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The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

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.

Anti-IL-12/IL-23 antibody therapy effectively treats psoriasiform skin lesions in IBD patients.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

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.

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.

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.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Early development of hair, teeth, and glands involves specific signaling pathways and cellular interactions.

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

Male pattern baldness involves hormones and cell signals affecting hair growth.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Men, especially older ones with health issues like prostate cancer, may have worse COVID-19 outcomes and could benefit from therapies targeting male hormones.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Animal models have helped understand hair loss from alopecia areata and find new treatments.

Blocking the virus's entry into cells by targeting certain pathways could lead to early COVID-19 treatments.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Hair can regrow after certain stem cells are lost because other stem cells can take over their role.

The drug enzalutamide may reduce the ability of the virus causing COVID-19 to enter lung cells.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

New genes found linked to balding, may help develop future treatments.

MicroRNAs play a crucial role in skin and hair health, affecting everything from growth to aging, and could potentially be used in treating skin diseases.

Dutasteride makes alcohol less sedating and may lead to less drinking in men.