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Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

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

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

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

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

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

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

A specific gene mutation causes long hair in Angora rabbits.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Activating Nrf2 can help protect against hearing loss.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Disrupting Stat3 in hair follicle stem cells greatly reduces skin tumor formation.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.