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Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

SDF-1/CXCL12 and its receptor CXCR4 are crucial for melanocyte movement in mouse hair follicles.

Skin problems are common in Bangladesh due to arsenic, prompt treatment of diabetic foot ulcers is crucial, maternal transmission causes most neonatal herpes, treatments for pediatric vasculitis are effective, the chickenpox vaccine works, more frequent UVB therapy helps psoriasis, certain jobs increase hand dermatitis risk, monoclonal antibodies treat psoriasis well, lifestyle affects psoriasis, alefacept improves psoriasis, imiquimod cream partially clears basal cell carcinoma, and iron may not help chronic hair loss.

The skin and thymus develop similarly to protect and support immunity.

Photobiomodulation therapy using red and near-infrared light can reduce inflammation and aid in healing various conditions.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Hair proteins have weak spots in their α-helical segments.

The study found that specific proteins are markers of hair follicle development in human fetuses.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

Scientists have improved 3D models of human skin for research and medical uses, but still face challenges in perfectly replicating real skin.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

The spiny mouse can regenerate its skin without scarring, which could help us learn how to heal human skin better.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

The document concludes that understanding tissue degeneration is crucial for diagnosing skin lesions.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Minoxidil may help prevent capsular opacification after cataract surgery.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Grape seed oil improved hair quality the most, followed by rosehip and safflower seed oils, and reduced damage from shampoo.

Burn reconstruction improves with new techniques, materials, and tissue engineering.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

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

Curly hair is mechanically different from straight hair and may need new testing methods.

Repeated hair dyeing significantly damages hair.