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R Bartram

Showing results (251-260 of 393) with videos related to

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British Journal of Haematology|February 1, 1994
The acute lymphoblastic leukaemia cell line SEM with t(4;11) chromosomal rearrangement is biphenotypic and responsive to interleukin-7J Greil, M Gramatzki, R Burger, et al.
Haematology and Blood Transfusion|January 1, 1990
Incidence and clinical implications of acute hybrid leukemia in childhoodW D Ludwig, E Thiel, U Köller, et al.
Cancer Research|July 4, 1998
Frequent loss of heterozygosity on the long arm of chromosome 6: identification of two distinct regions of deletion in childhood acute lymphoblastic leukemiaS Takeuchi, M Koike, T Seriu, et al.
Genomics|June 6, 1998
An evolutionarily conserved gene on human chromosome 5q33-q34, UBH1, encodes a novel deubiquitinating enzymeT E Hansen-Hagge, J W Janssen, H Hameister, et al.
Blood|April 15, 1996
Acute lymphoblastic leukemia of childhood: identification of two distinct regions of deletion on the short arm of chromosome 12 in the region of TEL and KIP1S Takeuchi, C R Bartram, C W Miller, et al.
Oncology Reports|June 18, 2004
Aberrant methylation in promoter-associated CpG islands of multiple genes in relapsed childhood acute lymphoblastic leukemiaChise Matsushita, Yang Yang, Seisho Takeuchi, et al.
Carcinogenesis|October 20, 2005
Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancerMichael Wirtenberger, Sandrine Tchatchou, Kari Hemminki, et al.
Carcinogenesis|June 25, 2005
Association of death receptor 4 haplotype 626C-683C with an increased breast cancer riskBernd Frank, Kari Hemminki, Kalai S Shanmugam, et al.
Leukemia|October 1, 1989
Phenotypic and genotypic heterogeneity in infant acute leukemia. II. Acute nonlymphoblastic leukemiaU Köller, O A Haas, W D Ludwig, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 1, 1991
Expansion of a maternally derived monoclonal T cell population with CD3+/CD8+/T cell receptor-gamma/delta+ phenotype in a child with severe combined immunodeficiencyV Wahn, S Yokota, K L Meyer, et al.
Pageof 40

Showing results (251-260 of 393) with videos related to

Sort By:
Pageof 40
British Journal of Haematology|February 1, 1994
The acute lymphoblastic leukaemia cell line SEM with t(4;11) chromosomal rearrangement is biphenotypic and responsive to interleukin-7J Greil, M Gramatzki, R Burger, et al.
Haematology and Blood Transfusion|January 1, 1990
Incidence and clinical implications of acute hybrid leukemia in childhoodW D Ludwig, E Thiel, U Köller, et al.
Cancer Research|July 4, 1998
Frequent loss of heterozygosity on the long arm of chromosome 6: identification of two distinct regions of deletion in childhood acute lymphoblastic leukemiaS Takeuchi, M Koike, T Seriu, et al.
Genomics|June 6, 1998
An evolutionarily conserved gene on human chromosome 5q33-q34, UBH1, encodes a novel deubiquitinating enzymeT E Hansen-Hagge, J W Janssen, H Hameister, et al.
Blood|April 15, 1996
Acute lymphoblastic leukemia of childhood: identification of two distinct regions of deletion on the short arm of chromosome 12 in the region of TEL and KIP1S Takeuchi, C R Bartram, C W Miller, et al.
Oncology Reports|June 18, 2004
Aberrant methylation in promoter-associated CpG islands of multiple genes in relapsed childhood acute lymphoblastic leukemiaChise Matsushita, Yang Yang, Seisho Takeuchi, et al.
Carcinogenesis|October 20, 2005
Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancerMichael Wirtenberger, Sandrine Tchatchou, Kari Hemminki, et al.
Carcinogenesis|June 25, 2005
Association of death receptor 4 haplotype 626C-683C with an increased breast cancer riskBernd Frank, Kari Hemminki, Kalai S Shanmugam, et al.
Leukemia|October 1, 1989
Phenotypic and genotypic heterogeneity in infant acute leukemia. II. Acute nonlymphoblastic leukemiaU Köller, O A Haas, W D Ludwig, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 1, 1991
Expansion of a maternally derived monoclonal T cell population with CD3+/CD8+/T cell receptor-gamma/delta+ phenotype in a child with severe combined immunodeficiencyV Wahn, S Yokota, K L Meyer, et al.
Pageof 40