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A new test more accurately detects citrulline in hair follicles and pilomatrixomas.

The observed "toughening" in keratin was actually due to water evaporation, not a real change in keratin.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

Human mitochondrial DNA polymerase makes very few errors, crucial for preventing degenerative diseases.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

PN hydrates skin; PDRN heals and regenerates skin and hair.

A reliable method was created to measure dutasteride and related molecules in capsules.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

A new method was developed to purify finasteride for better medical use.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

Scientists created 3D hair-like structures that could help study hair growth and test treatments.

SARM-induced changes in the androgen receptor are specific to each ligand and affect stability and protein interactions.

Yak hair stretches mainly due to macromolecules slipping past each other.

Dissolving microneedles can effectively deliver dutasteride for hair loss treatment.

The keratin network in mouse skin changes during cornification and affects the skin's protective barrier.

Decomposed tritiated thymidine is less accurate for DNA tracing, and hair changes can indicate malnutrition.

Hair follicles form hard α-keratin filaments in four steps, showing structural differences.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

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

Human hair keratins can be turned into useful 3D biomedical scaffolds through a freeze-thaw process.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

Hair structure forms the same way inside and outside the body.

Antizyme reduces tumor growth and normalizes skin cell development affected by MEK.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

The technique effectively shows how human skin and hair cells form into ball-like structures.

Human dermal fibroblasts help microvascular endothelial cells grow, but not vice versa.

GLABRA2 gene controls root-hair growth by regulating phospholipid signaling.