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Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

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

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

The document explains the genetic causes and characteristics of inherited hair disorders.

The study concluded that hair growth in mice is regulated by a stable interaction between skin cell types, and disrupting this can cause hair loss.

Human nails and hair follicles have similar gene activity, especially in the cells that contribute to their growth and development.

Certain DNA regions in alpacas are linked to fiber diameter.

Prolactin affects the production of different keratins in human hair, which could lead to new treatments for skin and hair disorders.

Different combinations of human hair keratins affect how hair fibers form.

Proteolytic enzymes damage hair follicles by detaching stem cells.

Good feather growth in poultry needs the right balance of proteins, amino acids, minerals, and vitamins.

A specific immune response helps control mite populations on the skin, maintaining healthy hair follicles.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

Hair and wool have diverse keratins and keratin-associated proteins.

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

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

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

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

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

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Different forms of FGF5 either promote or inhibit hair growth.

Keratin proteins in epithelial cells are dynamic and crucial for cell processes and disease understanding.

Gray hair may be caused by lower antioxidant activity in hair cells.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.