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DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

Prolactin levels and gene polymorphism are not linked to vitiligo severity but are related to BMI.

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.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

The Rotterdam Study investigates diseases in older adults and has produced many research findings.

Melatonin affects many body functions beyond sleep by interacting with specific receptors in various tissues.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

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.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

The Rotterdam Study aims to understand various diseases in older adults.

The document concludes that the 5 alpha-reductase enzymes are important in steroid metabolism and related to various human diseases, with inhibitors used to treat conditions like male pattern baldness and prostate issues.

Tight junctions are key for skin protection and controlling what gets absorbed or passes through the skin.

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.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

Antibiotics can reduce acne but may lead to resistant bacteria, and understanding the skin's bacteria is important for treatment.

A new gene, JMJD1C, may affect testosterone levels in men.

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

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

Scientists found a gene in mice that causes early hearing loss.

Lymphocytes, especially CD8+ T cells, play a key role in causing alopecia areata, and targeting them may lead to new treatments.

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

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

Current treatments for male pattern baldness include minoxidil and finasteride, with new options being developed.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Genetic marker rs12558842 strongly linked to male hair loss.

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

Hair loss risk is influenced by multiple genes.

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.