De Franceschi L - Search Results

1

NCOA4 Deficiency Impairs Systemic Iron Homeostasis.

Bellelli R, Federico G, Matte' A, Colecchia D, Iolascon A, Chiariello M, Santoro M, De Franceschi L, Carlomagno F. Bellelli R, et al. Among authors: de franceschi l. Cell Rep. 2016 Jan 26;14(3):411-421. doi: 10.1016/j.celrep.2015.12.065. Epub 2016 Jan 14. Cell Rep. 2016. PMID: 26776506 Free article.

2

Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects.

De Franceschi L, Olivieri O, Miraglia del Giudice E, Perrotta S, Sabato V, Corrocher R, Iolascon A. De Franceschi L, et al. Am J Hematol. 1997 Jul;55(3):121-8. doi: 10.1002/(sici)1096-8652(199707)55:3<121::aid-ajh1>3.0.co;2-u. Am J Hematol. 1997. PMID: 9256290 Free article.

3

Decreased band 3 anion transport activity and band 3 clusterization in congenital dyserythropoietic anemia type II.

De Franceschi L, Turrini F, del Giudice EM, Perrotta S, Olivieri O, Corrocher R, Mannu F, Iolascon A. De Franceschi L, et al. Exp Hematol. 1998 Aug;26(9):869-73. Exp Hematol. 1998. PMID: 9694508

4

Liver expression of hepcidin and other iron genes in two mouse models of beta-thalassemia.

De Franceschi L, Daraio F, Filippini A, Carturan S, Muchitsch EM, Roetto A, Camaschella C. De Franceschi L, et al. Haematologica. 2006 Oct;91(10):1336-42. Haematologica. 2006. PMID: 17018382

5

K-CL co-transport plays an important role in normal and beta thalassemic erythropoiesis.

De Franceschi L, Ronzoni L, Cappellini MD, Cimmino F, Siciliano A, Alper SL, Servedio V, Pozzobon C, Iolascon A. De Franceschi L, et al. Haematologica. 2007 Oct;92(10):1319-26. doi: 10.3324/haematol.11556. Haematologica. 2007. PMID: 18024369 Free article.

6

PTPepsilon has a critical role in signaling transduction pathways and phosphoprotein network topology in red cells.

De Franceschi L, Biondani A, Carta F, Turrini F, Laudanna C, Deana R, Brunati AM, Turretta L, Iolascon A, Perrotta S, Elson A, Bulato C, Brugnara C. De Franceschi L, et al. Proteomics. 2008 Nov;8(22):4695-708. doi: 10.1002/pmic.200700596. Proteomics. 2008. PMID: 18924107 Free PMC article.

7

A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis.

Iolascon A, De Falco L, Borgese F, Esposito MR, Avvisati RA, Izzo P, Piscopo C, Guizouarn H, Biondani A, Pantaleo A, De Franceschi L. Iolascon A, et al. Among authors: de franceschi l, de falco l. Haematologica. 2009 Aug;94(8):1049-59. doi: 10.3324/haematol.2008.002873. Haematologica. 2009. PMID: 19644137 Free PMC article.

8

Deoxygenation affects tyrosine phosphoproteome of red cell membrane from patients with sickle cell disease.

Siciliano A, Turrini F, Bertoldi M, Matte A, Pantaleo A, Olivieri O, De Franceschi L. Siciliano A, et al. Among authors: de franceschi l. Blood Cells Mol Dis. 2010 Apr 15;44(4):233-42. doi: 10.1016/j.bcmd.2010.02.007. Epub 2010 Mar 4. Blood Cells Mol Dis. 2010. PMID: 20206558

9

Peroxiredoxin-2 expression is increased in beta-thalassemic mouse red cells but is displaced from the membrane as a marker of oxidative stress.

Matte A, Low PS, Turrini F, Bertoldi M, Campanella ME, Spano D, Pantaleo A, Siciliano A, De Franceschi L. Matte A, et al. Among authors: de franceschi l. Free Radic Biol Med. 2010 Aug 1;49(3):457-66. doi: 10.1016/j.freeradbiomed.2010.05.003. Epub 2010 May 19. Free Radic Biol Med. 2010. PMID: 20488244 Free PMC article.

10

Heat-shock protein-27, -70 and peroxiredoxin-II show molecular chaperone function in sickle red cells: Evidence from transgenic sickle cell mouse model.

Biondani A, Turrini F, Carta F, Matté A, Filippini A, Siciliano A, Beuzard Y, De Franceschi L. Biondani A, et al. Among authors: de franceschi l. Proteomics Clin Appl. 2008 May;2(5):706-19. doi: 10.1002/prca.200780058. Proteomics Clin Appl. 2008. PMID: 21136868

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