Recessive congenital methaemoglobinaemia: cytochrome b5 reductase deficiency von Percy, Melanie J., Lappin, Terry R.

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HOXA/PBX3 knockdown impairs growth and sensitizes cytogenetically normal acute myeloid leukemia cells to chemotherapy von Dickson, G. J., Liberante, F. G., Kettyle, L. M., O'Hagan, K. A., Finnegan, D. P. J., Bullinger, L., Geerts, D., McMullin, M. F., Lappin, T. R. J., Mills, K. I., Thompson, A.

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Recessive congenital methaemoglobinaemia: cytochrome b(5) reductase deficiency von Percy, Melanie J, Lappin, Terry R

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Editorial: Sibling Synergy von Lappin, Terry R J

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A Tale of Two Sisters von Lappin, Terry R.J.

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Erythropoietin-induced activation of the JAK2/STAT5, PI3K/Akt, and Ras/ERK pathways promotes malignant cell behavior in a modified breast cancer cell line von Shi, Zhanzhong, Hodges, Vivien M, Dunlop, Elaine A, Percy, Melanie J, Maxwell, Alexander P, El-Tanani, Mohamed, Lappin, Terry R J

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Familial idiopathic methemoglobinemia revisited: original cases reveal 2 novel mutations in NADH-cytochrome b5 reductase von Percy, Melanie J., Gillespie, Matthew J.S., Savage, Geraldine, Hughes, Anne E., McMullin, Mary Frances, Lappin, Terry R.J.

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Sibling Synergy von Lappin, Terry R.J.

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GATA2 regulates the erythropoietin receptor in t(12;21) ALL von Gaine, Marie E, Sharpe, Daniel J, Smith, James S, Colyer, Hilary A A, Hodges, Vivien M, Lappin, Terry R, Mills, Ken I

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A Tale of Two Sisters von Lappin, Terry R.J.

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Disorders of oxidised haemoglobin von Percy, Melanie J., McFerran, Neil V., Lappin, Terry R.J.

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Editorial: Our Top 10 Developments in Stem Cell Biology over the Last 30 Years von Armstrong, Lyle, Lako, Majlinda, Buckley, Noel, Lappin, Terry R.J., Murphy, Martin J., Nolta, Jan A., Pittenger, Mark, Stojkovic, Miodrag

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The worldwide distribution of the VHL 598C>T mutation indicates a single founding event von Liu, Enli, Percy, Melanie J., Amos, Christopher I., Guan, Yongli, Shete, Sanjay, Stockton, David W., McMullin, Mary F., Polyakova, Lydia A., Ang, Sonny O., Pastore, Yves D., Jedlickova, Katerina, Lappin, TerryR.J., Gordeuk, Victor, Prchal, Josef T.

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Recessive congenital methaemoglobinaemia: cytochrome b 5 reductase deficiency von Percy, Melanie J., Lappin, Terry R.

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A Novel HIFalpha Mutation Associated with Familial Erythrocytosis Supports This Isoform Being the Major Regulator of Erythropoietin in Humans von Percy, Melanie J., Furlow, Paul W., Lucas, Guy S., Li, Xiping, Lappin, Terry R., McMullin, Mary F., Lee, Frank S.

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Peptide Leucine Arginine, a Potent Immunomodulatory Peptide Isolated and Structurally Characterized from the Skin of the Northern Leopard Frog, Rana pipiens von Salmon, Amanda L., Cross, Laurence J.M., Irvine, Alexandra E., Lappin, Terry R.J., Dathe, Margitta, Krause, Gerd, Canning, Paul, Thim, Lars, Beyermann, Michael, Rothemund, Sven, Bienert, Michael, Shaw, Chris

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GATA2 regulates the erythropoietin receptor in t(12;21) ALL von Gaine, Marie E, Sharpe, Daniel J, Smith, James S, Colyer, Hilary AA, Hodges, Vivien M, Lappin, Terry R, Mills, Ken I

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Hemoglobin Old Dominion/Burton-upon-Trent, (beta 143) (H21) His -> Tyr, Codon 143 CAC -> TAC--a variant with altered oxygen affinity that compromises measurement of glycated hemogl... von Elder, G Elizabeth, Lappin, Terry R J, Horne, Allen B, Fairbanks, Virgil F

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The worldwide distribution of the VHL 598C>T mutation indicates a single founding event von ENLI LIU, PERCY, Melanie J, JEDLICKOVA, Katerina, LAPPIN, Terry R. J, GORDEUK, Victor, PRCHAL, Josef T, AMOS, Christopher I, YONGLI GUAN, SHETE, Sanjay, STOCKTON, David W, MCMULLIN, Mary F, POLYAKOVA, Lydia A, ANG, Sonny O, PASTORE, Yves D

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Evaluating Elements of the Care Partner Experience in Individuals Who Care for People with Alzheimer's Disease Across the Severity Spectrum von Callahan, Leigh F., Samsell, Brian, DiBenedetti, Dana, Frangiosa, Terry, Slota, Christina, Biggar, Virginia, Paulsen, Russ, Lappin, Debra, Herring, William L., Romano, Carla

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