Search Results - "Heerema, N. A."

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    Long-term follow-up of imatinib in pediatric Philadelphia chromosome-positive acute lymphoblastic leukemia: Children's Oncology Group Study AALL0031 by Schultz, K R, Carroll, A, Heerema, N A, Bowman, W P, Aledo, A, Slayton, W B, Sather, H, Devidas, M, Zheng, H W, Davies, S M, Gaynon, P S, Trigg, M, Rutledge, R, Jorstad, D, Winick, N, Borowitz, M J, Hunger, S P, Carroll, W L, Camitta, B

    Published in Leukemia (01-07-2014)
    “…We previously reported preliminary findings that post induction imatinib mesylate (340 mg/m 2 /day), in combination with intensive chemotherapy, resulted in…”
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    Wwox–Brca1 interaction: role in DNA repair pathway choice by Schrock, M S, Batar, B, Lee, J, Druck, T, Ferguson, B, Cho, J H, Akakpo, K, Hagrass, H, Heerema, N A, Xia, F, Parvin, J D, Aldaz, C M, Huebner, K

    Published in Oncogene (20-04-2017)
    “…In this study, loss of expression of the fragile site-encoded Wwox protein was found to contribute to radiation and cisplatin resistance of cells, responses…”
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    Children's Cancer Group trials in childhood acute lymphoblastic leukemia : 1983-1995 by GAYNON, P. S, TRIGG, M. E, HEEREMA, N. A, SENSEL, M. G, SATHER, H. N, HAMMOND, G. D, BLEYER, W. A

    Published in Leukemia (01-12-2000)
    “…Since 1968, the Children's Cancer Group (CCG) has treated more than 16,000 children with acute lymphoblastic leukemia (ALL). Herein, we report improvements…”
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    Multiplex PCR: critical parameters and step-by-step protocol by Henegariu, O, Heerema, N A, Dlouhy, S R, Vance, G H, Vogt, P H

    Published in BioTechniques (01-09-1997)
    “…By simultaneously amplifying more than one locus in the same reaction, multiplex PCR is becoming a rapid and convenient screening assay in both the clinical…”
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    Genomic profiling in Down syndrome acute lymphoblastic leukemia identifies histone gene deletions associated with altered methylation profiles by Loudin, M G, Wang, J, Eastwood Leung, H-C, Gurusiddappa, S, Meyer, J, Condos, G, Morrison, D, Tsimelzon, A, Devidas, M, Heerema, N A, Carroll, A J, Plon, S E, Hunger, S P, Basso, G, Pession, A, Bhojwani, D, Carroll, W L, Rabin, K R

    Published in Leukemia (01-10-2011)
    “…Patients with Down syndrome (DS) and acute lymphoblastic leukemia (ALL) have distinct clinical and biological features. Whereas most DS-ALL cases lack the…”
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    Deletion of 7p or monosomy 7 in pediatric acute lymphoblastic leukemia is an adverse prognostic factor: a report from the Children's Cancer Group by HEEREMA, N. A, NACHMAN, J. B, SATHER, H. N, LA, M. K, HUTCHINSON, R, LANGE, B. J, BOSTROM, B, STEINHERZ, P. G, GAYNON, P. S, UCKUN, F. M

    Published in Leukemia (01-05-2004)
    “…Monosomy 7 or deletions of 7q are associated with many myeloid disorders; however, the significance of such abnormalities in childhood acute lymphoblastic…”
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    Maternal vitamin and iron supplementation and risk of infant leukaemia: a report from the Children's Oncology Group by Linabery, A M, Puumala, S E, Hilden, J M, Davies, S M, Heerema, N A, Roesler, M A, Ross, J A

    Published in British journal of cancer (23-11-2010)
    “…Background: Prenatal supplementation has been inversely associated with childhood, but not with infant, leukaemia. Methods: Mothers of 443 cases of infant…”
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    Expression of HOX11 in childhood T-lineage acute lymphoblastic leukaemia can occur in the absence of cytogenetic aberration at 10q24: a study from the Children's Cancer Group (CCG) by KEES, U. R, HEEREMA, N. A, KUMAR, R, WATT, P. M, BAKER, D. L, LA, M. K, UCKUN, F. M, SATHER, H. N

    Published in Leukemia (01-05-2003)
    “…Clonal genetic aberrations in tumour cells provide critical information for the development of new diagnostic and therapeutic strategies for patients. In…”
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    Cytogenetic studies of infant acute lymphoblastic leukemia : Poor prognosis of infants with t(4;11) : A report of the Children's Cancer Group by HEEREMA, N. A, SATHER, H. N, GE, J, ARTHUR, D. C, HILDEN, J. M, TRIGG, M. E, REAMAN, G. H

    Published in Leukemia (01-05-1999)
    “…Infants less than 1 year of age at diagnosis of acute lymphoblastic leukemia (ALL) have a poor prognosis, which has been attributed primarily to a breakpoint…”
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    Hypodiploidy With Less Than 45 Chromosomes Confers Adverse Risk in Childhood Acute Lymphoblastic Leukemia: A Report From the Children's Cancer Group by Heerema, Nyla A., Nachman, James B., Sather, Harland N., Sensel, Martha G., Lee, Mei K., Hutchinson, Raymond, Lange, Beverly J., Steinherz, Peter G., Bostrom, Bruce, Gaynon, Paul S., Uckun, Fatih

    Published in Blood (15-12-1999)
    “…We have determined the prognostic significance of hypodiploidy (<46 chromosomes) in a large cohort of children with acute lymphoblastic leukemia (ALL) treated…”
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    Filgrastim and alemtuzumab (Campath-1H) for refractory chronic lymphocytic leukemia by LIN, T. S, FLINN, I. W, LUCAS, M. S, PORCU, P, SICKLER, J, MORAN, M. E, LUCAS, D. M, HEEREMA, N. A, GREVER, M. R, BYRD, J. C

    Published in Leukemia (01-07-2005)
    “…Alemtuzumab (anti-CD52; Campath-1H) is effective in fludarabine-refractory chronic lymphocytic leukemia (CLL), but is associated with infection and early onset…”
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    Childhood and maternal infections and risk of acute leukaemia in children with Down syndrome: a report from the Children's Oncology Group by CANFIELD, K. N, SPECTOR, L. G, ROSS, J. A, ROBISON, L. L, LAZOVICH, D, ROESLER, M, OLSHAN, A. F, SMITHS, F. O, HEEREMA, N. A, BARNARD, D. R, BLAIR, C. K

    Published in British journal of cancer (29-11-2004)
    “…Children with Down syndrome (DS) are highly susceptible to acute leukaemia. Given the potential role of infections in the aetiology of leukaemia in children…”
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    Cytogenetic features of infants less than 12 months of age at diagnosis of acute lymphoblastic leukemia : impact of the 11q23 breakpoint on outcome : a report of the Childrens Cancer Group by HEEREMA, N. A, ARTHUR, D. C, SATHER, H, ALBO, V, FEUSNER, J, LANGE, B. J, STEINHERZ, P. G, ZELTZER, P, HAMMOND, D, REAMAN, G. H

    Published in Blood (15-04-1994)
    “…Cytogenetic analyses of pretreatment bone marrows were performed at local institutions as part of Childrens Cancer Group (CCG) protocol CCG-107 for infants…”
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