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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 leukemia
S 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 differentiation
K 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 disease
V 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 rRNA
C 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 deacetylase
U 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 formation
C 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 disease
M 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 patients
K 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 3q26
S 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 cALL
M Edelhäuser, W Raber, G Mitterbauer, et al.
Page
of 16
Search research articles
Search
Showing results (31-40 of 157) with videos related to
Sort By:
Page
of 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 leukemia
S 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 differentiation
K 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 disease
V 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 rRNA
C 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 deacetylase
U 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 formation
C 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 disease
M 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 patients
K 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 3q26
S 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 cALL
M Edelhäuser, W Raber, G Mitterbauer, et al.
Page
of 16