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The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

DNA methylation changes in women with PCOS could be used as disease markers and suggest new treatment targets.

Using protein degradation to fight cancer drug resistance shows promise but needs more precise targeting and fewer side effects.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

New understanding and treatments for hair loss are improving, but more research is needed.

Certain transporters are found in human hair follicles and may affect hair growth and loss.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Activating NRF2 might help treat hair disorders by improving antioxidant defenses.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Green tea component EGCG may help prevent hair loss by changing microRNA levels in certain scalp cells.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Researchers identified genes and proteins that may influence wool thickness in sheep.

Pig skin cells can turn into mesodermal cells but lose their ability to become neural cells.

Specific genes influence hair and cashmere growth in Laiwu black goats.

Sex steroids affect the MafB gene differently in male and female hamsters.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

EF and PXE not closely related.

Skin changes in Pseudoxanthoma elasticum patients can indicate the severity of related health issues.

Women treated with X-ray for scalp fungus as children had a higher chance of hair loss, especially with higher radiation doses and severe fungus infections.

EVG staining is a valuable, simple, and cost-effective method for diagnosing various skin conditions in dermatopathology.

Mice with autoimmune hair loss showed signs of heart problems.

Many research paper titles in dermatology journals lack scientific precision.

Early onset female hair loss is linked to lower hair density, scalp issues, and certain genetic factors.

Studying rare genetic disorders can help us understand and treat common diseases better.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

The document concludes that side effects from Smoothened inhibitor drugs for skin cancer are reversible and can be managed with a team approach to maintain quality of life.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

KATP channels are important for energy balance and are targeted by drugs for diabetes, hypoglycemia, hypertension, and hair loss.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.