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A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Ultrasound helps efficiently extract beneficial compounds from maidenhairtree for potential medicinal use.

Ginsenoside Rg3 combined with minoxidil was more effective in treating hair loss in mice.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Best results found using acetonitrile, water, and trifluoroacetic acid or methanol mixture.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

Cross-section trichometry is an accurate method to measure hair loss and growth.

Non-coding RNAs help control hair growth cycles in cashmere goats, suggesting ways to improve cashmere production.

Charnoly bodies could be a marker for cell damage, and certain nutrients and proteins might prevent them, potentially helping with brain diseases and cancer.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

MicroRNA-205 helps hair regrow by making hair follicle stem cells less stiff.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

CCC1 is essential for ion balance and proper plant cell function.

The HCR gene contributes to psoriasis risk.

Sheep hair follicle transglutaminases are calcium-dependent.

The study found potential new DNA patterns in fertility genes, but further testing is needed.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

The UHS promoter is specific to mouse hair follicles.

The new delivery system improved raloxifene's skin absorption and effectiveness against cancer cells.

miR-150 helps blood vessel cells develop and speeds up blood clot healing.

A systems biology approach helps improve mesenchymal stromal cell therapies by mapping interactions and identifying treatment targets.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Deleting MED1 in skin cells causes hair loss and skin changes.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

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

Caffeine and DMG increase calcium influx in hair follicle cells without being toxic.