Add BrightSurf on Google Email

Gene essential to making DNA appears to be a good target in minimizing pulmonary hypertension

Researchers discover that inhibiting a gene crucial for DNA production can significantly reduce destructive cell proliferation and disease progression in pulmonary hypertension. This finding presents a potential treatment target for the condition, which affects females aged 30-60 with limited treatment options.

SourceMedical College of Georgia at Augusta University·JournalEuropean Heart Journal·DateMar 14, 2023

Single gene causes stinging cell to lose its sting

A single gene controls a switch between two alternative cell fates in a species of sea anemone, enabling the transition from a piercing cell to a sticky cell. This finding suggests that the nematocyte cell may have evolved from a spirocyte thanks to the development of the NvSox2 gene.

SourceCornell University·JournalNature Communications·DateFeb 23, 2023

Deer carry SARS-CoV-2 variants that are extinct in humans

A study found white-tailed deer are harboring SARS-CoV-2 variants that were once widely circulated but no longer found in humans. The deer may have become infected through contact with humans, and the virus has adapted to the deer population, potentially making it more transmissible between them.

SourceCornell University·JournalProceedings of the National Academy of Sciences·DateJan 31, 2023

New zinc finger model shows promise for gene therapy

Researchers developed a novel technology to engineer proteins targeting specific DNA sequences, offering a new approach to gene therapies. The system generates engineered zinc fingers that bind to any given sequence of DNA, potentially treating diseases caused by genetic mutations.

SourceUniversity of Toronto·JournalNature Biotechnology·TypeExperimental study·DateJan 26, 2023

Stowers scientists use cavefish to learn more about metabolism and the evolutionary basis of being a couch potato

Researchers studied cavefish metabolism to understand how humans might adapt over long periods of inactivity, finding genetic changes that enable muscle endurance and efficient energy storage. The study suggests potential implications for understanding and mitigating the negative effects of sedentary lifestyles on human health.

SourceStowers Institute for Medical Research·JournalProceedings of the National Academy of Sciences·TypeExperimental study·DateJan 24, 2023

CABBI team achieves first precision gene editing in miscanthus

The CABBI team successfully demonstrated precision gene editing in miscanthus, a promising perennial crop for sustainable bioenergy production. The results will accelerate efforts to tap the huge potential of this highly productive but genetically complex grass as a source for biofuels, renewable bioproducts, and carbon sequestration.

SourceUniversity of Illinois at Urbana-Champaign Institute for Sustainability, Energy, and Environment·JournalBiotechnology for Biofuels and Bioproducts·TypeExperimental study·DateJan 19, 2023

Genetic diagnosis helps guide care of childhood hearing loss

A recent study found that genomic testing can identify genetic causes of childhood hearing loss and provide critical information on its clinical characteristics. The researchers detected variants responsible for hearing loss in 43 different genes, and the severity of hearing loss varied by gene.

SourceUniversity of Washington School of Medicine/UW Medicine·JournalJAMA Otolaryngology–Head & Neck Surgery·TypeObservational study·DateJan 18, 2023

Modified CRISPR-based enzymes improve the prospect of inserting entire genes into the genome to overcome diverse disease-causing mutations

Researchers at Massachusetts General Hospital created a new class of technologies called CRISPR-associated transposases (CASTs) to overcome diverse disease-causing mutations. The optimized approach improves product purity and genome-wide specificity, offering a potential solution for inserting entire genes into the genome.

SourceMassachusetts General Hospital·JournalNature Biotechnology·TypeExperimental study·DateJan 17, 2023

Molecular Tumor Board provides useful assist in cancer precision medicine

A multidisciplinary team reviews genomic test results and recommends treatment options for patients with gastrointestinal cancer, identifying clinical trials suitable for most patients. The program has been successful in providing expert treatment guidance for over 500 patients and can be a model for other cancer centers.

SourceDana-Farber Cancer Institute·JournalJCO Precision Oncology·TypeSystematic review·DateJan 12, 2023

Scientists sequence and annotate majority of Red Perilla’s genome, a step toward harnessing more of its medically valuable bioactive chemicals

Hiroshima University researchers have generated a high-quality genome assembly of red perilla, allowing scientists to harness its abundance of potentially useful bioactive chemicals. The study enables targeted gene editing for enhanced phytochemical production, paving the way for new medical applications.

SourceHiroshima University·JournalDNA Research·DateJan 11, 2023

Tailoring 'hollow' hydrogen molecule generation with two-color, bicircularly polarized laser pulses

A team of researchers has developed an experimental method to manipulate the Rydberg state excitation in hydrogen molecules using bicircular two-color laser pulses. By controlling the photon effect and field effect, they were able to generate Rydberg states while varying the extent to which each effect contributed to the process.

Toward standardized tests for assessing lidars in autonomous vehicles

The three-year effort aims to establish a widely accepted protocol for comparing lidar performance. The first year's tests evaluated range, accuracy, and precision of eight automotive-grade lidars using a survey-grade reference. Results showed the distribution of measured values was not Gaussian, with significant errors in some cases.

Weiss-Kruszka syndrome and the failure to establish neuronal identity

Researchers identified the molecular mechanism underlying Weiss-Kruszka syndrome, a rare neurodevelopmental disorder characterized by craniofacial anomalies and autistic features. The study reveals that the ZFP462 gene mutation leads to a failure to safeguard neural lineage specification during early embryonic development.

SourceIMBA- Institute of Molecular Biotechnology of the Austrian Academy of Sciences·JournalNature Cell Biology·TypeExperimental study·DateJan 5, 2023

New spectroscopy technique improves trace element detection in liquid

Researchers have developed a new spectroscopy technique called filament- and plasma-grating-induced breakdown spectroscopy (F-GIBS), which improves the sensitivity of trace metal detection in liquid samples. The technique uses fluid jets to analyze aqueous solutions and achieves high precision by avoiding detrimental influences of liqu...

SourceSPIE--International Society for Optics and Photonics·JournalAdvanced Photonics Nexus·DateJan 4, 2023

A potential screening method to support drug development for dementia treatment featured in the December issue of SLAS Discovery

A new neuronal cell-based reporter system has been developed to identify compounds that inhibit histone deacetylase 2 (HDAC2) with minimal effect on its partner enzyme HDAC1. This innovation holds promise for dementia drug development by targeting the root cause of memory impairment.

SourceSLAS (Society for Laboratory Automation and Screening)·JournalSLAS DISCOVERY·TypeExperimental study·DateDec 14, 2022

How selfish genes succeed

A study published in PLoS Genetics reveals the mechanism by which a selfish gene in yeast, wtf4, enables its function using a poison-antidote strategy. This strategy involves the production of poison protein that can kill spores, but is countered by an antidote protein produced only by those spores that inherit the drive allele.

SourceStowers Institute for Medical Research·JournalPLOS Genetics·TypeExperimental study·DateDec 8, 2022