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New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

New topical treatment using spherical nucleic acids shows promise in reducing psoriasis inflammation.

A specific genetic deletion in goats affects cashmere yield and thickness.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

The research found that certain microRNAs are important for human hair growth and health.

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

DHT reduces a cell's ability to promote hair growth, while 3D culture without DHT improves it.

The endocannabinoid system affects oil production and inflammation in skin cells.

Zinc deficiency disrupts hair growth and cycle, but zinc supplements can fix this.

Gene mutations can cause problems in male genital development.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

Parthenolide promotes hair growth in mice and may influence pathways related to male pattern baldness.

Stress in hair follicle cells increases certain immune-related proteins, which might contribute to hair loss conditions.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

Researchers found 19 genes important for root hair growth in a plant called Arabidopsis.

Men are more likely to have severe COVID-19 cases and fatalities than women due to factors like lifestyle, aging, and biological differences.

Skin-derived precursors in hair follicles come from different origins but function similarly.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Blocking Wnt signaling in young mice causes thymus shrinkage and cell loss, but recovery is possible when the block is removed.

Hoxc genes control hair growth through Wnt signaling.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Hair loss risk is influenced by multiple genes.