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Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

Reducing Zyxin may help treat hair loss.

A rabbit gene important for hair development was identified and detailed.

One type of progenitor cell can maintain normal skin in mice.

Early hair follicle development involves distinct cell populations and Wnt signaling influences cell identity.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Exosomes from Pinctada martensii mucus can safely reduce melanin production, offering a new treatment for skin pigment issues.

Pantothenic acid helps mink hair follicles grow by affecting certain cell signals.

Overexpressing PKCepsilon in mice reduces papillomas but increases carcinomas.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Wnt-10b helps skin cells and hair grow.

Integrin α6 helps identify different neural crest cell types in the skin.

Human thymus has stem cells that can self-renew and maintain their identity.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

YAP1 helps fat cell formation by influencing the Hippo pathway.

Wnt-10b is important for keeping mouse skin cells healthy for hair growth.

Ku80 is a key receptor for Thymosin β4, affecting cell migration and wound healing.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

Wnt10a may help regenerate dental pulp and form dentine.

Bim and Puma proteins are found in developing mouse hair follicles and are involved in more than just cell death.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

Kremen is crucial for proper development and preventing tumors by regulating Wnt signaling.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Dkk4 protein is necessary for the proper development and arrangement of hair follicles.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.