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Using quantitative traits in genetics can improve understanding and management of skin health and conditions.

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

Alopecia areata and vitiligo share immune system dysfunction but differ in specific immune responses and affected areas.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

Identified genes linked to male-pattern baldness may help develop new treatments.

New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

The conclusion is that obesity should be managed with a slow, balanced approach to diet and exercise, with medication and surgery as additional options, and education and access to care are important.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

Key genes and pathways improve wool quality in Zhexi Angora rabbits.

Men are more likely to have severe respiratory viral infections like COVID-19 due to hormonal and genetic differences, while women generally have stronger immune responses.

The document concludes that skin biopsies, genetic and environmental factors, and specific treatments are important in managing cutaneous lupus erythematosus.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Different species use the same genes for tooth regeneration.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

The skin systems of jawed vertebrates evolved diverse appendages like hair and scales from a common structure over 420 million years ago.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

Low-dose oral minoxidil improved hair growth in a woman with short anagen syndrome.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Key proteins and pathways regulate wool fiber diameter in Alpine Merino sheep.

The conference concluded with plans for joint research into children's skin conditions and emphasized the importance of collaboration and patient-focused research.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Low iron levels may be linked to some types of hair loss in women.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Polycystic Ovary Syndrome is linked to higher risk of hypertension and heart disease.

Despite progress in treatment, the exact cause of Alopecia areata is still unknown.