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Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

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

Hypertrichosis (excessive hair growth) can help diagnose superficial epidermolytic ichthyosis.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Hair follicle stem cells use specific chromatin changes to control their growth and differentiation.

Human head hair proteins can be typed into eight distinct patterns, useful for genetic and forensic investigations.

Sheet formation is key to macrofibril structure differences in wool.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

KRTAP2 genes are crucial for hair structure and may impact hair disorders and treatments.

Scientists identified and cloned specific keratin proteins in mouse hair.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

The EDA pathway plays a key role in bone development by interacting with other signaling pathways.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Scientists discovered two versions of a new human hair keratin gene.

The hairless protein is important for skin, hair, and may influence cancer development.

Four specific keratins in hair follicles help understand hair structure and function.

AgK114 protein helps in hamster skin injury recovery.

Intermediate filaments are crucial for cell differentiation and stem cell function.

The study found clear differences in lesion distribution and microscopic features among trichostasis spinulosa, keratosis pilaris, and eruptive vellus hair cysts.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Phospholipase A2 enzymes play key roles in skin health and disease.

A specific gene mutation causes sparse, brittle hair in a family.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.