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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.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

The SOSTDC1 gene is crucial for determining sheep wool type.

A new, efficient method creates sulfinimidate esters from sulfenamides and alcohols without metals.

Using focused ultrasound on the brain can help epilepsy medicine work better in rats.

Researchers found 44 proteins that change during different hair growth stages and may be important for hair follicle function.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

The research found how certain drugs and polymers form stable complexes, which could help develop new pharmaceutical forms.

Agarose/fucoidan hydrogels may help treat diabetes by supporting pancreatic cell growth.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

The research shows how certain drug molecules form stable structures with polymers, which could help create new drug forms.

The FOS gene helps hair growth in Tan sheep.

Inducing ferroptosis in hepatic stellate cells is crucial for treating liver fibrosis.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

LHX2, with other markers, can identify hair placodes in rats.

KATP channels are important for energy balance and are targeted by drugs for diabetes, hypoglycemia, hypertension, and hair loss.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

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

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

Fahr syndrome causes brain calcification and is managed by treating symptoms and underlying issues.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The combination of TACE and Donafenib is effective and tolerable for treating unresectable liver cancer.

Gut bacteria overgrowth may cause some Post-Finasteride Syndrome symptoms.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Profilin1 speeds up wound healing.