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Haematologica
|
November 4, 2005
Gene-expression profiles and their association with drug resistance in adult acute myeloid leukemia
Michael Heuser, Luzie U Wingen, Doris Steinemann, 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.
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.
Genes, Chromosomes & Cancer
|
March 4, 2008
Copy number alterations in childhood acute lymphoblastic leukemia and their association with minimal residual disease
Doris Steinemann, Gunnar Cario, Martin Stanulla, et al.
Genes, Chromosomes & Cancer
|
June 28, 2020
Frequency and prognostic impact of PAX5 p.P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP-BFM acute lymphoblastic leukemia protocol
Mareike Jung, Maximilian Schieck, Winfried Hofmann, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
September 19, 2006
Assessment of differentiation and progression of hepatic tumors using array-based comparative genomic hybridization
Doris Steinemann, Britta Skawran, Thomas Becker, et al.
Haematologica
|
May 10, 2007
Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle-cell lymphomas
Tim Ripperger, Nils von Neuhoff, Kathrin Kamphues, et al.
International Journal of Cancer
|
November 15, 2018
The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants
Stephanie Schubert, Jana L van Luttikhuizen, Bernd Auber, et al.
Scientific Reports
|
December 3, 2016
Improved bi-allelic modification of a transcriptionally silent locus in patient-derived iPSC by Cas9 nickase
Reto Eggenschwiler, Mohsen Moslem, Mariane Serra Fráguas, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Haematologica
|
November 4, 2005
Gene-expression profiles and their association with drug resistance in adult acute myeloid leukemia
Michael Heuser, Luzie U Wingen, Doris Steinemann, 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.
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.
Genes, Chromosomes & Cancer
|
March 4, 2008
Copy number alterations in childhood acute lymphoblastic leukemia and their association with minimal residual disease
Doris Steinemann, Gunnar Cario, Martin Stanulla, et al.
Genes, Chromosomes & Cancer
|
June 28, 2020
Frequency and prognostic impact of PAX5 p.P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP-BFM acute lymphoblastic leukemia protocol
Mareike Jung, Maximilian Schieck, Winfried Hofmann, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
September 19, 2006
Assessment of differentiation and progression of hepatic tumors using array-based comparative genomic hybridization
Doris Steinemann, Britta Skawran, Thomas Becker, et al.
Haematologica
|
May 10, 2007
Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle-cell lymphomas
Tim Ripperger, Nils von Neuhoff, Kathrin Kamphues, et al.
International Journal of Cancer
|
November 15, 2018
The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants
Stephanie Schubert, Jana L van Luttikhuizen, Bernd Auber, et al.
Scientific Reports
|
December 3, 2016
Improved bi-allelic modification of a transcriptionally silent locus in patient-derived iPSC by Cas9 nickase
Reto Eggenschwiler, Mohsen Moslem, Mariane Serra Fráguas, et al.
Page
of 2