Search

everythinglearnresearchcommunity

for

Search:↓

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.

Acne is caused by multiple factors including oil production, bacteria, inflammation, and possibly diet and environment.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Early signs of PCOS in girls, like irregular periods and polycystic ovaries, suggest a need for early diagnosis and intervention to prevent further health issues.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Hair loss in men is mainly caused by hormones and genes, and while current treatments can slow it down, they can't fully stop it.

Alopecia Areata is an autoimmune condition causing hair loss, influenced by genetics, environment, and possibly improved by anti-MIF therapy, with many patients experiencing regrowth within a year.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Female pattern hair loss involves hormonal factors, genetics, and may be linked to low ferritin levels.

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

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

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

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Men's hair loss is caused by hormones and genes, and can be treated with medication and surgery, while graying is due to aging and has no prevention except dyeing.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

Understanding where cancer cells come from helps create better prevention and treatment methods.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

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.

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

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.