List of works - N Scott Reading

5'-(RACE) identification of rare ALK fusion partner in anaplastic large cell lymphoma.

scientific article published on May 2003

A Novel Variant in G6PD (c.1375C>G) Identified from a Hispanic Neonate with Extreme Hyperbilirubinemia and Low G6PD Enzymatic Activity

scientific article published on 28 September 2020

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

scientific article published on 13 February 2017

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 curves

scientific article published on 8 January 2013

Acute kernicterus in a neonate with O/B blood group incompatibility and a mutation in SLC4A1.

scientific article published on 22 July 2013

Addition of veratryl alcohol oxidase activity to manganese peroxidase by site-directed mutagenesis

scientific article published on 01 March 1999

Angiogenic and inflammatory markers of cardiopulmonary changes in children and adolescents with sickle cell disease

scientific article

Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia

scientific article

CYB5R3c .350C>G and G6PD A Alleles Modify Severity of Anemia in Malaria and Sickle Cell Disease

scientific article published on 22 July 2020

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

scientific article published on 01 September 2014

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

scientific article

Detection of nine Mediterranean β-thalassemia mutations in Palestinians using three restriction enzyme digest panels: a reliable method for developing countries

scientific article published on 21 October 2013

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.

scientific article

Effect of modified hemes on the spectral properties and activity of manganese peroxidase

scientific article published on 01 November 1998

Engineering a disulfide bond in recombinant manganese peroxidase results in increased thermostability

scientific article published on 01 May 2000

Expression of the Rho-family GTPase gene RHOF in lymphocyte subsets and malignant lymphomas.

scientific article

Expression of the lignin peroxidase H2 gene from Phanerochaete chrysosporium in Escherichia coli

scientific article published on 01 August 1998

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

scientific article published on 22 February 2012

Mechanisms for protection against inactivation of manganese peroxidase by hydrogen peroxide

scientific article

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

scientific article published in December 2007

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

scientific article published on 5 July 2012

National G6PD neonatal screening program in Gaza Strip of Palestine: rationale, challenges and recommendations

scientific article published on 10 April 2016

Neonatal death suspected to be from sepsis was found to be kernicterus with G6PD deficiency

scientific article published on 11 November 2013

Relative stability of recombinant versus native peroxidases from Phanerochaete chrysosporium

scientific article published on 01 May 1999

Role of disulfide bonds in the stability of recombinant manganese peroxidase

scientific article published on 01 July 2001

The 'GGCC' haplotype of JAK2 confers susceptibility to JAK2 exon 12 mutation-positive polycythemia vera

scientific article

Unexplained extreme hyperbilirubinemia among neonates in a multihospital healthcare system.

scientific article

Variations in both α-spectrin (SPTA1) and β-spectrin ( SPTB ) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosis.

scientific article published on 31 October 2013

List of works by N Scott Reading

5'-(RACE) identification of rare ALK fusion partner in anaplastic large cell lymphoma.

A Novel Variant in G6PD (c.1375C>G) Identified from a Hispanic Neonate with Extreme Hyperbilirubinemia and Low G6PD Enzymatic Activity

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

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 curves

Acute kernicterus in a neonate with O/B blood group incompatibility and a mutation in SLC4A1.

Addition of veratryl alcohol oxidase activity to manganese peroxidase by site-directed mutagenesis

Angiogenic and inflammatory markers of cardiopulmonary changes in children and adolescents with sickle cell disease

Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia

CYB5R3c .350C>G and G6PD A Alleles Modify Severity of Anemia in Malaria and Sickle Cell Disease

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

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

Detection of nine Mediterranean β-thalassemia mutations in Palestinians using three restriction enzyme digest panels: a reliable method for developing countries

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.

Effect of modified hemes on the spectral properties and activity of manganese peroxidase

Engineering a disulfide bond in recombinant manganese peroxidase results in increased thermostability

Expression of the Rho-family GTPase gene RHOF in lymphocyte subsets and malignant lymphomas.

Expression of the lignin peroxidase H2 gene from Phanerochaete chrysosporium in Escherichia coli

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

Mechanisms for protection against inactivation of manganese peroxidase by hydrogen peroxide

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

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

National G6PD neonatal screening program in Gaza Strip of Palestine: rationale, challenges and recommendations

Neonatal death suspected to be from sepsis was found to be kernicterus with G6PD deficiency

Relative stability of recombinant versus native peroxidases from Phanerochaete chrysosporium

Role of disulfide bonds in the stability of recombinant manganese peroxidase

The 'GGCC' haplotype of JAK2 confers susceptibility to JAK2 exon 12 mutation-positive polycythemia vera

Unexplained extreme hyperbilirubinemia among neonates in a multihospital healthcare system.

Variations in both α-spectrin (SPTA1) and β-spectrin ( SPTB ) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosis.