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Scientists have developed a new method to detect steroid abuse in athletes using cell-based tests, which could be the future of anti-doping methods.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

Androgen receptor activity is influenced by hormones, co-factors, modifications, and mutations.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

New treatments targeting androgen receptors show promise for drug-resistant prostate cancer.

The research helps understand how finasteride works and aids drug development.

Dabrafenib was effective and well tolerated in treating thyroid cancer with a specific mutation.

Early recognition of symptoms is crucial for treating IPEX syndrome with a stem cell transplant.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

The new ddPCR method reliably detects unwanted viruses in CAR-T cell products, ensuring their safety for patients.

Non-coding RNAs help control hair growth in cashmere goats.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

QR678 Neo® improved seborrheic dermatitis symptoms in a small group of patients.

Calreticulin has roles in healing, immune response, and disease beyond its known functions in the endoplasmic reticulum.

NADPH oxidase 4 is key for stem cell activity and growth under low oxygen.

LHX2 and SOX9 identify unique hair follicle cell groups, crucial for hair maintenance.

RT1640 treatment reverses gray hair and promotes hair growth in mice.

Different lasers and radiofrequency affect skin differently, important for dermatologists to choose the right treatment.

A 50 mg non-loading dose of ritlecitinib is safe for adults and adolescents.

150 kHz electromagnetic radiation might help improve PCOS in rats.

FOXN1 duplication can cause excessive hair growth.

Lipid metabolism affects wool thickness in sheep.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Vemurafenib causes significant skin side effects, requiring regular dermatologist care and sun protection.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

The new sensor can detect a toxic chemical in water with high sensitivity and accuracy.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

The method accurately measures finasteride in skin after using special carriers.