Search Results - "Percy, M.J."

Establishing optimal quantitative-polymerase chain reaction assays for routine diagnosis and tracking of minimal residual disease in JAK2-V617F-associated myeloproliferative neoplasms: a joint European LeukemiaNet/MPN&MPNr-EuroNet (COST action BM0902) study by Jovanovic, J V, Ivey, A, Vannucchi, A M, Lippert, E, Oppliger Leibundgut, E, Cassinat, B, Pallisgaard, N, Maroc, N, Hermouet, S, Nickless, G, Guglielmelli, P, van der Reijden, B A, Jansen, J H, Alpermann, T, Schnittger, S, Bench, A, Tobal, K, Wilkins, B, Cuthill, K, McLornan, D, Yeoman, K, Akiki, S, Bryon, J, Jeffries, S, Jones, A, Percy, M J, Schwemmers, S, Gruender, A, Kelley, T W, Reading, S, Pancrazzi, A, McMullin, M F, Pahl, H L, Cross, N C P, Harrison, C N, Prchal, J T, Chomienne, C, Kiladjian, J J, Barbui, T, Grimwade, D

“…Reliable detection of JAK2 -V617F is critical for accurate diagnosis of myeloproliferative neoplasms (MPNs); in addition, sensitive mutation-specific assays…”
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Expression of a novel P275L variant of NADH:cytochrome b 5 reductase gives functional insight into the conserved motif important for pyridine nucleotide binding by Percy, M.J., Crowley, L.J., Boudreaux, J., Barber, M.J.

“…The clinical disorder of recessive congenital methemoglobinemia (RCM, OMIN 250800) is associated with mutations in NADH:cytochrome b 5 reductase (c b 5r) and…”
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Induction of signalling in non-erythroid cells by pharmacological levels of erythropoietin by Dunlop, E A, Percy, M J, Boland, M P, Maxwell, A P, Lappin, T R

“…Erythropoiesis is maintained by the hormone erythropoietin (Epo) binding to its cognate receptor (EpoR) on erythroid progenitor cells. The Epo-EpoR interaction…”
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Expression of a novel P275L variant of NADH:cytochrome b5 reductase gives functional insight into the conserved motif important for pyridine nucleotide binding by Percy, M J, Crowley, L J, Boudreaux, J, Barber, M J

“…The clinical disorder of recessive congenital methemoglobinemia (RCM, OMIN 250800) is associated with mutations in NADH:cytochrome b5 reductase (cb5r) and…”
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Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b5 reductase: An aid to determine recessive congenital methemoglobinemia status in an infant by Percy, M.J., Crowley, L.J., Roper, D., Vulliamy, T.J., Layton, D.M., Barber, M.J.

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Identification and characterization of the novel FAD-binding lobe G75S mutation in cytochrome b 5 reductase: An aid to determine recessive congenital methemoglobinemia status in an infant by Percy, M.J., Crowley, L.J., Roper, D., Vulliamy, T.J., Layton, D.M., Barber, M.J.

“…NADH–cytochrome b 5 reductase deficiency results clinically in either type I or type II recessive congenital methemoglobinemia. The more severe type II form is…”
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Oxygen Sensing-From Bedside to Bench: A Family with Erythrocytosis Establishes a Role for Prolyl Hydroxylase Domain Protein 2 in Oxygen Homeostasis. Proc National Acad Sci U S A 103: 654-659, 2006 by Percy, M J, Zhao, Q, Flores, A, Harrison, C, Lappin, T R, Maxwell, P H, McMullin, M F, Lee, F S

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Impact ionization experiments with low density conducting polymer-based micro-projectiles as analogues of solar system dusts by Burchell, M.J, Willis, M.J, Armes, S.P, Khan, M.A, Percy, M.J, Perruchot, C

“…Results for electrostatic acceleration of organic, silica- and metal-based micro-projectiles ( <1 μm diameter) are presented. These micro-projectiles, which…”
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Pyruvate kinase deficient hemolytic anemia in the Northern Irish population by Percy, M.J., van Wijk, R., Haggan, S., Savage, G.A., Boyd, K., Dempsey, S., Hamilton, J., Kettle, P., Kyle, A., Shepherd, C.W., van Solinge, W.W., Lappin, T.R.J., McMullin, M.F.

“…A common cause of hereditary nonspherocytic hemolytic anemia is pyruvate kinase deficiency, which is associated with lifelong chronic hemolysis. Pyruvate…”
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Novel and Mediterranean β thalassemia mutations in the indigenous Northern Ireland population by Knott, M., Ramadan, K.M.A., Savage, G., Jones, F.G.C., El-Agnaf, M., McMullin, M.F., Percy, M.J.

“…β thalassemia is one of the most common genetic diseases worldwide resulting from aberrant β-globin chain production. It is highly prevalent in regions with…”
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Intracellular antigenic changes associated with meiosis in the orthopteran Stauroderus scalaris by Percy, M J, Fletcher, H L, Trudgett, A

“…Monoclonal antibodies have been prepared against purified pachytene cells from grasshopper testes. Immunoblotting and immunofluorescence analyses identified…”
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