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Human placenta helps hair grow back after chemotherapy by blocking cell death and increasing hair follicle growth.

The study found nine new hair protein genes in human hair follicles.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

PC-associated alopecia has unique microscopic features.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

MPZL3 protein is important for controlling hair growth cycles.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

The hairless gene mutation causes baldness by disrupting hair follicle structure.

Phospholipid-coated nanoparticles penetrate hair follicles better than others, especially in pig ears.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

L-phenylalanine and hydrolyzed eggwhite protein deeply penetrate human hair.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

Arabidopsis Formin 2 stabilizes actin filaments, affecting cell-to-cell movement and virus susceptibility.

Slug (Snai2) helps regulate hair growth timing in mice.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

ELL is crucial for gene transcription related to skin cell growth.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

A specific gene mutation causes woolly hair and hair loss.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

The alpha-helix was confirmed as a key structure in proteins.