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Hair follicle bulge cells are important for hair survival and help heal the skin after injury, which might be relevant for understanding hidradenitis suppurativa.

Mutations in the hairless protein gene cause hair loss.

Triple H syndrome exists and can vary in symptoms.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Kikuchi–Fujimoto disease can cause scarring alopecia and should be considered in diagnosis.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Hair follicle stem cells may help treat strokes by improving brain recovery.

AgK114 protein helps in hamster skin injury recovery.

Stem cells show promise for hair regrowth, but challenges remain.

Low androgen levels can still cause female pattern hair loss.

Kdm6b is crucial for skin cell differentiation.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Two new gene clusters important for hair formation were found on human chromosome 11.

The hydrogel with 20% Hibiscus rosa-sinensis extract was the best for potential therapeutic use.

Immortalized hair follicle cells could be useful for regenerative medicine and treating inflammation and oxidative stress.

Sgk3 is essential for normal hair follicle growth and maintenance.

Skin can heal wounds without hair follicle stem cells, but it takes a bit longer.

Familial dyskeratotic comedones are a rare, benign skin disorder that is hard to treat.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

The HSVS-A is an effective tool for quickly screening hair shedding in Asian women.

Keratins are crucial for cell stability, wound healing, and cancer diagnosis.

Hirsutism affects many women and is managed with a combination of medical treatments and hair removal, tailored to individual needs.

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

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Two new gene clusters important for hair formation were found on human chromosome 11.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

The Spanish HSS-29 scale effectively measures changes in life quality due to female-pattern hair loss.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

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

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.