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Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Activated protein C helps protect mice from radiation damage.

The right dosage of CPA and TB can work as a safe and reversible male contraceptive in monkeys.

Hair manganese may relate to cardiometabolic health, not coronary artery disease severity.

Intramuscular cyproterone acetate effectively treats hirsutism and improves skin conditions in women with hyperandrogenism.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

The InCISE score is a promising tool for assessing wound healing in head and neck surgery but needs more research for broader use.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Early treatment of mixed connective tissue disease is crucial to prevent severe autoimmune conditions.

MG53 helps reduce skin damage caused by nitrogen mustard.

TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

New technologies replicate human skin for testing without animals.

Keratin treatment reduces astrocyte reactivity and inflammation.

CXCR2 in skin cells promotes tumor growth.

ARHGEF3 is essential for proper hair follicle development in mice.

Looser dietary restrictions can improve growth and reduce illness in methylmalonic acidemia patients.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

miR-370-3p slows sheep hair cell growth by blocking SMAD4.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

The mind and body don't directly interact; the mind acts as an interface linking abstract and physical data.

A baby had a rare case of widespread milia, which was treated and is being monitored.

A new model helps study acne and test treatments.

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

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

TLR3 signaling enhances the immunosuppressive properties of human periodontal ligament stem cells.