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Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

AKR1C enzymes in scalp glands decrease with age, possibly affecting hair loss.

A specific gene mutation causes woolly hair and hair loss.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

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The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

Hair follicle keratin may have been used in tooth enamel evolution.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

Dickkopf-related Protein 2 can help hair grow by activating a specific cell pathway.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

A substance called DKK-1 increases in balding areas and causes hair cells to die when exposed to DHT.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

DcR3 helps heal wounds and regrow hair by changing macrophages to a repair-focused type.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Keratoacanthoma comes from hair follicle cells.

QLT0267 stops hair follicle cell growth and movement.

A rare skin condition in a 17-year-old was diagnosed late, stressing the need for careful evaluation and genetic testing.

Four new cases confirmed the unique features of follicular porokeratosis.

The malignant pilomatricoma showed strong epithelial keratin expression, suggesting it may not calcify.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

Human-hair keratin artificial tendons are biocompatible and degrade well in rabbits.

A mutation in the KRT74 gene causes tightly curled hair.

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

Ritlecitinib was generally well tolerated in children with alopecia areata.

Seborrheic keratosis shows varied cell differentiation, and keratin analysis helps diagnose skin tumors.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.