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Polycomb Repressive Complex 2 is not needed for hair regeneration.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

A new gene variant causes glucocorticoid resistance in a mother and son.

Studying rare genetic disorders can help us understand and treat common diseases better.

Genes affect cytokine production, which can influence chronic diseases, and certain interventions may help prevent related molecular damage.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.

Normal levels of DHT can reduce belly fat and increase muscle, but too much can lead to hair loss, prostate issues, and possibly heart disease.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

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

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

The new microrhizotron tool effectively observes and measures pepper plant roots non-destructively.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Certain gene variations are not a major cause of male infertility in Nigerian men.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Lactate production is important for activating hair growth stem cells.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

Early-onset baldness is linked to genetics, lifestyle, and can indicate higher risk for heart and metabolic diseases, and affects mental health.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.