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A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

New treatments for skin conditions related to the sebaceous gland are being developed based on current research.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

The PP2A-B55α protein is essential for brain and skin development in embryos.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Beta-caryophyllene, found in essential oils, helps wounds heal better in multiple ways.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Human hair keratin might be good for filtering out harmful substances from water.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

K18® and Olaplex® both effectively repair bleached hair, improving its strength, smoothness, and overall health.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Different species use the same genes for tooth regeneration.

Corin helps control salt and sweat release in sweat glands.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

Activating β-catenin increases melanocytes and decreases Schwann cells.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

Injectables can feminize or masculinize a transgender person's face, but more research is needed for best practices.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Men need higher doses of botox than women and a different approach for facial aesthetics due to their unique facial features and muscle mass.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.