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Genes, Chromosomes & Cancer
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July 11, 2006
Quantitative microsatellite analysis to delineate the commonly deleted region 1p22.3 in mantle cell lymphomas
Asha 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 families
Stephanie 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 Progression
Sarah 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 type
Anna 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 neoplasms
Doris 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 ALL
Hanna 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 carcinoma
Matthias 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 cancer
Matthias 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 karyotype
Daria Warnstorf, Randa Bawadi, Andrea Schienke, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 138) with videos related to
Sort By:
Page
of 14
Genes, Chromosomes & Cancer
|
July 11, 2006
Quantitative microsatellite analysis to delineate the commonly deleted region 1p22.3 in mantle cell lymphomas
Asha 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 families
Stephanie 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 Progression
Sarah 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 type
Anna 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 neoplasms
Doris 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 ALL
Hanna 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 carcinoma
Matthias 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 cancer
Matthias 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 karyotype
Daria Warnstorf, Randa Bawadi, Andrea Schienke, et al.
Page
of 14