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The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Enzymatic phosphorylation of hair keratin improves the effectiveness of hair products with cationic ingredients.

PP405 shows promise as a new, effective treatment for hair loss with minimal side effects.

A woman developed a hair disorder after a bone marrow transplant, which improved with treatment.

Researchers found a new mutation causing total hair loss from birth.

Children with alopecia areata have lower BDNF levels, linked to worse symptoms and quality of life.

Hair plucking quickly increases antizyme, reducing a specific enzyme activity in rats.

Androgens increase norepinephrine release, promoting smooth muscle growth in male sex organs, which may contribute to benign prostatic hypertrophy.

A gene mutation in mice causes severe skin disorder similar to a human condition.

Thiourea compounds affect hair growth and pigmentation in black rats.

Oral pulse steroids reduce TNF-α levels, improving alopecia areata.

Changing Allopregnanolone levels in newborns affects adult behavior and anxiety.

Alopecia areata may be caused by antibodies targeting specific hair follicle proteins, hindering hair growth.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.

Upper eyelid hyperpigmentation can help diagnose facial lichen planus pigmentosus in patients with frontal fibrosing alopecia.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Researchers found two new genetic variants linked to Alzheimer's disease.

Eosinophilic esophagitis may trigger alopecia areata in some patients.

Increasing alkaline phosphatase in human skin cells helps to grow more hair.

The combination therapy may be more effective for mild alopecia areata, especially in patients with allergies.

Arginine converts to citrulline in hair follicles as proteins harden.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Nanozymes can restore hair growth by fixing peroxisomal function.

Hair can be used to measure cancer-related chemicals noninvasively.

FAPD and possibly CCCA may be AGA subtypes, and treatments combining antiandrogens, hair growth agents, hair transplants, and anti-inflammatories could be effective.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Alopecia areata involves specific immune cells, offering potential treatment targets.