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A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Activating autophagy might reverse skin fibrosis.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Serum granulysin levels can indicate the activity and prognosis of alopecia areata.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

Loss of Rap1 protein speeds up heart aging in mice.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

Nexin 1 may help control hair growth.

Trichoscopy helps diagnose and assess the severity of Frontal Fibrosing Alopecia.

Certain blood miRNAs are linked to severe alopecia areata and could lead to new treatments.

Stress in hair follicle cells increases certain immune-related proteins, which might contribute to hair loss conditions.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

PP2Acα is essential for proper hair and skin development.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

c-Myc, Max, and Bin1 help hair follicle cells mature and die.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Frontal fibrosing alopecia in men is often misdiagnosed and needs better diagnostic criteria and treatments.

The proteins transthyretin and megalin are more present in the growth phase of hair, suggesting they might affect hair health and growth.

Foreign-body granuloma may be a marker for late-stage Lichen Planopilaris and should be considered in diagnosis.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

A genetic variant in the KRT25 gene causes tightly curled hair.

Hair matrix cysts are rare skin nodules with unique features, often needing surgical removal.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Using facial sunscreen and moisturizer may increase the risk of frontal fibrosing alopecia.

Rats can develop an immune response to prion protein peptides, but it may cause severe skin issues in older rats.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

MMP-2 and MMP-9 help hair grow, while their inhibitors peak when hair growth slows.