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The research shows that hydrogen bonds greatly affect the crystal structure of a Finasteride derivative.

Keratins K4 and K13 form stable dimers in mature esophageal cells, aiding cell stability.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A new method speeds up insulin amyloid fibril growth, useful for studying diseases.

A truncated protein linked to breast cancer may change cell adhesion.

A unique gene mutation was found in a family with monilethrix.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

A new method creates valuable compounds for drug discovery by breaking traditional chemical rules.

Chirality influences the structure, strength, and biological uses of peptide-based hydrogels.

A gene mutation causes monilethrix in a Chinese family.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

Trichohyalin is found in non-hair tissues and works with filaggrin in certain skin areas and conditions.

A new method was developed to create complex molecular knots using iron ions.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Hard α-keratin in hair has a unique, nonordered structure, different from other fibers.

Sheet formation is key to macrofibril structure differences in wool.

The model shows that filament flexibility and amino acid differences affect how fast intermediate filament proteins assemble.

Dihydrotestosterone specifically binds to hamster sebaceous glands, with a higher affinity than testosterone.

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

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.