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Epirubicin and cyclophosphamide cause more anemia and side effects than docetaxel and cyclophosphamide, but both are equally effective.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

Hormone replacement therapy may lower the risk of severe COVID-19 outcomes in non-immunosuppressed people and male organ transplant recipients.

The new Brigatinib nanocarrier is more effective against lung cancer cells than the free drug.

Brazilian pepper tree leaf extract effectively protects skin cells from UVC damage and is a strong natural skincare option.

Botryococcus terribilis and its compounds may promote hair growth and improve hair health.

Hom Thong banana peels can help reduce skin pigmentation by inhibiting melanin production.

Genetic testing can identify causes of rare hair loss disorders in children, but no treatments exist.

Understanding genes and mutations can lead to new treatments for hair loss disorders.

The hairless protein is important for skin, hair, and may influence cancer development.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

Vitamin D helps protect skin, PSORS1 gene's risk interval for psoriasis is expanded, hair follicles can be generated from mouse cells, and interferon-γ may cause pigmented skin lesions.

The new method improves accuracy in segmenting scalp tissue layers.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.

Hair follicles could be used to noninvasively monitor our body's internal clock and help identify risks for related diseases.

Histone demethylases can change gene expression and may be linked to diseases like cancer.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

Next-generation sequencing greatly improves understanding and treatment of genetic hair disorders.

The study concludes that regulating apoptosis could lead to new treatments for various skin and hair conditions.

AUC and APL are distinct conditions needing careful clinical assessment.

This rare genetic disorder causes permanent hair loss and skin bumps from birth.

Genetic testing is crucial for diagnosing rare hair loss disorders.

Six genetic conditions are often linked to complete scalp hair loss in children.

Ets2 gene is crucial for placental development in mice.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.