Search

everythinglearnresearchcommunity

for

Search:↓

Anti-epileptic drugs may cause visual and hair side effects due to enzyme inhibition, especially in genetically predisposed individuals.

Scientists discovered a new way UVB light increases skin pigmentation through the ATP-P2X7 pathway.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

Liver damage in PCOS is linked to iron overload and cell death due to the miR-761-hepcidin/GPX4 pathway.

Acetate helps reduce depression in rats with PCOS by lowering specific gene expression and DNA changes in the brain.

Applying a specific inhibitor lightens skin and hair color.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

The UHS promoter is specific to mouse hair follicles.

The availability of certain hormones and specific stimulation patterns affect long-term synaptic changes in the male rat brain.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Presynaptic inhibition of certain nerve fibers in cats is mainly controlled by GABA and glycine.

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

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Marine sponges from Tabuhan Island can inhibit enzymes linked to Alzheimer's and hair loss.

PAD type III enzyme is specific to rat skin and hair follicles.

Targeting lipid metabolism can help treat advanced, resistant cancers.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Stopping finasteride improved seizure control, suggesting neurosteroids affect seizures and treatment.

TGFβ signaling prevents sebaceous gland cells from producing fats.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

5α-reduced neurosteroids may help regulate glial cell differentiation.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

The medicine Cyclosporin A might cause excessive hair growth by reducing a protein that controls hair growth.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.