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ADF8 and ADF11 help root hairs grow by responding to hormones and environmental signals.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Recombinant keratins can form useful structures for medical applications, overcoming natural keratin limitations.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.

Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

PTHrP and its receptor can control blood vessel growth and hair development in mouse skin.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Sheep breeds show different keratin gene expression in the groin, linked to hair follicle density.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Wool fiber curliness is linked to the presence of certain proteins and K38.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Blocking Wnt/β-catenin signaling with EGF receptor is necessary for proper hair growth.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

Nerve growth factor helps cashmere goat hair cells grow by activating a specific protein.

Monilethrix is linked to a gene cluster on chromosome 12.

Calretinin identifies the companion cell layer in human hair follicles.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

p2y5, now called LPA6, is a receptor important for human hair growth.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

ABCG2 protein marks stem-like skin cells in human epidermis.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.