Sfoglia per Autore
Blue light induced differentiation in Phycomyces blakesleeanus : The Blue Light Syndrome
1980 V.E.A. Russo, P. Galland, M. Toselli, L. Volpi
Carbon-dioxide inhibits phorogenesis in phycomyces and blue-light overcomes this inhibition
1981 V.E.A. Russo, U. Pohl, L. Volpi
Activation of c-fos and c-fes in metastatic lympho-macrophage hybrids
1992 S. Fumagalli, L. Volpi, D. Rossi, L. Larizza
On the paternal origin of the chromosomes in a 49,XXXXX fetus.
1994 L. Volpi, P. Riva, L. Dalprà, M.G. Tibiletti, P. Vergani, L. Larizza
Differential induction of the two early genes c-jun and c-fos in weakly and strongly metastatic murine lymphoma cell lines
1994 D. Rossi, S. Fumagalli, L. Volpi, L. Larizza
Isochromosome 15q of maternal origin in a Prader-Willi patient with pituitary adenoma
1996 D. Bettio, D. Giardino, N. Rizzi, P. Riva, L. Volpi, E. Barantani, A. Tagliaferri, L. Larizza
An improved procedure for in situ RTPCR
1996 L. Volpi, L. Doneda, M. G. Grimoldi, E. Pollina, L. Larizza
Microsatellite instability in IVS3 of murine c-fes gene: tumor-associated rearrangement and mammalian divergence
1996 L. Volpi, A. Beghini, D. Rossi, L. Larizza
Localization of fos, jun, kit and SCF mRNA in human placenta throughout gestation using in situ RT-PCR
1997 L. Doneda, G. Bulfamante, M.G. Grimoldi, L. Volpi, L. Larizza
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome
1998 M. Miozzo, P. Castorina, P. Riva, L. Dalprà, A. M. Fuhrman Conti, L. Volpi, T. S. Hoe, A. Khoo, J. Wiegant, C. Rosenberg, L. Larizza
A novel complex mutation of the OTC (ornithine transcarbamylase) gene in a Malaysian pedigree
1999 A.S. Khoo, P. Balraj, A. Rachedi, C.N. Chin, L. Volpi
A new BRCA1 germline mutation (E879X) in a Malaysian breast cancer patient of Chinese descent
2000 A.S. Khoo, P. Balraj, L. Volpi, S. Nair
Mutation analysis of the BRCA1 gene in Malaysian breast cancer patients
2002 P. Balraj, A.S.B. Khoo, L. Volpi, J.A.M.A. Tan, S. Nair, H. Abdullah
An unusual mutation in RECQ4 gene leading to Rothmund-Thomson syndrome
2002 P. Balraj, P. Concannon, R. Jamal, A. Beghini, T. S. Hoe, A. S. Khoo, L. Volpi
Letter in response to “RNA processing effects of the Helicase gene RECQL4 in a compound Heterozygous Rothmund-Thomson patient
2004 L. Volpi
Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene
2010 L. Volpi, G. Roversi, E.A. Colombo, N. Leijsten, D. Concolino, A. Calabria, M.A. Mencarelli, M. Fimiani, F. Macciardi, R. Pfundt, E.F. Schoenmakers, L. Larizza
Rothmund-Thomson syndrome
2010 L. Larizza, G. Roversi, L. Volpi
Clericuzio-Type Poikiloderma With Neutropenia Syndrome in Three Sibs With Mutations in the C16orf57 Gene : Delineation of the Phenotype
2010 D. Concolino, G. Roversi, G.L. Muzzi, S. Sestito, E.A. Colombo, L. Volpi, L. Larizza, P. Strisciuglio
Poikiloderma with neutropenia: Delineation of novel mutations and geographic clusters
2010 E. Colombo, G. Roversi, N. Elcioglu, G. Fremont, L. Volpi, L. Larizza
Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations
2012 E.A. Colombo, J..F. Bazan, G. Negri, C.C.G. Gervasini, N..H. Elcioglu, D. Yucelten, I. Altunay, U. Cetincelik, A. Teti, A. Del Fattore, M. Luciani, S..K. Sullivan, A..C. Yan, L. Volpi, L. Larizza
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile