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A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

The treatment was not recommended due to limited effectiveness and significant side effects.

Four keratin genes are crucial for hair growth in Xinji fine wool sheep.

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

LPA 4 helps control blood and lymph vessel development in zebrafish.

Certain genetic variants increase the risk of aggressive prostate cancer.

Premature graying of hair significantly harms psychological and social wellbeing.

Some people have a genetic variation that makes them less effective at breaking down drugs.

The protein p21 is more abundant in normal skin cells than in melanoma cells and may help protect against melanoma, with UVB light affecting its levels.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Increased LC3 gene expression may be linked to premature graying of hair.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

A new change in the WNT10A gene caused a condition leading to short hair growth in a Chinese family.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.

Basal cell carcinomas and squamous cell carcinomas have different gene activity patterns, suggesting unique treatment approaches.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

More severe hair loss worsens quality of life in men.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

GLABRA2 represses root hair formation by inhibiting a specific gene.

Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

The enzyme CD73 helps control human hair growth and could be targeted to treat hair growth disorders.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The PCOSQ-50 is a valid and reliable questionnaire for measuring quality of life in Iranian women with PCOS.

Middle-aged skin shows aging signs, and quercetin might help delay them.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.