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Mitochondrial problems in diabetic nerve damage might cause pain by lowering the production of certain nerve-related steroids.

Correct diagnosis and treatment are crucial for effective management of lipid storage myopathies.

New pyridine compounds effectively inhibit GSK3, a diabetes treatment target.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

MCP@G improves diabetic wound healing by reducing stress and promoting tissue repair.

Mitochondrial dysfunction contributes to ageing by causing DNA mutations and reduced cell function.

Glycogen metabolism is important for energy and processes in human hair follicles, and hair follicles may produce glucose from lactate.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Mitochondrial activity varies in cells before they stop growing, affecting their growth potential.

The man had myotonia, which caused delayed hand grip relaxation.

Early diagnosis and proper treatment improve outcomes for methylmalonic acidemia.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

PKM2 is a promising target for heart repair and regeneration.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

Glycated hemoglobin is not as effective as the oral glucose tolerance test for diagnosing blood sugar problems in women with PCOS in Southern Iraq.

PHGDH promotes cancer growth by aiding cell proliferation and tumor progression.

Glycogen helps E. coli cells divide unevenly and organize their contents.

Isolated amylase deficiency can cause failure to thrive and should be checked with specific tests.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Recognizing rare causes of MASLD is crucial for effective treatment and preventing complications.

Myotonic dystrophy may be classified as a segmental progeroid disorder.

Lack of a certain enzyme causes hair to grey early by damaging stem cells, but an antioxidant can help prevent this.

Engineered vesicles deliver mitochondria to improve diabetic wound healing.

Two calves died from ethylene glycol poisoning, a condition more common in pets.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

A pancreatic tumor caused high glucagon levels and symptoms, but treatment reduced glucagon and shrank liver tumors.