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HYDRO DELUXE BIO hyaluronic acid hydrogel is compatible with skin cells, may reduce inflammation, promote blood vessel growth, and protect against oxidative stress, suggesting it could help revitalize hair follicles.

Understanding proteins in skin structures like claws and hair is crucial for future research.

Combining proper shaving, topical treatments, and laser therapy effectively reduces Pseudofolliculitis Barbae.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Hair conditioners with argan oil or camellia oil improve the strength and color of bleached hair.

Hair and nail cells share similar proteins, indicating a common differentiation pathway.

Fox genes are important for hair growth and development in cashmere goats.

16-MHA can restore the barrier and moisture of damaged hair, making it similar to undamaged hair.

Cationic and nonionic surfactants provide better color intensity and resistance for semi-permanent hair dye than anionic surfactants.

Lower pH straighteners change hair more but weaken it.

Neonate scalp hair is thinner, lacks a medulla, and has smaller follicles compared to adult hair.

Hair growth environment recreated with challenges; stem cells make successful skin organoids.

Permanent hair dyes use chemicals that react with hydrogen peroxide to create color.

Healthy scalp leads to better hair quality and less damage.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Feed restriction in sheep leads to finer wool fibers but may reduce wool quality.

Hair absorbs molecules differently based on their size, charge, and love for water, and less at higher pH; this can help make better hair products.

Hair treatments cause significant structural changes, especially with excessive heat, regardless of ethnicity.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

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

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Light microscopy is useful for diagnosing different hair disorders.

Hair grays due to oxidative stress and fewer functioning melanocytes.

Human hair varies widely and should be classified by curl type rather than race.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

Hair follicle stem cells are key for hair and skin regeneration, can be reprogrammed, and have potential therapeutic uses, but also carry a risk of cancer.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.