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The enzyme Rand protease works well for leather dehairing and its stability is important, with Leu75 playing a key role.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

Prenatal THC exposure may harm ovarian health and fertility.

TRPV4 slows hair growth by affecting hair follicle cells.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

Lack of FPR2 slows hair growth by affecting hair cell activity.

MC-1R is present in skin cells and may help reduce inflammation.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.

Finasteride use in male rats may harm their male offspring's liver function.

dAR-6–1 is a promising new treatment for hair loss that works better than minoxidil.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Gene regulatory regions evolve faster than protein coding regions, allowing new gene relationships without changing transcription factors.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

TRPV1 is involved in pain, various body functions, and diseases, but targeting it for treatment is challenging.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

BMP signaling is essential for forming skin structures called rete ridges, aiding skin thickness and regeneration.

RNA-based treatments show promise for managing Hutchinson-Gilford Progeria Syndrome.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

Inhibiting mTORC2 can reduce DNA repair and increase cancer cell death, suggesting potential for targeted brain cancer treatments.

FOL-026 peptide can help repair blood vessels and promote growth, offering potential treatment for vascular diseases.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.