Biblioteca Digital

496 resultados para Cronyn, Terence

Erythrocytosis caused by mutations in the PHD2 and VHL genes

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Growth factor-independent cell lines derived from retrovirally-infected TF-1 cells exhibit a selective block in erythropoietin-induced differentiation.

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A novel Arg371His mutation in the HIF prolyl hydroxylase PHD2 is associated with erythrocytosis

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Alternative splicing targets PBX3 mrna for nonsense mediated decay

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Investigation of HOXA6 as a candidate gene in AML

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Artificial neural network analysis identifies novel patterns of HOX gene expression in prognostic subgroups of acute myeloid leukaemia

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HOXA6: A novel candidate gene in AML.

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Artificial neural NetworkAnalysis of HOX gene expression profiles predicts prognostic subgroups in acute myeloid leukemia.

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A novel mutation in the HIF prolyl hydroxylase, PHD2, associated with familial erythrocytosis

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Expression of NADH-cytochrome b(5) reductase variants provides important functional insights into recessive congenital methaemoglobinaemia

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The spectrum of molecular defects in idiopathic erythrocytosis

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Familial erythrocytosis associated with a mutation in the HIF prolyl hydroxylase, PHD2.

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Mutations in the VHL gene are the major identified cause of inherited erythrocytosis.

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Type I methemoglobinemia arising due to a change in cofactor specificity of cytochrome B5 reductase

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The C598T VHL mutation arose in an ancestor common to Asian and Caucasian populations

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