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pCLCA2 protein may help maintain skin structure and function.

Some diseases can improve the outcomes of other diseases, leading to new treatment possibilities.

The 2024 guideline updates recommendations for genetic testing, imaging, and sperm retrieval in male infertility.

LEF1 is essential for the development of airway glands and is regulated by the Wnt/ß-catenin pathway.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Osthole inhibits the TRPV3 channel by binding to specific sites, potentially aiding drug development for skin diseases and cancers.

More high-quality research is needed to recommend flavonoids and saponins for clinical use.

A 70-year-old woman with bronchiectasis developed a rare immune disease due to a bacterial infection, requiring a difficult balance of treatments.

Lung and liver macrophages protect our tissues and their dysfunction can cause various diseases.

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

Potassium channel openers are effective in treating heart conditions, high blood pressure, pulmonary diseases, bladder issues, and hair loss, but more selective drugs are needed.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Neurosteroids can influence behavior by modulating brain inhibition, with potential for treating psychiatric disorders.

Cantú syndrome is caused by mutations in the ABCC9 gene.

CDP is crucial for lung and hair follicle cell development.

Neurosteroids change how GABA_A receptors work in the brain, which could be important for treating temporal lobe epilepsy.

Elevated CO2 can lessen the negative impact of water shortage on soybean roots and affects specific genes.

Neuroactive steroids show promise for treating mental and neurological disorders by targeting GABA_A receptors.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Nanocarrier technology in cosmetics improves ingredient delivery and effectiveness while reducing side effects.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Gene therapy shows promise for treating skin disorders and cancer, but faces technical challenges.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

Blocking the Wnt pathway could lead to new treatments for cancer and tissue repair but requires careful development to avoid side effects.

Activin helps skin growth and healing mainly through stromal cells and affects keratinocytes based on its amount.

Spironolactone might help protect against severe lung problems in COVID-19 patients.

Existing drug dexamethasone may lower death risk in severe COVID-19 cases; more research needed for other drugs.