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Scalp hair follicle cells help protect and heal skin in certain skin conditions.

A woman with a rare autoimmune disorder had a blister on her eye and unique immune reaction, which was effectively treated with medication.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

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

Glycerol is essential for skin hydration in mice without sebaceous glands.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

NG2 is crucial for normal skin and hair development in mice.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

GPC1 is important for hair growth by helping blood vessels form around hair follicles.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

The Gsdma3 gene is essential for normal hair development in mice.

Meis1 is crucial for skin health and tumor development.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

Human dermal fibroblast proteins help restore nerves during healing.

GLI2 activates GLI1, promoting skin tumor growth and hair development.

Antibodies help identify glycoproteins in normal skin and tumor cells.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

MARCKSL1 is important for wound healing and could be a target to reduce scarring.

The protein SLC1A3 is important for activating skin stem cells and is necessary for normal hair and skin growth in mice.

SCD1 is crucial for skin health and overall energy balance.

Sebum from sebocytes is important for skin health and linked to conditions like acne and hair loss.