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Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Reducing FOXA2 in skin cells lowers their ability to grow hair.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

TCDD reduces EGF receptors in the liver, affecting growth and development.

Ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes and influencing hair follicle phases.

Certain gene variations may increase the risk of PCOS in South Indian women.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Ocu-miR-205 affects hair density in Rex rabbits by promoting cell changes and influencing hair follicle phases.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Human bone cells mainly produce a type 1 enzyme that may help regulate bone health.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

The research found specific genes that are more active in balding cells, which could be causing hair loss.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.

The FOS gene helps hair growth in Tan sheep.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

Mice without certain skin proteins had abnormal skin and hair development.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

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

A mutation in the VDR gene affects hair cycling without needing ligand binding.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

OsUEV1B protein is essential for controlling phosphate levels in rice.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.