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Surgery on a baby with a skin disorder improved eyelid position and eye health.

A 73-year-old man's grey-white hair turned dark brown after eczema treatment.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

Men are more likely to have severe COVID-19 cases and fatalities than women due to factors like lifestyle, aging, and biological differences.

Transplant success has improved with better immunosuppressive drugs and donor matching.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Air pollution (PM10) increases skin inflammation and aging by reducing collagen and may trigger a repair response in skin cells.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Reduced AR gene methylation may cause early pubic hair growth in girls.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

DHT affects hair follicle cells by changing microRNA levels, leading to less cell growth and more cell death.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

A young man with an eating disorder had a life-threatening adrenal crisis due to an autoimmune condition, highlighting the need for better education on managing hormone treatments.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

The lotion and shampoo effectively treated scalp seborrheic dermatitis.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Androgen receptors in the mouse brain may explain cognitive and mood changes in prostate cancer treatment.

The gene Prss53 affects hair shape and bone development in rabbits.

Genetic mutations can affect female sexual development, requiring personalized medical care.

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

Men with early hair loss may have a higher risk of enlarged prostate and possibly prostate cancer due to shared hormonal factors.

New skin treatments in 1987-1988 showed effectiveness for various conditions, but some had side effects or risks.

Finasteride may effectively treat hair loss in Klinefelter Syndrome patients.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.