What is cbl blood test?
Drets, M. E., & Shaw, M. W. Specific banding patterns of human chromosomes. Proceedings of the National Academy of Sciences 68, 2073–2077 (1971)
Druker, B. J. Perspectives on the development of a molecularly targeted agent. Cancer Cell 1, 31–36 (2002)
Parra, I., & Windle, B. High resolution visual mapping of stretched DNA by fluorescent hybridization. Nature Genetics 5, 17–21 (1993) doi:10.1038/ng0993-17
Pinkel, D., et al. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nature Genetics 20, 207–211 (1998) doi:10.1038/2524
Speicher, M. R., et al. Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nature Genetics 12, 368–375 (1996) doi:10.1038/ng0496-368
Papaemmanuil, E., Gerstung, M., Malcovati, L., Tauro, S., Gundem, G., Van Loo, P., ... & Shlien, A. (2013). Clinical and biological implications of driver mutations in myelodysplastic syndromes. Blood, 122(22), 3616-3627.
Pardanani, A. D., Lasho, T. L., Finke, C., Zblewski, D. L., Abdelrahman, R. A., Wassie, E. A., ... & Tefferi, A. (2015). ASXL1 and CBL mutations are independently predictive of inferior survival in advanced systemic mastocytosis. British journal of haematology.
Score, J., Chase, A., Forsberg, L. A., Feng, L., Waghorn, K., Jones, A. V., ... & Cross, N. C. P. (2015). Detection of leukemia-associated mutations in peripheral blood DNA of hematologically normal elderly individuals. Leukemia, 29(7), 1600.
Stockton, S. S., Malhotra, V., Lu, X., Thangavelu, M., Albitar, M., & Cogle, C. R. (2015). Gene Mutations in MDS Associating with Peripheral Blood Count Abnormalities. Blood, 126(23), 1685-1685.
Park, S. H., Lee, H. J., Kim, I. S., Kang, J. E., Lee, E. Y., Kim, H. J., ... & Song, M. K. (2015). Incidences and prognostic impact of c-KIT, WT1, CEBPA, and CBL mutations, and mutations associated with epigenetic modification in core binding factor acute myeloid leukemia: a multicenter study in a Korean population. Annals of laboratory medicine, 35(3), 288-297.
Hansen, J. W., Westman, M. K., Sjö, L. D., Saft, L., Kristensen, L. S., Ørskov, A. D., ... & Grønbæk, K. (2016). Mutations in idiopathic cytopenia of undetermined significance assist diagnostics and correlate to dysplastic changes. American journal of hematology, 91(12), 1234-1238.
CBL : The dimorphic fungus, Blastomyces dermatitidis, causes blastomycosis. Detection of antibodies in spinal fluid specimens from patients with blastomycosis. This is a clinical test intended for HelpPurposes or indications for the test. The specimen sample requirements may vary from lab to lab. Cobalamin, Cbl, folic acid, FA, B12. The meaning of CBL is Circulating Blood Lymphocytes and other meanings are located at the bottom which take place within Blood Test terminology and CBL.
Drets, M. E., & Shaw, M. W. Specific banding patterns of human chromosomes. Proceedings of the National Academy of Sciences 68, 2073–2077 (1971)
Druker, B. J. Perspectives on the development of a molecularly targeted agent. Cancer Cell 1, 31–36 (2002)
Parra, I., & Windle, B. High resolution visual mapping of stretched DNA by fluorescent hybridization. Nature Genetics 5, 17–21 (1993) doi:10.1038/ng0993-17
Pinkel, D., et al. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nature Genetics 20, 207–211 (1998) doi:10.1038/2524
Speicher, M. R., et al. Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nature Genetics 12, 368–375 (1996) doi:10.1038/ng0496-368
Papaemmanuil, E., Gerstung, M., Malcovati, L., Tauro, S., Gundem, G., Van Loo, P., ... & Shlien, A. (2013). Clinical and biological implications of driver mutations in myelodysplastic syndromes. Blood, 122(22), 3616-3627.
Pardanani, A. D., Lasho, T. L., Finke, C., Zblewski, D. L., Abdelrahman, R. A., Wassie, E. A., ... & Tefferi, A. (2015). ASXL1 and CBL mutations are independently predictive of inferior survival in advanced systemic mastocytosis. British journal of haematology.
Score, J., Chase, A., Forsberg, L. A., Feng, L., Waghorn, K., Jones, A. V., ... & Cross, N. C. P. (2015). Detection of leukemia-associated mutations in peripheral blood DNA of hematologically normal elderly individuals. Leukemia, 29(7), 1600.
