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

Different PIN proteins affect plant root hair growth by changing how auxin is transported.

A gene mutation in mice causes permanent hair loss and skin issues.

Follicular structures help differentiate keratoacanthoma from squamous cell carcinoma.

K15 gene is mainly active in the basal layers of hair follicles and epithelia, aiding early skin cell development.

Hair follicles and sweat glands show different keratin staining patterns.

Tumor cells in calcifying epithelioma of Malherbe resemble hair follicle cells.

Genetic variants in specific genes cause a type of hair loss.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

The ventral matrix is the main source of the nail plate.

Keratin 79 cells help form and regenerate hair canals.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Mutations in the hairless protein gene cause hair loss.

Abnormal gene expression related to keratin causes hair loss in certain mice.

A new keratin gene was found in mice, explaining hair growth.

The hair keratin variant is mostly found in Caucasians.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Lipase H is important for hair follicle function and shaping hair fibers.

Mouse keratin 6 isoforms have different expression patterns in various tissues.

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

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.