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The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

Cannabinoid receptor-1 signaling is essential for the survival and growth of human hair follicle stem cells.

A new mouse mutation causes skin and hair defects due to a gene change.

Changing the C-ring structure in certain compounds can make them better at blocking a specific human enzyme.

1α,25-dihydroxyvitamin D3 directly affects cartilage growth and development.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Vitamin D compounds may help treat psoriasis by promoting skin cell differentiation.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

New compounds were made that effectively block enzymes related to prostate issues and hair loss.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

New chemical compounds were made that effectively block an enzyme linked to prostate growth.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

The compound 4c effectively inhibits the enzyme linked to hair loss.

Compound 15a was effective in inhibiting 5α-reductase.

Cyproterone acetate can effectively treat idiopathic hirsutism, but ethinyl oestradiol and lynoestrenol may not always reduce hair growth.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Finasteride showed limited hair growth and low patient compliance in treating male pattern baldness.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Blocking Janus kinase 1 helps stop inflammation and regrow hair, making it a good treatment for hair loss from alopecia areata.

XMU-MP-1 stops cell growth in a human mini-organ and reduces the effectiveness of the chemotherapy drug paclitaxel.

Higher levels of MiR-92a-1-5p and miR-328-3p found in female hair loss patients.

Using an anti-ICAM-1 antibody with rapamycin improves hair transplant survival in monkeys.

Certain genes controlled by OVOL1 are crucial for creating new hair follicles.