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Neutrophil elastase mutations and risk of leukaemia in severe congenital neutropenia

dc.contributor.authorRosenberg, Philip S.en_US
dc.contributor.authorAlter, Blanche P.en_US
dc.contributor.authorLink, Daniel C.en_US
dc.contributor.authorStein, Stevenen_US
dc.contributor.authorRodger, Elinen_US
dc.contributor.authorBolyard, Audrey Annaen_US
dc.contributor.authorAprikyan, Andrew A.G.en_US
dc.contributor.authorBonilla, Mary A.en_US
dc.contributor.authorDror, Yigalen_US
dc.contributor.authorKannourakis, Georgeen_US
dc.contributor.authorNewburger, Peter E.en_US
dc.contributor.authorBoxer, Laurence A.en_US
dc.contributor.authorDale, David C.en_US
dc.date.accessioned2010-06-01T20:41:20Z
dc.date.available2010-06-01T20:41:20Z
dc.date.issued2008-01en_US
dc.identifier.citationRosenberg, Philip S.; Alter, Blanche P.; Link, Daniel C.; Stein, Steven; Rodger, Elin; Bolyard, Audrey A.; Aprikyan, Andrew A.; Bonilla, Mary A.; Dror, Yigal; Kannourakis, George; Newburger, Peter E.; Boxer, Laurence A.; Dale, David C. (2008). "Neutrophil elastase mutations and risk of leukaemia in severe congenital neutropenia." British Journal of Haematology 140(2): 210-213. <http://hdl.handle.net/2027.42/73793>en_US
dc.identifier.issn0007-1048en_US
dc.identifier.issn1365-2141en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/73793
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18028488&dopt=citationen_US
dc.format.extent148954 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rightsJournal Compilation 2007 Blackwell Publishing Ltd No claim to original US government worksen_US
dc.subject.otherSevere Congenital Neutropeniaen_US
dc.subject.otherNeutrophil Elastase ELA2en_US
dc.subject.otherAcute Myeloid Leukaemiaen_US
dc.subject.otherMyelodysplastic Syndromesen_US
dc.subject.otherGranulocyte Colony-stimulating Factoren_US
dc.titleNeutrophil elastase mutations and risk of leukaemia in severe congenital neutropeniaen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pediatrics, University of Michigan Medical Center, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherBiostatistics Branch, Division of Cancer Epidemiology and Genetics, Department of Health and Human Services, National Cancer Institute, National Institutes of Healthen_US
dc.contributor.affiliationotherClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, Department of Health and Human Services, National Cancer Institute, National Institutes of Health, Rockville, MDen_US
dc.contributor.affiliationotherDepartment of Medicine, Washington University School of Medicine, St Louis, MOen_US
dc.contributor.affiliationotherDepartment of Medicine, University of Washington, Seattle, WAen_US
dc.contributor.affiliationotherDepartment of Pediatric Hematology Oncology, St. Joseph’s Children’s Hospital, Paterson, NJ, USAen_US
dc.contributor.affiliationotherHospital for Sick Children, Toronto, ON, Canadaen_US
dc.contributor.affiliationotherBallarat Cancer Research Centre, University of Ballarat, Wendouree, Vic., Australiaen_US
dc.contributor.affiliationotherDepartment of Pediatrics, University of Massachusetts Medical School, Worcester, MAen_US
dc.identifier.pmid18028488en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/73793/1/j.1365-2141.2007.06897.x.pdf
dc.identifier.doi10.1111/j.1365-2141.2007.06897.xen_US
dc.identifier.sourceBritish Journal of Haematologyen_US
dc.identifier.citedreferenceAncliff, P.J. ( 2003 ) Congenital neutropenia. Blood Reviews, 17, 209 – 216.en_US
dc.identifier.citedreferenceAncliff, P.J., Gale, R.E., Liesner, R., Hann, I. & Linch, D.C. ( 2003 ) Long-term follow-up of granulocyte colony-stimulating factor receptor mutations in patients with severe congenital neutropenia: implications for leukaemogenesis and therapy. British Journal of Haematology, 120, 685 – 690.en_US
dc.identifier.citedreferenceBellanne-Chantelot, C., Clauin, S., Leblanc, T., Cassinat, B., Rodrigues-Lima, F., Beaufils, S., Vaury, C., Barkaoui, M., Fenneteau, O., Maier-Redelsperger, M., Chomienne, C. & Donadieu, J. ( 2004 ) Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia Register. Blood, 103, 4119 – 4125.en_US
dc.identifier.citedreferenceBoxer, L.A. & Newburger, P.E. ( 2007 ) A molecular classification of congenital neutropenia syndromes. Pediatric Blood & Cancer, 49, 609 – 614.en_US
dc.identifier.citedreferenceDale, D.C., Bonilla, M.A., Davis, M.W., Nakanishi, A.M., Hammond, W.P., Kurtzberg, J., Wang, W., Jakubowski, A., Winton, E. & Lalezari, P. ( 1993 ) A randomized controlled phase III trial of recombinant human granulocyte colony-stimulating factor (filgrastim) for treatment of severe chronic neutropenia. Blood, 81, 2496 – 2502.en_US
dc.identifier.citedreferenceDale, D.C., Person, R.E., Bolyard, A.A., Aprikyan, A.G., Bos, C., Bonilla, M.A., Boxer, L.A., Kannourakis, G., Zeidler, C., Welte, K., Benson, K.F. & Horwitz, M. ( 2000 ) Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood, 96, 2317 – 2322.en_US
dc.identifier.citedreferenceDale, D.C., Cottle, T.E., Fier, C.J., Bolyard, A.A., Bonilla, M.A., Boxer, L.A., Cham, B., Freedman, M.H., Kannourakis, G., Kinsey, S.E., Davis, R., Scarlata, D., Schwinzer, B., Zeidler, C. & Welte, K. ( 2003 ) Severe chronic neutropenia: treatment and follow-up of patients in the Severe Chronic Neutropenia International Registry. American Journal of Hematology, 72, 82 – 93.en_US
dc.identifier.citedreferenceHorwitz, M.S., Duan, Z., Korkmaz, B., Lee, H.H., Mealiffe, M.E. & Salipante, S.J. ( 2007 ) Neutrophil elastase in cyclic and severe congenital neutropenia. Blood, 109, 1817 – 1824.en_US
dc.identifier.citedreferenceKlein, C., Grudzien, M., Appaswamy, G., Germeshausen, M., Sandrock, I., Schaffer, A.A., Rathinam, C., Boztug, K., Schwinzer, B., Rezaei, N., Bohn, G., Melin, M., Carlsson, G., Fadeel, B., Dahl, N., Palmblad, J., Henter, J.I., Zeidler, C., Grimbacher, B. & Welte, K. ( 2007 ) HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Nature Genetics, 39, 86 – 92.en_US
dc.identifier.citedreferenceRosenberg, P.S., Alter, B.P., Bolyard, A.A., Bonilla, M.A., Boxer, L.A., Cham, B., Fier, C., Freedman, M., Kannourakis, G., Kinsey, S., Schwinzer, B., Zeidler, C., Welte, K. & Dale, D.C. ( 2006 ) The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy. Blood, 107, 4628 – 4635.en_US
dc.identifier.citedreferenceTouw, I.P. & Bontenbal, M. ( 2007 ) Granulocyte colony-stimulating factor: key (f)actor or innocent bystander in the development of secondary myeloid malignancy? Journal of the National Cancer Institute, 99, 183 – 186.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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