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Sphaeranthus indicus and silver nanoparticles can help treat liver cancer by killing cancer cells.

Ethylenthiourea is toxic to the liver and nervous system, especially with alcohol.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

A woman with EMS showed unusual skin mucinosis without the typical hard skin syndrome, suggesting EMS can cause skin mucinosis.

Hair follicles have unique proteins that vary by species and are influenced by nutrition.

Superoxide dismutases help balance cell stress and may aid cancer treatment.

ISCK03 stops melanin production in human melanoma cells and lightens skin color in mice and guinea pigs.

Cell junctions are crucial for healthy skin by supporting sebaceous gland function and sebum production.

SLC45A2 and GPNMB genes help control chicken feather color by promoting melanin.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Silibinin-loaded micelles significantly protect hair from UV-B damage.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

Transglutaminases work through a ping-pong mechanism, and human plasma and platelet transglutaminases have similar catalytic subunits.

A man in Japan got better from a scalp fungal infection using terbinafine.

Contaminated wheat caused hair loss and other symptoms due to high selenium, but washing it with alkaline water helped.

A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

A woman's cyclic Cushing syndrome was caused by a tumor in her adrenal gland that produced ACTH.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

Nano-liposol with astaxanthin may improve antioxidant and wound healing effects.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

The supplement significantly improves hair density and appearance in people with hair loss.

Autophagy is crucial for normal sebaceous gland function and sebum composition.

TTD symptoms vary widely, requiring thorough evaluations.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

PEG and keratin scaffolds can effectively deliver protein drugs by controlling release based on pH levels.

Ceramide Synthase 4 is crucial for maintaining hair follicle stem cells and preventing hair loss.