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The conventional extraction method with 50% ethanol was the most effective for antioxidant activity.

Gefitinib and Sasam-Kyeongokgo together significantly reduce cancer growth and improve immune response in mice.

UHP-sCESr is as effective as HESr for treating BPH symptoms.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

Lupus is a complex disease that requires personalized treatment because it varies greatly between individuals.

The 755 nm laser is more effective and safer for hair removal than the dual-wavelength laser.

Follicular Unit Hair Transplantation is a method for restoring hair by transplanting individual hair follicles.

Some patients fail bladder function tests due to lower flow rates and higher remaining urine volumes, but the exact reasons for failure are unclear.

Promising cancer treatments were found, but the manufacturer closed.

The film-trigger applicator improves microneedle skin delivery and drug efficiency using simple finger force.

New hydrogel sensors can be quickly made and customized for wearable devices.

Selaginella doederleinii extract shows potential for cervical cancer treatment but needs more research.

The research developed new fortilin protein constructs for potential heart disease treatments.

LDE225 is a promising skin-applied treatment for basal cell carcinoma with good skin penetration and effectiveness.

EF and PXE not closely related.

Finasteride and tamsulosin hydrochloride can be safely taken together without significant interaction.

A specific gene mutation causes a severe skin disorder in a family.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Errors found in identifying furosemide and finasteride polymorphs due to incomplete data.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

The nanofibers effectively fight bacteria and help wounds heal faster.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

pbn-STAC effectively finds strategies for cellular reprogramming using deep reinforcement learning.