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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Folliculin slows hair growth, and blocking it might help treat hair loss.

Rabies virus was found in specific skin cells of rabid dogs' muzzles, suggesting these cells could help diagnose rabies.

Hair shaft miniaturization leads to hair follicle stem cell loss, suggesting Piezo1 as a potential treatment target.

SK2 channels help control sensory signals in rat muscle spindles and hair follicles.

Older women's scalp cells show changes that could contribute to hair thinning.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

Stem cell factor and certain proteins help melanocytes from hair follicles move and attach better, aiding vitiligo repigmentation.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

Methylene blue staining effectively reveals detailed nerve structures in rat snouts.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A genetic hair protein variant is more common in Japanese people and is inherited.

Senescent fibroblasts can help start tumors in normal skin cells.

Cosmeceuticals like sunscreens may trigger frontal fibrosing alopecia, but more research is needed.

Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.

Monotreme and marsupial skin proteins show primitive features and species-specific differences compared to placental mammals.

Increased cell death and reduced cell growth in hair follicles contribute to baldness.

Tenascin-C and tenascin-W help control stem cell movement and growth in whisker follicles.

Keratin structure changes during keratinization, but the exact model remains uncertain.

JAK inhibitors may help treat certain types of hair loss, but more research is needed.

Some skin growths with mucin can form hair follicles and resemble skin cancer, but a special stain can help tell them apart.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

A new method quickly extracts and identifies proteins from hair and other keratin sources.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Hard α-keratins stay stiff in water because the surrounding matrix keeps them dehydrated and strong.

Genetic hair shaft abnormalities can be seen with microscopes and often affect scalp hair.

FGF20 is essential for hair follicle stem cell growth and development in fine-wool sheep.

MicroRNAs play a key role in controlling hair growth and quality in sheep and goats.

Combining anti-androgenic, anti-inflammatory, and anti-fibrotic treatments may improve hair loss outcomes, but more testing is needed.