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Your search keyword '"Alikarami, Fatemeh"' showing total 28 results

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28 results on '"Alikarami, Fatemeh"'

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1. CAR T-cell-mediated delivery of bispecific innate immune cell engagers for neuroblastoma

3. Single-cell multiomics reveals increased plasticity, resistant populations, and stem-cell–like blasts in KMT2A-rearranged leukemia

4. Targeting GPC2 on intraocular and CNS metastatic retinoblastomas with local and systemic delivery of CAR T-cells

5. ZMYND8-regulated IRF8 transcription axis is an acute myeloid leukemia dependency

8. The Human Tumor Atlas Network: Charting Tumor Transitions across Space and Time at Single-Cell Resolution

9. Oncogenic RAS-Pathway Activation Drives Oncofetal Reprogramming and Creates Therapeutic Vulnerabilities in Juvenile Myelomonocytic Leukemia

14. Data from Small-Molecule Inhibition of the Acyl-Lysine Reader ENL as a Strategy against Acute Myeloid Leukemia

15. Supplementary Data from Small-Molecule Inhibition of the Acyl-Lysine Reader ENL as a Strategy against Acute Myeloid Leukemia

16. Clonal evolution mediates Menin-inhibitor resistance in KMT2A-rearranged leukemias.

17. The Role of GATA2 in Drug Resistance in AML

18. Small-Molecule Inhibition of the Acyl-Lysine Reader ENL as a Strategy against Acute Myeloid Leukemia

19. Single-Cell Multiomics Reveals Increased Plasticity, Resistant Populations and Stem-Cell-like Blasts in KMT2A-Rearranged Leukemia

21. Single-cell multi-omics reveals elevated plasticity and stem-cell-like blasts relevant to the poor prognosis of KMT2A-rearranged leukemia

22. The Human Tumor Atlas Network: Charting Tumor Transitions across Space and Time at Single-Cell Resolution

25. The Immunosuppressive Activity of Amniotic Membrane Mesenchymal Stem Cells on T Lymphocytes.

26. GATA2 links stemness to chemotherapy resistance in acute myeloid leukemia.

27. Overexpression of MiR-138 Inhibits Cell Growth and Induces Caspase-mediated Apoptosis in Acute Promyelocytic Leukemia Cell Line.

28. Rapid Induction of Neural Differentiation in Human Umbilical Cord Matrix Mesenchymal Stem Cells by cAMP-elevating Agents.

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