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The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Increased 14-3-3 proteins may block hair cycle regression, causing hair loss.

Recombinant keratins can form useful structures for medical applications, overcoming natural keratin limitations.

The Glu413Lys mutation in keratin affects hair stability, while Glu413Asp does not.

Using special RNA to target a mutant gene fixed hair problems in mice.

CIPK13 and CIPK18 genes are crucial for root hair growth in plants.

Matriptase is crucial for skin barrier, hair growth, and may contribute to skin cancer.

Hedgehog signaling is essential for normal sebaceous gland development and affects keratin 6a expression.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

Abnormal gene expression related to keratin causes hair loss in certain mice.

The HCR gene contributes to psoriasis risk.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

A gene mutation in mice causes permanent hair loss and skin issues.

PAK4 is crucial in cancer progression, brain development, and could be a therapeutic target, especially through the PAK4-CREB axis.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

Claudin-1 is important for the barrier function and growth of hair.

Certain genetic variants in keratins increase the risk of tooth decay.

Cannabinoid receptor-1 signaling is essential for the survival and growth of human hair follicle stem cells.

Keratin 17 is important for skin development and may help define skin cell types.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Lack of Crif1 in hair follicle stem cells slows down hair growth in mice.

EGF and KGF signalling prevent hair follicle formation and promote skin cell development in mice.

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

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.