Search

everythinglearnresearchcommunity

for

Search:↓

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

Certain long non-coding RNAs are important for the growth of hair follicles in Inner Mongolian cashmere goats.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

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.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

Ozone and procaine boost the release of healing factors in platelet-rich plasma.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

The document concludes that pig iPSCs show promise for transplant therapies and the field is advancing in controlling cell behavior for biology and medicine.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

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

Excess androgens may cause PCOS, not just be a symptom.

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

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

A group has developed therapies that show promise for treating cancer and various other conditions.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

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.

Genetic mutations can affect female sexual development, requiring personalized medical care.

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

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

ATP-sensitive K+ channel subunits, particularly Sur2A, play a significant role in various cancers.

EGFR helps control how hair grows and forms without needing p53 protein.