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IL-17 and certain immune cells are linked to more severe alopecia areata.

Lack of cystatin M/E causes thin hair and dry skin.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

The enzyme for activating vitamin D is found in many body tissues, not just the kidneys.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

A 22-year-old woman with a rare genetic condition was successfully treated to develop normal female characteristics and regular menstruation.

17α-Estradiol solution safely improves hair density and thickness in female pattern hair loss.

1′S-1′-Acetoxychavicol acetate may help treat hair loss by reducing oxidative stress.

CNGC14 is crucial for calcium entry needed for root hair growth in plants.

Different conditions affect how hair proteins assemble, and certain mutations can change their structure.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Skin changes in Pseudoxanthoma elasticum patients can indicate the severity of related health issues.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

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

Certain genetic variants in keratins increase the risk of tooth decay.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

Type 3 5α-reductase is more common and finasteride and dutasteride strongly inhibit it.