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Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

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

Neuronatin is found in various cells of rat tissues and has a unique location in sperm cells.

The hair follicle structure is more complex than thought, with new findings on protein formation.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

Rat vibrissae have sensory terminals with specific structures that help detect hair movements.

Methylene blue staining effectively highlights detailed nerve structures in rat fur.

The big-clawed shrew's sinus hair follicles are highly specialized for sensing vibrations.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

A unique skin cell similar to hair bulb melanocytes was identified, with better preservation using permanganate fixation.

Mouse tail skin has different keratinization near hair follicles and scales.

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

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Rat hair follicle bulge cells can become nerve and glial cells, showing potential for neuroprotection.

Hard α-keratin has a universal molecular structure with a specific superlattice arrangement.

Finding eosinophils near hair bulbs helps diagnose alopecia areata.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Human hair follicles have their own thyroid hormone system.

Recent findings in cell biology help understand cell roles in health and disease.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Hairless mice have longer hair follicles and abnormal structures during the catagen phase.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

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

Mutations in the hHb6 gene cause the hair disorder monilethrix.