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

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

EBF1 controls hair type and length.

A genetic hair protein variant is more common in Japanese people and is inherited.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Hyper-keratinisation in Meibomian glands contributes to gland dysfunction.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

Granzyme B is important in autoimmune skin diseases and could be a new treatment target.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Ultra-high molecular weight poly-γ-glutamic acid may help promote hair growth.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

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

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

Mutations in the DSG4 gene cause specific hair and scalp issues.

Transglutaminase activity is important for skin and is found in both mammals and birds.

The gene GJA1 is important for regulating coarse hair density in goats.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

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

A specific gene mutation causes congenital hair loss.

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

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.