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Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Female pattern hair loss involves hormonal factors, genetics, and may be linked to low ferritin levels.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Genetics affect early female hair loss, severity depends on duration, and low ferritin levels not significant.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Scalp basal cell carcinoma may be more aggressive and harder to treat than other types, requiring special attention and further research.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Some women with PCOS have rare genetic variants linked to the condition.

Neuroactive steroids may affect the risk and treatment of alcohol use disorders.

Genetic factors could lead to personalized treatments for hair loss.

Alopecia Areata affects people of all ages worldwide, is likely caused by genetic and environmental factors, and can lead to stress and depression, highlighting the need for treatments that address both physical and mental health.

The study suggests that hypothyroidism may cause alopecia areata.

The guidelines suggest using various treatments, including antidepressants and steroids, for alopecia areata and discuss the condition's genetic and immune aspects.

Immune cells are essential for early hair and skin development and healing.

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

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Researchers developed reliable models to predict how well certain compounds bind to androgen receptors, emphasizing the importance of atomic electronegativity.

PCOS may have evolved as an advantage in past environments with food scarcity.

Early signs of PCOS in girls, like irregular periods and polycystic ovaries, suggest a need for early diagnosis and intervention to prevent further health issues.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.