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A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

The study aims to create a model to predict health attributes using diverse health data from Japanese adults.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

Vitamin D receptors in hair follicles change with the hair cycle, affecting hair growth.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Certain histamine receptors (H2R, H3R, H4R) have unique roles in treating skin diseases, with H2R helping with chronic urticaria and other conditions, H3R providing pain relief and allergy benefits, and H4R reducing inflammation and itchiness.

Women with excessive hair growth or polycystic ovary disease may more often carry a gene variant for 21 hydroxylase deficiency.

The vellus index is a simple, quick, and reliable method to assess and monitor hair growth, especially in hirsutism.

A young woman with late-stage Vogt-Koyanagi-Harada disease was successfully treated at a hospital.

The HSVS-A is an effective tool for quickly screening hair shedding in Asian women.

VKHD can include rare oral symptoms like discolored teeth.

The lower part of rat vibrissa hair gets more blood and is well-protected for growth.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

The system helps monitor hair properties using RGB video microscopy.

hHbl gene is active in hair shaft cells and some pilomatricomas.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Human hair follicles have their own thyroid hormone system.

Natural α-hydroxyl acids cause skin exfoliation by activating TRPV3 channels.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

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