Found: 19
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Total Synthesis of (−)-Spiroleucettadine.
- Published in:
- Angewandte Chemie, 2017, v. 129, n. 46, p. 14855, doi. 10.1002/ange.201708110
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- Article
BCL-2 family antagonists for cancer therapy.
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- Nature Reviews Drug Discovery, 2008, v. 7, n. 12, p. 989, doi. 10.1038/nrd2658
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- Article
Analysis of Ca<sup>2</sup><sup>+</sup> mediated signaling regulating Toxoplasma infectivity reveals complex relationships between key molecules.
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- Cellular Microbiology, 2017, v. 19, n. 4, p. n/a, doi. 10.1111/cmi.12685
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- Article
Total Synthesis of (−)-Spiroleucettadine.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 46, p. 14663, doi. 10.1002/anie.201708110
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- Article
Insights into the evolution of divergent nucleotide-binding mechanisms among pseudokinases revealed by crystal structures of human and mouse MLKL.
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- Biochemical Journal, 2014, v. 457, n. 3, p. 369, doi. 10.1042/BJ20131270
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- Article
Computationally designed high specificity inhibitors delineate the roles of BCL2 family proteins in cancer.
- Published in:
- eLife, 2016, p. 1, doi. 10.7554/eLife.20352
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- Article
Human RIPK3 maintains MLKL in an inactive conformation prior to cell death by necroptosis.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-27032-x
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- Article
Synthesis and Biological Evaluation of (−) and (+)‐Spiroleucettadine and Analogues.
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- ChemMedChem, 2021, v. 16, n. 8, p. 1308, doi. 10.1002/cmdc.202000954
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- Article
BCL‐XL exerts a protective role against anemia caused by radiation‐induced kidney damage.
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- EMBO Journal, 2020, v. 39, n. 24, p. 1, doi. 10.15252/embj.2020105561
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- Article
Control of apoptosis by the BCL-2 protein family: implications for physiology and therapy.
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- Nature Reviews Molecular Cell Biology, 2014, v. 15, n. 1, p. 49, doi. 10.1038/nrm3722
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- Article
Structures of BCL-2 in complex with venetoclax reveal the molecular basis of resistance mutations.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-10363-1
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- Article
Key residues in the VDAC2-BAK complex can be targeted to modulate apoptosis.
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- PLoS Biology, 2024, v. 22, n. 5, p. 1, doi. 10.1371/journal.pbio.3002617
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- Article
Dual drug targeting to kill colon cancers.
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- Cancer Medicine, 2022, v. 11, n. 13, p. 2612, doi. 10.1002/cam4.4641
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- Article
Improved drug target deconvolution with PISA‐DIA using an extended, overlapping temperature gradient.
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- Proteomics, 2024, v. 24, n. 16, p. 1, doi. 10.1002/pmic.202300644
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- Article
The Lck inhibitor, AMG-47a, blocks necroptosis and implicates RIPK1 in signalling downstream of MLKL.
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- Cell Death & Disease, 2022, v. 13, n. 4, p. 1, doi. 10.1038/s41419-022-04740-w
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- Article
Defining the susceptibility of colorectal cancers to BH3-mimetic compounds.
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- Cell Death & Disease, 2020, v. 11, n. 9, p. 1, doi. 10.1038/s41419-020-02815-0
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- Article
Conformational switching of the pseudokinase domain promotes human MLKL tetramerization and cell death by necroptosis.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04714-7
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- Article
Simplified Silvestrol Analogues with Potent Cytotoxic Activity.
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- ChemMedChem, 2014, v. 9, n. 7, p. 1556, doi. 10.1002/cmdc.201400024
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- Article
Structure-guided design of a selective BCL-X<sub>L</sub> inhibitor.
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- Nature Chemical Biology, 2013, v. 9, n. 6, p. 390, doi. 10.1038/nchembio.1246
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- Article