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Doris Steinemann

Showing results (61-70 of 138) with videos related to

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Genes, Chromosomes & Cancer|July 11, 2006
Quantitative microsatellite analysis to delineate the commonly deleted region 1p22.3 in mantle cell lymphomasAsha Balakrishnan, Nils von Neuhoff, Cornelia Rudolph, et al.
Genes & Cancer|April 25, 2017
<i>GT198 (PSMC3IP)</i> germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer familiesStephanie Schubert, Tim Ripperger, Melanie Rood, et al.
Neuropediatrics|May 22, 2012
A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?Cengiz Yalcinkaya, Ozdem Erturk, Beyhan Tuysuz, et al.
Frontiers in Oncology|July 25, 2022
Clonal Evolution at First Sight: A Combined Visualization of Diverse Diagnostic Methods Improves Understanding of Leukemic ProgressionSarah Sandmann, Yvonne Lisa Behrens, Claudia Davenport, et al.
International Journal of Oncology|May 15, 2012
A tumor-derived population (SCCOHT-1) as cellular model for a small cell ovarian carcinoma of the hypercalcemic typeAnna Otte, Gudrun Göhring, Doris Steinemann, et al.
Genes, Chromosomes & Cancer|June 12, 2003
Identification of candidate tumor-suppressor genes in 6q27 by combined deletion mapping and electronic expression profiling in lymphoid neoplasmsDoris Steinemann, Stefan Gesk, Yanming Zhang, et al.
Blood|January 29, 2021
Venetoclax and dexamethasone synergize with inotuzumab ozogamicin-induced DNA damage signaling in B-lineage ALLHanna Kirchhoff, Uemran Karsli, Caroline Schoenherr, et al.
The Journal of Pathology. Clinical Research|August 4, 2017
Subclonal analysis in a lobular breast cancer with classical and solid growth pattern mimicking a solid-papillary carcinomaMatthias Christgen, Stephan Bartels, Jana Lisa van Luttikhuizen, et al.
The Journal of Pathology|February 5, 2009
Comprehensive genetic and functional characterization of IPH-926: a novel CDH1-null tumour cell line from human lobular breast cancerMatthias Christgen, Henriette Bruchhardt, Catarina Hadamitzky, et al.
Genes, Chromosomes & Cancer|January 24, 2021
Unbalanced translocation der(5;17) resulting in a TP53 loss as recurrent aberration in myelodysplastic syndrome and acute myeloid leukemia with complex karyotypeDaria Warnstorf, Randa Bawadi, Andrea Schienke, et al.
Pageof 14

Showing results (61-70 of 138) with videos related to

Sort By:
Pageof 14
Genes, Chromosomes & Cancer|July 11, 2006
Quantitative microsatellite analysis to delineate the commonly deleted region 1p22.3 in mantle cell lymphomasAsha Balakrishnan, Nils von Neuhoff, Cornelia Rudolph, et al.
Genes & Cancer|April 25, 2017
<i>GT198 (PSMC3IP)</i> germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer familiesStephanie Schubert, Tim Ripperger, Melanie Rood, et al.
Neuropediatrics|May 22, 2012
A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?Cengiz Yalcinkaya, Ozdem Erturk, Beyhan Tuysuz, et al.
Frontiers in Oncology|July 25, 2022
Clonal Evolution at First Sight: A Combined Visualization of Diverse Diagnostic Methods Improves Understanding of Leukemic ProgressionSarah Sandmann, Yvonne Lisa Behrens, Claudia Davenport, et al.
International Journal of Oncology|May 15, 2012
A tumor-derived population (SCCOHT-1) as cellular model for a small cell ovarian carcinoma of the hypercalcemic typeAnna Otte, Gudrun Göhring, Doris Steinemann, et al.
Genes, Chromosomes & Cancer|June 12, 2003
Identification of candidate tumor-suppressor genes in 6q27 by combined deletion mapping and electronic expression profiling in lymphoid neoplasmsDoris Steinemann, Stefan Gesk, Yanming Zhang, et al.
Blood|January 29, 2021
Venetoclax and dexamethasone synergize with inotuzumab ozogamicin-induced DNA damage signaling in B-lineage ALLHanna Kirchhoff, Uemran Karsli, Caroline Schoenherr, et al.
The Journal of Pathology. Clinical Research|August 4, 2017
Subclonal analysis in a lobular breast cancer with classical and solid growth pattern mimicking a solid-papillary carcinomaMatthias Christgen, Stephan Bartels, Jana Lisa van Luttikhuizen, et al.
The Journal of Pathology|February 5, 2009
Comprehensive genetic and functional characterization of IPH-926: a novel CDH1-null tumour cell line from human lobular breast cancerMatthias Christgen, Henriette Bruchhardt, Catarina Hadamitzky, et al.
Genes, Chromosomes & Cancer|January 24, 2021
Unbalanced translocation der(5;17) resulting in a TP53 loss as recurrent aberration in myelodysplastic syndrome and acute myeloid leukemia with complex karyotypeDaria Warnstorf, Randa Bawadi, Andrea Schienke, et al.
Pageof 14