Search

everythinglearnresearchcommunity

for

Search:↓

Endocrine-disrupting chemicals cause irreversible harm to children's development, increasing disease risk.

A group has developed therapies that show promise for treating cancer and various other conditions.

A neurodivergent physiologist reflects on how his unique perspective benefits his research, despite facing challenges with tasks and communication.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

Myhre syndrome symptoms worsen over time, with specific genetic variants affecting severity.

Men in the U.S. have more health issues, higher death rates from various diseases, lower life expectancy, and are less likely to seek healthcare.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

PolyQ repeats in neural proteins evolve together, affecting brain function and disease.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

AI is revolutionizing healthcare by improving diagnosis, treatment, and monitoring, but still needs close supervision.

Different medications can cause serious side effects in some people.

Toxoplasma gondii infection may increase testosterone levels in males.

Children with Parry Romberg Syndrome had successful facial fat-grafting surgeries after disease stabilization with no complications.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

iPSCs help understand and treat neurodevelopmental disorders.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A 3-year-old girl developed scurvy symptoms that improved with vitamin C but relapsed when supplementation stopped.

Finger length ratio may indicate male hair loss.

Trichotillomania is a challenging-to-treat impulse-control disorder where individuals pull out their hair, more common in females, with some treatments showing benefits.

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.

Dental amalgam releases harmful mercury, posing health risks, and should be replaced with safer materials.

A 3.75-year-old girl showed that different body organs can grow at different rates.

Pharmacists play a crucial role in customizing treatments and ensuring medication safety.

Basaloid follicular hamartoma is a rare, benign skin growth often misdiagnosed.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

Dental amalgam releases harmful mercury, posing health risks, and should be replaced with safer materials.

Sodium valproate is effective in treating epilepsy, especially in patients who don't respond to other medications.

Injecting alpha-melanocyte-stimulating hormone in mice improved skin healing and reduced scarring.