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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

miR-200c-3p could help diagnose and treat alopecia areata.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Ritlecitinib effectively regrows scalp, eyebrow, and eyelash hair in Asians with alopecia areata and is safe.

Higher SRD5A2 expression predicts better response to finasteride in treating urinary symptoms.

KSR1 is crucial for certain skin tumor formation and could be a cancer therapy target.

NXC736 significantly reduced hair loss in mice with alopecia areata.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

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Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

PF-05314882 selectively activates androgen receptors without much effect on prostate and may help in prostate cancer treatment and hair loss prevention.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.