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The document concluded that stem cells are crucial for skin repair, regeneration, and may help in developing advanced skin substitutes.

Polycystic Ovary Syndrome (PCOS) is a common condition in women that can cause metabolic, reproductive, and psychological issues, and requires lifestyle changes and medication for management.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

Tofacitinib temporarily regrew hair in a man with alopecia, but its effects didn't last.

Testosterone therapy is beneficial for women's health and does not cause masculinization or liver damage, and it protects the heart and breasts.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Many patients on new leukemia drugs had mild to moderate skin reactions.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

PRP treatment may promote hair growth and improve hair density in women with AGA, but more research is needed.

Certain gene variations might be linked to severe acne in women but not in men.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Relatives of women with PCOS symptoms are more likely to have similar health issues.

The document concludes that more research is needed to create suitable diagnostic criteria and understand PCOS in Korean women, and genetics may allow for personalized treatment.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Adequate vitamin D might lower, and high hair chromium might increase DNA damage in obese women.

The document is a detailed medical reference on skin and genetic disorders.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

Plant steroid hormones show growth, health, and medicinal benefits in various organisms, including potential for treating diseases.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Mutations in certain receptors can cause diseases and offer new treatment options.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Familial factors affect hair loss types in Koreans, with M type in men, L type in women, and paternal factors influencing male hair loss more.

lncRNAs may regulate hair follicle development in Hu sheep.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

The PP2A-B55α protein is essential for brain and skin development in embryos.

The research identified genes that explain why some sheep have curly wool and others have straight wool.

Key genes linked to hair growth and cancer were identified in hairless mice.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Spironolactone might lower the chance of getting rosacea.