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The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

Sulfur-containing radioprotectors can protect hair from X-ray damage if given before exposure but worsen damage if given after.

Effective treatment for UFT overdose includes antibiotics and G-CSF, with bone marrow biopsy and transfusion as backup options.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Steroid sulfatase in hair follicles may be a target for treating hair loss.

5α-reductase enzymes are crucial in certain disorders, and while treatment advances exist, more research on SRD5A3 is needed.

Compound 1 showed promising anticancer activity.

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

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

The research found enzymes in Stephania epigaea that help make cepharanthine.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

ETS2 is crucial in squamous cell carcinoma development and could be a therapeutic target.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Cysteines in wool fibers are accessible and form important disulfide bonds.

CYP154C7 enzyme can effectively modify steroids and is promising for commercial use.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

PROTACs offer new ways to treat hard-to-target diseases, with promising drugs for cancer in advanced trials.

The Enterobacter isolate AMS1-S8 is effective for removing selenium from wastewater.

Improving PROTAC delivery systems can enhance their effectiveness and speed up their use in medicine.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

Very-long-chain acyl-CoA synthetases and fatty acid transport proteins play key roles in fatty acid metabolism and lipid processing in different tissues.

The infant with a urea cycle disorder improved with treatment and a liver transplant.

Low-sulfur hair syndrome can cause UVB sensitivity and testicular failure.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Sebaceous glands help study fatty acid transporters and binding proteins.