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The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

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

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

The article concludes that understanding the molecular processes in hair follicle development can improve the quality of fibers like Angora and cashmere.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Certain genetic variations are linked to hair loss in Mexican men.

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Hair color production is closely linked to the active growth phase of hair in mice and may also influence hair growth itself.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

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

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.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

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

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

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.