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Leukemia Research|February 4, 2010
Quantification of fibrosis and osteosclerosis in myeloproliferative neoplasms: a computer-assisted image studyCarolin J Teman, Andrew R Wilson, Sherrie L Perkins, et al.
Blood|July 22, 2008
Hematopoiesis is not clonal in healthy elderly womenSabina I Swierczek, Neeraj Agarwal, Roberto H Nussenzveig, et al.
The Journal of Molecular Diagnostics : JMD|January 15, 2013
A quantitative allele-specific PCR test for the BRAF V600E mutation using a single heterozygous control plasmid for quantitation: a model for qPCR testing without standard curvesPhilippe Szankasi, N Scott Reading, Cecily P Vaughn, et al.
International Journal of Medical Sciences|October 24, 2007
Familial polycythemia caused by a novel mutation in the beta globin gene: essential role of P50 in evaluation of familial polycythemiaNeeraj Agarwal, Mariluz P Mojica-Henshaw, Elizabeth D Simmons, et al.
Blood Cells, Molecules & Diseases|October 20, 2009
Erythropoietin receptor signaling regulates both erythropoiesis and megakaryopoiesis in vivoXiaosong Huang, L Jeanne Pierce, George L Chen, et al.
Human Mutation|July 24, 2013
β-Thalassemia due to intronic LINE-1 insertion in the β-globin gene (HBB): molecular mechanisms underlying reduced transcript levels of the β-globin(L1) alleleLucie Lanikova, Jana Kucerova, Karel Indrak, et al.
Blood Cells, Molecules & Diseases|March 13, 2014
High altitude genetic adaptation in Tibetans: no role of increased hemoglobin-oxygen affinityTsewang Tashi, Tang Feng, Parvaiz Koul, et al.
Blood|October 2, 2004
Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overloadMartha P Mims, Yongli Guan, Dagmar Pospisilova, et al.
Leukemia & Lymphoma|October 1, 2015
Increased frequency of co-existing JAK2 exon-12 or MPL exon-10 mutations in patients with low JAK2(V617F) allelic burdenRoberto H Nussenzveig, Ha T Pham, Sherrie L Perkins, et al.
Neonatology|November 7, 2013
Variations in both α-spectrin (SPTA1) and β-spectrin ( SPTB ) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosisRobert D Christensen, Roberto H Nussenzveig, N Scott Reading, et al.
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