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Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.

The PP2A-B55α protein is essential for brain and skin development in embryos.

GFC injections significantly improved hair growth and quality with minimal side effects.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

MAEG helps in mouse hair follicle development by aiding cell adhesion.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

VEGF promotes hair follicle cell growth through the VEGFR-2/ERK pathway.

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

Gefitinib can cause hair loss without scarring.

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

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

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

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Frontal Fibrosing Alopecia involves disrupted cholesterol pathways, fibrosis, and increased mast cells.

Endoglin is important for proper hair growth cycles and stem cell activation in hair follicles.

EGF and EGFR are important for goat skin development, increasing from weeks 6 to 21.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

A male patient developed frontal fibrosing alopecia after antiandrogen therapy for prostate cancer.

A unique gene mutation was found in a family with monilethrix.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

A new gene mutation causes long hair in some Maine Coon cats.

Frontal fibrosing alopecia mostly affects postmenopausal women, with diagnosis often delayed by 3 years.

TGF-β1 and 2 in hair follicles may be linked to hair loss in AGA.

The mineralocorticoid receptor temporarily affects mouse skin development, but the glucocorticoid receptor has a more lasting impact.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.