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A balance between BMP and Wnt signals is crucial for hair follicle stem cell function and hair growth.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

AgK114 protein helps in hamster skin injury recovery.

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Certain genes control the color of human hair by affecting pigment production.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

BMP signaling is crucial for skin and hair growth.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

4-O-Methylhonokiol helps protect skin cells from growth-stopping effects of a protein by regulating growth-related pathways.

Iron deficiency in mothers causes hair loss in their baby mice.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

Keratin-associated proteins help link filaments and affect keratin's strength.

DHEA boosts bone cell growth and differentiation in elderly stem cells.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Hair follicles have unique proteins that vary by species and are influenced by nutrition.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.