Search

everythinglearnresearchcommunity

for

Search:↓

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Insulin resistance is linked to PCOS and can lead to other health issues, but treatments like metformin can help manage symptoms.

Men are more likely to have severe COVID-19 cases and fatalities than women due to factors like lifestyle, aging, and biological differences.

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

Skin problems in COVID-19 patients are rare and may be due to the body's complex immune response or blood clotting issues.

Advanced human skin models improve drug development and could replace animal testing.

Researchers found 15 new genetic links to skin traits in Japanese women.

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

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

Si Jun Zi Tang may slow aging by affecting specific cell signaling pathways.

Understanding skin structure and development helps diagnose and treat skin disorders.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Vitiligo is linked to autoimmune diseases and hearing issues, so hearing tests are recommended for patients.

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

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.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

CaV1.2 helps activate hair follicle stem cells without calcium flux.

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

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

FGF13 gene changes cause excessive hair growth in a rare condition.

Gut health affects skin diseases, and probiotics might help.

Some women with PCOS have rare genetic variants linked to the condition.

Personalized treatments for hair loss are becoming more effective by using genetic information.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Men and women respond differently to drugs for COVID-19, high cholesterol, and diabetes, which suggests a need for personalized treatments.

Restoring mitochondrial function in mice reversed their skin wrinkling and hair loss.