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Women in STEM July: Meet Michelle Arkin

Drug Target Review

For my PhD project, I chose an advisor who worked on DNA and I started working with her on the physical properties of DNA. I worked with Jackie Barton in the early days of what’s now called DNA-mediated electron transfer. And that was a very controversial idea.

DNA 98
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#WhyIScience Q&A: A cell biologist now helps recent college graduates launch their scientific careers

Broad Institute

in cell biology. During graduate school at MIT and the Whitehead Institute, my interest in cell division came full circle and I was able to explore how a cell divides to make two cells that are genetically identical. Each cell needs the same amount of DNA so they can function like each other.

Science 111
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How nucleolar stress accelerates aging in mice

Drug Target Review

For his postdoctoral stay he joined the group of André Nussenzweig, where he started to work on DNA repair, particularly focusing on the role of histone H2AX. In 2005, he joined CNIO to lead the Genomic Instability Group where he has been ever since.

RNA 64
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Reinventing the small molecule toolbox: from proteins to RNA

Dark Matter Blog

The tools in this kit fall into a few broad categories: understanding protein structures and their functional significance, identifying ligands that bind into functionally significant pockets, and developing assays that confirm target engagement along with demonstrating the anticipated impact on cell biology.

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Precision Medicine in the Genomic Era

DrugBank

In contrast, non-coding mutations have effects on gene expression, transcript stability, and the physical state of the DNA itself (e.g., Network expansion of genetic associations defines a pleiotropy map of human cell biology. Coding mutations have a more direct effect through direct alteration of a gene product.

Disease 98
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AI At The Frontier: Empowering Early Career Professionals In Drug Discovery

Elrig

Srinivasan has led the development of multiple computational pipelines to process data from different next generation sequencing techniques with applications in oncology, genome editing systems including CRISPR-Cas mediated DNA editing, and ADAR-mediated RNA editing.

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TACACICLIB, AUR-102, AURIGENE

New Drug Approvals

As such, it has been proposed that inhibiting CDK7 would provide a potent means of inhibiting cell cycle progression, which may be especially relevant given that there is compelling evidence from gene knockout studies in mice for lack of an absolute requirement for CDK2, CDK4 and CDK6 for the cell cycle at least in most cell types (M alumbres et al.,