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CD28 is a promising target for treating alopecia areata with belatacept.

CD28 is a promising target for treating alopecia areata with belatacept.

CD99 is highly present in certain skin cells and could help treat skin conditions.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

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

Lack of certain fatty acids causes skin, immune, and fertility issues in mice.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

OX40-targeted therapies may help treat skin diseases by reducing inflammation and balancing immune responses.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

Increasing PDCD4 protein may help prevent or treat some skin cancers.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

ARQ-234, a protein designed to treat atopic dermatitis, shows increased effectiveness in early testing.

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

Mice genetically modified to produce more CD109 in their skin had less inflammation and better healing with less scarring.

CD271 is crucial for maintaining healthy skin and preventing inflammation.

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

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

A gene mutation causes monilethrix in a Chinese family.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A mutation in mice causes hair loss and immune problems.