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The fragrance cyclohexyl salicylate helps promote hair growth and increase hair stem cell numbers.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Scientists found genes linked to the growth of high-quality brush hair in Chinese Haimen goats.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

Specific keratin gene mutations can cause monilethrix.

Reduced AhR signaling in HS tunnels leads to persistent inflammation and microbial imbalance.

Most 46XX CAH patients have female identity, but a few identify as male and may need treatment and surgery.

Hyaluronic acid microneedles help deliver minoxidil derivatives effectively for hair regrowth.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

HIF-1A may aid hair growth, Backhousia citriodora improves skin, autologous cells stabilize hair loss, infrared thermography assesses alopecia, and a new treatment preserves hair.

Hair diameter diversity helps assess hair loss, but its standard measure varies by individual and ethnicity.

Exclamation mark hairs and broken hairs best indicate active alopecia areata.

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Blue honeysuckle fruit extract helps hair grow by activating a specific signaling pathway.

ANXA1 influences hair growth in mice through the EGF signaling pathway.

Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

The study created a new type of microsphere that effectively regrows hair.

LSD1 and HSP90 help heal skin wounds by changing hair follicle stem cells' metabolism.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Hydrogen sulfide disrupts protein function and root hair growth in plants by modifying proteins.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.