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PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

Linagliptin slows down premature aging in certain mice.

AD198 is more effective than doxorubicin in stopping certain dog cancer cells.

Allopregnanolone changes gene expression in glioblastoma cells.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

The rare cliff plant Oresitrophe rupifraga has diverse metabolites, with leaves rich in phenolic acids and rhizomes and bulblets high in terpenoids, aiding its growth and potential use.

Dental care may help improve hair loss in alopecia patients.

Forskolin-loaded hydrogels improve wound healing and skin repair.

New methods to test hair growth treatments have been developed.

Early intervention in patch-type alopecia may prevent progression to more severe forms by targeting immune pathways and preserving keratin.

Fermented grapeseed oil effectively repairs and protects chemically damaged hair.

In alopecia areata, certain immune cells increase and express a protein linked to immune activation.

Fisetin, found in fruits and vegetables, may help treat various health conditions like inflammation, diabetes, heart issues, cancer, and hair loss.

Melatonin affects specific gene patterns and biological processes in goat hair growth.

Shikimic acid can promote hair growth and may help treat hair loss.

Polyunsaturated fatty acids, especially arachidonic acid and eicosapentaenoic acid, can promote hair growth.

Recent findings advanced understanding of cancer mechanisms and potential treatments.

ILC1-like cells can cause alopecia areata by themselves.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

The cross beam laser is a useful tool for safely measuring scalp stretchiness to improve hair transplant results.

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Fibroblasts from healthy donors can prevent changes seen in recessive epidermolysis bullosa simplex.

Corneous beta-proteins evolved uniquely in reptiles and birds, forming scales, claws, beaks, and feathers.

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

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

A specific gene mutation causes a severe skin disorder in a family.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.