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Researcher at Research Department
Ask questions about Justin Ainscough's research, publications, and ongoing work
Identified Piezo1 as a key mechanotransducer integrating vascular architecture with physiological force, influencing vascular development and function.
Showed that the H19 gene acts as a trans regulator of the imprinted gene network, controlling growth in mice.
Determined that the nuclear matrix protein CIZ1 facilitates the localization of Xist RNA to the inactive X-chromosome territory, contributing to X-chromosome inactivation.
Discovered that variant Ciz1 is a circulating biomarker for early-stage lung cancer, suggesting its potential for diagnostic applications.
Demonstrated that TRPM2 channel deficiency prevents delayed cytosolic Zn2+ accumulation and CA1 pyramidal neuronal death after transient global ischemia, suggesting a therapeutic target for stroke.
Demonstrated that maintenance of epigenetic landscape requires CIZ1 and is corrupted in differentiated fibroblasts in long-term culture.
Showed that prion-like domains drive CIZ1 assembly formation at the inactive X chromosome, contributing to understanding of chromosome inactivation.
Dr. Ainscough is a leading researcher in genomic imprinting, stem cell biology, and the role of CIZ1 in DNA replication and cancer. His work has significantly advanced our understanding of epigenetic mechanisms and their implications for development and disease.
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