Mirabile E - Search Results

1

Genetic characterization of general transcription factors TFIIF and TFIIB of Homo sapiens sapiens.

Purrello M, Di Pietro C, Rapisarda A, Mirabile E, Motta S, Sichel G, Grzeschik KH. Purrello M, et al. Among authors: mirabile e. Cytogenet Cell Genet. 1995;69(1-2):75-80. doi: 10.1159/000133942. Cytogenet Cell Genet. 1995. PMID: 7835093

2

Physical mapping at 6q27 of the locus for the TATA box-binding protein, the DNA-binding subunit of TFIID and a component of SL1 and TFIIIB, strongly suggests that it is single copy in the human genome.

Purrello M, Di Pietro C, Mirabile E, Rapisarda A, Rimini R, Tinè A, Pavone L, Motta S, Grzeschik KH, Sichel G. Purrello M, et al. Among authors: mirabile e. Genomics. 1994 Jul 1;22(1):94-100. doi: 10.1006/geno.1994.1349. Genomics. 1994. PMID: 7959796

3

The gene for SP-40,40, human homolog of rat sulfated glycoprotein 2, rat clusterin, and rat testosterone-repressed prostate message 2, maps to chromosome 8.

Purrello M, Bettuzzi S, Di Pietro C, Mirabile E, Di Blasi M, Rimini R, Grzeschik KH, Ingletti C, Corti A, Sichel G. Purrello M, et al. Among authors: mirabile e. Genomics. 1991 May;10(1):151-6. doi: 10.1016/0888-7543(91)90495-z. Genomics. 1991. PMID: 2045098

4

Presence of hemoglobinopathies in Sicily: a historic perspective.

Schilirò G, Mirabile E, Testa R, Russo-Mancuso G, Dibenedetto SP. Schilirò G, et al. Among authors: mirabile e. Am J Med Genet. 1997 Mar 17;69(2):200-6. doi: 10.1002/(sici)1096-8628(19970317)69:2<200::aid-ajmg17>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9056562

5

Genetic heterogeneity of beta-thalassemia in southeast Sicily.

Schilirò G, Di Gregorio F, Samperi P, Mirabile E, Liang R, Cürük MA, Ye Z, Huisman TH. Schilirò G, et al. Among authors: mirabile e. Am J Hematol. 1995 Jan;48(1):5-11. doi: 10.1002/ajh.2830480103. Am J Hematol. 1995. PMID: 7530406

6

Association of Hb S/Hb lepore and delta beta-thalassemia/Hb lepore in Sicilian patients: review of the presence of Hb lepore in Sicily.

Mirabile E, Testa R, Consalvo C, Dickerhoff R, Schilirò G. Mirabile E, et al. Eur J Haematol. 1995 Aug;55(2):126-30. doi: 10.1111/j.1600-0609.1995.tb01822.x. Eur J Haematol. 1995. PMID: 7543057

7

Phenotype-genotype correlation in Sicilian patients with Hb H.

Mirabile E, Samperi P, Di Cataldo A, Poli A, La Spina M, Schilirò G. Mirabile E, et al. Eur J Haematol. 2000 Nov;65(5):306-9. doi: 10.1034/j.1600-0609.2000.065005306.x. Eur J Haematol. 2000. PMID: 11092460

8

A mild form of Hb S-beta-thalassemia syndrome is assured in Sicilian patients by beta+mutant IVS-I nt 6(T-->C).

Mirabile E, Testa R, Samperi P, Consalvo C, Romano V, Schilirò G. Mirabile E, et al. Eur J Haematol. 1997 Jan;58(1):67-9. doi: 10.1111/j.1600-0609.1997.tb01412.x. Eur J Haematol. 1997. PMID: 9020376 No abstract available.

9

Application of a chemiluminescent methodology for detection of minimal residual disease in childhood acute lymphoblastic leukemia.

Lo Nigro L, Poli A, Mirabile E, Costantino F, Schilirò G. Lo Nigro L, et al. Among authors: mirabile e. Haematologica. 2001 Dec;86(12):1314-6. Haematologica. 2001. PMID: 11726326 No abstract available.

10

Use of PEG-interferon alfa-2a plus ribavirin as treatment for chronic HCV hepatitis in a child cured of ALL.

Lo Nigro L, La Spina M, Mirabile E, Pisana P, Schilirò G, Guardo P. Lo Nigro L, et al. Among authors: mirabile e. Pediatr Blood Cancer. 2004 Aug;43(2):185. doi: 10.1002/pbc.20084. Pediatr Blood Cancer. 2004. PMID: 15236293 No abstract available.

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