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Men with early balding should be checked for metabolic syndrome, as there's a link between the two.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

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

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

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.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Using special RNA to target a mutant gene fixed hair problems in mice.

The authors maintain that shorter androgen receptor alleles may lead to milder COVID-19 by positively affecting the immune response, not due to changes in testosterone levels or activity.

Certain gene variations increase the risk of alopecia areata in Koreans.

Gene variant linked to prostate cancer, hormone levels, and hair loss.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Men with Kennedy disease have less chance of hair loss.

Estrogen and androgenic hair increase melanoma risk, especially in European-ancestry individuals.

Neuroactive steroids may affect the risk and treatment of alcohol use disorders.

Some African American women's central scalp hair loss is linked to genetics and past fungal scalp infections, with more research needed on other causes.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

Certain hairstyles, diabetes, scalp infections, and vitamin D deficiency may increase the risk of hair loss in Black women; more research is needed for better treatment.

Alopecia areata patients have varied cancer risks, with some cancers being lower and others higher.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

People with common hair loss conditions may have a higher risk of heart disease and related health issues.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.