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UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

The document concludes that managing skin conditions during pregnancy is important and requires specialized care.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Dehydroepiandrosterone (DHEA) is a prohormone important for producing sex steroids and has potential health benefits.

Some viruses can cause cancer by changing cell processes and avoiding the immune system; vaccines and targeted treatments help reduce these cancers.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Hedychium spicatum has medicinal properties but needs more research for scientific validation and use.

Androgens and androgen receptors are important for metabolic health, affecting how the body uses glucose and fats through mitochondrial function.

Skin stem cells are crucial for maintaining and repairing skin, with potential for treating skin disorders and improving wound healing.

The vitamin D receptor has many roles in the body beyond managing calcium, affecting the immune system, hair growth, muscles, fat, bone marrow, and cancer cells.

Genomic research can help improve the quality and production of natural fibers in animals.

Sex hormones' effects on COVID-19 are unclear and more research is needed to understand their potential as treatment.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

Some existing medicines show promise as safe treatments to protect against the side effects of radiation therapy.

A protein called IL-36γ causes skin side effects from certain cancer treatments when combined with a common skin bacteria.

Hedgehog pathway inhibitors can treat certain aggressive cancers but face limitations like resistance and side effects.

Caspases are enzymes important for both cell death and various non-lethal cell functions, affecting head development and hair growth, with different caspases playing specific roles.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

Topical finasteride might be a good alternative for hair loss treatment with fewer side effects, but more research is needed.

Using protein degradation to fight cancer drug resistance shows promise but needs more precise targeting and fewer side effects.

Plant sterols have health benefits like lowering cholesterol, but more research is needed to understand their effects and improve their extraction and sustainability.

Testosterone replacement can help women with low libido and mood, but they need to have enough estrogen first to avoid side effects.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Gene therapy shows promise for healing chronic wounds but needs more research to overcome challenges.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

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