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

Hair proteins have weak spots in their α-helical segments.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

A peptide from hair follicle stem cells promotes hair growth by activating specific skin cells.

The Itpr3 gene causes a specific hair pattern in mice.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Mutations in the KRT16 gene can cause skin and nail disorders.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Dkk4 protein is necessary for the proper development and arrangement of hair follicles.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

TRPS1 loss in balding scalp areas contributes to hair loss in androgenic alopecia.

Keratin is crucial for skin barrier formation and affects mitochondrial function.

Nexin 1 may help control hair growth.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

TR3 is mainly found in hair follicle stem cells and may be involved in hair loss.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

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

New mutations in the hairless gene may cause hair loss and affect bone development.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Gene expression in wool follicles changes with growth cycles, offering insights into wool and human hair growth.