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Adult stem cells are effective and ethically acceptable for treating various diseases.

Blocking the Wnt/β‐catenin pathway can speed up wound healing, reduce scarring, and improve cartilage repair.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Targeted anticancer therapies in children often cause skin side effects like rash and dry skin.

COVID-19 infection can significantly cause temporary hair loss.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

Neuroactive steroids and the enzyme 5α-reductase might be involved in the development of Tourette's syndrome.

Skin organoids from stem cells could better mimic real skin but face challenges.

OCT4 helps granulosa cell growth in early-stage follicles, and FSH increases OCT4 through specific pathways.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Oleanolic acid promotes hair growth by increasing cell proliferation through the Wnt/β-catenin pathway.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Men in the U.S. have more health issues, higher death rates from various diseases, lower life expectancy, and are less likely to seek healthcare.

Injecting newborn mice with a niacin blocker caused skin, gut, and brain damage similar to human pellagra.

Ban Tu Wan, a Chinese herbal supplement, can cause severe liver damage.

Gloriosa superba poisoning can mimic severe tropical infections and cause rapid hair loss.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Intermediate filaments are crucial for cell differentiation and stem cell function.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Researchers identified five new potential targets for leishmaniasis treatment, suggesting repurposing existing drugs could be effective.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

Older, obese people with many COVID-19 symptoms are more likely to suffer from severe long-term COVID-19 effects.

Long COVID-19 patients with skin pain might have a nerve condition that responds to a medication called gabapentin.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Linoleic acid (Vitamin F) can help protect against the harmful effects of acrylamide.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Paeonia lactiflora and Poria cocos extracts can potentially increase hair growth and reduce hair loss symptoms by lowering testosterone and inflammation levels.

5-alpha reductase inhibitors, like finasteride and dutasteride, may cause depression, but more research is needed to understand why.