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Skin problems in COVID-19 patients are rare and may be due to the body's complex immune response or blood clotting issues.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Men with Kennedy disease have less chance of hair loss.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

AGA treatments like minoxidil and LLLLT are safe and effective for gender minority patients.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

Human skin makes sexual hormones that affect hair growth, skin health, and healing; too much can cause acne and hair loss, while treatments can manage these conditions.

Pregnancy can cause various skin changes and diseases, with PUPPP being the most common skin condition specific to pregnancy.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Animals that change color with the seasons mainly do so in response to daylight changes, but climate change is causing camouflage problems that may require evolutionary changes.

Androgens can both stimulate and cause hair loss, and understanding their effects is key to treating hair disorders.

Fatty acid transport protein 4 is essential for skin and hair development.

Animal models have helped understand hair loss from alopecia areata and find new treatments.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

AR polyglycine repeat doesn't cause baldness.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

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

Different species and human skin models vary in their skin enzyme activities, with pig skin and some models closely matching human skin, useful for safety assessments and understanding the skin's protective roles.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

DHT's role in hair loss is important, but measuring its level for diagnosis is questionable.

Cellular senescence has both cancer-blocking and cancer-promoting effects, and targeting senescent cells may improve health and lifespan.

Early onset hair loss linked to genetics and androgen levels.

Two gene areas linked to male pattern baldness found, more research needed.

R-spondins and their receptors help increase bone growth and may be used to treat bone loss diseases.