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Melatonin can increase cashmere yield by altering gene expression and restarting the growth cycle early.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Cathepsin L is essential for normal hair growth and development.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

Some heart drugs show promise for other conditions, but more research is needed to confirm their effectiveness and safety.

Researchers found 15 new genetic links to skin traits in Japanese women.

Eating healthy, exercising, and taking certain supplements can help manage Polycystic Ovary Syndrome symptoms.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

Explosions don't stop hair proteins from being used to identify people.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Aquaporins could be new drug targets for treating polycystic ovary syndrome.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.