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Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

The study found that nerve signals are stronger when there are more connection points, but not necessarily denser, along the nerve's path in the spine.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Genetic factors influence growth and brain development in children.

Targeting Keratin 17 may help overcome cancer therapy resistance.

ASH2L is essential for skin and hair development.

A rabbit gene important for hair development was identified and detailed.

A gene mutation causes curly hair and hair loss in rats.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

SOX9 is essential for the development of various organs and hair follicles.

A new protein, mK6irs, is found in specific hair layers and may help understand hair growth and diseases.

FGF20 is essential for hair follicle stem cell growth and development in fine-wool sheep.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Finasteride helps female-pattern hair loss.

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.

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

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

Heat shock proteins help basal cell carcinoma grow by responding to inflammation signals.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Collagen VI is crucial for nerve function and affects wound-induced hair regrowth.

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

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

The rat vibrissa follicle can quickly remodel its basement membrane during hair growth, affecting cell signaling and activity.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

The LTF gene may help predict and manage nonspecific orbital inflammation.

The Foxn1 gene is essential for normal nail and hair development.