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2011 Enero Erythrophagocytosis by neutrophils. Blood. 2011 Jan 20;117(3):753. PubMed PMID: 21309135. Vogel G. Cell biology. Telling time without turning on genes. Science. 2011 Jan 28;331(6016):391. PubMed PMID: 21273463. Hickey MJ. MPO and neutrophils: a magnetic attraction. Blood. 2011 Jan 27;117(4):1103-4. PubMed PMID: 21273327. Castella M, Pujol R, Callén E, Trujillo JP, Casado JA, Gille H, Lach FP, Auerbach AD, Schindler D, Benitez J, Porto B, Ferro T, Muñoz A, Sevilla J, Madero L, Cela E, Beléndez C, Díaz de Heredia C, Olivé T, Sánchez de Toledo J, Badell I, Torrent M, Estella J, Dasí A, Rodríguez-Villa A, Gómez P, Barbot J, Tapia M, Molinés A, Figuera A, Bueren JA, Surrallés J. Origin, functional role and clinical impact of Fanconi anemia FANCA mutations. Blood. 2011 Jan 27. [Epub ahead of print] PubMed PMID: 21273304. Satta S, Perseu L, Moi P, Asunis I, Cabriolu A, Maccioni L, Demartis FR, Manunza L, Cao A, Galanello R. Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin. Haematologica. 2011 Jan 27. [Epub ahead of print] PubMed PMID: 21273267. O'Neill JS, Reddy AB. Circadian clocks in human red blood cells. Nature. 2011 Jan 27;469(7331):498-503. PubMed PMID: 21270888. Bass J, Takahashi JS. Circadian rhythms: Redox redux. Nature. 2011 Jan 27;469(7331):476-8. PubMed PMID: 21270881. Merryweather-Clarke AT, Atzberger A, Soneji S, Gray N, Clark K, Waugh C, McGowan SJ, Taylor S, Nandi AK, Wood WG, Roberts DJ, Higgs DR, Buckle VJ, Robson KJ. Global gene expression analysis of human erythroid progenitors. Blood. 2011 Jan 26. [Epub ahead of print] PubMed PMID: 21270440. Weatherall DJ. Systems biology and red cells. N Engl J Med. 2011 Jan 27;364(4):376-7. PubMed PMID: 21268732. Astwood E, Vora A. Erythroblastic islands. Blood. 2011 Jan 6;117(1):10. PubMed PMID: 21265064. Cantù C, Ierardi R, Alborelli I, Fugazza C, Cassinelli L, Piconese S, Bosè F, Ottolenghi S, Ferrari G, Ronchi A. Sox6 enhances erythroid differentiation in
human erythroid progenitors. Blood. 2011 Jan 24. [Epub ahead of print] PubMed PMID: 21263153. Farha S, Asosingh K, Xu W, Sharp J, George D, Comhair S, Park M, Tang WH, Loyd JE, Theil K, Tubbs R, Hsi E, Lichtin A, Erzurum SC. Hypoxia-inducible factors in human pulmonary arterial hypertension: a link to the intrinsic myeloid abnormalities. Blood. 2011 Jan 21. [Epub ahead of print] PubMed PMID: 21258008. Georgitsi M, Papachatzopoulou A, Linardaki E, Maroulis V, Papadakis MN, Patrinos GP. First report of Hb A2-NYU (HBD:c.39T>A) in the Hellenic population. Hemoglobin. 2011;35(1):91-5. PubMed PMID: 21250887. Liao C, Zhou JY, Xie XM, Li DZ. Screening for Hb Constant Spring in the Guangdong Province, South China, using the Sebia capillary electrophoresis system. Hemoglobin. 2011;35(1):87-90. PubMed PMID: 21250886. Waye JS, Nakamura-Garrett LM, Eng B, Kanavakis E, Traeger-Synodinos J. β+- Thalassemia trait due to a novel mutation in the β-globin gene promoter: -26 (A>C) [HBB c.-76A>C]. Hemoglobin. 2011;35(1):84-6. PubMed PMID: 21250885. Guzmán LF, Perea FJ, Morales-González KR, Sánchez-López JY, de la Cruz EI, Chávez-Velasco ML, Ibarra CB. Characterization of the 5' and 3' breakpoints of the Spanish (δβ)0-thalassemia deletion in Mexican patients. Hemoglobin. 2011;35(1):80-3. PubMed PMID: 21250884. Abdalla MY, Fawzi M, Al-Maloul SR, El-Banna N, Tayyem RF, Ahmad IM. Increased oxidative stress and iron overload in Jordanian β-thalassemic children. Hemoglobin. 2011;35(1):67-79. PubMed PMID: 21250883. Zachaki S, Vrettou C, Destouni A, Kokkali G, Traeger-Synodinos J, Kanavakis E. Novel and known microsatellite markers within the β-globin cluster to support robust preimplantation genetic diagnosis of β-thalassemia and sickle cell syndromes. Hemoglobin. 2011;35(1):56-66. PubMed PMID: 21250882. Mendilcioglu I, Yakut S, Keser I, Simsek M, Yesilipek A, Bagci G, Luleci G. Prenatal diagnosis of β-thalassemia and other hemoglobinopathies in southwestern Turkey. Hemoglobin. 2011;35(1):47-55. PubMed PMID: 21250881. Ebrahimkhani S, Azarkeivan A, Bayat N, Houry-Parvin M, Jalil-Nejad S, Zand S, Golkar Z, Hadavi V, Imanian H, Oberkanins C, Najmabadi H. Genotypephenotype correlation in Iranian patients with Hb H disease. Hemoglobin. 2011;35(1):40-6. PubMed PMID: 21250880.
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