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Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

Autologous growth factor concentrate therapy shows promise for treating early-stage hair loss safely and effectively.

Glycogen metabolism is important for energy and processes in human hair follicles, and hair follicles may produce glucose from lactate.

CGF treatment effectively and safely improves hair loss in androgenic alopecia patients.

LSCI-HR is reliable for monitoring blood flow in wound healing in mice.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Black hairy tongue can be an early sign of graft-versus-host disease after stem cell transplants.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

Surgical face-lifts are more effective, but fractional radiofrequency is a good, less invasive alternative for treating skin laxity.

A new one-step test can quickly identify skin cancer during surgery.

The Laxometer helps make hair transplants with many grafts safer.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

A new method using a microfluidic device can prepare hair follicle germs efficiently for potential use in hair loss treatments.

Hormone-replacement therapy improved a woman's skin condition known as lymphomatoid papulosis.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

Chemotherapy successfully treated both Hodgkin's disease and skin lesions.

FGF5 gene mutations cause long hair in domestic cats.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

The conclusion is that using light-sheet fluorescence microscopy with a special solution can effectively create detailed 3D images of human skin for dermatological research.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

Nrf-2-modified stem cells from hair follicles significantly improve ulcerative colitis in rats.

Hair follicle stem cell research has advanced in understanding and using these cells for hair growth and skin repair.

RC48 shows promise for treating certain advanced cancers, but more research is needed.

Hispanic patients in the USA have lower survival rates for melanoma compared to non-Hispanic Whites.