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Androgen-deprivation therapies increase the risk of certain heart conditions, but testosterone treatment may help.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

The KDM1 gene helps Venus flytraps close by managing potassium ions.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

Ketoconazole's structure and dynamics are linked, aiding antifungal drug development.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

TAK-279 effectively reduces psoriasis symptoms and is safe.

K10 may not prevent tumors as previously thought and might increase benign tumor risk.

Testosterone reduces knee movement, while flutamide and finasteride increase it.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Krt15+ cells in mice can resist radiation, regenerate tissue, and start tumors, suggesting new cancer treatment targets.

Reducing PIEZO1 speeds up wound healing.

TEC kinases may help cause inflammation in vitiligo and could be targeted for treatment.

Megavoltage radiation therapy extended survival in rabbits with thymomas, especially in those weighing more than 1.57 kg.

A sugar glider had a rare skin cancer that worsened despite treatment, highlighting the need for thorough checks in exotic pets.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

The research found specific genes that may cause longer hair in Tianzhu White Yak.