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Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

Methotrexate side effects vary by race and sex.

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

The document concludes that more research is needed to create suitable diagnostic criteria and understand PCOS in Korean women, and genetics may allow for personalized treatment.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

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.

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

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.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

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 human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

COVID-19 can cause various skin lesions, which may result from the virus and immune response, and are not directly linked to illness severity.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Fetal cells could improve skin repair with minimal scarring and are a potential ready-to-use solution for tissue engineering.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Macrophage-stimulating protein helps hair grow and can start hair growth phase in mice and human hair samples.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Some drugs can cause skin and hair color changes, often reversible when the drug is stopped.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

Symmetrical Acrokeratoderma (SAK) may be a unique skin condition in China, lacking specific treatment and needing long-term monitoring.

Most hirsutism patients had idiopathic hirsutism or PCOS, with hormonal imbalances and signs like acne and irregular periods.

Reversing female hair loss.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.