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The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

A man developed male breast cancer after four years of finasteride treatment for an enlarged prostate.

Radiation therapy with chemotherapy can cause severe, long-lasting hair loss.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Catalase in processed meats may increase cancer risk due to electromagnetic emissions.

Brepocitinib improves cicatricial alopecia and reduces key immune markers.

Mutant stem cells adapt their metabolism differently to outcompete normal cells in the skin.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

Men with baldness at the front and top of their head at age 45 may have a higher risk of aggressive prostate cancer.

Overexpressing GLI-1 in mice skin can cause tumors like human basal cell carcinomas.

A new method, iSiMPRe, effectively identifies key protein regions in cancer genes, highlighting potential drug targets.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

Lifestyle factors like BMI at young adulthood can increase cancer risk in women with Lynch Syndrome, but diet and height don't seem to affect this risk.

CCCA affects adolescents too, with genetic and environmental links, requiring careful diagnosis.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

RXRα is crucial for hair growth and skin cell function.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

CDK4/6 inhibitors may cause hair loss in breast cancer patients.

DNA analysis can help tailor alopecia treatment.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Androgens increase cervical cancer risk and affect its development.

Some breast cancer treatments cause hair loss similar to male pattern baldness, which can be improved with minoxidil.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.