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SOX2 helps reduce wound size and pressure ulcer formation by suppressing oxidative stress and increasing antioxidant activity in mice.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The research helps improve wool quality and aids human hair research.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Researchers created a new mouse model for studying scleroderma.

CD10 helps distinguish between basal cell carcinoma and benign hair follicle tumors.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

Pig skin is similar to human skin, with no major changes as they age.

C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Higher levels of MIG and IP-10 may help diagnose and monitor Alopecia Areata.

Dermal lymphatic vessels help hair growth by affecting hair cycle phases.

The combination therapy of PEG-IFN α-2a and Ribavirin can cause widespread hair loss and skin reactions.

A new mouse model for vitiligo helps study immune responses and potential treatments.

ICAM-1 helps regulate hair growth cycles and skin remodeling.

New sensor detects minoxidil accurately and effectively.

Androgens and estrogens are crucial for insulin secretion in males.

A gene mutation in mice causes severe skin disorder similar to a human condition.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

The tool iCOUNT helps understand how stem cells divide and affect tissue development and repair.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

MEX3A is crucial for maintaining intestinal stem cells in mice.

The IPL device is safe, effective, and has high patient satisfaction for hair removal.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.