Moi P - Search Results

1

Genetic modifying factors in beta-thalassemia.

Cao A, Moi P. Cao A, et al. Among authors: moi p. Clin Chem Lab Med. 2000 Feb;38(2):123-32. doi: 10.1515/CCLM.2000.019. Clin Chem Lab Med. 2000. PMID: 10834399 Review.

2

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.

Uda M, Galanello R, Sanna S, Lettre G, Sankaran VG, Chen W, Usala G, Busonero F, Maschio A, Albai G, Piras MG, Sestu N, Lai S, Dei M, Mulas A, Crisponi L, Naitza S, Asunis I, Deiana M, Nagaraja R, Perseu L, Satta S, Cipollina MD, Sollaino C, Moi P, Hirschhorn JN, Orkin SH, Abecasis GR, Schlessinger D, Cao A. Uda M, et al. Among authors: moi p. Proc Natl Acad Sci U S A. 2008 Feb 5;105(5):1620-5. doi: 10.1073/pnas.0711566105. Epub 2008 Feb 1. Proc Natl Acad Sci U S A. 2008. PMID: 18245381 Free PMC article.

3

Normal delta-globin gene sequences in Sardinian nondeletional delta beta-thalassemia.

Loudianos G, Moi P, Lavinha J, Galanello R, Cao A, Pirastu M. Loudianos G, et al. Among authors: moi p. Hemoglobin. 1992;16(6):503-9. doi: 10.3109/03630269208993118. Hemoglobin. 1992. PMID: 1487421

4

Interaction of heterozygous beta zero-thalassemia with single functional alpha-globin gene.

Galanello R, Paglietti E, Melis MA, Crobu MG, Addis M, Moi P, Cao A. Galanello R, et al. Among authors: moi p. Am J Hematol. 1988 Oct;29(2):63-6. doi: 10.1002/ajh.2830290202. Am J Hematol. 1988. PMID: 3189303

5

Delineation of the molecular basis of delta- and normal HbA2 beta-thalassemia.

Moi P, Paglietti E, Sanna A, Brancati C, Tagarelli A, Galanello R, Cao A, Pirastu M. Moi P, et al. Blood. 1988 Aug;72(2):530-3. Blood. 1988. PMID: 3401592 Free article.

6

Regulation of the globin genes.

Cao A, Moi P. Cao A, et al. Among authors: moi p. Pediatr Res. 2002 Apr;51(4):415-21. doi: 10.1203/00006450-200204000-00003. Pediatr Res. 2002. PMID: 11919323 Review.

7

A novel silent beta-thalassemia mutation in the distal CACCC box affects the binding and responsiveness to EKLF.

Moi P, Faà V, Marini MG, Asunis I, Ibba G, Cao A, Rosatelli MC. Moi P, et al. Br J Haematol. 2004 Sep;126(6):881-4. doi: 10.1111/j.1365-2141.2004.05146.x. Br J Haematol. 2004. PMID: 15352994 Free article.

8

The distal beta-globin CACCC box is required for maximal stimulation of the beta-globin gene by EKLF.

Marini MG, Asunis I, Porcu L, Salgo MG, Loi MG, Brucchietti A, Cao A, Moi P. Marini MG, et al. Among authors: moi p. Br J Haematol. 2004 Oct;127(1):114-7. doi: 10.1111/j.1365-2141.2004.05153.x. Br J Haematol. 2004. PMID: 15384985 Free article.

9

Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin.

Satta S, Perseu L, Moi P, Asunis I, Cabriolu A, Maccioni L, Demartis FR, Manunza L, Cao A, Galanello R. Satta S, et al. Among authors: moi p. Haematologica. 2011 May;96(5):767-70. doi: 10.3324/haematol.2010.037333. Epub 2011 Jan 27. Haematologica. 2011. PMID: 21273267 Free PMC article.

10

Recent advances in β-thalassemias.

Cao A, Moi P, Galanello R. Cao A, et al. Among authors: moi p. Pediatr Rep. 2011 Jun 16;3(2):e17. doi: 10.4081/pr.2011.e17. Pediatr Rep. 2011. PMID: 21772954 Free PMC article.

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