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A new method using gold nanoshells and infrared light effectively delivers siRNA to cancer and stem cells with precision and minimal damage.

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

NFATc1 is crucial for keeping hair follicle stem cells inactive.

Physical inactivity is a primary cause of many human illnesses.

lncRNAs are important for understanding and treating skin diseases.

A new, quick method accurately detects minoxidil in drugs and cosmetics.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

MicroRNA miR-22 causes hair loss by making hair follicles regress early.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Netherton's disease causes multiple hair defects.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Nanostructured lipid carriers improve anti-aging drug delivery and effectiveness in cosmetics.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

Negative Pressure Wound Therapy speeds up wound healing by reducing inflammation and promoting skin cell growth.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

Wnt and Shh signaling are key in noggin-induced tumors, and blocking them can slow tumor growth.

LncRNA RP11-818024.3 helps hair growth and recovery in hair loss by boosting cell survival and reducing cell death.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

The microneedles effectively kill MRSA and improve wound healing.

Nelfb is essential for dermal fat development and survival.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

MG53 helps reduce skin damage caused by nitrogen mustard.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.