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A new genetic tool improves the study of hair growth and potential hair disorder treatments.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

The developed nasal gel improves cilostazol delivery to the brain, enhancing its effectiveness and reducing side effects.

Topical putrescine and spermine increased DNA synthesis in hairless mouse skin.

A new mutation in mice causes crooked whiskers and messy hair.

The pony's skin condition improved significantly with prednisolone treatment.

Copper supplements during pregnancy improve survival and development in mutant mice.

A new method can detect mutations in mice by observing changes in hair follicle cells.

Overexpressing a specific enzyme in mice causes hair loss and female infertility.

A mutation in the Sgkl gene causes defective hair growth in mice.

Espumil foam base allows easy preparation of skin medications for hairy areas.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

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

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Activating the sonic hedgehog pathway in chicken embryos can permanently change scales to feathers.

These temporary hair dyes may be harmful to human health.

The study found markers indicating that cells responsible for hair color are differentiating in specific areas of the hair follicle.

The African spiny mouse can fully regenerate its muscle without scarring, unlike the common house mouse.

ZPK helps skin cells mature and may affect skin health.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

The conclusion is that a new test was created to find substances that affect specific ion channels, and it works well for drug discovery.

Mice with a virus similar to COVID-19 had skin damage, but a special treatment helped repair it.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

Anti-SRP myopathy can be linked to systemic lupus erythematosus and may improve with specific treatment.

Imatinib mesylate can cause skin lightening, especially in Chinese patients, due to its effect on pigment production.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.