Moi P - Search Results

1

An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotype.

Moi P, Cash FE, Liebhaber SA, Cao A, Pirastu M. Moi P, et al. J Clin Invest. 1987 Nov;80(5):1416-21. doi: 10.1172/JCI113220. J Clin Invest. 1987. PMID: 3680504 Free PMC article.

2

Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene.

Moi P, Loudianos G, Lavinha J, Murru S, Cossu P, Casu R, Oggiano L, Longinotti M, Cao A, Pirastu M. Moi P, et al. Blood. 1992 Jan 15;79(2):512-6. Blood. 1992. PMID: 1309671 Free article.

3

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.

4

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

5

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

6

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.

7

Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian family.

Oggiano L, Pirastu M, Moi P, Longinotti M, Perseu L, Cao A. Oggiano L, et al. Among authors: moi p. Br J Haematol. 1987 Oct;67(2):225-9. doi: 10.1111/j.1365-2141.1987.tb02331.x. Br J Haematol. 1987. PMID: 3676110

8

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.

9

Molecular pathology of haemoglobin H disease in Sardinians.

Paglietti E, Galanello R, Moi P, Pirastu M, Cao A. Paglietti E, et al. Among authors: moi p. Br J Haematol. 1986 Jul;63(3):485-96. doi: 10.1111/j.1365-2141.1986.tb07525.x. Br J Haematol. 1986. PMID: 3015190

10

Phenotype-genotype correlation in haemoglobin H disease in childhood.

Galanello R, Pirastu M, Melis MA, Paglietti E, Moi P, Cao A. Galanello R, et al. Among authors: moi p. J Med Genet. 1983 Dec;20(6):425-9. doi: 10.1136/jmg.20.6.425. J Med Genet. 1983. PMID: 6317863 Free PMC article.

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