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C Fonatsch

Showing results (31-40 of 157) with videos related to

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Cancer Genetics and Cytogenetics|November 3, 1998
Fluorescence in situ hybridization characterization of the chromosomal breakpoints in a case with ins(17;3)(q11.2;q21q26.3) and acute monocytic leukemiaS Schnittger, E Joachimmayer, C Schoch, et al.
Biochemical and Biophysical Research Communications|December 5, 1998
Comparative expression analysis of the antagonistic transcription factors EVI1 and MDS1-EVI1 in murine tissues and during in vitro hematopoietic differentiationK Wimmer, U Vinatzer, P Zwirn, et al.
Haematology and Blood Transfusion|January 1, 1981
Lymphoproliferation and heterotransplantation in nude mice: tumor cells in Hodgkin's diseaseV Diehl, H H Kirchner, M Schaadt, et al.
Human Genetics|April 1, 1990
Chromosomal in situ hybridization of a Hodgkin's disease-derived cell line (L540) using DNA probes for TCRA, TCRB, MET, and rRNAC Fonatsch, G Gradl, U Kolbus, et al.
British Journal of Haematology|September 13, 2001
The leukaemia-associated transcription factors EVI-1 and MDS1/EVI1 repress transcription and interact with histone deacetylaseU Vinatzer, J Taplick, C Seiser, et al.
Cancer Genetics and Cytogenetics|February 1, 1986
Cytogenetic investigations in Hodgkin's disease: I. Involvement of specific chromosomes in marker formationC Fonatsch, V Diehl, M Schaadt, et al.
International Journal of Cancer|December 15, 1980
Two neoplastic cell lines with unique features derived from Hodgkin's diseaseM Schaadt, V Diehl, H Stein, et al.
Human Mutation|June 30, 2000
Three different premature stop codons lead to skipping of exon 7 in neurofibromatosis type I patientsK Wimmer, M Eckart, P F Stadler, et al.
Leukemia|December 1, 1996
Refined chromosomal localization of the human thrombopoietin gene to 3q27-q28 and exclusion as the responsible gene for thrombocytosis in patients with rearrangements of 3q21 and 3q26S Schnittger, F J de Sauvage, D Le Paslier, et al.
Cancer Genetics and Cytogenetics|December 7, 2000
Variant intra philadelphia translocation with rearrangement of BCR-ABL and ABL-BCR within the same chromosome in a patient with cALLM Edelhäuser, W Raber, G Mitterbauer, et al.
Pageof 16

Showing results (31-40 of 157) with videos related to

Sort By:
Pageof 16
Cancer Genetics and Cytogenetics|November 3, 1998
Fluorescence in situ hybridization characterization of the chromosomal breakpoints in a case with ins(17;3)(q11.2;q21q26.3) and acute monocytic leukemiaS Schnittger, E Joachimmayer, C Schoch, et al.
Biochemical and Biophysical Research Communications|December 5, 1998
Comparative expression analysis of the antagonistic transcription factors EVI1 and MDS1-EVI1 in murine tissues and during in vitro hematopoietic differentiationK Wimmer, U Vinatzer, P Zwirn, et al.
Haematology and Blood Transfusion|January 1, 1981
Lymphoproliferation and heterotransplantation in nude mice: tumor cells in Hodgkin's diseaseV Diehl, H H Kirchner, M Schaadt, et al.
Human Genetics|April 1, 1990
Chromosomal in situ hybridization of a Hodgkin's disease-derived cell line (L540) using DNA probes for TCRA, TCRB, MET, and rRNAC Fonatsch, G Gradl, U Kolbus, et al.
British Journal of Haematology|September 13, 2001
The leukaemia-associated transcription factors EVI-1 and MDS1/EVI1 repress transcription and interact with histone deacetylaseU Vinatzer, J Taplick, C Seiser, et al.
Cancer Genetics and Cytogenetics|February 1, 1986
Cytogenetic investigations in Hodgkin's disease: I. Involvement of specific chromosomes in marker formationC Fonatsch, V Diehl, M Schaadt, et al.
International Journal of Cancer|December 15, 1980
Two neoplastic cell lines with unique features derived from Hodgkin's diseaseM Schaadt, V Diehl, H Stein, et al.
Human Mutation|June 30, 2000
Three different premature stop codons lead to skipping of exon 7 in neurofibromatosis type I patientsK Wimmer, M Eckart, P F Stadler, et al.
Leukemia|December 1, 1996
Refined chromosomal localization of the human thrombopoietin gene to 3q27-q28 and exclusion as the responsible gene for thrombocytosis in patients with rearrangements of 3q21 and 3q26S Schnittger, F J de Sauvage, D Le Paslier, et al.
Cancer Genetics and Cytogenetics|December 7, 2000
Variant intra philadelphia translocation with rearrangement of BCR-ABL and ABL-BCR within the same chromosome in a patient with cALLM Edelhäuser, W Raber, G Mitterbauer, et al.
Pageof 16