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Jennifer Doudna

Jennifer Doudna

Jennifer Doudna

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Jennifer Anne Doudna is an American biochemist who has pioneered work in CRISPR gene editing, and made other fundamental contributions in biochemistry and genetics. She received the 2020 Nobel Prize in Chemistry, with Emmanuelle Charpentier, "for the development of a method for genome editing." She is the Li Ka Shing Chancellor's Chair Professor in the department of chemistry and the department of

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"... CRISPR is, in fact, a bacterial immune system. It’s an ancient system that evolved in microbes to allow prevention of viral infection. Our interest in this started with that fundamental biology, asking, “How does this work?” We did a collaborative research project with Emmanuelle Charpentier, a medical microbiologist, and our work with her laboratory revealed that one of the components of this CRISPR immune system is, in fact, a protein that’s called , that can be programmed to find and cut virus DNA. We published this work back in the summer of 2012, and for me, life hasnt been the same since."
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Jennifer Doudna
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"... I just think you have to embrace your passions. You have to really go for it. People that have been less successful, in my opinion, are those that dabble in something, but then don’t really give it their all. They almost never give themselves a chance to succeed, as they back off too soon. I think for young people, I tell them go for it, find supportive mentors who will help you through the tough times, and then just keep going. Because if you have a good idea, it’s probably going to work out in some way. You may not be able to predict how, but you should just keep pursuing it."
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Jennifer Doudna
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"Two years ago, I was working on my laptop in an airport lounge in Newark, New Jersey, when I glanced up and saw a couple walking with their two boys. The younger boy slowly made his way on crutches, displaying the telltale signs of a hereditary disease called muscular dystrophy. Generally manifesting in childhood, the disease steadily robs those who have it of their ability to walk. Eventually, I knew, the crutches would no longer be enough. My heart skipped a beat. Most types of muscular dystrophy originate with genetic mutations that weaken key muscle proteins, and I had just come from a meeting where a cure appeared possible, using CRISPR technology to rewrite the DNA of kids just like him. Imagining how the technology I’d helped create could change this boy’s life, I was overwhelmed with emotion. Beyond hope and wonder, I was filled with a sense of fierce urgency to expand CRISPR’s impact to the people around the world who need it most."
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Jennifer Doudna

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