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Most people in Turkey start getting gray hair around 33 years old, with factors like age, education, hair loss, skin type, family history, and anxiety playing a role.

Most people using minoxidil for hair loss probably won't see significant improvement.

Early-onset hair loss in young males is linked to a higher risk of metabolic syndrome.

PRP therapy is more effective than minoxidil for treating hair loss from androgenetic alopecia.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Men generally have more severe COVID-19 cases and higher death rates than women due to biological differences.

Androgens may influence T cells, contributing to higher autoimmune liver disease risk in women.

Stem cell research and regenerative medicine have made significant advancements in treating various diseases and conditions.

Multimodal recruitment effectively gathered a diverse group for an online survey on ovulation and menstruation health.

The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Humans lost body hair relatively recently in evolution.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.

Genetic differences may affect COVID-19 deaths; anti-androgens could be potential treatment.

Msx2 and Foxn1 are both crucial for hair growth and health.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

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

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

The document concludes that the androgen receptor's structure and function are complex, affecting how it regulates genes and is involved in diseases like prostate cancer.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.