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Keratin biomaterials from human hair help nerve regeneration by activating Schwann cells.

TRPS1 is crucial for bone, kidney, and hair follicle development.

A stable, active version of a growth factor was made in bacteria, showing promise for medical use.

A 31-year-old man's hair turned white suddenly, likely due to alopecia areata.

Tooth loss can cause premature gray hair due to less chewing.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

Two patients with a rare scalp fungus in Poland were successfully treated with griseofulvin and ciclopirox.

Stem cells in eccrine glands could be used for regenerative medicine.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Aconiti Lateralis Preparata Radix helps mouse stem cells grow and turn into bone cells faster than usual methods.

Non-motor symptoms in myasthenia gravis are common and need early diagnosis for better management.

A possible link exists between hair follicle abnormalities, hair loss, and muscle weakness.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

A new method using a microfluidic device can prepare hair follicle germs efficiently for potential use in hair loss treatments.

The Graft Quality Index grades hair transplant grafts to predict placement difficulty and surgery results.

New mutations in the DSG4 gene cause a rare hair condition.

The mouse model helps study and develop treatments for radiation-induced saliva reduction.

Graves' disease is a common cause of hyperthyroidism, mainly in women, treated with medication, iodine, or surgery, with varying outcomes.

Iron supplements may reverse premature hair graying caused by iron deficiency.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

TG5 helps maintain hair follicle health, while TG3 aids in hair shaft development.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

The Gsdma3 gene is essential for normal hair development in mice.

KSR1 is crucial for certain skin tumor formation and could be a cancer therapy target.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.