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Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

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

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Sox9 is important in the development of tumors in domestic animals.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Antibodies help identify glycoproteins in normal skin and tumor cells.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

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

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Sgk3 is essential for normal hair follicle growth and maintenance.

New genetic mutations causing hair loss were found in a Chinese family.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Increasing SSAT makes skin more prone to cancer.

Researchers identified promising inhibitors for the BRD4 protein, including finasteride and amentoflavone.

WNT10A gene mutations cause short anagen hair syndrome.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

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

ICAM-1 helps regulate hair growth cycles and skin remodeling.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Keratin proteins in hair are complex and come from multiple gene families.