All Stories

  1. A patient with both methemoglobinemia and G6PD deficiency: A therapeutic conundrum

    Article • American Journal of Hematology, March 2017, Wiley

    Dr. Noel S. Reading

  2. A novel approach to quantitating leukemia fusion transcripts by qRT-PCR without the need for standard curves

    Article • Experimental and Molecular Pathology, August 2015, Elsevier

    Dr. Noel S. Reading

  3. Calreticulin mutated prefibrotic-stage myelofibrosis and PMF represent an independent clone from coexisting CLL

    Article • Blood, September 2014, American Society of Hematology

    Dr. Noel S. Reading

  4. Variations in Both a-Spectrin(SPTA1)and �-Spectrin (SPTB) in a Neonate with Prolonged Jaundice in a Family where Nine Individuals Had Hereditary Elliptocytosis

    Article • Neonatology, January 2014, Karger Publishers

    Dr. Noel S. Reading

  5. Neonatal Death Suspected To Be From Sepsis Was Found To Be Kernicterus With G6PD Deficiency

    Article • PEDIATRICS, November 2013, American Academy of Pediatrics (AAP)

    Dr. Noel S. Reading

  6. Detection of Nine Mediterranean β-Thalassemia Mutations in Palestinians Using Three Restriction Enzyme Digest Panels: A Reliable Method for Developing Countries

    Article • Hemoglobin, October 2013, Taylor & Francis

    Dr. Noel S. Reading

  7. Acute Kernicterus in a Neonate With O/B Blood Group Incompatibility and a Mutation in SLC4A1

    Article • PEDIATRICS, July 2013, American Academy of Pediatrics (AAP)

    Dr. Noel S. Reading

  8. A Quantitative Allele-Specific PCR Test for the BRAF V600E Mutation Using a Single Heterozygous Control Plasmid for Quantitation

    Article • Journal of Molecular Diagnostics, March 2013, Elsevier

    Dr. Noel S. Reading

  9. Unexplained extreme hyperbilirubinemia among neonates in a multihospital healthcare system

    Article • Blood Cells Molecules and Diseases, February 2013, Elsevier

    Dr. Noel S. Reading

  10. Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Gaza Strip Palestinians

    Article • Blood Cells Molecules and Diseases, October 2012, Elsevier

    Dr. Noel S. Reading

  11. Development of a rapid multiplex PCR assay for identification of the three common Hemoglobin-Lepore variants (Boston-Washington, Baltimore, and Hollandia) and identification of a new Lepore variant

    Article • American Journal of Hematology, August 2012, Wiley

    Dr. Noel S. Reading

  12. Hemolysis and Mediterranean G6PD mutation (c.563 C>T) and c.1311 C>T polymorphism among Palestinians at Gaza Strip

    Article • Blood Cells Molecules and Diseases, April 2012, Elsevier

    Dr. Noel S. Reading

  13. Association of G6PD202A,376G with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia

    Article • British Journal of Haematology, May 2010, Wiley

    Dr Seyed Mehdi Nouraie, Dr. Noel S. Reading

  14. Angiogenic and Inflammatory Markers of Cardiopulmonary Changes in Children and Adolescents with Sickle Cell Disease

    Article • PLoS ONE, November 2009, PLOS

    Dr Seyed Mehdi Nouraie, Dr. Noel S. Reading

  15. The ‘GGCC’ haplotype of JAK2 confers susceptibility to JAK2 exon 12 mutation-positive polycythemia vera

    Article • Leukemia, May 2009, Nature

    Dr. Noel S. Reading

  16. Concordance of assays designed for the quantification of JAK2V617F: a multicenter study

    Article • Haematologica, January 2009, Ferrata Storti Foundation (Haematologica)

    Dr. Noel S. Reading

  17. Missense mutation of the last nucleotide of exon 1 (G->C) of globin gene not only leads to undetectable mutant peptide and transcript but also interferes with the expression of wild allele

    Article • Haematologica, December 2007, Ferrata Storti Foundation (Haematologica)

    Dr. Noel S. Reading

  18. Detection of Acquired Janus Kinase 2 V617F Mutation in Myeloproliferative Disorders by Fluorescence Melting Curve Analysis

    Article • Molecular Diagnosis & Therapy, September 2006, Springer Science + Business Media

    Dr. Noel S. Reading

  19. Expression of the Rho-family GTPase geneRHOFin lymphocyte subsets and malignant lymphomas

    Article • British Journal of Haematology, May 2005, Wiley

    Dr. Noel S. Reading

  20. 5′-(RACE) Identification of Rare ALK Fusion Partner in Anaplastic Large Cell Lymphoma

    Article • Journal of Molecular Diagnostics, May 2003, Elsevier

    Dr. Noel S. Reading

  21. Role of Disulfide Bonds in the Stability of Recombinant Manganese Peroxidase †

    Article • Biochemistry, July 2001, American Chemical Society (ACS)

    Dr. Noel S. Reading

  22. Engineering a Disulfide Bond in Recombinant Manganese Peroxidase Results in Increased Thermostability

    Article • Biotechnology Progress, June 2000, Wiley

    Dr. Noel S. Reading

  23. Substrate Specificity of Lignin Peroxidase and a S168W Variant of Manganese Peroxidase

    Article • Archives of Biochemistry and Biophysics, January 2000, Elsevier

    Dr. Noel S. Reading

  24. Relative Stability of Recombinant Versus Native Peroxidases fromPhanerochaete chrysosporium

    Article • Archives of Biochemistry and Biophysics, May 1999, Elsevier

    Dr. Noel S. Reading

  25. Addition of Veratryl Alcohol Oxidase Activity to Manganese Peroxidase by Site-Directed Mutagenesis

    Article • Biochemical and Biophysical Research Communications, March 1999, Elsevier

    Dr. Noel S. Reading

  26. Effect of Modified Hemes on the Spectral Properties and Activity of Manganese Peroxidase

    Article • Archives of Biochemistry and Biophysics, November 1998, Elsevier

    Dr. Noel S. Reading

  27. Mechanisms for Protection against Inactivation of Manganese Peroxidase by Hydrogen Peroxide

    Article • Archives of Biochemistry and Biophysics, August 1998, Elsevier

    Dr. Noel S. Reading

  28. Expression of the Lignin Peroxidase H2 Gene fromPhanerochaete chrysosporiuminEscherichia coli

    Article • Biochemical and Biophysical Research Communications, August 1998, Elsevier

    Dr. Noel S. Reading