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A special receptor in sensory nerve endings helps control how they respond to stretching.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

Dimethylarsinic acid speeds up skin tumor growth in certain mice.

A new gene variant causes curly coats in some dog breeds.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

CaM7 and CNGC14 interaction controls root hair growth in Arabidopsis.

Janus kinase inhibitors may help treat lichen planopilaris.

The KRTAP gene family helps understand hair evolution and hair disorders.

Confocal Laser Scanning Microscopy (CLSM) is a useful tool for studying how drugs interact with skin and diagnosing skin disorders, despite some limitations.

KFSD causes scarring hair loss and skin roughness, mainly in males.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

KRTAP10 proteins help form the hair shaft's tough outer layer by interacting with specific hair keratins.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

Injecting specific cells into the skin can help improve skin structure and reduce blisters in a genetic skin disorder.

Some CKD patients' kidney function remains stable over time.

A specific gene mutation causes a severe skin disorder in a family.

A specific DNA region controls skin cell gene expression by working with certain proteins.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

LPA 4 helps control blood and lymph vessel development in zebrafish.