Zobrazeno 1 - 10 of 27 pro vyhledávání: '"N A, Heerema"'
2
Interferon-alpha-2b downregulation of oncogenes H-ras, c-raf-2, c-kit, c-myc, c-myb and c-fos in eskol, a hairy cell leukemic line, results in temporal perturbation of signal transduction cascade
Autor: L R Lowe, Steven T. Kosak, J C Sheaffer, N A Heerema, William H. Harvey, Omar S. Harb
Publikováno v: Leukemia Research. 18:577-585
ESKOL, a B-lymphoblastoid cell line consisting of late differentiated cells, resembles hairy cell leukemia (HCL). It is pseudodiploid with a deleted 7q and an unbalanced translocation between chromosomes 4 and 6. It was screened by Northern hybridiza
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6241f003abcc5e581121e2dea511a1c
https://doi.org/10.1016/0145-2126(94)90039-6
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3
Multifocal primary neuroblastoma
Autor: Mervyn D. Cohen, N. A. Heerema, S. T. Auringer, Jay L. Grosfeld, Carlos A. Galliani
Publikováno v: Pediatric Radiology. 23:463-466
The purpose of this study is to present three patients with multifocal primary neuroblastoma, to review the literature, and describe the radiographic findings.Subjects and methods. Three children with multifocal neuroblastoma have been identified. Th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5e1b24cac4e1abfd0c78abec69e2728
https://doi.org/10.1007/bf02012454
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5
Improvements in cytogenetic slide preparation: controlled chromosome spreading, chemical aging and gradual denaturing
Autor: O, Henegariu, N A, Heerema, L, Lowe Wright, P, Bray-Ward, D C, Ward, G H, Vance
Publikováno v: Cytometry. 43(2)
Metaphase spreading is an essential technique for clinical and molecular cytogenetics. Results of classical banding techniques as well as complex fluorescent in situ hybridization (FISH) applications, such as comparative genomic hybridization (CGH) o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c57ea90ad870d51e586c728ea0bb9ac7
https://pubmed.ncbi.nlm.nih.gov/11169574
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6
Prognostic significance of cytogenetic abnormalities of chromosome arm 12p in childhood acute lymphoblastic leukemia: a report from the Children's Cancer Group
Autor: N A, Heerema, H N, Sather, M G, Sensel, M K, Lee, R, Hutchinson, J B, Nachman, B J, Lange, P G, Steinherz, B, Bostrom, P S, Gaynon, F M, Uckun
Publikováno v: Cancer. 88(8)
The authors have determined the prognostic significance of cytogenetically detectable 12p abnormalities, which are frequent in children with acute lymphoblastic leukemia (ALL), in a large cohort of patients treated on risk-adjusted protocols of the C
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9c716874775b29b3b9a359b79d5e630e
https://pubmed.ncbi.nlm.nih.gov/10760773
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7
Detection of monosomy 7 in bone marrow by fluorescence in situ hybridization. A study of Fanconi anemia patients and review of the literature
Autor: V C, Thurston, T M, Ceperich, G H, Vance, N A, Heerema
Publikováno v: Cancer genetics and cytogenetics. 109(2)
Monosomy 7 is frequently found in the bone marrow of patients with Fanconi anemia (FA), marrow myelodysplasia, or acute myelogenous leukemia and is associated with poor prognosis. In our laboratory, cytogenetic analysis of bone marrow from an FA pati
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6a6f0c3dcb70d19e9cb8a8d4e6e3fae6
https://pubmed.ncbi.nlm.nih.gov/10087952
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8
Cytogenetic analyses of 85 testicular germ cell tumors: comparison of postchemotherapy and untreated tumors
Autor: T A, Smolarek, R I, Blough, R S, Foster, T M, Ulbright, C G, Palmer, N A, Heerema
Publikováno v: Cancer genetics and cytogenetics. 108(1)
Cytogenetic analyses of 85 testicular germ cell tumors, of which 54 were karyotypically abnormal, showed recurrent breakpoints at chromosome bands 1p36, 1p13-1qh, 11q23, 19q13, and the pericentromeric regions of the acrocentric chromosomes. Postchemo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2494cee08cf7bb740b96bb142973c121
https://pubmed.ncbi.nlm.nih.gov/9973926
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9
Clinical significance of Philadelphia chromosome positive pediatric acute lymphoblastic leukemia in the context of contemporary intensive therapies: a report from the Children's Cancer Group
Autor: F M, Uckun, J B, Nachman, H N, Sather, M G, Sensel, P, Kraft, P G, Steinherz, B, Lange, R, Hutchinson, G H, Reaman, P S, Gaynon, N A, Heerema
Publikováno v: Cancer. 83(9)
Children with Philadelphia (Ph) chromosome positive (+) acute lymphoblastic leukemia (ALL) represent a subgroup at very high risk for treatment failure. In this report, the authors assessed the outcome of Ph+ ALL in a large cohort of children treated
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ec053a10d3e235dcada5db827abc9411
https://pubmed.ncbi.nlm.nih.gov/9806664
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10
The association of aneuploidy and unexplained elevated maternal serum alpha-fetoprotein
Autor: A K, Hiett, C M, Callaghan, H L, Brown, A M, Golichowski, N A, Heerema
Publikováno v: Journal of perinatology : official journal of the California Perinatal Association. 18(5)
The purpose of this study was to examine fetal chromosomal abnormalities in pregnancies complicated by unexplained elevated maternal serum alpha-fetoprotein (MSAFP).We reviewed, using a computerized database, 58,162 obstetrical ultrasounds that were
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b5b9af0fc81bbebfbec707c00c1db104
https://pubmed.ncbi.nlm.nih.gov/9766408
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