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The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A woman's severe hirsutism was caused by Leydig cell tumors in her ovaries, which improved after surgery.

Nutrease powder, a high-protein, low-carb supplement, can help manage Polycystic Ovary Syndrome symptoms, regulate periods, improve ovulation, and restore fertility.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

Specialized ribosomes affect aging in human skin cells.

Mouse skin glands need healthy nerves to grow properly during hair growth phases.

Hair follicles repair 3D injuries using a 2D healing process.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Using old drugs for new uses can help treat rare immune deficiencies.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

The review explains how hair products work and the science of different hair types to help improve hair care research.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

Pregnant women with Systemic Lupus Erythematosus have a higher risk of blood clotting problems.

Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Cow milk sugars increase fat production and inflammation in skin oil cells.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Scientists created a tiny, 3D model of a hair follicle that grows and acts like a real one.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.