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A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Keratins K4 and K13 form stable dimers in mature esophageal cells, aiding cell stability.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

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K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

S100A7 and IL-17 may contribute to inflammation in lichen planopilaris.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

Hair care products used for 4 weeks made hair smoother.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

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Keratin 6a is important for quick wound healing from hair follicles.

DHHB from Platycladus orientalis L. promotes hair growth and could be a natural alternative to current treatments.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

The RHD4 gene is crucial for consistent root hair growth in Arabidopsis thaliana.

Too much Smad7 changes skin and hair development by breaking down a protein called β-catenin, leading to more oil glands and fewer hair follicles.

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CDH3-related disease causes worsening eye and hair issues.

CK 5/6 expression in breast cancer is linked to negative hormone receptor status and higher tumor grade.

HPE may help treat osteoarthritis by promoting cartilage regeneration.

A young man had a rare case of hair cysts on his elbows, which was hard to diagnose and treat.

The model can effectively test gene functions and drug responses in human skin.

A new mutation in mice causes crooked whiskers and messy hair.