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Keratin 2e shows a unique pattern in developing fetal skin, different from other keratins.

Normal skin results from interactions between EGF and the Tabby mutation.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Nail stem cells help nail and finger regeneration through BMP signaling.

Dkk4 protein helps control how hair grows and its arrangement.

Mouse tail skin has different keratinization near hair follicles and scales.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

The research concluded that hyaluronic acid affects the formation and growth of hair follicle-like structures in a lab setting.

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

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Monotreme and marsupial skin proteins show primitive features and species-specific differences compared to placental mammals.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

A specific gene mutation causes severe skin and nail issues and hair loss.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

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

Corneodesmosin is crucial for skin and hair health, and its dysfunction can cause skin and hair disorders.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

Researchers created early-stage hair-like structures from skin cells, showing how these cells can self-organize, but more is needed for complete hair growth.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Defects in certain proteins cause major heart abnormalities during early development.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.