4D Printing Time Lapsed
Engineers at George Tech and Singapore University of Technology and Design have built a 4-D printer: “The [MORE]
Artificial Organelle
In many gene therapy trials, viral vectors transform producer cells. But from the beginning, researchers knew viruses were not [MORE]
3D Image of Hungtington Gene
Researchers at Northwestern University have discovered that the trinucleotide repeats (TNRs) associated with Huntington’s disease also [MORE]
Sandia Theranostics
Sandia National Laboratories engineers have developed rare-earth “metal-organic framework” materials that have unusual properties such as different color fluorescence, [MORE]
Vessel Damage Model
Chemical engineers at ITMO University (St. Petersburg, Russia) have developed intravenously injected nanoparticles that can be moved to [MORE]
Using Magnets to Heal Myocardial Cells
The previous piece is about protecting stem cell-derived cardiomyocytes so they survive when transplanted. This [MORE]
CU Boulder Researcher at Boulder at the BioFrontiers Institute
Drug resistance in several pathogenic species have raised alarms and stimulated a [MORE]
CAR-Engineered T-Cell
Some of the excitement over chimeric antigen receptor T cell therapy for cancer has diminished following the first patient [MORE]
Endothelial Cells Treated with Drug-Loaded Nanoparticles Saltzman
Preventing organ rejection because of an immune response to a transplant remains a major [MORE]
Nanoparticles Loaded with Chemotherapy
Quoting directly: “To improve the low efficacy and toxic side effects of chemotherapies that rely on this [MORE]
Lab Scale Prototype for Tumors
This piece leaves out two critical pieces of information: what kind of skin tumors are being [MORE]
Nanoparticles Reprogram Immune Cells
Here’s a good question: can nanoparticle technology transform immunotherapy for cancer? From researchers at the Fred Hutchinson [MORE]
Nasal Spray
Compared to injecting a drug into the blood stream for treating problems beyond the blood-brain barrier, a nasal spray [MORE]
CRISPR Delivery Mechanism
Getting CRISPR-Cas 9 molecules to their target cells without damage or off-targeting has been an obstacle for gene [MORE]