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Hair loss was found in 37.4% of surveyed rural high-school students in Eskisehir, Turkey, affecting their quality of life, especially in general health and mental well-being.

miRNA-based therapies show promise for treating skin diseases, including hair loss, in animals.

Chemicals and body size might change when puberty starts and progresses, but more research is needed to confirm this.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Androgens are important for normal ovarian function and estrogen production, but may not be the main cause of follicle death.

Use specific tools to measure quality of life in alopecia areata patients and improve future treatments.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Engineered skin substitutes can grow hair but have limitations like missing sebaceous glands and hair not breaking through the skin naturally.

Certain drugs that block specific enzymes can help treat prostate diseases.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Oral and maxillofacial surgery has advanced with fluoride reducing tooth decay and high-speed handpieces aiding in more aesthetic procedures, leading to changes in practice and training.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Children's skin diseases and treatments differ from adults and require specific approaches.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

5α-reductase is essential for male sexual development and its inhibitors have potential in treating various conditions related to hormone action.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.

Tofacitinib may help regrow hair in severe alopecia areata, but results differ greatly between people.

Checking family social conditions in tourniquet syndrome cases can help find neglect.

Scientists have developed a new method to detect steroid abuse in athletes using cell-based tests, which could be the future of anti-doping methods.

The document explains different types of hair loss, their causes, and treatments, and suggests future research areas.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Genetics and nutritional deficiencies are key factors in premature graying of hair.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

The conclusion is that tissue structure is key for stem cell communication and maintaining healthy tissues.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

The document concludes that a complete skin restoration biomaterial does not yet exist, and more clinical trials are needed to ensure these therapies are safe and effective.

Exosomes may improve skin, scars, hair growth, and fat grafts in plastic surgery, but more research is needed.

Women with PCOS face higher risks of diabetes and heart disease, and these risks increase with obesity.