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Cell Cyde/DNA Damage

Cell cycle/DNA damage signaling pathways are crucial for maintaining genomic stability and regulating cell division. When DNA damage occurs, these pathways are activated to either repair the damage or induce cell death to prevent the propagation of mutations.

Key players in these pathways include cell cycle checkpoints, DNA repair enzymes, and signaling molecules that coordinate the appropriate cellular response to DNA damage. Dysregulation of these pathways can result in various diseases, including cancer and genetic disorders.

Cell cycle/DNA damage signaling pathways are tightly regulated and interconnected to ensure proper responses to DNA damage during different phases of the cell cycle. For example, the activation of checkpoint proteins like p53 and ATM can lead to cell cycle arrest to allow for DNA repair before cell division proceeds.

Understanding the intricate mechanisms of cell cycle/DNA damage signaling pathways is essential for developing targeted therapies to effectively treat diseases associated with genomic instability. Researchers continue to investigate these pathways to uncover potential drug targets and improve treatment outcomes for patients with DNA damage-related conditions.

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Raspberry ketone, C7133, C10H12O2,
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6-Bromo-2-hydroxy-3-methoxybenzaldehyde, C7073, C8H7BrO3,
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Nicotinamide Riboside Chloride (NIAGEN), C7038, C11H15ClN2O5,
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5-Methylcytosine, C7031, C5H7N3O,
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Isocytosine, C7013, C4H5N3O,
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Beaucage reagent, C6991, C7H4O3S2,
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6-(Dimethylamino)purine, C6989, C7H9N5,
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4-Phenylbutyric acid, C6831, C10H12O2,
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Tempo, C6812, C9H18NO,
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Maleic hydrazide, C6727, C4H4N2O2,

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