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A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

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.

Men generally have more severe COVID-19 cases and higher death rates than women due to biological differences.

Three genes linked to the development of trichilemmal cysts were found.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

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

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

The skin and thymus develop similarly to protect and support immunity.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Tumor suppressors help control inflammation in cancer and restoring their function could lead to new treatments.

MicroRNAs play a crucial role in skin and hair health, affecting everything from growth to aging, and could potentially be used in treating skin diseases.

Genetic marker rs12558842 strongly linked to male hair loss.

The research suggests that the ZP4 gene is linked to egg development in women with PCOS but requires more study to understand its role in infertility.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Women with hair loss have more androgen receptors in certain hair follicles.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Hedgehog signaling in certain cells is crucial for hair growth during wound healing.