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Hani Goodarzi on Muck Rack

Hani Goodarzi

As seen in: Nature, EurekAlert!, Flipboard, Science Magazine, Medical Xpress, BioRxiv, Cell Press, Cell Reports, Cell Reports Medicine, The Scientist and
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Articles

The Quiet Loss of Iranian Scientific Talent in US Labs

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By Hani Goodarzi
| The Scientist Verified
The Trump administration’s ongoing freeze on visa applications for nationals of 39 countries has extended into a fifth month, with no sign of relief. For Iranian scientists already in the US, this stranglehold on immigration is not only sending a strong signal to scientific talentthat they are not welcome, but it’s also compounded by the strain of an ongoing war affecting their families andcolleagues abroad.
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Pervasive and programmed nucleosome distortion on single chromatin fibres

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By Marty G. Yang, Hannah Richter, Simai Wang, Colin P. McNally, Camille Moore, Ali Emadi, Nicole Harris, Michela Maresca, Huimin Pan, Hayden Saunders, Megan S. Ostrowski, Erika Anderson, Elzo de Wit, Jacquelyn J. Maher, Yuhong Fan, Geeta J. Narlikar, Elphège P. Nora, Holger Willenbring, Hani Goodarzi, Vijay Ramani, Simaron Dhillon, Ruiqiao Yang
| Nature Verified
Abstract Despite decades of biochemical and structural studies of the nucleosome1, researchers lack genome-scale methods to determine variability in nucleosome structure along individual chromatin fibres. To address this, here we present Iteratively Defined Lengths of Inaccessibility (IDLI), a computational method that maps the single-molecule co-occupancy of structurally distinct nucleosomes, subnucleosomes and other protein–DNA interactions through long-read single-molecule footprinting2,3.
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Programmable RNA translation through deep learning-driven IRES discovery and de novo generation

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By Yanyi Chu, Di Yin, Dan Yu, Guangxue Xu, Junze Zhang, Xiaotong Wang, Yue Shen, Yupeng Li, Ning Zhao, Yi Zhu, Jason Zhang, Hani Goodarzi, Mengdi Wang, Le Cong
| Nature Verified
Abstract The precise control of protein expression is a major bottleneck in the development of RNA therapeutics. Internal ribosome entry sites (IRES) overcome traditional limitations by enabling cap-independent translation initiation, making them highly desirable tools for synthetic biology and therapeutic payload expression. However, the complex structure-function relationship of IRES elements has historically hindered their rational design.
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