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A runner developed tangled armpit hairs from shirt friction, preventable by shaving or wearing smooth shirts.

Women's hair has more sulfur, and black hair has more calcium than white hair.

Trichohyalin granules help inner root sheath cells in hair follicles harden by integrating with keratin filaments.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

The study concluded that hair growth in mice is regulated by a stable interaction between skin cell types, and disrupting this can cause hair loss.

Premature infants have less elastic hair than full-term infants.

German shepherd hair varies in color and pattern but is flat with a consistent internal structure.

Hair loss is caused by the breakdown of a protein called COL17A1 in hair follicle stem cells.

Bubble hair damage is caused by high heat from styling tools, and trichoscopy helps diagnose it.

Understanding hair follicle anatomy helps diagnose hair disorders.

Keratin 17 is crucial for early hair strength and cell survival.

The study found that hair follicles are above muscle connections in the scalp, which may help protect stem cell areas.

The document concluded that certain clinical signs and hair growth tests help diagnose Short Anagen Syndrome.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

A new change in the WNT10A gene caused a condition leading to short hair growth in a Chinese family.

A protein called COMP is part of the connective tissue in normal human hair follicles and may be important for hair health.

Hair medulla patterns vary by Prakruti type, affecting hair strength.

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

Researchers developed a new model for more realistic computer graphics of hair by considering how light scatters on hair fibers.

Foxc1 helps keep hair follicle stem cells inactive, preventing hair loss.

The document concludes that different patterns of hair thickness and scalp changes can help diagnose types of non-scarring hair loss.

Recognizing ultrastructures of cashmere goat hair follicles helps identify and locate follicle layers.

Claudin-1 is important for the barrier function and growth of hair.

Keratin-based hydrogels from human hair help nerve repair better than traditional methods.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Abnormal contraction of connective tissue in hair follicles causes hair loss by killing off important cells, and treating this could improve hair growth.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Hair is a complex organ, and understanding its detailed structure and growth phases is crucial for analyzing substances within it.