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Activating the Nrf2 pathway reduces inflammation and cell activation in human hair follicles, suggesting a potential treatment for certain hair loss conditions.

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

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Far-infrared radiation improves stem cell growth and movement, helping heart therapy.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Understanding snoRNA regulation may help slow skin aging.

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

ROR2 is crucial for hair follicle stem cell maintenance and self-renewal.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

Localized ROS production is essential for cell growth and movement in plants and animals.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

FGF signaling is a promising target for developing treatments for wounds, metabolic diseases, and cancer.

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

Disabling the FGF5 gene in sheep leads to longer wool.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

Blocking certain immune signals can reduce skin damage from radiation therapy.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Sheep cells were successfully modified to include a spider silk protein gene.

The study created special nanoparticles that effectively deliver an anti-inflammatory drug to treat skin inflammation in psoriasis.

Removing SIX1 in fat cells reduces skin fibrosis.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.