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Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

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.

Pityriasis rubra pilaris is a rare skin disorder with reddish-orange patches and thickened skin, needing better treatment understanding.

A woman with HIV had a severe skin condition that improved with antiretroviral therapy.

A specific gene variant may increase the risk of developing Alopecia Areata.

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

Blocking certain immune signals can reduce skin damage from radiation therapy.

S1PR1 helps control inflammation in blood vessel cells by affecting gene activity differently in various cell types and locations.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

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

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

PPARs help regulate skin health and could be used to treat skin disorders.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

B blood type has the highest growth factors and cytokines in umbilical cord blood-derived PRP.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Upadacitinib effectively treats pyoderma gangrenosum.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Immortalized human dermal papilla cells were created that grow better and can still help form hair.

The research identified genes and non-coding RNAs in cells that could be affected by testosterone, which may help understand hair loss and prostate cancer.

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

A gene mutation causes monilethrix in a Chinese family.

A new gene variant causes glucocorticoid resistance in a mother and son.

EREG therapy may help treat hair loss by promoting hair growth.

Allopregnanolone increases growth and changes gene activity in human brain cancer cells.