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A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Optimizing the structure of a specific compound greatly improved its effectiveness and precision for treating diabetic complications.

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Newly made nicotinamide compounds could potentially treat cancer.

K10 may not prevent tumors as previously thought and might increase benign tumor risk.

Scientists found new, better-working inhibitors for a hormone-related enzyme.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

Mice hair follicles take in the amino acid cystine.

A specific mutation in PA-PLA1α causes abnormal hair growth.

A boy's hair turned red because of genetic mutations, not lack of zinc.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

A new gene mutation is linked to monilethrix in the studied family.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

New compounds were made that block an enzyme linked to breast cancer better than existing treatments.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

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