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The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Nilotinib can cause skin issues like red bumps and hair loss.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Ritlecitinib is effective and safe for long-term treatment of alopecia areata.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

CCC1 is essential for ion balance and proper plant cell function.

Nexin 1 helps control hair growth in young rats.

JMJD3 and NF-κB activate Notch1, which is essential for skin cell movement and wound healing.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

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Certain long non-coding RNAs are important for the growth of hair follicles in Inner Mongolian cashmere goats.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

A mutation in the KRTHB5 gene causes hair and nail issues.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

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.

RALF22 is essential for root hair growth in response to fungal emissions in Arabidopsis.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Different parts of the nail express different keratins, showing unique patterns of differentiation.