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The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Glutamine metabolism affects hair stem cell maintenance and their ability to change back to stem cells.

Skin tumor regression is helped by retinoic acid signaling blocking Wnt signaling.

The drug enzalutamide may reduce the ability of the virus causing COVID-19 to enter lung cells.

Finasteride for hair loss may cause persistent sexual symptoms, depression, anxiety, and lower quality of life.

Skin fat plays a key role in immune defense and healing beyond just storing energy.

Selective non-steroidal inhibitors of 5α-reductase type 1 can help treat DHT-related disorders.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

Researchers created rat liver stem cells that could help repair liver failure in rats and may be useful for studying human liver diseases.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Endocrine therapies for cancer significantly increase the risk of hair loss.

Chemokine signaling is important for hair development.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

COVID-19 might affect male fertility, but more research is needed to understand the full impact.

Scientists have created a new hair loss treatment using ultrasound to deliver gene-editing particles, which resulted in up to 90% hair regrowth in mice.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Noncoding dsRNA boosts hair growth by activating TLR3 and increasing retinoic acid.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Phosphorylation of certain parts of the PIN3 protein is crucial for its role in plant root growth and response to gravity.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Natural 5α-reduced glucocorticoids might be anti-inflammatory with fewer side effects than current options.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Researchers developed a new method to identify animal hair in textiles, which is effective for various fibers and more reliable than previous methods.

FLRG and follistatin have different roles in wound healing.

Some natural compounds may help overcome drug resistance in certain cancers, but more research is needed.