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Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

The document concluded that more research is needed to understand how estrogen affects the enzyme involved in hirsutism development.

People still turn to witchcraft for help with modern problems despite technological advances.

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.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Recent progress has been made in understanding inherited hair and nail disorders.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

Early onset hair loss linked to genetics and androgen levels.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.