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Combining microneedle-delivered ECM and radiofrequency improves skin elasticity and thickness more than ECM alone.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

Finasteride may help reduce COVID-19 infection by altering a key gene.

Zfp462 deficiency in mice causes anxiety-like behaviors and excessive self-grooming.

Forsythiaside A helps reduce brain damage from lack of blood flow by activating certain protective pathways.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

RF energy is used in medical and beauty treatments to heat tissues, tighten skin, and reduce fat safely.

Editing the FGF5 gene in sheep increases wool length, confirming its role in hair growth.

The WIF1 gene is crucial for hair growth in Angora rabbits.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Patients often overestimate their skin type, affecting sun protection and treatment plans.

Rb-bFGF improves hair transplant results and patient satisfaction with fewer complications.

Different types of human skin cells respond uniquely to various colors and doses of light, which could lead to specialized light treatments for skin conditions.

The model can effectively test gene functions and drug responses in human skin.

Ginsenoside F2 may help prevent hair loss and promote hair growth better than finasteride.

Editing the FGF5 gene in sheep increases fine wool growth.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

IFAP syndrome is a rare genetic disorder causing skin, hair, and eye issues, with limited treatment options.

RSPO1 could help create new diabetes treatments by increasing pancreatic β cells.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Plasma Rich in Growth Factors may help reduce hair loss in Frontal Fibrosing Alopecia.

Combining Endo-RF with PRP may improve acne scars better than Endo-RF alone.

Non-coding RNAs help control hair growth in cashmere goats.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.