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Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.

Human hair is made up of different keratins, some strong and some weak, with specific types appearing at various stages of hair growth.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

New treatments targeting specific genes show promise for treating keratin disorders.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Human beard hair medulla contains a unique and complex mix of keratins not found in other human tissues.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Oral minoxidil shows promise in treating monilethrix-related hair loss.

Only a few hair-specific keratins are linked to inherited hair disorders.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Human hair follicles grown in vitro maintain normal keratin patterns and structure.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

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

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Storing hair follicle micrografts for longer times can cause them to enter a state similar to the natural hair shedding phase, which might impact hair transplant results.

Cysteine-rich keratins evolved independently in mammals, reptiles, and birds for hard skin structures like hair, claws, and feathers.

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

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Epithelial-mesenchymal interactions control hair growth cycles through specific molecular signals.

Human hair keratins can self-assemble and support cell growth, useful for biomedical applications.

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

Poor maternal nutrition can lead to fewer wool follicles in Chinese Merino sheep.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

Hair protein composition is similar across different races and shapes.

The p75 neurotrophin receptor is important for hair follicle regression by controlling cell death.

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