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Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The zinc finger protein 3 in Arabidopsis thaliana reduces plant growth and root hair development.

The enzyme PA-PLA1α is important for proper hair follicle development.

Tranexamic acid turns white hair brown in certain mice by affecting specific proteins.

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

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

Fatp4 is crucial for healthy skin development and function.

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

The HCR gene contributes to psoriasis risk.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

The Gsdma3 gene is essential for normal hair development in mice.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

Giving immune serum from vaccinated mice to mice without T cells prevents infection and tumor growth.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

A new keratin gene was found in mice, explaining hair growth.

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