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Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

Early-onset hair loss is linked to Parkinson's disease and decreased fertility.

Human hair keratin has a 40% α-helix structure that changes to a random coil in 8 M urea.

PPAR-γ may be a key target for treating alopecia areata and other skin conditions.

Hair glycation can indicate long-term blood sugar levels and diabetic nerve issues.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Hair examination helps diagnose rare neurological diseases in children.

The research found specific proteins that affect fiber characteristics and hair growth in sheep and goats.

Lykoi cats' unique sparse hair is linked to specific genetic variants in the Hairless gene.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

DNA analysis can help tailor alopecia treatment.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Genetic variants in CYP genes may worsen PCOS symptoms.

Genetic factors might cause fibrosing alopecia linked to hair shaft abnormalities.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.