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Patients with RASopathies are at risk for autoimmune disorders and should be routinely screened.

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

Biomimetic scaffolds are better than traditional methods for growing cells and could help regenerate various tissues.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Certain vitamins in wrong amounts, alcohol abuse, metals, and other toxins can cause serious brain and nerve damage.

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

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Facial plastic surgery has evolved to focus on less invasive techniques and innovative technologies for cosmetic and reconstructive procedures.

Retinoids are effective for skin conditions like severe acne and psoriasis but must be used with caution due to potential side effects and risks during pregnancy.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Oral retinoids can cause side effects ranging from mild to severe, including birth defects, and require careful monitoring and contraception.

Medical tattooing improves appearance and quality of life, but has potential risks.

Hair follicle transplantation can hide scars but often needs more than one surgery for better results.

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

Children with Parry Romberg Syndrome had successful facial fat-grafting surgeries after disease stabilization with no complications.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

The conclusion is that acne, alopecia, and hyperhidrosis are common skin issues with various treatments available, and accurate diagnosis is key for effective management.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Skin needs dermal β-catenin activity for hair growth and skin cell multiplication.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

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

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

ΔNp63α helps control a protein that stops cancer cells from spreading.

Researchers identified specific genes that are important for mouse skin cell development and healing.

New treatments targeting the Hedgehog pathway can help treat advanced skin cancer but may have side effects and their effectiveness in early stages is unknown.

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.