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A two-step method was created in 2015 to make more cells that help with hair growth, but they need to be combined with other cells for 4 days to actually form new hair.

A new method was developed to grow and maintain human hair follicle stem cells for hair reconstruction.

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

Scientists can grow human hair follicle stem cells in a lab without changing their nature, which could help treat hair loss.

Platelet-rich plasma can speed up bone healing and shows promise in orthopaedic treatments.

Human epidermal neural crest stem cells could be used for therapies, drug discovery, and disease modeling.

A dog's skin calcification condition resolved without treatment after a bacterial infection.

A new patch can deliver stable antibodies over time for potential HIV treatment.

Scientists made stem cells that can grow hair by adding three specific factors to them.

Platelet-rich fibrin (PRF) is better for natural healing, especially in dental and medical treatments.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Tissue expanders effectively repair large scalp defects and restore a natural-looking scalp.

More research is needed to improve wool and cashmere quality through genetics.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Two cows had a rare hair disorder causing hair loss but were otherwise healthy.

Hair restoration surgery has improved with better techniques for natural looks and managing patient expectations, but it remains labor-intensive and requires careful consideration of potential complications.

Mesenchymal stromal cell therapies show promise for treating various diseases but need more research and standardization.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Different problems with hair stem cell renewal can lead to hair loss.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

LLLT devices for hair loss need more research to define proper guidelines.

New treatments for atopic dermatitis and alopecia areata have been developed using a targeted approach.

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

An 8-year-old girl had a rare, benign skin tumor on her forehead.

Surgery for scar-related hair loss on the scalp and eyebrow was successful in 75% of patients.