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Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Increased FGFR2b signaling, influenced by androgens, plays a role in causing acne.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

Significant progress was made in understanding PXE, but effective treatments are still needed.

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

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Genetic marker rs12558842 strongly linked to male hair loss.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

New models predict male pattern baldness better than old ones but still need improvement.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Light affects skin health, aging, and cancer risk, and new light-based treatments and imaging are promising for skin care.

Monitor for early signs of azathioprine toxicity and check blood counts regularly.

Genetic factors could lead to personalized treatments for hair loss.

Topical finasteride might be a good alternative for hair loss treatment with fewer side effects, but more research is needed.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

The document discussed hair loss causes and treatments but didn't give a final summary.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Developing microRNA-based treatments is hard but has potential.

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

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

Mutations in specific llama genes may affect fiber quality for textiles.

Certain fats in the blood are linked to an increased risk of male pattern baldness.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

Sox6 is important in heart and kidney health, affecting diseases like diabetes, heart disease, and high blood pressure.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

Hair follicle stem cells from Arbas Cashmere goats can become fat, nerve, and liver cells.