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A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Scientists created a functional 3D skin system from stem cells that can be transplanted into wounds.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Deleting the scd1 gene in mice prevents obesity by disrupting skin lipids and improving heat regulation.

Sca-1+ cells in newborn mouse skin may become fat cells.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Breathing in high levels of certain air pollutants significantly increases women's risk of developing Polycystic Ovary Syndrome.

Orf infections can happen during the Muslim event 'Aid el Kebir' due to close contact with sheep.

Oral contraceptives with CPA improve overall quality of life for women with PCOS.

S-1 treatment led to a complete response in pancreatic cancer with manageable side effects.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Women with PCOS have higher xanthine oxidase activity linked to inflammation and heart disease risks.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Satoyoshi syndrome can occur without causing premature ovarian failure.

ETS2 is crucial in squamous cell carcinoma development and could be a therapeutic target.

Vitamin D supplements should be used cautiously in sarcoidosis patients, with regular monitoring to avoid high calcium levels.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

The Siah1 and Siah2 genes are active in mouse skin development and hair growth, especially right after birth.

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

The BHBS is a valid tool to study cultural norms and breast cancer risk in Black women.

Argentine-cross polo ponies commonly develop sarcoid tumors with distinct types and histopathological features.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Super-enhancers controlled by pioneer factors like SOX9 are crucial for stem cell adaptability and identity.

Early genetic testing and new therapies like secukinumab are crucial for managing Netherton syndrome effectively.

ZSYY001 is safe, well-tolerated, and shows promise for treating advanced solid tumors.