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Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Alopecia areata in these mice is inherited, more common in young females, and can be treated with triamcinolone acetonide.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

Mouse touch-sensitive nerve cells adjust their connections based on competition with other similar cells.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

TLR2 is crucial for hair growth and regeneration, and boosting it can help prevent hair loss.

Thymus-derived Tregs, not peripherally-derived Tregs, primarily regulate type 1 diabetes in the NOD mouse model.

IL-3 worsens lupus nephritis and blocking it improves kidney health.

Use ethical and humane practices in mouse research.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

TCDD changes skin cell growth and keratin production in mice.

A new enzyme in rats may help regulate hair growth.

Lack of TrkC receptor delays hair follicle development.

The improved genome of the African spiny mouse will help understand its tissue regeneration abilities.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

A new imaging method helps see and study touch nerve endings in mouse skin.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Activating Tgr5 may help treat hair loss and bone loss.

A gene mutation causes curly hair and hair loss in rats.

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

Transferrin receptor 1 is essential for normal function in the intestines, pancreas, and skin.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.