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TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

Trichoscopy effectively diagnoses temporal triangular alopecia in children.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

Facial trichostasis spinulosa is a chronic condition with significant cosmetic impact, especially in young women.

Trichostasis spinulosa is a common but often unnoticed skin condition involving bundled vellus hairs, especially in people with darker skin or UV exposure.

A unique gene mutation was found in a family with monilethrix.

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

Low testosterone can cause a heart rhythm problem in men, but fixing it can prevent the issue.

A new method allows for controlled, long-lasting delivery of retinoic acid through the skin with fewer side effects.

TR3 is mainly found in hair follicle stem cells and may be involved in hair loss.

Trichotillomania can occur in unusual patterns and sites, highlighting the need for awareness and treatment options.

Isolated rheumatic tricuspid valve disease is very rare.

A rare hair regrowth pattern can occur in some people with alopecia areata.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

Tay syndrome is a unique genetic disorder causing skin, hair, and developmental issues.

Nested PCR can reliably identify fungal infections when traditional methods fail.

TRH stimulates human hair growth and extends the hair growth phase.

Tph cells are linked to the severity of systemic lupus erythematosus.