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

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

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*Acorus calamus* has many medicinal benefits but needs more safety research.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Cosmetic products or emotional factors might contribute to Frontal Fibrosing Alopecia, and trichoscopy is useful for diagnosis.

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Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.

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

Fibrosing alopecia in a pattern distribution is a new type of scarring hair loss that resembles common baldness and an autoimmune skin disease.

Brunfelsia uniflora has good antioxidant properties and moderate antibacterial activity.

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DHT enhances androgen receptor activity more than testosterone, and MAGE-11 influences this activity through specific interactions.

VESALT improves alopecia areata assessment by including non-scalp areas and is reliable and user-friendly.

A20 protein is crucial for normal skin and hair development.

A specific gene change is linked to severe hair loss.

The ISHRS standardized FUE terminology for global use in hair restoration.

FFA in men, often mistaken for other hair loss types, may be more common than thought and needs larger studies for confirmation.