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New technologies show potential for better understanding and treating skin conditions with abnormal mucin, but more research is needed for clinical use.

MENT could be a better option than testosterone for male hormone therapy and birth control because it works well at lower doses and has fewer side effects on the prostate.

Microneedling and oral tranexamic acid both improve facial melasma, but microneedling shows more sustained benefits.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

Trichophyton mentagrophytes genotype VII is a sexually transmitted fungus causing skin issues, mainly among men who have sex with men in Europe, and requires quick treatment.

Amotosalen-treated donor T-cells can prevent late CMV infection after bone marrow transplants.

New therapies and trials are needed for Merkel cell carcinoma, a tough skin cancer.

Midazolam reduces PTSD-like behavior in rats by acting on specific brain receptors.

Mrp3 may aid in wound healing and hair growth.

Minoxidil prevents serotonin loss from MDMA by affecting potassium channels and increasing Akt phosphorylation.

Sebaceous glands help study fatty acid transporters and binding proteins.

Ultrasound helps efficiently extract beneficial compounds from maidenhairtree for potential medicinal use.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

Fluoxetine's effectiveness as an antidepressant in mice depends on a specific protein activity and a 5-minute pretest.

Majocchi's granuloma can occur in kidney transplant patients on tacrolimus and can be treated with antifungal medication.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

Ets2 gene is crucial for placental development in mice.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

Mrp3 helps in wound healing and hair growth.

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

MPZL3 is crucial for seborrheic dermatitis development.

A specific gene mutation causes different hair defects in Indian monilethrix families.

A rare type of skin cancer with mucosal involvement was partially treated but eventually relapsed.