Search Results - N. Scott Reading
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Missense mutation of the last nucleotide of exon 1 (G->C) of β globin gene not only leads to undetectable mutant peptide and transcript but also interferes with the expression of w... by Neeraj Agarwal, Ferdane Kutlar, Mariluz P. Mojica-Henshaw, Ching N. Ou, Amos Gaikwad, N. Scott Reading, Lakeia Bailey, Abdullah Kutlar, Josef T. Prchal
Published 2007-12-01
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Clinical, metabolic, and genetic characterization of hereditary methemoglobinemia caused by cytochrome b5 reductase deficiency in cats by Jared A. Jaffey, N. Scott Reading, Urs Giger, Osheiza Abdulmalik, Ruben M. Buckley, Sophie Johnstone, Leslie A. Lyons, the 99 Lives Cat Genome Consortium
Published 2019-11-01
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Angiogenic and inflammatory markers of cardiopulmonary changes in children and adolescents with sickle cell disease. by Xiaomei Niu, Mehdi Nouraie, Andrew Campbell, Sohail Rana, Caterina P Minniti, Craig Sable, Deepika Darbari, Niti Dham, N Scott Reading, Josef T Prchal, Gregory J Kato, Mark T Gladwin, Oswaldo L Castro, Victor R Gordeuk
Published 2009-11-01
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Concordance of assays designed for the quantification of JAK2V617F: a multicenter study by Eric Lippert, François Girodon, Emma Hammond, Jaroslav Jelinek, N. Scott Reading, Boris Fehse, Katy Hanlon, Mirjam Hermans, Céline Richard, Sabina Swierczek, Valérie Ugo, Serge Carillo, Véronique Harrivel, Christophe Marzac, Daniela Pietra, Marta Sobas, Morgane Mounier, Marina Migeon, Sian Ellard, Nicolaus Kröger, Richard Herrmann, Josef T. Prchal, Radek C. Skoda, Sylvie Hermouet
Published 2009-01-01
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