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

XMU-MP-1 stops cell growth in a human mini-organ and reduces the effectiveness of the chemotherapy drug paclitaxel.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

Keratin 17 is crucial for early hair strength and cell survival.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

Mice lacking steroid 5α-reductase 2 show less aggression and better impulse control.

Bim and Puma proteins are found in developing mouse hair follicles and are involved in more than just cell death.

Two new gene mutations cause a rare hair disorder.

Blocking mTORC1 reduces skin tumor growth in mice.

BMP2 helps hair follicle stem cells become specialized by increasing PTEN, which causes autophagy.

Blocking hair follicle development stops key gene signals needed for hair growth in mice.

Deleting MPZL3 increases skin oil production and reduces body fat.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

PINCH-1 is crucial for skin cell adhesion and movement, working with EPLIN and ILK.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

A gene mutation causes monilethrix in a Chinese family.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Deleting TNFα gene reduces skin cancer risk in certain mice.

The hairless mutant gene causes early hair loss and affects skin and thymus development in mice.

A new gene mutation causes a rare type of hair loss.

PKM2 is a promising target for heart repair and regeneration.

Lack of functional CYLD in mice leads to early aging and cancer.