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Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Unique microRNA patterns can help diagnose and treat severe alopecia areata.

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

An 18-year-old girl was diagnosed with a rare hereditary hair loss condition, despite no family history.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

miR-199a-3p controls hair growth and is linked to alopecia areata.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

PAON shows skin patterns due to genetic mosaicism.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

A new mutation in mice causes crooked whiskers and messy hair.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Nevus comedonicus can sometimes grow terminal hair, challenging previous beliefs.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

Aging reduces stem cell activation, leading to hair loss in mice lacking a specific enzyme.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

A substance called miR-1246 may help treat severe hair loss by reducing certain immune cell activities.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

Topical minoxidil may help improve hair growth in rare congenital hypotrichosis.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

ILC1-like cells can independently cause alopecia areata by affecting hair follicles.

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

No clear link between specific gene and hair loss in Mexican brothers.

Researchers found four genes that could help diagnose severe alopecia areata early.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Imatinib can cause hair loss due to lichen planopilaris.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

Arteannuin might work against cancer and Alzheimer's by targeting neprilysin.