Proteomic and phosphoproteomic profiling of AML
收藏integrated proteome resources2026-02-07 收录
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Proteomic and phosphoproteomic profiling of AML
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2025-05-26
相关数据集
Thirty-five proteins identified with altered levels of expression in response to transport stress (stressed) compared to non-stressed birds, as revealed by label-free MS/MS analysis using progenesis QI for proteomics.
Thirty-five proteins identified with altered levels of expression in response to transport stress (stressed) compared to non-stressed birds, as revealed by label-free MS/MS analysis using progenesis Q
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Number of cords, number of litters, pooled tissue weight and total protein concentration of samples obtained for each group of animals used in the proteomic study.
+1d and +7d refer to days after injury at either P7 or P28. P8, P14, p29 and P35 are age-matched controls.
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Bleximenib, the novel menin-KMT2A inhibitor JNJ-75276617, impairs long-term proliferation and immune evasion in acute myeloid leukemia. Bleximenib, the novel menin-KMT2A inhibitor JNJ-75276617, impairs long-term proliferation and immune evasion in acute myeloid leukemia
Acute myeloid leukemia (AML) remains challenging to treat, which in part relates to genetic heterogeneity of the disease, to the protective tumor microenvironment driving resistance to therapy, and al
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TrypOx, a novel eukaryotic homologue of the redox-regulated chaperone Hsp33 in Trypanosoma brucei
In this study, we describe a novel eukaryotic homologue of Hsp33 in Trypanosoma brucei.Bioinformatics analysis of the Hsp33 family suggested that eukaryotic pathogens belonging to the kinetoplastids,
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S1 Table - Uncovering the antifungal potential of Cannabidiol and Cannabidivarin
A. Differentially abundant proteins in C. neoformans H99 in response to CBD treatment. B. Differentially abundant proteins in C. neoformans H99 in response to CBDV treatment. C. Significantly enriched
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