# | Title | Journal | Year | Citations |
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1 | The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis | Blood Cells, Molecules, and Diseases | 2009 | 533 |
2 | Mutation Analysis in Hereditary Hemochromatosis | Blood Cells, Molecules, and Diseases | 1996 | 377 |
3 | Tumor exosomes expressing Fas ligand mediate CD8+ T-cell apoptosis | Blood Cells, Molecules, and Diseases | 2005 | 350 |
4 | The ferroportin disease | Blood Cells, Molecules, and Diseases | 2004 | 337 |
5 | Genetic and Physical Mapping of theLpsLocus: Identification of the Toll-4 Receptor as a Candidate Gene in the Critical Region | Blood Cells, Molecules, and Diseases | 1998 | 328 |
6 | Vascular endothelial growth factor family of ligands and receptors: Review | Blood Cells, Molecules, and Diseases | 2007 | 304 |
7 | Exosomes biological significance: A concise review | Blood Cells, Molecules, and Diseases | 2006 | 300 |
8 | Understanding the biology of angiogenesis: Review of the most important molecular mechanisms | Blood Cells, Molecules, and Diseases | 2007 | 299 |
9 | Hepcidin, A New Iron Regulatory Peptide | Blood Cells, Molecules, and Diseases | 2002 | 288 |
10 | The Human Nramp2 Gene: Characterization of the Gene Structure, Alternative Splicing, Promoter Region and Polymorphisms | Blood Cells, Molecules, and Diseases | 1998 | 282 |
11 | Inhibition of the ABL Kinase Activity Blocks the Proliferation of BCR/ABL+Leukemic Cells and Induces Apoptosis | Blood Cells, Molecules, and Diseases | 1997 | 273 |
12 | Thalassemia intermedia: Revisited | Blood Cells, Molecules, and Diseases | 2006 | 269 |
13 | Mature dendritic cells secrete exosomes with strong ability to induce antigen-specific effector immune responses | Blood Cells, Molecules, and Diseases | 2005 | 249 |
14 | Role of exosomes in sperm maturation during the transit along the male reproductive tract | Blood Cells, Molecules, and Diseases | 2005 | 247 |
15 | Glucose-6-phosphate dehydrogenase (G6PD) mutations database: Review of the “old” and update of the new mutations | Blood Cells, Molecules, and Diseases | 2012 | 241 |
16 | Decreased Liver Hepcidin Expression in the Hfe Knockout Mouse | Blood Cells, Molecules, and Diseases | 2002 | 237 |
17 | Tissue-specific muscle, neural and liver stem/progenitor cells reside in the bone marrow, respond to an SDF-1 gradient and are mobilized into peripheral blood during stress and tissue injury | Blood Cells, Molecules, and Diseases | 2004 | 214 |
18 | The Bigger the C-Value, the Larger the Cell: Genome Size and Red Blood Cell Size in Vertebrates | Blood Cells, Molecules, and Diseases | 2001 | 210 |
19 | Posttranslational processing of hepcidin in human hepatocytes is mediated by the prohormone convertase furin | Blood Cells, Molecules, and Diseases | 2008 | 206 |
20 | Clustered CD20 Induced Apoptosis: Src-Family Kinase, the Proximal Regulator of Tyrosine Phosphorylation, Calcium Influx, and Caspase 3-Dependent Apoptosis | Blood Cells, Molecules, and Diseases | 2000 | 200 |
21 | Imaging red blood cell dynamics by quantitative phase microscopy | Blood Cells, Molecules, and Diseases | 2008 | 200 |
22 | Very Short Telomeres in the Peripheral Blood of Patients with X-Linked and Autosomal Dyskeratosis Congenita | Blood Cells, Molecules, and Diseases | 2001 | 196 |
23 | Surface Antigen Changes during Normal Neutrophilic Development: A Critical Review | Blood Cells, Molecules, and Diseases | 2002 | 194 |
24 | Activity of Drugs from Traditional Chinese Medicine toward Sensitive and MDR1- or MRP1-Overexpressing Multidrug-Resistant Human CCRF-CEM Leukemia Cells | Blood Cells, Molecules, and Diseases | 2002 | 190 |
25 | Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) gene☆ | Blood Cells, Molecules, and Diseases | 2003 | 187 |
26 | Facilitative glucose transporter gene expression in human lymphocytes, monocytes, and macrophages: a role for GLUT isoforms 1, 3, and 5 in the immune response and foam cell formation | Blood Cells, Molecules, and Diseases | 2004 | 181 |
27 | Emerging role of nitrite in human biology | Blood Cells, Molecules, and Diseases | 2004 | 181 |
28 | The orchestration of body iron intake: how and where do enterocytes receive their cues? | Blood Cells, Molecules, and Diseases | 2003 | 180 |
29 | Hematologically important mutations: X-linked chronic granulomatous disease (third update) | Blood Cells, Molecules, and Diseases | 2010 | 179 |
30 | GA-binding protein transcription factor: a review of GABP as an integrator of intracellular signaling and protein–protein interactions | Blood Cells, Molecules, and Diseases | 2004 | 174 |
31 | Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure | Blood Cells, Molecules, and Diseases | 2005 | 174 |
32 | Platelet Microparticles Bind, Activate and Aggregate Neutrophils In Vitro | Blood Cells, Molecules, and Diseases | 1995 | 171 |
33 | Application of multipotent mesenchymal stromal cells in pediatric patients following allogeneic stem cell transplantation | Blood Cells, Molecules, and Diseases | 2008 | 171 |
34 | Adult Rat and Human Bone Marrow Stromal Stem Cells Differentiate into Neurons | Blood Cells, Molecules, and Diseases | 2001 | 170 |
35 | Deferiprone versus Deferoxamine in Patients with Thalassemia Major: A Randomized Clinical Trial | Blood Cells, Molecules, and Diseases | 2002 | 165 |
36 | Mitochondrial Ferritin: A New Player in Iron Metabolism | Blood Cells, Molecules, and Diseases | 2002 | 165 |
37 | BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies | Blood Cells, Molecules, and Diseases | 2008 | 158 |
38 | Pathways of Iron Absorption | Blood Cells, Molecules, and Diseases | 2002 | 157 |
39 | Revisiting the road to the discovery of exosomes | Blood Cells, Molecules, and Diseases | 2005 | 156 |
40 | Hematologically important mutations: Gaucher disease | Blood Cells, Molecules, and Diseases | 2005 | 154 |
41 | Genetic and Clinical Description of Hemochromatosis Probands and Heterozygotes: Evidence That Multiple Genes Linked to the Major Histocompatibility Complex Are Responsible for Hemochromatosis | Blood Cells, Molecules, and Diseases | 1997 | 153 |
42 | Increased incidence of cancer in adult Gaucher disease in Western Europe | Blood Cells, Molecules, and Diseases | 2006 | 153 |
43 | The chronic wound: impaired healing and solutions in the context of wound bed preparation | Blood Cells, Molecules, and Diseases | 2004 | 152 |
44 | Exosome Display technology: Applications to the development of new diagnostics and therapeutics | Blood Cells, Molecules, and Diseases | 2005 | 152 |
45 | Two Novel Missense Mutations of the HFE Gene (I105T and G93R) and Identification of the S65C Mutation in Alabama Hemochromatosis Probands | Blood Cells, Molecules, and Diseases | 1999 | 150 |
46 | Hematologically Important Mutations: Glucose-6-phosphate Dehydrogenase | Blood Cells, Molecules, and Diseases | 2002 | 147 |
47 | Hematologically important mutations: Leukocyte adhesion deficiency (first update) | Blood Cells, Molecules, and Diseases | 2012 | 147 |
48 | Transferrin receptor 2 is frequently expressed in human cancer cell lines | Blood Cells, Molecules, and Diseases | 2007 | 145 |
49 | Exosomes contain ubiquitinated proteins | Blood Cells, Molecules, and Diseases | 2005 | 144 |
50 | Hematologically important mutations: The autosomal recessive forms of chronic granulomatous disease (second update) | Blood Cells, Molecules, and Diseases | 2010 | 143 |