Chronic lymphocytic leukemia cells with allelic deletions at 13q14 commonly have one intact RB1 gene : evidence for a role of an adjacent locus
- Author
- YIE LIU1 ; SZEKELY, L; GRANDER, D1 ; SÖDERHÄLL, S; JULIUSSON, G; GAHRTON, G; LINDER, S1 ; EINHORN, S1
[1] Radiumhemmet, div. exp. oncology, 104 01 Stockholm, Sweden - Source
Proceedings of the National Academy of Sciences of the United States of America. 1993, Vol 90, Num 18, pp 8697-8701 ; ref : 20 ref
- CODEN
- PNASA6
- ISSN
- 0027-8424
- Scientific domain
- Multidisciplinary
- Publisher
- National Academy of Sciences of the United States of America, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Allèle Chromosome D13 Délétion Gène suppresseur tumeur Homme Leucémie lymphoïde Mutation Pathogénie Séquence adjacente Transformation cellulaire Gène RB1 Hémopathie maligne Hémopathie
- Keyword (en)
- Allele D13-Chromosome Deletion Tumor suppressor gene Human Chronic lymphocytic leukemia Mutation Pathogenesis Flanking sequence Cell transformation Malignant hemopathy Hemopathy
- Keyword (es)
- Alelo Cromosoma D13 Deleción Gen supresor tumor Hombre Leucemia linfoidea Mutación Patogenia Secuencia adyacente Transformación celular Hemopatía maligna Hemopatía
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19B Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
- Discipline
- Blood diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3773135
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
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DOI
10.1073/pnas.90.18.8697 
https://dx.doi.org/10.1073/pnas.90.18.8697
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