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Genetic Research

Scientists unveil terbium-161 breakthrough in targeted lymphoma treatment

A groundbreaking study from the Paul Scherrer Institute (PSI) in collaboration with Inselspital–Bern University Hospital has unveiled a promising new therapy for lymphoma using the radioactive isotope terbium-161.

AI deciphers plant DNA: Language models set to transform genomics and agriculture

Groundbreaking AI models are now deciphering plant DNA, treating genetic sequences like language. This innovation promises to revolutionise genomics and agriculture, offering unprecedented insights into plant biology and accelerating crop improvement for global food security.

Combination drug therapy increases longevity by 30% in mice

According to a study, a combination of two cancer drugs, rapamycin and trametinib, can increase longevity in mice by 30%.

New blood test rapidly diagnoses rare genetic diseases in children and infants

A new rapid blood test promises to improve the diagnosis of rare genetic diseases in children significantly.

Understanding age-related macular degeneration and emerging treatments

Steven T. Reed, O.D., President of the American Optometric Association, discusses age-related macular degeneration (AMD), the leading cause of severe vision loss in adults over 50, and the importance of early diagnosis and preventive care.

FDA approves clinical trial for groundbreaking Hereditary Spastic Paraplegia treatment

BlackfinBio Limited has received approval from the FDA to trial a novel therapy for Hereditary Spastic Paraplegia.

$2.7 Million NIH grant fuels development of first comprehensive syphilis test

Amidst a stark rise in US syphilis cases, researchers have secured a $2.7 million NIH grant to develop the first comprehensive, rapid test for active infection that aims to deliver accurate results within 10 minutes.

Common genetic variants linked to drug resistance in focal epilepsy

A new global study has found genetic changes that may make individuals with focal epilepsy less responsive to seizure medications.

New tool detects cancer tumours with faulty DNA repair

Researchers from the University of Cambridge and the NIHR Cambridge Biomedical Research Centre have created an algorithm that finds vulnerable cancer tumours.

How cancer cells trick the immune system by altering mitochondria

Cancer cells are masters of disguise, evading immune destruction through cunning mechanisms. Groundbreaking research reveals a novel tactic: mitochondrial transfer. Cancer cells cripple immune cells by donating their damaged mitochondria, hindering the immune response and fostering tumour growth.

New genetic mutation linked to drug resistance in non-small cell lung cancer

A new case report details a novel genetic mutation linked to drug resistance in a non-small cell lung cancer patient. Researchers identified a RUFY1-RET fusion, highlighting the need for advanced genetic testing to guide treatment strategies and combat evolving resistance.

New insights into insulin production deciphered

The University of Würzburg has shed light on the intricate mechanisms of insulin production in fruit flies, revealing surprising parallels with human physiology. This study offers crucial insights into how insulin-producing cells respond to metabolic changes, with potential implications for understanding and treating diabetes.

Engineered apatite nanoparticles enhance the biocompatibility of medical implants

Biocompatibility is a key challenge for medical implants. Researchers have engineered apatite nanoparticles with enhanced cell adhesion via pH-controlled synthesis. This breakthrough promises more effective implant coatings, improving integration and reducing inflammation.

NHS genetic testing programme could potentially offer lifesaving cancer prevention

A new NHS genetic testing programme has identified hundreds of people with Jewish ancestry at increased risk of cancer.

Epigenetic map creates new insights into the cause of cancer and dementia

A new project is expected to help us understand diseases such as cancer and dementia. A major partnership involving Oxford Nanopore Technologies, UK Biobank, NHS England, Genomics England, and the UK government has made this possible.

Harnessing genomic data for early disease detection

Lorna Rothery spoke to Heidi Rehm, Chair of the Global Alliance for Genomics and Health, about steps to harness quality genomic data to support disease detection and the importance of collaboration in this endeavour.

Common Agricultural Policy post-2027 strategies

Stoyan Tchoukanov, EESC member and Rapporteur for the EESC opinion on Promoting autonomous and sustainable food production, shares with us strategies for the Common Agricultural Policy post-2027.

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