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

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

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.

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

BAF200 is essential for proper heart and coronary artery formation.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Women with high androgen levels may have more severe COVID-19 symptoms.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

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

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Loss of Fz6 disrupts hair follicle and associated structures' orientation.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.

A protein called PLC2 is important for the growth and development of plant roots influenced by auxin.

Removing vitamin D and calcium receptors in mice skin cells slows down skin wound healing.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

Activin activation in skin cells speeds up wound healing without affecting scar quality.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Suppressing certain hormones might help prevent prostate cancer.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

High levels of auxin increase root hair growth by activating RSL2 and producing ROS, while high phosphate levels hinder growth by repressing RSL2.

Finasteride use may lead to less alcohol consumption in men with lasting sexual side effects.

Mice that can regenerate tissue have cells that pause in the cell cycle, which is important for healing, similar to axolotls.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Stump-tailed macaque best for researching hair loss causes and treatments.

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

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.