Moi P - Search Results

1

A New Intronic Variant in ECEL1 in Two Patients with Distal Arthrogryposis Type 5D.

Alesi V, Sessini F, Genovese S, Calvieri G, Sallicandro E, Ciocca L, Mingoia M, Novelli A, Moi P. Alesi V, et al. Among authors: moi p. Int J Mol Sci. 2021 Feb 20;22(4):2106. doi: 10.3390/ijms22042106. Int J Mol Sci. 2021. PMID: 33672664 Free PMC article.

2

Induction of therapeutic levels of HbF in genome-edited primary β⁰ 39-thalassaemia haematopoietic stem and progenitor cells.

Mingoia M, Caria CA, Ye L, Asunis I, Marongiu MF, Manunza L, Sollaino MC, Wang J, Cabriolu A, Kurita R, Nakamura Y, Cucca F, Kan YW, Marini MG, Moi P. Mingoia M, et al. Among authors: moi p. Br J Haematol. 2021 Jan;192(2):395-404. doi: 10.1111/bjh.17167. Epub 2020 Nov 20. Br J Haematol. 2021. PMID: 33216968 Free article.

3

Lentiviral globin gene therapy with reduced-intensity conditioning in adults with β-thalassemia: a phase 1 trial.

Boulad F, Maggio A, Wang X, Moi P, Acuto S, Kogel F, Takpradit C, Prockop S, Mansilla-Soto J, Cabriolu A, Odak A, Qu J, Thummar K, Du F, Shen L, Raso S, Barone R, Di Maggio R, Pitrolo L, Giambona A, Mingoia M, Everett JK, Hokama P, Roche AM, Cantu VA, Adhikari H, Reddy S, Bouhassira E, Mohandas N, Bushman FD, Rivière I, Sadelain M. Boulad F, et al. Among authors: moi p. Nat Med. 2022 Jan;28(1):63-70. doi: 10.1038/s41591-021-01554-9. Epub 2022 Jan 3. Nat Med. 2022. PMID: 34980909 Free PMC article. Clinical Trial.

4

A novel splicing defect (IVS6+1G>T) in a patient with pseudovitamin D deficiency rickets.

Porcu L, Meloni A, Casula L, Asunis I, Marini MG, Cao A, Moi P. Porcu L, et al. Among authors: moi p. J Endocrinol Invest. 2002 Jun;25(6):557-60. doi: 10.1007/BF03345500. J Endocrinol Invest. 2002. PMID: 12109629

5

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.

6

Regulation of the human HBA genes by KLF4 in erythroid cell lines.

Marini MG, Porcu L, Asunis I, Loi MG, Ristaldi MS, Porcu S, Ikuta T, Cao A, Moi P. Marini MG, et al. Among authors: moi p. Br J Haematol. 2010 Jun;149(5):748-58. doi: 10.1111/j.1365-2141.2010.08130.x. Epub 2010 Mar 15. Br J Haematol. 2010. PMID: 20331458 Free article.

7

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.

8

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.

9

Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation.

Satta S, Paglietti ME, Sollaino MC, Barella S, Moi P, Desogus MF, Demartis FR, Manunza L, Origa R. Satta S, et al. Among authors: moi p. Blood Cells Mol Dis. 2017 May;64:30-32. doi: 10.1016/j.bcmd.2017.03.007. Epub 2017 Mar 18. Blood Cells Mol Dis. 2017. PMID: 28342932

10

Synergistic enhancement of globin gene expression by activator protein-1-like proteins.

Moi P, Kan YW. Moi P, et al. Proc Natl Acad Sci U S A. 1990 Nov;87(22):9000-4. doi: 10.1073/pnas.87.22.9000. Proc Natl Acad Sci U S A. 1990. PMID: 2123346 Free PMC article.

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