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A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

The Ovol2-Zeb1 circuit is crucial for skin healing and hair growth by guiding cell movement and growth.

Finasteride doesn't affect omeprazole metabolism in Japanese people.

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

Obesity is linked to various skin problems and may increase the risk of skin cancer.

No link found between new male baldness genes and female hair loss.

Skin symptoms can indicate endocrine disorders and have various treatments.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

Spironolactone might lower the chance of getting rosacea.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Vitamin C deficiency changes gene expression, affecting skin and hair health.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Wnt signaling is crucial for skin development and hair growth.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

Dermal papillae cells, important for hair growth, come from multiple cell lines and can be formed by skin cells, regardless of their origin or hair cycle phase. These cells rarely divide, but their ability to shape tissue may contribute to their efficiency in inducing hair growth.

Mice without the enzyme HSD17B3 still produce normal testosterone, suggesting they have different ways to make it compared to humans.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

GPR39 is linked to certain cells in the sebaceous gland and helps with skin healing.

Hdac1 and Hdac2 help maintain and protect the cells that control hair growth.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

m-Aminophenol in hair dye can cause skin cell toxicity and stress responses.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.