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Early onset hair loss linked to genetics and androgen levels.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Skin problems are common in lupus, important for diagnosis, and can be triggered by sunlight.

β-blockers can cause skin problems like psoriasis and vitiligo, and doctors should tell patients about these risks.

Certain signals are important for reducing specific chemical markers on hair follicle stem cells during rest periods, which is necessary for healthy hair growth.

Psychotropic medications can cause skin reactions, including severe conditions like SJS and TEN, and it's important for psychiatrists to recognize and manage these side effects.

Smad1 and Smad5 are essential for hair follicle development and stem cell sleepiness.

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.

Stress in mice delays hair growth and treatments blocking substance P can partly reverse this effect.

WAA-QOL measures impact of hair loss on women's well-being.

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.

Continuous light exposure in rats leads to PCOS-like symptoms and suggests sleep habits might affect the disorder's development.

BAF200 is essential for proper heart and coronary artery formation.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

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.

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

Oral zinc sulphate reduces dark hair color in mice.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

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

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Meis1 is crucial for skin health and tumor development.

Alopecia areata is an autoimmune hair loss condition treated with corticosteroids, and histologic confirmation is the best diagnosis method.

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

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

Adult stem cells are important for tissue repair and have therapeutic potential, but more research is needed to fully use them.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Some stem cells in the body rarely divide, which could help create better treatments for diseases and aging.

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