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New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

Dermoscopy improves diagnosis and treatment monitoring for children's skin infections, inflammations, and hair disorders.

The conclusion is that exogen is a unique hair cycle phase and the new sampling method specifically targets this stage, which may help in future hair loss research.

Smad4 is important for healthy hair follicles because it helps produce a protein needed for hair to stick together and grow.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

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

Different skin diseases show unique patterns of skin cell separation, cell death, and granular layer changes.

The X5 Hairlaser might help treat male hair loss, but more research is needed.

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Terbinafine is more effective than itraconazole for toenail fungus, especially in older patients, and debridement improves its effectiveness.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

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

HOXC13 is essential for hair and nail development by regulating Foxn1.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Bone marrow stem cells and their medium help hair regrowth.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.