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Tributyltin exposure causes sex changes, sterilization, and decline in the snail Ocinebrina aciculata, risking its extinction.

AKN might be a skin marker for metabolic syndrome.

Tenascin is present in normal skin and certain skin tumors but not in sebaceous glands or their tumors.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

A person had two different benign skin tumors, a trichoadenoma and melanocytic naevi, at the same time but in different places on the face.

Targeting NETs may help reduce fibrosis in Crohn's disease.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Netherton syndrome in a boy caused skin and hair issues, and treatment didn't work.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

Cernitin™, a pollen extract, was found to significantly reduce pain and inflammation in rats with chronic prostatitis, suggesting it could be a useful alternative to certain anti-inflammatory drugs.

These gene variations are not linked to alopecia areata in Egyptians.

A new method helps detect androgen receptor movement in cells, aiding research on hair loss treatments.

High-throughput LC-MS screening is effective for finding new autotaxin inhibitors for asthma treatment.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Both penicillamine and tiopronin have significant side effects, but trying the alternative drug can be beneficial if the first is not tolerated.

TNFα, IFNγ, and Substance P significantly affect prolactin levels in human skin, suggesting new treatments for skin and hair conditions.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

NIPT can help detect potential maternal cancer, and GIPXplore can identify immune diseases in pregnancies.

The N-K GM Series offers a new method to reduce aflatoxin poisoning and cancer, improving health and saving costs in affected regions.

Oral Acitretin effectively resolved symptoms in a child with Netherton syndrome.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Netherton syndrome causes specific skin and hair changes that help in early diagnosis.

Trichohyalin is a versatile protein involved in hair and skin structure.

Chronic tonsillitis is linked to NETosis activity, which may help tailor treatments and reduce tonsil removal surgeries.

Equilibrium dialysis can accurately measure testosterone levels when lab results are inconsistent.