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Blue helices connected by a blue ribbon with a white illumination pinpointing one section of the ribbon.
The Wonderfully Shrunken Cas13
Scientists removed unnecessary sections of the Cas13 enzyme, creating a mini-enzyme that works and fits with other CRISPR elements into a single gene therapy vector.
The Wonderfully Shrunken Cas13
The Wonderfully Shrunken Cas13

Scientists removed unnecessary sections of the Cas13 enzyme, creating a mini-enzyme that works and fits with other CRISPR elements into a single gene therapy vector.

Scientists removed unnecessary sections of the Cas13 enzyme, creating a mini-enzyme that works and fits with other CRISPR elements into a single gene therapy vector.

CRISPR

Biosensors for Colorectal Cancer
Hannah Thomasy, PhD | Nov 1, 2023 | 4 min read
Engineered bacteria sound the alarm on a common oncogenic mutation.
Venus flytrap plants grow in the lab, trigger hairs at the ready.
How the Venus Flytrap Captures Its Prey
Rachael Moeller Gorman | Oct 16, 2023 | 4 min read
Scientists used CRISPR-Cas9 for the first time in a carnivorous plant to prove the role of two ion channels in closing the Venus flytrap’s trap.
<em >The Scientist</em>&rsquo;s Journal Club: Detecting Nucleic Acids with CRISPR
The Scientist’s Journal Club: Detecting Nucleic Acids with CRISPR
The Scientist’s Creative Services Team | 1 min read
Kuangwen Hsieh will discuss his research understanding CRISPR-based nucleic acid detection assays.
A three-dimensional rendered image of neuron cell network on black background.
Assembloids Unlock the Roles of Key Neurodevelopment Disease Genes
Aparna Nathan, PhD | Sep 27, 2023 | 3 min read
Brain-like tissue grown in a dish mimics critical periods for development and reveals how it can go wrong.
Image of <em >Candida albicans</em> fungus.
A Fungus Plays Tug-of-war for Metal Ions
Laura Tran, PhD | Sep 14, 2023 | 3 min read
In the fight between hosts and fungal pathogens, scientists discovered how withholding manganese can cripple Candida albicans.
David Liu
Targeting a Genetic Accident to Treat Disease
Deanna MacNeil, PhD | 2 min read
David Liu shares how integrating chemistry and evolution in his research has directed his work on base editing techniques aimed at developing new therapeutics.
This shows a cryo-EM map of a Fanzor protein in complex with its guiding RNA (in purple) and DNA (target strand in red, complementary strand in blue).
CRISPR-like Abilities in Eukaryotic Proteins
Ida Emilie Steinmark, PhD | Sep 8, 2023 | 4 min read
Two groups independently discovered that Fanzor proteins in eukaryotic organisms are CRISPR’s genome-editing cousins.
A dart board with on dart on the bullseye and several scattered darts that missed the target
Predicting the Next Level of CRISPR Control
Deanna MacNeil, PhD | Aug 28, 2023 | 3 min read
Scientists combine the power of genome-wide screens and machine learning to unlock the secrets of transcriptome engineering with Cas13.
Cell division abstract image
Versatile and Sustainable: Cell Counting for the 21st Century
The Scientist’s Creative Services Team and DeNovix Inc. | 3 min read
Discover how the latest cell counting technology is reshaping a mundane task for the future.
Blood vessel with flowing red blood cells and white immune cells.
New CRISPR Treatment Could Prevent HIV Reinfection after Viral DNA Excision
Jennifer Zieba, PhD | Aug 21, 2023 | 3 min read
Researchers design dual CRISPR treatments to remove HIV DNA and prevent reinfection in vitro.
A transverse section of stem wood from the researchers&rsquo; greenhouse-grown poplar tree.
CRISPR Trees Could Improve Paper Production
Alejandra Manjarrez, PhD | Aug 15, 2023 | 3 min read
Researchers edited several tree genes to improve suitability and sustainability in the pulp and paper industry.
COVID-19: Lessons Learned
COVID-19: Lessons Learned
The Scientist’s Creative Services Team | 2 min read
An expert panel will discuss what researchers have learned from the COVID-19 pandemic and what lessons remain for the future. 
Photo of Rosa Bacchetta, associate professor of pediatrics at Stanford University
The Future of Gene Therapy for a Rare Pediatric Autoimmune Disease
Niki Spahich, PhD | Jul 10, 2023 | 3 min read
By editing a mutated immune regulatory gene in patient cells, Rosa Bacchetta brings hope to those suffering from IPEX syndrome.
Chromosome with gold band
Immunity Genes May Play a Role in Down Syndrome
Kamal Nahas, PhD | Jul 6, 2023 | 4 min read
Extra copies of four interferon receptor genes found on human chromosome 21 trigger developmental changes in a mouse model of Down syndrome.
3d render illustration of Single strand ribonucleic acid.
Message in a Bottle: Developing mRNA Therapeutics
The Scientist’s Creative Services Team and Mirus Bio | 3 min read
A high efficiency, low toxicity method for direct RNA delivery into cells.
Illustration of glowing fireflies
Glow-in-the-dark Diagnostics
Danielle Gerhard, PhD | Jul 5, 2023 | 2 min read
A nucleic acid detection platform that marries CRISPR diagnostic tools with bioluminescence could accelerate treatment decisions in the clinic.
Glowing red DNA on bluish background
Redesigning Medicine Using Synthetic Biology
Alison Halliday, PhD, Technology Networks | Jun 21, 2023 | 5 min read
Drawing inspiration from nature, synthetic biology offers exciting opportunities to transform the future of medicine.
Technique Talk: Understanding Cancer One Base Edit at a Time
Technique Talk: Understanding Cancer One Base Edit at a Time
The Scientist’s Creative Services Team | 1 min read
Francisco J. Sánchez-Rivera will discuss strategies to design CRISPR base editor libraries for in vivo applications.
mosquito on leaf
Combating Mosquito-Borne Diseases with CRISPR
Niki Spahich, PhD | Jun 1, 2023 | 4 min read
As alternatives to insecticides, Omar Akbari uses sophisticated genetic engineering methods to solve the world’s mosquito problems.
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