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FLCN helps control iron levels in cells.

A boy with toxic shock syndrome had severe heart rhythm problems but recovered with treatment.

Women with telogen effluvium have an imbalance in thiol-disulphide, suggesting oxidative stress may contribute to hair loss.

Adding a second method to PROTACs could improve cancer treatment.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Scientists made a sensor that can detect a specific type of RNA related to androgen receptors quickly and accurately.

The activity of a specific rat enzyme in the prostate and epididymis is highly dependent on the acidity level.

A new triple drug system using nanoparticles effectively targets breast tumors in 3D models.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

KRTAP genes evolved early in mammals, leading to diverse hair traits.

Sulphur in hair follicles increases from the bulb and then levels off, while other elements vary in distribution.

PROTACs have become a breakthrough in medicine by effectively targeting and degrading specific proteins to treat diseases.

Combining TUSV with finasteride effectively treats recurrent hemospermia.

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

Different animals have unique versions of the enzyme that changes testosterone into another hormone, which is important for creating effective treatments for prostate and hair loss conditions.

Researchers developed new compounds that target the androgen receptor effectively with fewer side effects.

Ethylenthiourea is toxic to the liver and nervous system, especially with alcohol.

Lower SOD enzyme levels are linked to more severe hair loss in men.

Early diagnosis, genetic testing, and personalized care are essential for managing tuberous sclerosis.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Transglutaminase-3 is often reduced in esophageal cancer.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Genosomes are promising for safe and effective gene delivery in therapy.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Using existing drugs for new purposes can effectively treat infections resistant to multiple antibiotics.

The new fluoroquinolone effectively fights certain bacteria.