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Chinese scientists find structural variation that boosts grain number in sorghum

Researchers have uncovered two major genes responsible for sorghum's double-grain spikelet, leading to a significant increase in grain number and crop yield. The study found that the DG1 gene regulates floret meristem formation and differentiation, restoring fertility to the lower floret and resulting in the double-grain trait.

Boosting plant health: the role of gene exchange with bacteria

Researchers have discovered a dynamic cross-kingdom horizontal gene transfer between plants and bacteria, transferring 75 genes that enhance carbohydrate metabolism and hormone synthesis. This finding opens up exciting possibilities for biotechnological applications in agriculture.

Apple iPhone 17 Pro

Apple iPhone 17 Pro delivers top performance and advanced cameras for field documentation, data collection, and secure research communications.

Transformation-associated recombination (TAR) cloning and its applications

Researchers have developed a novel tool for the selective and efficient recovery of large DNA molecules using TAR cloning. This technique has been applied to isolate individual gene alleles, study genome architecture and evolution, and engineer synthetic viruses with novel properties, including vaccine development.

GQ GMC-500Plus Geiger Counter

GQ GMC-500Plus Geiger Counter logs beta, gamma, and X-ray levels for environmental monitoring, training labs, and safety demonstrations.

Evolution: Larger datasets unravel deep roots

Researchers introduce a new approach to analyzing genome content in animals, resolving long-standing debates about the origin and development of tissues and organ systems. The method yields consistent results with classical views of animal phylogeny, shedding light on early evolutionary history.

Garmin GPSMAP 67i with inReach

Garmin GPSMAP 67i with inReach provides rugged GNSS navigation, satellite messaging, and SOS for backcountry geology and climate field teams.

First human circadian rhythm gene identified

Researchers have pinpointed the first human gene that controls circadian rhythm, a discovery that raises hopes for treating sleep problems in adolescents, the elderly, and shift workers. The study found a mutation in the hPer2 gene, which is responsible for familial advanced sleep-phase syndrome.

One-two punch knocks out fly genes

Scientists have developed a method to 'knock out' fruit fly genes, allowing researchers to study their functions and identify corresponding human diseases. The technique, also applicable to fixing faulty genes, has the potential to revolutionize gene therapy.

Drosophilagenome sequence completed

The Drosophila genome sequence has been completed, providing valuable insights into human diseases and animal development. The sequence data reveals homologues for 60% of known genetic flaws causing disease in humans and 70% of genes involved in human cancers.

GoPro HERO13 Black

GoPro HERO13 Black records stabilized 5.3K video for instrument deployments, field notes, and outreach, even in harsh weather and underwater conditions.

Gene protects tubby mouse strain from hearing loss

Researchers at The Jackson Laboratory have identified a chromosomal region that interacts with the tub mutation to prevent deafness in the tubby mouse model. The region, known as moth1, maps to mouse Chromosome 2 and was found to protect C57BL/6J mice from hearing loss.

Genome Research July tipsheet

Scientists map lung cancer gene Pas1 to mouse chromosome 6, shedding light on human lung cancers. The researchers also study the evolution of trichromatic vision in humans and primates, revealing gene duplication events that confer color vision abilities.

Jackson Laboratory Researchers Identify Neuromuscular Degeneration Gene

Scientists at The Jackson Laboratory have cloned the gene for mouse neuromuscular degeneration, a devastating neurological disease that affects humans such as amyotrophic lateral sclerosis and spinal muscular atrophy. The discovery provides an additional tool for understanding motor neuron death and may lead to new treatments.

SAMSUNG T9 Portable SSD 2TB

SAMSUNG T9 Portable SSD 2TB transfers large imagery and model outputs quickly between field laptops, lab workstations, and secure archives.

Blindness Linked To The Cytoskeleton?

A gene defect has been identified as causing a form of hereditary blindness, retinitis pigmentosa. The discovery links the disease to a malfunction of the cytoskeleton, which forms the skeleton of cells and affects internal transport and cell division.

Hopkins Researchers Identify Saethre-Chotzen Disease Gene

Researchers at Johns Hopkins Medicine identify TWIST gene as cause of Saethre-Chotzen syndrome, a rare genetic disorder characterized by craniofacial abnormalities and limb defects. The study confirms the role of the TWIST protein in human development and provides insight into the confusion with Crouzon syndrome.

Apple MacBook Pro 14-inch (M4 Pro)

Apple MacBook Pro 14-inch (M4 Pro) powers local ML workloads, large datasets, and multi-display analysis for field and lab teams.