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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.

Apple iPhone 17 Pro

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

A new approach to high insulin levels

Congenital hyperinsulinism is caused by a genetic mutation that leads to permanent activation of the GDH protein, resulting in excessive insulin production. This triggers chronic hypoglycaemia, brain damage, and intellectual retardation. A new study may pave the way for novel therapies, including a drug that inhibits the GDH accelerator.

New test could identify infants with rare insulin disease

A new test developed by researchers at the University of Manchester can identify congenital hyperinsulinism in some patients without known genetic causes. The test measures hormone levels and may influence treatment options, including avoiding pancreatic removal.

Aranet4 Home CO2 Monitor

Aranet4 Home CO2 Monitor tracks ventilation quality in labs, classrooms, and conference rooms with long battery life and clear e-ink readouts.

Treatment breakthrough for rare disease linked to diabetes

Researchers at University of Manchester discover new treatments for congenital hyperinsulinism by correcting gene defects in insulin-producing cells. The breakthrough has the potential to reverse cellular defects and pave way for new drugs, offering real hope for devastating condition.

Treatment corrects severe insulin imbalance in animal studies

Researchers have successfully treated congenital hyperinsulinism, a rare genetic disease causing insulin imbalance, using a peptide called exendin-(9-39) that blocks hormone receptor action. This could lead to an innovative medicine for children with this condition.

Enzyme defect leads to hyperinsulinism

A genetic disorder causing hypoglycemia, congenital hyperinsulinism is linked to defects in insulin secretion by pancreatic cells. Mutations in the glutamate dehydrogenase gene impair enzyme sensitivity, leading to excessive insulin release and hypoglycemia.