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Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

The Foxn1 gene is essential for normal nail and hair development.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

UV radiation may cause DNA changes in skin, certain UVB therapy helps psoriasis, a new gene mutation is linked to mild piebaldism, different immune cells affect psoriasis, a drug promotes hair growth, and some cancer drugs could treat skin barrier issues.

Epigenetic changes in blood cells may contribute to alopecia areata.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Targeting IL-15 may help treat Alopecia Areata.

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

Allopregnanolone changes gene expression in glioblastoma cells.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

The N gene affects the protein makeup of mouse hair.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

Vitamin D receptor mutations can cause alopecia by affecting hair growth genes.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.