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Stress can cause hair loss by negatively affecting hair follicles and this effect might be reversed with specific treatments.

Oxytocin receptor changes in hair cells may help identify autism, especially in males.

Hair grows when stem cell offspring in the follicle base proliferate, influenced by the dermal papilla.

Tianzhu white yak hair varies in structure and density between fuzz and coarse hair.

Mouse skin fibroblasts vary in function and adaptability based on their environment.

Dogs could be good models for studying human hair growth and hair loss.

M2 macrophages help hair regrowth in wounds by making growth factors.

Human hair follicles can provide stem cells for regenerative medicine.

Excessive body hair can signal complex health issues.

Rodent spiny hair traits are due to genetic factors other than the Edar gene.

A certain type of skin cell, marked by EGFR, produces a lot of IGF1 and helps hair follicles grow back faster.

Activating certain hair follicle cells could prevent hair loss from cancer treatments.

Stem cells improve nerve repair by enhancing blood vessel growth.

Basal cell carcinoma may start from parts of tiny hair follicles.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Major histocompatibility antigens are found in specific skin cells and structures, but not in sweat glands.

Adult vibrissa follicle stem cells can regenerate hair follicles, glands, and skin.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

A young man developed a rare, bilateral scalp condition after head trauma, causing hair loss but no neurological or eye issues.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Heterotypic cell contacts likely help hair matrix cells differentiate during mouse hair follicle development.

Telocytes in the scalp may help with skin regeneration and maintenance.

Ichthyosis serpentina may be a variant linked to bamboo hair, with a possible genetic component.

Ovalbumin–aluminum sensitization causes increased pain sensitivity and nerve changes in mice.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Human hair has bipolar electrical charges due to gaps in the hair follicle's electromagnetic fields.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

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