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Blood Cells, Molecules & Diseases|December 12, 2018
Analysis of clinical and molecular features of MDS patients with complex karyotype in ChinaYanling Ren, Chen Mei, Li Ye, et al.Blood Cells, Molecules & Diseases|February 10, 2018
Combinations of antioxidants and/or of epigenetic enzyme inhibitors allow for enhanced collection of mouse bone marrow hematopoietic stem cells in ambient airQingchun Cai, Maegan Capitano, Xinxin Huang, et al.Blood Cells, Molecules & Diseases|November 1, 2019
Allergy and inhibitors in hemophilia - a rare complication with potential novel solutionsSarina Levy-Mendelovich, Tami Livnat, Assaf Arie Barg, et al.Blood Cells, Molecules & Diseases|November 1, 2019
Polymorphisms in genes that affect the variation of lipid levels in a Brazilian pediatric population with sickle cell disease: rs662799 APOA5 and rs964184 ZPR1Thaisa Netto Souza Valente-Frossard, Nilcemar Rodrigues Carvalho Cruz, Fernanda Oliveira Ferreira, et al.Blood Cells, Molecules & Diseases|November 1, 2019
Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutationKarolina Maciak, Anna Adamowicz-Salach, Alicja Siwicka, et al.Blood Cells, Molecules & Diseases|November 22, 2007
p15Ink4b: dual function in myelopoiesis and inactivation in myeloid diseaseMichael Rosu-Myles, Linda WolffBlood Cells, Molecules & Diseases|October 6, 2007
Hematologically important mutations: Shwachman-Diamond syndromeElísio Costa, Rosário SantosBlood Cells, Molecules & Diseases|August 5, 2008
Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretionManuela Platè, Rosanna Asselta, Silvia Spena, et al.Blood Cells, Molecules & Diseases|April 24, 2009
Post-translational modifications of Runx1 regulate its activity in the cellLan Wang, Gang Huang, Xinyang Zhao, et al.Blood Cells, Molecules & Diseases|April 28, 2009
Glucocerebrosidase gene mutations in black South Africans with Gaucher diseaseSilke Arndt, Rene Heitner, Anthony Lane, et al.Pageof 220