Bottini F - Search Results

1

Identification of an AP-1-like sequence in the promoter region of calcyclin, a S-100-like gene. Enhancement of binding during retinoic acid-induced neuroblastoma cell differentiation.

Bottini F, Mazzocco K, Abbondi T, Tonini GP. Bottini F, et al. Neurosci Lett. 1994 Nov 7;181(1-2):35-8. doi: 10.1016/0304-3940(94)90554-1. Neurosci Lett. 1994. PMID: 7898765

2

Distribution of retinoic Acid receptor-alpha, receptor-Beta and receptor-gamma messenger-rnas in neuroblastoma-derived cell-lines and in fresh tumors.

Ferrari N, Tonini G, Briata A, Bottini F, Vidali G. Ferrari N, et al. Among authors: bottini f. Int J Oncol. 1994 Nov;5(5):1019-22. doi: 10.3892/ijo.5.5.1019. Int J Oncol. 1994. PMID: 21559674

3

The use of antisense oligodeoxynucleotides (aODNs) for the therapy of cancer.

Alama A, Barbieri F, Bottini F, Nicolin A. Alama A, et al. Among authors: bottini f. Drugs Exp Clin Res. 1991;17(12):575-9. Drugs Exp Clin Res. 1991. PMID: 1841051

4

Detection of T cell receptor delta gene rearrangements in childhood B and T lineage acute lymphoblastic leukaemia by southern blot and PCR: technical comparison of two methods of analysis.

Valetto A, Di Martino D, Scuderi F, Lanza T, Lanciotti M, Bottini F, Dini G. Valetto A, et al. Among authors: bottini f. Clin Lab Haematol. 2000 Oct;22(5):263-9. doi: 10.1046/j.1365-2257.2000.00317.x. Clin Lab Haematol. 2000. PMID: 11122266

5

Rapid detection of gammaT cell receptor gene rearrangements in acute lymphoblastic leukemia by electrophoresis and silver staining: implications for detection of minimal residual disease.

Valetto A, Lanciotti M, Di Martino D, Anselmi G, Bottini F, Mori P, Candiano G. Valetto A, et al. Among authors: bottini f. Electrophoresis. 1998 Jun;19(8-9):1385-7. doi: 10.1002/elps.1150190831. Electrophoresis. 1998. PMID: 9694286

6

Germ-line origin of intron 1 inversion in two haemophilia A families.

Acquila M, Pasino M, Santoro C, Lanza T, Molinari AC, Bottini F, Bicocchi MP. Acquila M, et al. Among authors: bottini f. Haemophilia. 2003 Nov;9(6):717-20. doi: 10.1046/j.1351-8216.2003.00818.x. Haemophilia. 2003. PMID: 14750938

7

Insight into molecular changes of the FIX protein in a series of Italian patients with haemophilia B.

Bicocchi MP, Pasino M, Rosano C, Molinari AC, Della Valle E, Lanza T, Bottini F, Acquila M. Bicocchi MP, et al. Among authors: bottini f. Haemophilia. 2006 May;12(3):263-70. doi: 10.1111/j.1365-2516.2006.01275.x. Haemophilia. 2006. PMID: 16643212

8

Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A.

Bicocchi MP, Migeon BR, Pasino M, Lanza T, Bottini F, Boeri E, Molinari AC, Corsolini F, Morerio C, Acquila M. Bicocchi MP, et al. Among authors: bottini f. Eur J Hum Genet. 2005 May;13(5):635-40. doi: 10.1038/sj.ejhg.5201386. Eur J Hum Genet. 2005. PMID: 15741993

9

Inversion mutation as a major cause of severe hemophilia A in Italian patients.

Mori PG, Caprino D, Bicocchi MP, Valetto A, Bottini F, Aquila M. Mori PG, et al. Among authors: bottini f. Haematologica. 1997 Jan-Feb;82(1):75-6. Haematologica. 1997. PMID: 9107090

10

A new strategy for prenatal diagnosis in a sporadic haemophilia B family.

Acquila M, Bottini F, Valetto A, Caprino D, Mori PG, Bicocchi MP. Acquila M, et al. Among authors: bottini f. Haemophilia. 2001 Jul;7(4):416-8. doi: 10.1046/j.1365-2516.2001.00514.x. Haemophilia. 2001. PMID: 11442646

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