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The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Chicken feather gene mutation helps understand human hair disorders.

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

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

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

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Mutant mice help researchers understand hair growth and related genetic factors.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

Alopecia areata causes hair loss due to an immune attack on hair follicles, influenced by genetics and environment.

Fetal scalp cells have more regenerative genes than adult cells, and decellularized muscle matrix is better for muscle repair than commercial alternatives.

Insulin resistance is a key factor in polycystic ovary syndrome, but genetics may also contribute.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Researchers created a model to understand heart aging, highlighting the role of microRNAs and identifying key genes and pathways involved.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

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

The document concludes that new treatments for hair loss may involve a combination of cosmetics, clinical methods, and genetic approaches.

Some skin conditions may increase the risk of heart disease, but are not yet included in cardiovascular prevention guidelines.

Long-term finasteride treatment reduces depression and brain issues in obese male rats.

Male hormones affect COVID-19 severity and certain drugs targeting these hormones could help reduce the risk.

Zinc supplementation may help improve treatment outcomes for chronic hepatitis C.

Immunomodulatory therapies are effective for treating cutaneous lymphoma, particularly in early stages.

Alopecia areata involves immune activation in the scalp, suggesting treatments targeting TH1, TH2, and IL-23 pathways.