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Three molecular subtypes of advanced skin T-cell lymphoma were identified, with potential biomarkers for predicting treatment response and disease progression.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

Minoxidil helps restore thymus size in 22q11.2 deletion syndrome.

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

Staphylococcus aureus delays wound healing by disrupting lipid metabolism in skin cells.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

Blocking YAP/TAZ could be a new way to treat skin cancer.

Scientists can control how skin stem cells divide by using different treatments.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

Mutations in keratin genes can cause skin and mucosa disorders.

MPZL3 is crucial for seborrheic dermatitis development.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

Disrupting β-catenin signaling in certain cells causes anorectal malformations.

Keratin 15 cells from hair follicles help develop and maintain skin tumors in mice.

Lack of certain cells causes abnormal nipple development and nursing failure.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Overexpression of COX-2 in mice skin causes abnormal skin and hair development.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

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

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Grasp protein helps maintain skin health after UVB exposure.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.