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Proceedings of the National Academy of Sciences of the United States of America|June 12, 2020
Functional interplay of Epstein-Barr virus oncoproteins in a mouse model of B cell lymphomagenesisThomas Sommermann, Tomoharu Yasuda, Jonathan Ronen, et al.Cancer Genetics and Cytogenetics|August 17, 2005
High incidence and intraclonal heterogeneity of chromosome 11 aberrations in patients with newly diagnosed multiple myeloma detected by multiprobe interphase FISHFriedrich W Cremer, Mutlu Kartal, Dirk Hose, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 25, 2013
Clonal heterogeneity as detected by metaphase karyotyping is an indicator of poor prognosis in acute myeloid leukemiaTilmann Bochtler, Friedrich Stölzel, Christoph E Heilig, et al.Genes, Chromosomes & Cancer|August 1, 2020
A versatile system to introduce clusters of genomic double-strand breaks in large cell populationsThorsten Kolb, Umar Khalid, Milena Simović, et al.Frontiers in Oncology|November 11, 2021
Prevalence of the GFI1-36N SNP in Multiple Myeloma Patients and Its Impact on the PrognosisCyrus Khandanpour, Christine Eisfeld, Subbaiah Chary Nimmagadda, et al.American Journal of Medical Genetics. Part A|September 27, 2014
3p25.3 microdeletion of GABA transporters SLC6A1 and SLC6A11 results in intellectual disability, epilepsy and stereotypic behaviorNicola Dikow, Bianca Maas, Stephanie Karch, et al.Haematologica|March 22, 2015
A magnetic resonance imaging-based prognostic scoring system to predict outcome in transplant-eligible patients with multiple myelomaElias K Mai, Thomas Hielscher, Jost K Kloth, et al.European Radiology|January 16, 2016
Association between magnetic resonance imaging patterns and baseline disease features in multiple myeloma: analyzing surrogates of tumour mass and biologyElias K Mai, Thomas Hielscher, Jost K Kloth, et al.Molecular Cancer Research : MCR|May 14, 2009
High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarrayDong Yin, Seishi Ogawa, Norihiko Kawamata, et al.Stem Cell Reports|September 25, 2020
Precise Correction of Heterozygous SHOX2 Mutations in hiPSCs Derived from Patients with Atrial Fibrillation via Genome Editing and Sib SelectionSimon Alexander Sumer, Sandra Hoffmann, Svenja Laue, et al.Pageof 19