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Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

NSC167409 can effectively inhibit the virus causing hand, foot, and mouth disease.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Chirality affects the structure, strength, and function of peptide-based hydrogels.

PROTACs offer new ways to treat hard-to-target diseases, with promising drugs for cancer in advanced trials.

FOXN1 duplication can cause excessive hair growth.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

MOF controls skin development by regulating genes for mitochondria and cilia.

A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

The new hydrogel is good for wound dressing because it absorbs water quickly, has high porosity, can release drugs, fights bacteria, and helps wounds heal with less scarring.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

Chitosan-based hydrogels effectively control bleeding and have promising medical uses.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Researchers created an efficient method to extract DNA from marmoset hair, reducing blood chimerism.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

Fz3 and Fz6 can partially replace each other in tissue polarity and axon guidance.

Hepatitis C treatment may cause frontal fibrosing alopecia.

Hypoxic preconditioning helps human hair follicle stem cells survive oxidative stress.

Unique genes in hair follicle cells help tissue regeneration.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Transplanting a mix of specific skin cells can significantly improve the repair of damaged hair follicles.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Hair follicle cells help maintain and support stem cells and blood cell formation.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Human stem cells can help form hair follicles in mice.

The fuzzy gene is crucial for controlling hair growth cycles.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

Human hair follicle organ culture is a useful model for hair research with potential for studying hair biology and testing treatments.

Neural crest-derived progenitor cells in the cornea could help treat corneal issues without transplants.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.