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Trichohyalin and peptidylarginine deiminase type III are found together in rat hair follicles, with trichohyalin being modified after expression.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

Selenium in proteins helps prevent over-oxidation and supports chemical reversibility.

ROXY proteins help plants respond to nitrate shortage by affecting nutrient sensing and growth.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

The anti-hangover product may boost enzyme activity to help prevent brain damage.

Inhibiting ODC can prevent UV-induced skin cancer.

The enzyme system in hair follicles is similar to the liver's and is inhibited by certain substances.

Oxidation changes the structure of hair protein filaments, causing them to compact and rearrange.

Mutants of CYP154C2 enzyme significantly improved steroid conversion efficiency.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

Efficient enzyme function relies on specific residue interactions and structural coordination.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

A new method efficiently modifies alkenes to create useful medicinal compounds.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

Removing part of the vitamin D receptor stops vitamin D from working properly.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

New method makes important drug ingredients more easily without needing extra purification steps.

A specially designed molybdenum oxide nanozyme can treat and monitor acute kidney injury effectively.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

The structure of SRD5A reveals how it reduces steroids, aiding drug design for related health conditions.

Oxidized trichocyte keratin has a helical dislocation in its structure.

CDH3-related disease causes worsening eye and hair issues.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

Mutations in the hHb6 gene cause the hair disorder monilethrix.