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Centella asiatica extract may help promote hair growth by blocking a specific cell signaling pathway.

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

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PAS III can cause multiple autoimmune diseases with noticeable skin issues.

Methyl pyropheophorbide A from Sansevieria trifasciata leaves may help treat hair loss.

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The new microneedle patch effectively treats alopecia areata with fewer side effects than oral medication.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

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The method effectively reduces and hides scalp defects after surgery.

This new method makes checking for female infertility less painful, less invasive, and doesn't use radiation.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

The new device improves surgical accuracy by using a special dye and camera to see inside tissues.

The procedure effectively improved facial appearance with high satisfaction and low complications.

Using a collagen sponge scaffold helps stem cells become more like skin cells.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

A 16-year-old boy with lupus had a rare brain artery issue but fully recovered with treatment.

A 2-year-old girl had a hair disorder not shared by her identical twin.

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PCOS in Karnataka is influenced by genetics, lifestyle, obesity, and diabetes.

Saw palmetto cream for hair loss works better with glycerol and sorbitol.

Somatic BHD mutations are rare in Japanese renal tumors.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Early detection of Graham-Little-Piccardi-Lasseur syndrome is key for better management.

Sorafenib can cause a temporary skin condition that goes away after stopping the drug.

The new system greatly improves carvedilol's solubility and effectiveness.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

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About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Living Skin Equivalent transplantation helps heal ischemic non-healing wounds.