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Frontiers in Cell and Developmental Biology|April 27, 2026
Histone acetylation and methylation in rare diseases: from molecular mechanisms to clinical presentationsBurcu Akman, Semra Gürsoy, Pınar Gençpınar, et al.Current Issues in Molecular Biology|July 23, 2025
Genetic and Epigenetic Aberrations of SOX7 in Newly Diagnosed and Relapsed Multiple Myeloma as Well as Related NeoplasmsCan Küçük, Burcu Akman, Xiaozhou Hu, et al.European Journal of Human Genetics : EJHG|July 9, 2026
Integrative and systematic genomic approaches to improve diagnosis in rare and undiagnosed diseases: results from the RareBoost projectAyca Yigit, Mert Pekerbas, Baris Salman, et al.Cells|November 11, 2022
Whole Transcriptome Sequencing Reveals Cancer-Related, Prognostically Significant Transcripts and Tumor-Infiltrating Immunocytes in Mantle Cell LymphomaEsra Esmeray Sönmez, Tevfik Hatipoğlu, Deniz Kurşun, et al.Frontiers in Oncology|July 7, 2022
Plasma Concentrations and Cancer-Associated Mutations in Cell-Free Circulating DNA of Treatment-Naive Follicular Lymphoma for Improved Non-Invasive Diagnosis and PrognosisTevfik Hatipoğlu, Esra Esmeray Sönmez, Xiaozhou Hu, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2026
Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumedSilvestre Cuinat, Valérie Cormier-Daire, Jeremie Rosain, et al.Pageof 3