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A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

The peptide IMT-P8 can effectively deliver proteins into the skin and cells for potential skin treatments.

Overexpressing Tβ4 in cashmere goats improves hair fiber traits and increases cashmere yield.

Different types of atopic dermatitis were linked to specific genetic and immune changes, suggesting that severe cases might need stronger immune-targeting treatments.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Sacituzumab govitecan improves quality of life and symptoms in breast cancer patients, except for causing more diarrhea.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

CNGA3, GLUD1, and SIRT1 are promising targets for treating aging and glioblastoma.

The ABI1 gene contributes to prostate cancer progression and treatment resistance.

Chronic T. gondii infection may harm male fertility.

Finasteride helps female-pattern hair loss.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

IL-18 signaling helps mature Tregs move into the thymus.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Gambogic Amide may prevent hair greying and promote hair growth by maintaining hair pigmentation.

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

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

TGFβ-2 may cause hair loss in androgenetic alopecia.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

BST2 is highly expressed in certain immune cells in alopecia areata, suggesting a role in the disease.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Tyrosinase and gp100 proteins can help diagnose and treat melanoma.

Blocking interferon-gamma might help treat various autoimmune diseases.

A new carrier improves skin delivery of tofacitinib for treating inflammatory skin diseases.