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Prolactin contributes to hair loss by promoting hair follicle shrinkage and cell death.

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

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

Two new gene clusters important for hair formation were found on human chromosome 11.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

PLIN2 affects hair growth in cashmere goats, potentially improving cashmere quality.

The patient's hair has unique structural differences with alternating bright and dark bands.

HAPLN1 can promote hair growth and may help treat hair loss.

Chemical treatments on bleached black hair change its internal structure by breaking and reforming bonds, and treatments with hydrolyzed eggwhite protein help repair it.

Finasteride crystals are held together by hydrogen bonds and weak interactions, forming synthon pseudopolymorphs.

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

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Dimeric peptide derivatives could help hair growth and treat hair loss safely.

Keratinous tissues have multiple structural layers, including ordered keratin and lipid granules.

A new compound, HTPI, promotes hair growth by protecting cells from damage and regulating energy use.

Netherton's disease causes multiple hair defects.

Human hair has different protein structures in its cuticle and cortex.

Peptide hydrogels show promise for healing skin, bone, and nerves but need improvement in stability and compatibility.

New hair perming method using tyrosine is gentler and can be done with a blow-dryer.

1,2,3,4-tetrahydroquinoline compounds are great for stable, pure blue hair dye.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

Hair medullary cells in mammals vary in complexity, with humans having more structured cells similar to inner root sheath cells.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Family members have similar hair protein patterns, which could be useful for genetic studies.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

Keratin structure changes during keratinization, but the exact model remains uncertain.