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Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Cross-section trichometry is an accurate method to measure hair loss and growth.

Different keratins have unique expression patterns in mouse skin cells.

Different growth patterns in thyroid tumors are influenced by where cell growth and death occur.

Thymic LCH may be underdiagnosed, so thymic ultrasound should be considered in infants with cutaneous LCH.

HPV8 E6 gene causes growth of certain skin stem cells.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

A new gene mutation is linked to monilethrix in the studied family.

Trichilemmal carcinoma shares genetic changes with other skin cancers, suggesting similar causes and potential treatments.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

Removing certain immune cells in mice causes their hair to enter the growth phase earlier than usual.

Breast cancer alters specific molecular structures in hair, which revert after cancer removal.

CD2 might be a new treatment target for patchy alopecia areata.

Three molecular subtypes of advanced skin T-cell lymphoma were identified, with potential biomarkers for predicting treatment response and disease progression.

Both induced and spontaneous AA lymphocytes can cause alopecia areata in mice.

The study mapped genetic variations in sheep, linking them to traits like milk production and growth.

No clear link between androgen receptor variation and hair loss, but more research needed.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

A gene mutation causes monilethrix in a Chinese family.

DNA virus-induced tumors have consistent isozyme profiles, unlike other tumor types.

Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

The CD44-CD49d complex boosts T cell activation and survival in autoimmune disease.

A patient with a rare chromosome condition also had a rare type of hair loss.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

A genetic variant linked to hair thinning in Japanese women was found.

Alopecia areata involves complex immune responses, suggesting broader treatments could help.

CMV infection increases the risk of GvHD after bone marrow transplants.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.