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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

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Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Keratin hydrogels can slowly release effective ciprofloxacin to prevent infections.

CUX1 boosts sheep hair cell growth and affects curl patterns.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

Paeoniflorin protects brain cells by involving a specific protein and neurosteroids.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

A genetic marker linked to a type of hair loss was found in most patients studied.

Cyproterone acetate improves skin symptoms and quality of life in women with androgen-related issues.

A new compound was made to detect copper ions effectively.

A method was found to select hair follicle stem cells, and beta-catenin helps them grow and change.

Lysine carboxymethyl cysteinate (LCC) protects skin from UVB damage by activating autophagy.

A rigid compound with a common structural motif was successfully synthesized.

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K6hf is a unique protein found only in a specific layer of hair follicles.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

CCC1 is essential for pH balance and normal cell function in plants.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.