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Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.

Majocchi’s granuloma should be considered when rashes don't improve with typical treatments.

Devon Rex cats with skin issues were successfully treated with antifungal medication.

Damaging mitochondrial DNA in mice speeds up aging due to increased reactive oxygen species, not through the p53/p21 pathway.

Deleting Rac1 in the skin depletes stem cells and damages hair follicles.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Zebrafish help understand genetic causes of skin pigment disorders like albinism.

A gene mutation in mice causes skin defects and early death.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

ODC transgenic mice can model human hair loss with skin lesions.

Treatment with prednisolone and dapsone stopped new blisters and partially healed previous ones.

A girl had rickets due to a gene mutation affecting vitamin D response.

The monkey's hair loss was due to an autoimmune disease, not genetics.

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

Melanocyte stem cells hold promise for skin regeneration and treating pigmentation issues.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Aged corneal cells can revert to a stem-like state to help repair tissue.

Moles may stop growing because of cell cooperation, not just because of aging cells.

Intersex frogs have different brain gene activity related to sex and thyroid hormones.

Wrinkled skin in Xiang pigs is linked to gene changes related to oxidative stress and the extracellular matrix.

Alopecia can be reversed with timely steroid treatment in VKH and SO diseases.

A rare benign skin growth called melanocytic matricoma was identified in a 69-year-old man.

Mirvetuximab soravtansine improves quality of life and reduces symptoms more than standard chemotherapy in ovarian cancer patients.

Mefloquine, an antimalarial drug, is effective in killing melanoma cells resistant to other treatments by causing lethal stress in the cells.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Topiramate impairs gene transmission in zebrafish, while Ginkgo biloba reduces harmful effects of high β-catenin levels.

Retinoic acid can change skin development, like turning scales into feathers or forming glands.