Pascal and Francis Bibliographic Databases

Help

Export

Selection :

Permanent link
http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18245601

Rationale for the recommendations for harmonizing current methodology for detecting BCR-ABL transcripts in patients with chronic myeloid leukaemia

Author
BRANFORD, S1 ; CROSS, N. C. P2 ; HOCHHAUS, A3 ; RADICH, J4 ; SAGLIO, G5 ; KAEDA, J6 ; GOLDMAN, J7 ; HUGHES, T8
[1] Division of Molecular Pathology, Institute of Medical and Veterinary Science, Adelaide, South Australia, Australia
[2] National Genetics Reference Laboratory, University of Southampton, Salisbury, United Kingdom
[3] Faculty of Clinical Medicine Mannheim, University of Heidelberg, Mannheim, Germany
[4] Divisions of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, United States
[5] Division of Hematology and Internal Medicine, University of Turin, Orbassano, Italy
[6] Department of Haematology, Imperial College at Hammersmith Hospital, London, United Kingdom
[7] Hematology Branch, National Heart, Lung & Blood Institute, NIH, Bethesda, MD, United States
[8] Division of Haematology, Institute of Medical and Veterinary Science, Adelaide, South Australia, Australia
Source

Leukemia. 2006, Vol 20, Num 11, pp 1925-1930, 6 p ; ref : 41 ref

CODEN
LEUKED
ISSN
0887-6924
Scientific domain
Medical oncology; Hematology
Publisher
Nature Publishing, London
Publication country
United Kingdom
Document type
Article
Language
English
Author keyword
BCR-ABL measurement reliability quality assurance real-time quantitative PCR
Keyword (fr)
Analyse quantitative Assurance qualité Chromosome C9 anormal Chromosome G22 anormal Chromosome Ph1 Chronique Fiabilité Gène hybride Homme Leucémie myéloïde Méthodologie Protein kinase RNA messager Recommandation Réaction chaîne polymérase Temps réel Translocation chromosomique Gène abl Gène bcr Hémopathie maligne myéloïde Leucémie myéloïde chronique Protéine bcr-abl Aberration chromosomique Biologie moléculaire Chromosome anormal Enzyme Hémopathie maligne Myéloprolifératif syndrome Transferases
Keyword (en)
Quantitative analysis Quality assurance Abnormal chromosome C9 Abnormal chromosome G22 Philadelphia chromosome Chronic Reliability Hybrid gene Human Chronic myelocytic leukemia Methodology Protein kinase Messenger RNA Recommendation Polymerase chain reaction Real time Chromosome translocation Myeloid neoplasm Chronic myelocytic leukemia Bcr-abl protein Chromosomal aberration Molecular biology Abnormal chromosome Enzyme Malignant hemopathy Myeloproliferative syndrome Transferases
Keyword (es)
Análisis cuantitativo Aseguración calidad Cromosoma C9 anormal Cromosoma G22 anormal Cromosoma Ph1 Crónico Fiabilidad Gen híbrido Hombre Leucemia mieloidea Metodología Protein kinase RNA mensajero Recomendación Reacción cadena polimerasa Tiempo real Translocación cromosómica Leucemia mieloidea Aberración cromosómica Biología molecular Cromosoma anormal Enzima Hemopatía maligna Mieloproliferativo síndrome Transferases
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19B Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23B Chromosome aberrations

Discipline
Blood diseases Medical genetics
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
18245601

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

Access to the document

Searching the Web