Diagnostic Utility of Multiprobe Fluorescence in situ Hybridization Assay for Detecting Cytogenetic Aberrations in Acute Leukemia

논문상세정보
' Diagnostic Utility of Multiprobe Fluorescence in situ Hybridization Assay for Detecting Cytogenetic Aberrations in Acute Leukemia' 의 주제별 논문영향력
논문영향력 선정 방법
논문영향력 요약
주제
  • 의학
  • acuteleukemia
  • cytogeneticaberration
  • multiprobefish
동일주제 총논문수 논문피인용 총횟수 주제별 논문영향력의 평균
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' Diagnostic Utility of Multiprobe Fluorescence in situ Hybridization Assay for Detecting Cytogenetic Aberrations in Acute Leukemia' 의 참고문헌

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    김석란 Annals of Laboratory Medicine 29 5 371-378 [2009]
  • The World Health Organization (WHO) classification of tumors of the hematopoietic and lymphoid tissues: an overview with emphasis on the myeloid neoplasms
    Vardiman JW Chem Biol Interact 184 16-20 [2010]
  • The BCR-ABL1 kinase bypasses selection for the expression of a pre-B cell receptor in pre-B acute lymphoblastic leukemia cells
    Klein F J Exp Med 199 673-685 [2004]
  • TP53 in hematological cancer: low incidence of mutations with significant clinical relevance
    Peller S Hum Mutat 21 277-284 [2003]
  • TEL/AML-1 fusion gene. its frequency and prognostic significance in childhood acute lymphoblastic leukemia
    Jamil A Cancer Genet Cytogenet 122 73-78 [2000]
  • Section E9 of the American College of Medical Genetics technical standards and guidelines: fluorescence in situ hybridization
    Mascarello JT Genet Med 13 667-675 [2011]
  • Proposals for the classification of the acute leukemias. French-American-British (FAB) co-operative group
    Bennett JM Br J Haematol 33 451-458 [1976]
  • Proposals for standardized protocols for cytogenetic analyses of acute leukemias, chronic lymphocytic leukemia, chronic myeloid leukemia, chronic myeloproliferative disorders, and myelodysplastic syndromes
    Haferlach C Genes Chromosomes Cancer 46 494-499 [2007]
  • Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B (CALGB 8461)
    Byrd JC Blood 100 4325-4336 [2002]
  • Preclinical validation of fluorescence in situ hybridization assays for clinical practice
    Wiktor AE Genet Med 8 16-23 [2006]
  • Karyotyping, FISH, and PCR in acute lymphoblastic leukemia: competing or complementary diagnostics?
    Olde Nordkamp L J Pediatr Hematol Oncol 31 930-935 [2009]
  • Improved outcome in adult B-cell acute lymphoblastic leukemia
    Hoelzer D Blood 87 495-508 [1996]
  • Guidance for fluorescence in situ hybridization testing in hematologic disorders
    Wolff DJ J Mol Diagn 9 134-143 [2007]
  • FISH panels for hematologic malignancies
    Sreekantaiah C Cytogenet Genome Res 118 284-296 [2007]
  • Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: report of the BIOMED-2 Concerted Action BMH4-CT98-3936
    van Dongen JJ Leukemia 17 2257-2317 [2003]
  • Cytogenetics in acute leukemia
    Mrózek, Heerema NA Blood Rev 18 115-136 [2004]
  • Clinical utility of FISH analysis in addition to G-banded karyotype in hematologic malignancies and proposal of a practical approach
    Won Kyung Kwon Blood Research 45 3 171-176 [2010]
  • Clinical importance of cytogenetics in acute myeloid leukaemia
    Mrózek K Best Pract Res Clin Haematol 14 19-47 [2001]
  • Analysis of discrepancies between G-banding and FISH in hematologic abnormalities
    Lee DY Korean J Clin Pathol 21 445-450 [2001]
  • An international system for human cytogenetic nomenclature
    Shaffer LG - [2005]
  • An international system for human cytogenetic nomenclature
    Shaffer LG - [2009]
  • A new reliable fluorescence in situ hybridization method for identifying multiple specific cytogenetic abnormalities in acute myeloid leukemia
    Valencia A Leuk Lymphoma 51 680-685 [2010]
  • A new nonrandom unbalanced t(17;20) in myeloid malignancies
    Patsouris C Cancer Genet Cytogenet 138 32-37 [2002]