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

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Methylene blue staining effectively highlights detailed nerve structures in rat fur.

New micelle solutions greatly improve skin delivery of certain antifungal drugs.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Wnt1a from stem cells boosts hair growth and regeneration in mice.

A gene mutation causes curly hair and hair loss in rats.

Nails are essential for fingertip regeneration.

Flubendazole in a nanoemulsion can potentially treat lung cancer and cryptococcal meningitis effectively and safely.

KRTAP10 proteins help form the hair shaft's tough outer layer by interacting with specific hair keratins.

Darkened knuckles can be an early sign of insulin resistance.

PIEZO1 helps keep hair follicle stem cells inactive, affecting hair growth.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Blocking CXXC5 speeds up diabetic wound healing by improving blood vessel growth and skin repair.

A protein-based hydrogel helps heal diabetic wounds and repair nerves.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Mutations in the SNRPE gene cause hereditary hair loss.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A KRT32 gene variant causes loose anagen hair syndrome.

The cuneate nucleus has two main neuron types: relay neurons and interneurons.

Neuropeptides affect hair growth and could be used to control it.

Root hairs help barley grow better in zinc-deficient soil.

The XBB lineage of the Omicron variant spread rapidly in Southeastern Wisconsin.

Zebrafish skin regeneration relies on cell behaviors and reactive oxygen species, with antioxidants reducing and hydrogen peroxide increasing regeneration.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

The EDAR V370A allele in East Asians likely evolved due to reliance on aquatic resources providing essential nutrients.