How 3-D Printing Could Help Shape Surgery
What you see in the image above is a lobe of a liver, times two—on the right, a flesh-and-blood one, removed from a transplant donor,
What you see in the image above is a lobe of a liver, times two—on the right, a flesh-and-blood one, removed from a transplant donor,
Researchers have developed lab-generated lymph node–like organoids that, when transplanted into mice in place of lymph nodes that have been removed, drain fluid and connect
Vaccines prevent millions of deaths a year and have pushed some diseases to the edge of existence. Yet it’s proven highly challenging, if not impossible,
By tweaking the chimeric antigen receptor or CAR engineered into T cells to treat patients’ lymphoma, scientists have avoided side effects common to the immunotherapy,
Keep hepatocytes fresh Freshly isolated primary human hepatocytes (PHHs) quickly lose their identity and function in vitro, limiting their application in modeling infectious liver diseases
Sientists have used CRISPR technology to edit out a lung-disease–causing gene while mice were in utero, rescuing the function of the lung and not affecting
Highlights • Glioma stem cells home toward, invade, and proliferate in human cerebral organoids • GLICO (cerebral organoid glioma) tumors phenocopy patient glioblastoma • Tumor
Current genetic testing methods often fall short in diagnosing pediatric patients with developmental delay, intellectual disability, or congenital abnormalities. Sometimes, this is because certain genetic
A one-of-a-kind rhesus macaque named Grady is growing up under intense scrutiny at the Oregon National Primate Research Center in Beaverton. That’s because she has
Genetically engineered yeast produce the cannabinoids THC and CBD, researchers reported today (February 27) in Nature. Much like in their typical application of brewing beer,
Without night vision goggles, mammals have no hope of seeing infrared light, which has wavelengths longer than light on the visible spectrum. But in a
Fetal DNA that is circulating in the blood of pregnant women is frequently extracted noninvasively and screened for common chromosome aneuploidies that cause disease such
The DNA of life on Earth naturally stores its information in just four key chemicals — guanine, cytosine, adenine and thymine, commonly referred to as
A new type of vaccine vehicle—this one literally has a teeny tiny motor—can drive itself to the mucosal linings of mouse intestines, potentially allowing for
ABOVE: A healthy adult bimaternal mouse with offspring of her own LEYUN WANG Mice with same-sex parents In research published in October in Cell Stem
A new technique that makes dead mice transparent and hard like plastic is giving researchers an unprecedented view of how different types of cell interact
The world’s first gene-edited babies were announced early this week not in a scientific publication or at a conference, but in news reports. He Jiankui,
In October, researchers at Kyoto University transplanted cells generated from induced pluripotent stem cells into the brain of a man with Parkinson’s disease, the scientists
There were just eight ingredients: two proteins, three buffering agents, two types of fat molecule and some chemical energy. But that was enough to create
For the first time, researchers have used the DNA from two mouse mothers to create healthy pups, some of which matured and had their own
A consortium of 17 laboratories worldwide has presented results contradicting a highly cited study that described a technique to create conditional knockout mice using CRISPR.
Using CRISPR, researchers have crafted a technique to study mammalian development in exceptional detail, according to a report published in Science yesterday (August 9). “This
Two gene injections reprogram Müller glia into rod photoreceptors in the retinas of blind mice and partially restore the animals’ vision, researchers report today (August
Immunotherapies that genetically modulate the antigenic receptors on a patient’s T cells—so-called CAR-T therapy—to seek out and destroy cancer have been met with favorable success
Immunotherapies that genetically modulate the antigenic receptors on a patient’s T cells—so-called CAR-T therapy—to seek out and destroy cancer have been met with favorable success
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