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New treatments for skin and hair disorders in women of color address unique biological differences and include specific acne medications, sunscreens, skin lighteners, and hair care adjustments.

Involucrin helps strengthen the inner parts of human hair.

UVB radiation changes the chemical makeup and dries out human hair but doesn't alter its appearance or texture.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

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

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Signaling pathways are crucial for hair growth in goats.

Nanoemulsions improve stability and delivery of active ingredients in cosmetics for skin and hair care.

Keratoacanthoma comes from hair follicle cells.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

African hair has the most lipids, while Caucasian hair is more hydrated and stronger.

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

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

Mice lacking a key DNA methylation enzyme in skin cells have a lower chance of activating stem cells necessary for hair growth, leading to progressive hair loss.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

Hair follicle cells can help heal wounds and study skin diseases.

DNA methylation is essential for skin and hair follicle development, and could be a target for treating skin diseases.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Keratose, derived from human hair, is a non-toxic biomaterial good for tissue regeneration and integrates well with body tissues.

Human liver cells stick to hair protein materials mainly through the liver's asialoglycoprotein receptor.

Sex hormones affect hair and feather growth and may help manage alopecia and hormone-dependent cancers.

The research found that postmortem root bands in hair are likely caused by the breakdown of a specific part of the hair's inner structure after death.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

Heating hair proteins changes their structure and may improve their blood clotting ability.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.