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Researchers found four genes that could help diagnose severe alopecia areata early.

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

STIM1 is essential for sweat secretion.

People with alopecia areata have higher levels of a heart disease marker in their blood.

Alopecia Areata is an autoimmune condition causing hair loss with no cure and treatments that often don't work well.

Cyclosporine A may help treat hair loss by blocking a protein that inhibits hair growth.

Apoptosis is crucial for healthy skin and treating skin diseases.

Thyroid hormone affects skin health, with too little causing rough, pale skin and too much leading to smooth, thin skin, and may also impact wound healing and skin conditions.

Mice skin has components that could help with hair growth and might be used for diabetes treatment.

DNA methylation and long non-coding RNAs are key in controlling hair growth in Cashmere goats.

lncRNAs may regulate hair follicle development in Hu sheep.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

Fat-derived stem cells show promise for skin repair and reducing aging signs but need more research for consistent results.

Fluorescent proteins help visualize and understand tumor blood vessel growth.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Spermidine may help reduce hair loss and deserves further testing as a treatment.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

t-Flavanone helps improve male pattern hair loss by making hair roots stronger.

Terbinafine can cause hair loss.

Hair disease research is a growing and evolving field in dermatology, with recent significant advances.