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The film-trigger applicator improves microneedle skin delivery and drug efficiency using simple finger force.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

SCDSFs from zebrafish embryos are beneficial for treating cancer, regenerating tissues, and improving conditions like psoriasis and alopecia.

A Korean girl developed kinky hair without known cause or effective treatment.

HSPGs help control stem cell behavior, affecting hair growth and offering a target for hair loss treatments.

Keratin hydrogel from human hair is a promising biocompatible material for soft tissue fillers.

Targeting hair follicle stem cell and lymphatic vessel signaling may help treat hair loss and improve wound healing.

Targeting hair follicle stem cell and lymphatic vessel signaling may help treat hair loss and improve wound healing.

A trial showed that a new treatment is safe and effective for male pattern baldness, with most participants growing new hair.

Y-27632 helps hair follicle stem cells grow and keep their abilities.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

Chemical modifications can alter hair's stability and flexibility, with hydrophobic interactions helping maintain structure in humid conditions.

EFFC might be common but underreported.

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

Skin cells and immune cells change in a skin condition called hidradenitis suppurativa, and a certain treatment can improve these changes.

A new method was developed to create better skin models for healing and reconstruction.

Mutations in the HOXC13 gene cause hair and nail development issues.

Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

Researchers created a 3D-printed skin model that grew human hair when grafted onto mice by improving blood supply to the grafts.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Female pattern hair loss often starts in teenage years, reduces hair density, and can impact quality of life.

Four new cases confirmed the unique features of follicular porokeratosis.

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

High levels of cortisol in hair show long-term stress which can lower fertility in animals.

Epidermal growth factor helps hair stem cells grow by activating specific cell pathways.

Mackerel fermented fish oil protects skin cells from damage by UVB light.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.