTR NEPHR, 136, 2001, pp. 306-311
Two different types of renal involvement in tuberous sclerosis complex
Authors: Scolari, F Viola, BF Grazioli, L Longa, L Migone, N Maiorca, R
Citation: F. Scolari et al., Two different types of renal involvement in tuberous sclerosis complex, CONTR NEPHR, 136, 2001, pp. 318-324
Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease
Authors: Janssens, K Gershoni-Baruch, R Guanabens, N Migone, N Ralston, S Bonduelle, M Lissens, W Van Maldergem, L Vanhoenacker, F Verbruggen, L Van Hul, W
Citation: K. Janssens et al., Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease, NAT GENET, 26(3), 2000, pp. 273-275
Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13
Authors: Janssens, K Gershoni-Baruch, R Van Hul, E Brik, R Guanabens, N Migone, N Verbruggen, LA Ralston, SH Bonduelle, M Van Maldergem, L Vanhoenacker, F Van Hul, W
Citation: K. Janssens et al., Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13, J MED GENET, 37(4), 2000, pp. 245-249
Polycystin-1 expression in PKD1, early-onset PKD1, and TSC2/PKD1 cystic tissue
Authors: Ong, ACM Harris, PC Davies, DR Pritchard, L Rossetti, S Biddolph, S Vaux, DJT Migone, N Ward, CJ
Citation: Acm. Ong et al., Polycystin-1 expression in PKD1, early-onset PKD1, and TSC2/PKD1 cystic tissue, KIDNEY INT, 56(4), 1999, pp. 1324-1333
The SH3 domains of endophilin and amphiphysin bind to the proline-rich region of synaptojanin 1 at distinct sites that display an unconventional binding specificity
Authors: Cestra, G Castagnoli, L Dente, L Minenkova, O Petrelli, A Migone, N Hoffmuller, U Schneider-Mergener, J Cesareni, G
Citation: G. Cestra et al., The SH3 domains of endophilin and amphiphysin bind to the proline-rich region of synaptojanin 1 at distinct sites that display an unconventional binding specificity, J BIOL CHEM, 274(45), 1999, pp. 32001-32007
Risultati: 1-8 |