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The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

CARASIL can cause different symptoms even with the same genetic mutation.

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

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

New genes linked to male pattern baldness were found on chromosome 20p11.

K15 staining helps distinguish basal cell carcinoma from trichoepithelioma.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

The Hedgehog signaling pathway is linked to cancer development, and targeting it with inhibitors shows promise but faces challenges like resistance.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

Stabilizing HIF1A in hair follicles increases glycolysis, which may help reduce oxidative stress and support hair growth.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

Some cancer treatments can cause abnormal fine hair growth.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A woman with a long-term skin condition developed a serious skin cancer that led to her death.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

Mouse hair follicle stem cells have a flexible chromatin state that supports skin health and hair growth.

A specific gene change in APCDD1 increases the risk of hair loss.

Genetic marker rs12558842 strongly linked to male hair loss.

The enzyme PA-PLA1α is important for proper hair follicle development.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

The new antibody, TYHF-1, specifically targets certain hair-related structures.