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Researchers found a specific T cell receptor linked to severe drug reactions like Stevens-Johnson syndrome when patients take carbamazepine.

A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

The rs1128977 gene variant may affect cholesterol and body measurements.

Four specific keratins in hair follicles help understand hair structure and function.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Activating Kras in mouse skin causes excess skin and hair loss.

The keratin network in mouse skin changes during cornification and affects the skin's protective barrier.

A new one-step test can quickly identify skin cancer during surgery.

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Cadd4 effectively reduces cholesterol levels without side effects.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

Recombinant keratins can form useful structures for medical applications, overcoming natural keratin limitations.

A new mouse mutation causes skin and hair defects due to a gene change.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

DermaCult™ Keratinocyte Expansion Medium allows human skin cells to grow longer while keeping their ability to develop properly.

A man with Cronkhite-Canada syndrome improved significantly with immunosuppressive therapy.

GKLF/KLF4 and Sp1 control Keratin 19 gene activity, influencing cancer-related changes.

Recombinant keratin materials may better promote skin cell differentiation than natural keratin.

CLE14 peptide promotes root hair growth in Arabidopsis.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.

Keratin 19 forms less stable and shorter filaments than keratin 14, giving unique traits to certain skin cells.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.