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The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

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

c-Maf positive macrophages help form hypertrophic scars by affecting fibroblasts and collagen production.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Long-standing benign tumors can become cancerous, especially in people with weakened immune systems.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Trichoscopy can help diagnose and decide when to biopsy folliculotropic mycosis fungoides.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Lack of functional CYLD in mice leads to early aging and cancer.

Tofacitinib effectively treated a woman's complex autoimmune and autoinflammatory disorders.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

A mother and her two daughters got a skin infection from their cat.

Pemigatinib may be effective for treating ZMYM2::FGFR1 fusion-positive leukemia.

Loss of Dnmt3a and Dnmt3b leads to more aggressive skin tumors, but blocking PPAR-γ can reduce this effect.

Four new FGF5 gene variants cause long hair in dogs.

Mycophenolate mofetil is a good alternative for autoimmune hepatitis patients who can't tolerate azathioprine.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

Introducing the rat OTC gene normalized hair growth in SPF-ASH mice.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

Folate receptor β helps suppress the immune system in macrophages and affects cancer growth and hair health.

FoxN1 overexpression in young mice harms immune cell and skin development.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.

The study developed a successful mouse model to study skin infections, highlighting the importance of choosing the right fungal strains.

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

Tofacitinib is more effective than methotrexate for treating moderate-to-severe alopecia areata.