Published in Pediatr Blood Cancer on December 13, 2011
Red cell membrane: past, present, and future. Blood (2008) 3.11
Hereditary spherocytosis. Lancet (2008) 2.37
Seventy-five years of neonatal sepsis at Yale: 1928-2003. Pediatrics (2005) 2.22
Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site. Blood (2008) 2.12
Sites of regulated phosphorylation that control K-Cl cotransporter activity. Cell (2009) 1.93
Changing patterns in neonatal Escherichia coli sepsis and ampicillin resistance in the era of intrapartum antibiotic prophylaxis. Pediatrics (2008) 1.91
Single-lineage transcriptome analysis reveals key regulatory pathways in primitive erythroid progenitors in the mouse embryo. Blood (2011) 1.79
Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis. Blood (2012) 1.76
Novel role for EKLF in megakaryocyte lineage commitment. Blood (2007) 1.53
Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiation. Blood (2011) 1.50
Altered subcellular localization of transcription factor TEAD4 regulates first mammalian cell lineage commitment. Proc Natl Acad Sci U S A (2012) 1.44
The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation. Blood (2013) 1.43
Failure of terminal erythroid differentiation in EKLF-deficient mice is associated with cell cycle perturbation and reduced expression of E2F2. Mol Cell Biol (2008) 1.42
Alterations in expression and chromatin configuration of the alpha hemoglobin-stabilizing protein gene in erythroid Kruppel-like factor-deficient mice. Mol Cell Biol (2006) 1.26
Major erythrocyte membrane protein genes in EKLF-deficient mice. Exp Hematol (2006) 1.23
Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfolding. Blood (2006) 1.22
Chromatin boundaries require functional collaboration between the hSET1 and NURF complexes. Blood (2011) 1.17
Imaging of the diffusion of single band 3 molecules on normal and mutant erythrocytes. Blood (2009) 1.12
Marrow stem cells shift gene expression and engraftment phenotype with cell cycle transit. J Exp Med (2003) 1.12
Downstream targets of HOXB4 in a cell line model of primitive hematopoietic progenitor cells. Blood (2010) 1.10
Expression of Pitx2 in stromal cells is required for normal hematopoiesis. Blood (2005) 1.07
Chromatin architecture and transcription factor binding regulate expression of erythrocyte membrane protein genes. Mol Cell Biol (2009) 1.06
Antibiotic-resistant organisms in the neonatal intensive care unit. Semin Perinatol (2007) 1.05
Identification of biologically relevant enhancers in human erythroid cells. J Biol Chem (2013) 1.03
USF1 and hSET1A mediated epigenetic modifications regulate lineage differentiation and HoxB4 transcription. PLoS Genet (2013) 1.03
An 11-amino acid beta-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytes. Proc Natl Acad Sci U S A (2007) 1.02
Applications of high-throughput DNA sequencing to benign hematology. Blood (2013) 1.01
Multiple isoforms of the KC1 cotransporter are expressed in sickle and normal erythroid cells. Exp Hematol (2005) 0.99
A decline in the frequency of neonatal exchange transfusions and its effect on exchange-related morbidity and mortality. Pediatrics (2007) 0.99
A novel mutation in the erythropoietin receptor gene is associated with familial erythrocytosis. Blood (2002) 0.97
A comprehensive model of the spectrin divalent tetramer binding region deduced using homology modeling and chemical cross-linking of a mini-spectrin. J Biol Chem (2010) 0.95
Erythrocyte peripheral type benzodiazepine receptor/voltage-dependent anion channels are upregulated by Plasmodium falciparum. Blood (2011) 0.95
Teleost growth factor independence (gfi) genes differentially regulate successive waves of hematopoiesis. Dev Biol (2012) 0.94
An insulator with barrier-element activity promotes alpha-spectrin gene expression in erythroid cells. Blood (2008) 0.93
A novel splicing mutation of the alpha-spectrin gene in the original hereditary pyropoikilocytosis kindred. Blood (2005) 0.91
Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing. Mov Disord (2011) 0.90
Sequences downstream of the erythroid promoter are required for high level expression of the human alpha-spectrin gene. J Biol Chem (2004) 0.89
A fused alpha-beta "mini-spectrin" mimics the intact erythrocyte spectrin head-to-head tetramer. J Biol Chem (2010) 0.88
Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function. Am J Hematol (2008) 0.88
Matched case-control analysis of polymicrobial bloodstream infection in a neonatal intensive care unit. Infect Control Hosp Epidemiol (2008) 0.88
Erythroid expression of the human alpha-spectrin gene promoter is mediated by GATA-1- and NF-E2-binding proteins. J Biol Chem (2002) 0.88
Induced pluripotent stem cells in regenerative medicine: an argument for continued research on human embryonic stem cells. Regen Med (2009) 0.87
Conjunctival colonization of infants hospitalized in a neonatal intensive care unit: a longitudinal analysis. Infect Control Hosp Epidemiol (2004) 0.87
Methicillin-resistant Staphylococcus aureus in the neonatal intensive care unit. Semin Perinatol (2012) 0.87
The GPA-dependent, spherostomatocytosis mutant AE1 E758K induces GPA-independent, endogenous cation transport in amphibian oocytes. Am J Physiol Cell Physiol (2009) 0.87
Clinical and laboratory factors that predict death in very low birth weight infants presenting with late-onset sepsis. Pediatr Infect Dis J (2014) 0.86
Granulicatella adiacens and early-onset sepsis in neonate. Emerg Infect Dis (2011) 0.86
Erythrocyte disorders in the perinatal period. Semin Perinatol (2007) 0.86
Hematopoiesis following disruption of the Pitx2 homeodomain gene. Exp Hematol (2006) 0.85
Probing large conformational rearrangements in wild-type and mutant spectrin using structural mass spectrometry. Proc Natl Acad Sci U S A (2014) 0.84
Determinants of erythrocyte hydration. Curr Opin Hematol (2010) 0.83
Patterns of histone H3 lysine 27 monomethylation and erythroid cell type-specific gene expression. J Biol Chem (2011) 0.82
Aplastic crisis revealing the diagnosis of Hb Evans [alpha62(E11)Val-->Met, GTG-->ATG (alpha2)] in a Hispanic kindred: case report and review. Hemoglobin (2007) 0.81
Cytokine signals through STAT3 promote expression of granulocyte secondary granule proteins in 32D cells. Exp Hematol (2005) 0.81
Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S. Am J Physiol Cell Physiol (2011) 0.81
Case-control analysis of endemic Serratia marcescens bacteremia in a neonatal intensive care unit. Arch Dis Child Fetal Neonatal Ed (2006) 0.80
A tissue-specific chromatin loop activates the erythroid ankyrin-1 promoter. Blood (2012) 0.80
Genome-wide detection of a TFIID localization element from an initial human disease mutation. Nucleic Acids Res (2010) 0.79
Perinatal onset mevalonate kinase deficiency. Pediatr Dev Pathol (2011) 0.79
Human and murine erythropoiesis. Curr Opin Hematol (2015) 0.78
Ankyrin-linked hereditary spherocytosis in an African-American kindred. Am J Hematol (2008) 0.78
A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis. Blood (2007) 0.78
Progress in understanding the hemoglobin switch. N Engl J Med (2011) 0.78
Nonsense mutations of the alpha-spectrin gene in hereditary pyropoikilocytosis. Haematologica (2008) 0.77
Bi-allelic deletions within 13q14 and transient trisomy 21 with absence of GATA1s in pediatric acute megakaryoblastic leukemia. Pediatr Blood Cancer (2011) 0.76
Human potassium chloride cotransporter 1 (SLC12A4) promoter is regulated by AP-2 and contains a functional downstream promoter element. Blood (2004) 0.76
Vancomycin-resistant enterococcal bacteremia and necrotizing enterocolitis in a preterm neonate. Pediatr Infect Dis J (2005) 0.76
Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the alpha beta spectrin self-association binding site. Lab Invest (2004) 0.76
Functional analysis of a novel cis-acting regulatory region within the human ankyrin gene (ANK-1) promoter. Mol Cell Biol (2010) 0.76
Partial exchange transfusion for polycythemia hyperviscosity syndrome. Am J Perinatol (2011) 0.75
Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia. Hemoglobin (2014) 0.75
Hereditary pyropoikilocytosis and the spectrin St. Claude allele. Br J Haematol (2004) 0.75
Picture of the month. Blueberry muffin baby (extramedullary hematopoiesis) due to congenital cytomegalovirus infection. Arch Pediatr Adolesc Med (2007) 0.75
Canine elliptocytosis due to a mutant beta-spectrin. Vet Clin Pathol (2008) 0.75