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The conclusion is that better understanding and more research are needed to effectively manage follicular and scarring disorders in skin of color, with an emphasis on patient education and cultural awareness.

Gene network oscillations inside hair stem cells are key for hair growth regulation and could help treat hair loss.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

Chicken feather gene mutation helps understand human hair disorders.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Polycystic Ovary Syndrome (PCOS) affects 6%-15% of women of reproductive age, causing symptoms like acne and hair loss, and increasing the risk of type 2 diabetes and heart disease; it's managed through diet, exercise, and medications like Metformin and hormonal contraceptives.

Certain immune cells are linked to non-scarring hair loss, suggesting potential for immune-targeted treatments.

Many women with hair loss also have thyroid issues, high blood pressure, and low Vitamin D.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

The study suggests that analyzing DNA can help treat hair loss, but more research is needed.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

Reactive oxygen species (ROS) help control plant growth and development.

The study created 3D-printed pills that effectively release a hair loss treatment drug over 24 hours.

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

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.

Minoxidil can reduce functions related to androgen receptors.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

Combined arsenic and low oxygen stress alters root growth to help plants absorb nutrients.

DNA methylation changes in women with PCOS could be used as disease markers and suggest new treatment targets.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

Hair follicle stem cells change states with age, affecting hair growth and aging.

Tadalafil and Finasteride may help treat aggressive melanoma.