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Inositol and arginine solutions improve hair follicle health and turnover.

Non-immune factors play a significant role in alopecia areata.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Nanomaterials can significantly improve wound healing and future treatments may include smart, real-time monitoring.

Radiotherapy effectively treated a large scalp tumor in an elderly woman, avoiding surgery.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

Human hair keratins can be turned into useful 3D biomedical scaffolds through a freeze-thaw process.

Good feather growth in poultry needs the right balance of proteins, amino acids, minerals, and vitamins.

Nanomaterials can improve hair care products and treatments, including hair loss and alopecia, by enhancing stability and safety, and allowing controlled release of compounds, but their safety in cosmetics needs more understanding.

Feather growth and regeneration involve complex patterns, stem cells, and evolutionary insights.

Ornithine decarboxylase is crucial for hair growth and follicle development.

Hair analysis is better than urine and blood for detecting past drug use.

WS Biotin, a new form of D-Biotin, improves water solubility and shows potential for hair and skin care without being toxic at low levels.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Lung repair involves both dedicated and flexible stem cells, important for developing new treatments.

Melanin density affects hair color, and this method can help in cosmetic assessments and diagnosing hair diseases.

CD2 might be a new treatment target for patchy alopecia areata.

Eucalyptus and Tween 80 most effectively increase cetirizine skin absorption.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

A specific type of skin cell creates an opening for hair to grow out, and problems with this process can lead to skin conditions.

The document concludes that more research is needed to understand airway repair and to improve tissue engineering for lung treatments.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

Type 2 diabetes slows down skin and hair renewal by blocking important stem cell activation in mice.

The research found specific genes and pathways that control fur development and color in young American minks.

Low-molecular weight hyaluronate can make damaged hair stronger.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

Iris germanica rhizome-derived exosomes help protect skin cells from oxidative stress and aging.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.