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Marcel Tauscher

Showing results (11-20 of 19) with videos related to

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Haematologica|November 4, 2005
Gene-expression profiles and their association with drug resistance in adult acute myeloid leukemiaMichael 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 familiesStephanie 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 karyotypeDaria 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 diseaseDoris 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 protocolMareike 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 hybridizationDoris Steinemann, Britta Skawran, Thomas Becker, et al.
Haematologica|May 10, 2007
Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle-cell lymphomasTim 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 variantsStephanie 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 nickaseReto Eggenschwiler, Mohsen Moslem, Mariane Serra Fráguas, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 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 leukemiaMichael 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 familiesStephanie 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 karyotypeDaria 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 diseaseDoris 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 protocolMareike 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 hybridizationDoris Steinemann, Britta Skawran, Thomas Becker, et al.
Haematologica|May 10, 2007
Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle-cell lymphomasTim 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 variantsStephanie 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 nickaseReto Eggenschwiler, Mohsen Moslem, Mariane Serra Fráguas, et al.
Pageof 2