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Yvonne Lisa Behrens

Showing results (1-10 of 28) with videos related to

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Bioinformatics (Oxford, England)|September 2, 2025
Scafari: Exploring scDNA-seq dataSophie-Marie Wind, Thea Reinkens, Yvonne Lisa Behrens, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 6, 2024
Ronja Hollstein, Nina Ishorst, Annette Lischka, et al.
Best Practice & Research. Clinical Haematology|March 15, 2024
The landscape of cytogenetic and molecular genetic methods in diagnostics for hematologic neoplasiaYvonne Lisa Behrens, Stefan Pietzsch, Željko Antić, et al.
Stem Cell Research|June 21, 2024
CRISPR/Cas9-based GLA knockout to generate the female Fabry disease human induced pluripotent stem cell line MHHi001-A-15Malte Juchem, Nele Lehmann, Yvonne Lisa Behrens, et al.
Annals of Hematology|August 19, 2020
Histiocytic sarcoma progressing from follicular lymphoma and mimicking acquired hemophagocytic lymphohistiocytosisChristoph Schünemann, Gudrun Göhring, Yvonne Lisa Behrens, et al.
Genes, Chromosomes & Cancer|June 9, 2017
Comparison of different methods for telomere length measurement in whole blood and blood cell subsets: Recommendations for telomere length measurement in hematological diseasesYvonne Lisa Behrens, Kathrin Thomay, Maike Hagedorn, et al.
Leukemia & Lymphoma|February 1, 2018
Octasomy 21 in a patient with secondary AML after CMML: the role of acquired NRAS mutations in triggering aneuploidyKathrin Thomay, Yvonne Lisa Behrens, Jana Lentes, et al.
Cancers|May 14, 2022
Optical Genome Mapping as a Diagnostic Tool in Pediatric Acute Myeloid LeukemiaJulia Suttorp, Jonathan Lukas Lühmann, Yvonne Lisa Behrens, et al.
Genes, Chromosomes & Cancer|January 8, 2019
Jumping translocations: Short telomeres or pathogenic TP53 variants as underlying mechanism in acute myeloid leukemia and myelodysplastic syndrome?Yvonne Lisa Behrens, Kathrin Thomay, Maike Hagedorn, et al.
Plos One|May 9, 2017
Human CD8+ CD57- TEMRA cells: Too young to be called "old"Kriti Verma, Justyna Ogonek, Pavankumar Reddy Varanasi, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Bioinformatics (Oxford, England)|September 2, 2025
Scafari: Exploring scDNA-seq dataSophie-Marie Wind, Thea Reinkens, Yvonne Lisa Behrens, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 6, 2024
Ronja Hollstein, Nina Ishorst, Annette Lischka, et al.
Best Practice & Research. Clinical Haematology|March 15, 2024
The landscape of cytogenetic and molecular genetic methods in diagnostics for hematologic neoplasiaYvonne Lisa Behrens, Stefan Pietzsch, Željko Antić, et al.
Stem Cell Research|June 21, 2024
CRISPR/Cas9-based GLA knockout to generate the female Fabry disease human induced pluripotent stem cell line MHHi001-A-15Malte Juchem, Nele Lehmann, Yvonne Lisa Behrens, et al.
Annals of Hematology|August 19, 2020
Histiocytic sarcoma progressing from follicular lymphoma and mimicking acquired hemophagocytic lymphohistiocytosisChristoph Schünemann, Gudrun Göhring, Yvonne Lisa Behrens, et al.
Genes, Chromosomes & Cancer|June 9, 2017
Comparison of different methods for telomere length measurement in whole blood and blood cell subsets: Recommendations for telomere length measurement in hematological diseasesYvonne Lisa Behrens, Kathrin Thomay, Maike Hagedorn, et al.
Leukemia & Lymphoma|February 1, 2018
Octasomy 21 in a patient with secondary AML after CMML: the role of acquired NRAS mutations in triggering aneuploidyKathrin Thomay, Yvonne Lisa Behrens, Jana Lentes, et al.
Cancers|May 14, 2022
Optical Genome Mapping as a Diagnostic Tool in Pediatric Acute Myeloid LeukemiaJulia Suttorp, Jonathan Lukas Lühmann, Yvonne Lisa Behrens, et al.
Genes, Chromosomes & Cancer|January 8, 2019
Jumping translocations: Short telomeres or pathogenic TP53 variants as underlying mechanism in acute myeloid leukemia and myelodysplastic syndrome?Yvonne Lisa Behrens, Kathrin Thomay, Maike Hagedorn, et al.
Plos One|May 9, 2017
Human CD8+ CD57- TEMRA cells: Too young to be called "old"Kriti Verma, Justyna Ogonek, Pavankumar Reddy Varanasi, et al.
Pageof 3