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Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

Changing YBX1 protein activity affects skin stem cell function and aging.

Fzd2 is important for skin and hair development through various signaling ways.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

Thuja orientalis extract significantly promotes hair growth in mice with hair loss.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

The protein's size was reduced, but more work is needed to confirm its function.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Human skin cells contain Protease Nexin-1, and male hormones can decrease its levels, potentially affecting hair growth.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Thymosin β4 helps with healing, inflammation, and organ protection.

XEDAR triggers a specific signaling pathway in cells.

The Bethesda system is effective for identifying thyroid cancer but has low sensitivity.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

PLX, a tomato extract mix, may help treat prostate issues like BPH.

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Polydopamine is promising for personalized medicine and biomedical technology due to its strong adhesion and biocompatibility.

A brominated phenoxy compound effectively inhibits a human enzyme and shows potential for clinical use.

ARQ-234, a protein designed to treat atopic dermatitis, shows increased effectiveness in early testing.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Two new gene mutations cause a rare hair disorder.

THH and PAD type III appear together early in hair growth, but deiminated THH appears later, suggesting another factor is involved.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.