Search

everythinglearnresearchcommunity

for

Search:↓

Nanoparticles improve drug delivery through the skin but more research is needed on their long-term effects and skin penetration challenges.

Hairlessness in mammals is caused by combined changes in genes and regulatory regions.

Compartmentalized organization might be crucial for stem cells to effectively respond to growth or injury.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

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

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

New treatments for vitiligo may focus on protecting melanocyte stem cells from stress and targeting specific pathways involved in the condition.

A new botanical treatment improved hair growth and symptoms in lichen planopilaris patients.

Diet changes can protect against harmful environmental effects on fetal development.

Humans lost body hair relatively recently in evolution.

The conclusion is that Treg-targeted therapies have potential, but more knowledge of Treg biology is needed for effective treatments, including for cancer.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Combining lifestyle changes and medication is most effective for managing PCOS symptoms.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

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

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Current treatments for male pattern baldness include minoxidil and finasteride, with new options being developed.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Leontopodium alpinum extract may help reduce hair shedding by keeping hair in the growth phase longer.

Differences in growth factors in platelet-rich plasma therapy for hair loss can vary between patients and can be influenced by the devices used, possibly leading to inconsistent results.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.