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A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

S100A3 protein is crucial for hair shaft formation in mice.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

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

SM04755 may be an effective topical treatment for psoriasis.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

MsPG3 protein gathers at root hair tips, aiding growth.

Keratin 17 is crucial for early hair strength and cell survival.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

A certain gene variation can affect protein production and is linked to male pattern baldness.

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

miR-29 is a key factor that accelerates aging.

Somatic BHD mutations are rare in Japanese renal tumors.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

HLD10 can include increased body hair and Mongolian spots.

miR-199a-3p controls hair growth and is linked to alopecia areata.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.