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March 2015 in “Neurological Sciences” A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.
The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.
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April 2011 in “British Journal of Dermatology” New mutations in the DSG4 gene cause a rare hair condition.
Keratin peptide signatures in hair may help identify gender and ethnicity.
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September 2015 in “Elsevier eBooks” SOX2 is crucial for skin cell function and hair growth, and it plays a role in skin cancer and wound healing.
January 2026 in “Frontiers in Medicine” A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.
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Human scalp hair follicles have PGE2 and its receptors, which might affect hair growth.
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