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Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Fibronectin is essential for hair follicle regeneration by supporting stem cells.

The cause of Frontal fibrosing alopecia, a type of hair loss, is complex, likely involving immune responses and genetics, but is not fully understood.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

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

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

FOXC1 boosts SFRP1 in hair loss, suggesting new treatments.

Researchers found specific genes in the part of hair follicles that could help treat hair disorders.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

NFIB and STAT5 work together to control specific genetic programs in cells.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Different forms of FGF5 either promote or inhibit hair growth.

Nfib in hair follicle stem cells boosts melanocyte stem cell growth and differentiation.

WNT10A and EBF1 interaction affects hair growth in male-pattern baldness.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

MAD2B slows down the growth of skin cells that are important for hair development by interacting with TCF4.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

The method successfully created stable transfection donor cells for goat hair follicle research.

Gene sequencing is essential for diagnosing Junctional epidermolysis bullosa.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

FGF18 helps hair follicles resist radiation by stopping hair growth cycles.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.