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Doris Steinemann

Showing results (71-80 of 138) with videos related to

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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.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 24, 2020
E-cadherin to P-cadherin switching in lobular breast cancer with tubular elementsMatthias Christgen, Stephan Bartels, Jana L van Luttikhuizen, et al.
Breast Cancer Research and Treatment|September 8, 2018
A tandem duplication of BRCA1 exons 1-19 through DHX8 exon 2 in four families with hereditary breast and ovarian cancer syndromeChen Du, Dorothea Mark, Barbara Wappenschmidt, et al.
Nucleic Acids Research|January 1, 2013
Sleeping Beauty transposon-based system for cellular reprogramming and targeted gene insertion in induced pluripotent stem cellsIvana Grabundzija, Jichang Wang, Attila Sebe, et al.
Stem Cells Translational Medicine|August 9, 2013
Sustained knockdown of a disease-causing gene in patient-specific induced pluripotent stem cells using lentiviral vector-based gene therapyReto Eggenschwiler, Komal Loya, Guangming Wu, et al.
NPJ Breast Cancer|June 30, 2026
Multi-omics analysis in suspected hereditary breast and ovarian cancer cases reveals novel candidate susceptibility factorsB Aldrige Allister, Winfried Hofmann, Jonathan L Lühmann, et al.
The Journal of Pathology. Clinical Research|December 31, 2020
Chromosome 2q gain and epigenetic silencing of GATA3 in microglandular adenosis of the breastMartin Radner, Jana Lisa van Luttikhuizen, Stephan Bartels, 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.
Journal of Clinical Immunology|April 29, 2022
Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and GainsRensheng Wan, Maximilian Schieck, Andrés Caballero-Oteyza, et al.
Genes, Chromosomes & Cancer|August 30, 2021
Cryptic TCF3 fusions in childhood leukemia: Detection by RNA sequencingMustafa Salim, Frederik Heldt, Kathrin Thomay, et al.
Pageof 14

Showing results (71-80 of 138) with videos related to

Sort By:
Pageof 14
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.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 24, 2020
E-cadherin to P-cadherin switching in lobular breast cancer with tubular elementsMatthias Christgen, Stephan Bartels, Jana L van Luttikhuizen, et al.
Breast Cancer Research and Treatment|September 8, 2018
A tandem duplication of BRCA1 exons 1-19 through DHX8 exon 2 in four families with hereditary breast and ovarian cancer syndromeChen Du, Dorothea Mark, Barbara Wappenschmidt, et al.
Nucleic Acids Research|January 1, 2013
Sleeping Beauty transposon-based system for cellular reprogramming and targeted gene insertion in induced pluripotent stem cellsIvana Grabundzija, Jichang Wang, Attila Sebe, et al.
Stem Cells Translational Medicine|August 9, 2013
Sustained knockdown of a disease-causing gene in patient-specific induced pluripotent stem cells using lentiviral vector-based gene therapyReto Eggenschwiler, Komal Loya, Guangming Wu, et al.
NPJ Breast Cancer|June 30, 2026
Multi-omics analysis in suspected hereditary breast and ovarian cancer cases reveals novel candidate susceptibility factorsB Aldrige Allister, Winfried Hofmann, Jonathan L Lühmann, et al.
The Journal of Pathology. Clinical Research|December 31, 2020
Chromosome 2q gain and epigenetic silencing of GATA3 in microglandular adenosis of the breastMartin Radner, Jana Lisa van Luttikhuizen, Stephan Bartels, 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.
Journal of Clinical Immunology|April 29, 2022
Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and GainsRensheng Wan, Maximilian Schieck, Andrés Caballero-Oteyza, et al.
Genes, Chromosomes & Cancer|August 30, 2021
Cryptic TCF3 fusions in childhood leukemia: Detection by RNA sequencingMustafa Salim, Frederik Heldt, Kathrin Thomay, et al.
Pageof 14