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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

Mimosine dipeptides are promising for treating hyperpigmentation and inflammation.

A gene mutation in mice causes permanent hair loss and skin issues.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Stopping mitochondrial respiration can prevent brain cancer spread in skin cancer patients, and plant compound β-sitosterol could help achieve this.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

Methotrexate is not proven to maintain remission in ulcerative colitis.

MicroRNA-200 prevents sebaceous gland development by inhibiting SOX9 and cell cycle progression.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

miRNA-211 reduces melanin in Cashmere goats by suppressing AP1S2.

Genetic disorders can disrupt mineral and trace element metabolism, affecting health.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.

Certain chelators lighten mink skin and hair, increase skin elasticity, and disrupt hair growth without affecting fur quality.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

Selenium deficiency can cause skin and hair color loss, muscle weakness, and blood cell changes, but these improve with selenium supplements.

Fatty acid transport protein 4 is essential for skin and hair development.

Methotrexate treatment for rheumatoid arthritis has a serious infection rate of about two per 100 patient-years.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

Both enzyme forms can sulfate minoxidil.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

A new mutation in the KRT86 gene causes monilethrix in a Han family.