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Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

Inhibiting Zyxin may help treat androgenetic alopecia by promoting hair growth.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Researchers found a non-functional sheep keratin gene due to mutations.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

ILC1-like cells can cause alopecia areata by themselves.

Hoxc13 gene is essential for hair, nail, and papilla development.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Certain genetic markers may increase or decrease prostate cancer risk.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Lack of Crif1 in hair follicle stem cells slows down hair growth in mice.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

A rabbit gene important for hair development was identified and detailed.

FLCN helps control iron levels in cells.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

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

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

Mutations in the HOXC13 gene cause hair and nail development issues.

Tight junctions create a barrier in pig hair follicles that controls what can enter the skin.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

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

Vitamin C derivative may promote hair growth by activating specific genes.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.