Neutrophil elastase mutations and risk of leukaemia in severe congenital neutropenia
dc.contributor.author | Rosenberg, Philip S. | en_US |
dc.contributor.author | Alter, Blanche P. | en_US |
dc.contributor.author | Link, Daniel C. | en_US |
dc.contributor.author | Stein, Steven | en_US |
dc.contributor.author | Rodger, Elin | en_US |
dc.contributor.author | Bolyard, Audrey Anna | en_US |
dc.contributor.author | Aprikyan, Andrew A.G. | en_US |
dc.contributor.author | Bonilla, Mary A. | en_US |
dc.contributor.author | Dror, Yigal | en_US |
dc.contributor.author | Kannourakis, George | en_US |
dc.contributor.author | Newburger, Peter E. | en_US |
dc.contributor.author | Boxer, Laurence A. | en_US |
dc.contributor.author | Dale, David C. | en_US |
dc.date.accessioned | 2010-06-01T20:41:20Z | |
dc.date.available | 2010-06-01T20:41:20Z | |
dc.date.issued | 2008-01 | en_US |
dc.identifier.citation | Rosenberg, 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.issn | 0007-1048 | en_US |
dc.identifier.issn | 1365-2141 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/73793 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18028488&dopt=citation | en_US |
dc.format.extent | 148954 bytes | |
dc.format.extent | 3109 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.publisher | Blackwell Publishing Ltd | en_US |
dc.rights | Journal Compilation 2007 Blackwell Publishing Ltd No claim to original US government works | en_US |
dc.subject.other | Severe Congenital Neutropenia | en_US |
dc.subject.other | Neutrophil Elastase ELA2 | en_US |
dc.subject.other | Acute Myeloid Leukaemia | en_US |
dc.subject.other | Myelodysplastic Syndromes | en_US |
dc.subject.other | Granulocyte Colony-stimulating Factor | en_US |
dc.title | Neutrophil elastase mutations and risk of leukaemia in severe congenital neutropenia | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Oncology and Hematology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Pediatrics, University of Michigan Medical Center, Ann Arbor, MI, USA | en_US |
dc.contributor.affiliationother | Biostatistics Branch, Division of Cancer Epidemiology and Genetics, Department of Health and Human Services, National Cancer Institute, National Institutes of Health | en_US |
dc.contributor.affiliationother | Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, Department of Health and Human Services, National Cancer Institute, National Institutes of Health, Rockville, MD | en_US |
dc.contributor.affiliationother | Department of Medicine, Washington University School of Medicine, St Louis, MO | en_US |
dc.contributor.affiliationother | Department of Medicine, University of Washington, Seattle, WA | en_US |
dc.contributor.affiliationother | Department of Pediatric Hematology Oncology, St. Joseph’s Children’s Hospital, Paterson, NJ, USA | en_US |
dc.contributor.affiliationother | Hospital for Sick Children, Toronto, ON, Canada | en_US |
dc.contributor.affiliationother | Ballarat Cancer Research Centre, University of Ballarat, Wendouree, Vic., Australia | en_US |
dc.contributor.affiliationother | Department of Pediatrics, University of Massachusetts Medical School, Worcester, MA | en_US |
dc.identifier.pmid | 18028488 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/73793/1/j.1365-2141.2007.06897.x.pdf | |
dc.identifier.doi | 10.1111/j.1365-2141.2007.06897.x | en_US |
dc.identifier.source | British Journal of Haematology | en_US |
dc.identifier.citedreference | Ancliff, P.J. ( 2003 ) Congenital neutropenia. Blood Reviews, 17, 209 – 216. | en_US |
dc.identifier.citedreference | Ancliff, 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.citedreference | Bellanne-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.citedreference | Boxer, L.A. & Newburger, P.E. ( 2007 ) A molecular classification of congenital neutropenia syndromes. Pediatric Blood & Cancer, 49, 609 – 614. | en_US |
dc.identifier.citedreference | Dale, 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.citedreference | Dale, 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.citedreference | Dale, 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.citedreference | Horwitz, 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.citedreference | Klein, 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.citedreference | Rosenberg, 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.citedreference | Touw, 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.owningcollname | Interdisciplinary and Peer-Reviewed |
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