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The anti-viral drug Elvitegravir may protect brain cells from damage related to neurodegenerative diseases.

More human hair protein makes the films weaker and less clear.

Lipid–polymer hybrid nanoparticles can improve genome editing delivery and outcomes.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Pregnancy increases certain GABA_A receptors in rat brains, influenced by steroid levels.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

The solution increased hair density safely and effectively for hair loss.

Hydrophilic carbon dots cause one protein to clump more and prevent another from clumping.

Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

Proteomic analysis can identify genetic differences in mouse hair, helping understand hair defects and variations.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

KAP6 genes are conserved across species and active in hair follicles.

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

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

P2X₃-IR fibers are widespread in rat skin and likely help detect pain.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Collagen XVIII is crucial for maintaining tissue structure and function in the brain, kidneys, and hair.

The hexosamine pathway helps maintain healthy skin by affecting the skin's structure and possibly increasing hair follicle stem cells.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Polyamidoamine dendrimers can change the strength and direction of electroosmotic flow through the skin, affecting drug delivery.

The research shows how certain drug molecules form stable structures with polymers, which could help create new drug forms.

Solid-state NMR can effectively study keratin structure and treatment effects in fur.