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The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

The skin protects the body, regulates temperature, senses touch, and makes vitamin D.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

The document explains the genetic causes and characteristics of inherited hair disorders.

The document concludes that understanding how hair follicles naturally die and regenerate is important for insights into organ development and could impact health and disease treatment.

CD4+ skin cells may be precursors to basal cell carcinoma.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The document concludes that stem cells and their environments are crucial for skin and hair health and have potential for medical treatments.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

No FDA-approved treatments for chemotherapy-induced hair loss existed in 2006; more research was needed.

Too much β-catenin activity can mess up the development of mammary glands and make them more like hair follicles.

The mesenchyme can start hair growth, but the exact signal that causes this is still unknown.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Activating β-catenin increases melanocytes and decreases Schwann cells.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

The vitamin D receptor helps maintain hair and bone health even without binding vitamin D.

Cancer rates are increasing in developed countries, with estrogen, aging, low vitamin D3, and HPV infection as common causes.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

The document lists various dermatology topics, treatments, and diagnostic methods.

Melatonin directly affects mouse hair follicles and may influence hair growth.

Understanding the scalp's five-layer structure is crucial for better surgical outcomes and fewer complications.

No link between hair loss and blood groups or Rhesus factor.

Dermal stem cells help regenerate hair follicles and heal skin wounds.