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A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The research found specific genes and pathways that control fur development and color in young American minks.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

DHT in the human prostate is produced through multiple pathways, not just from testosterone.

Zinc can both inhibit and stimulate mouse hair growth, and might help recover hair after chemotherapy.

Minoxidil 2% effectively treats Monilethrix without side effects.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Iron deficiency might contribute to hair loss in women.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

The protein Gnαs is found more in black mice than white mice and may influence their coat color.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Gene differences may affect baldness treatment response in Korean men.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

The document concludes that blocking the internal pathways that create androgens might help treat cancers that depend on sex hormones.

Methionine restriction works better than betaine for treating CBS deficiency symptoms in mice.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

Key genes and pathways improve wool quality in Zhexi Angora rabbits.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.