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Platelet-rich plasma (PRP) can help with hair loss and improve hair transplant results.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

TRP-hair essence protects hair from heat damage, maintains color, and strengthens hair.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

4-(Ethoxycarbophenyl) retinamide is much less toxic than other retinoids.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

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

Mutations in the LIPH gene cause woolly hair in a child.

AtZP1 protein stops root hair growth in plants by blocking certain genes.

Nocturnal calcium infusions improved a boy's severe rickets without causing hair loss.

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LY191704 is a compound that effectively blocks a specific enzyme involved in hormone conversion and could help treat enlarged prostate and hair loss.

The PHAT technique effectively rejuvenates lips and face.

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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

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

Temporary scalp trichopigmentation creates a shaved hair look on the scalp using pigments that fade over time.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Mutations in the hairless gene cause a rare form of permanent hair loss.

IL-1β inhibits human hair follicle growth.

Blocking mTORC1 activity could increase hair pigmentation and potentially reverse greying.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.