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The compound (NH4)2Mn0.17Cu0.83Cl4.2H₂O has a specific structure, shows weak magnetism at low temperatures, and undergoes phase changes at high temperatures.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

The upper hair follicle is stable, while the lower part allows movement during hair growth.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

The Cell Membrane Complex in hair has both water-attracting and water-repelling layers.

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

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

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Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

HKN-2 antibody targets specific skin and hair cells, showing keratin complexity.

Keratin 75 might be important in oral cancer progression.

The new composite scaffold may effectively treat chronic and deep wounds.

Alpha 6 + /MHCI - cells have stem cell traits and are similar to mouse hair follicle stem cells.

Whn is crucial for hair growth in certain areas by controlling a specific gene.

Vesicles made of behenyltrimethylammonium chloride and stearic acid can triple the skin absorption of hinokitiol, which may help with hair growth.

Hair follicle dermal stem cells help control hair growth timing by regulating signals at the hair germ–dermal papilla interface.

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

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

INT effectively shows enzyme activity and protein groups in wool and hair follicles.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

Different body parts have varying levels of certain hair follicle markers.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

K6hf is a unique protein found only in a specific layer of hair follicles.

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