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

There's no significant genetic link between male pattern baldness and COVID-19.

Autoimmune skin disorders are caused by genetic and environmental factors and are treated with various medications and preventative strategies.

Environmental factors like smoking, UV exposure, and poor diet contribute to hair loss and graying, and lifestyle changes can help manage it.

The study suggests that hypothyroidism may cause alopecia areata.

The document concludes that a new biosensor can efficiently detect prostate cancer cells and that standardized referrals help find significant cancers effectively.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

The document concludes that more research is needed to fully understand the causes of PCOS.

Hidradenitis Suppurativa is likely an autoinflammatory disease, and better understanding its causes could improve treatments.

Jieduquyuziyin prescription helps treat SLE with atherosclerosis by improving cholesterol removal and reducing inflammation.

The article suggests using four questions to tell apart necessary medicalization from excessive medicalization, focusing on problem significance, social expectations, medical understanding, and effective resolution.

Gray hair is caused by reduced melanin production or transfer issues, linked to aging and possibly health conditions, with treatments focusing on color camouflage.

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.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Metabolic syndrome linked to urinary symptoms; hair loss not significant.

Patients with RASopathies have a higher risk of autoimmune disorders and should be routinely screened.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

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

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Physical activity, height, and smoking affect prostate cancer risk.

After chemotherapy for a gestational trophoblastic tumor, normal pregnancy rates are possible, but there's a slightly higher risk of the tumor reoccurring in future pregnancies.

Gene variation affects prostate issues and hair loss.

Women with PCOS face higher risks of diabetes and heart disease, and these risks increase with obesity.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.