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New genetic locations explain much of hair color variation in Europeans.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

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

Hair loss gene found on chromosome 3q26.

New genes linked to male pattern baldness were found on chromosome 20p11.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

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

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

No clear link between androgen receptor variation and hair loss, but more research needed.

Early hair loss common in Chinese males, linked to family history and smoking; early treatment advised.

Higher sebum levels are linked to more severe male baldness.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

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

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Hormones and genes affect hair growth and male baldness.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

The study suggests smoking is common in HS patients but its role is unclear, and more research is needed to understand HS causes.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Dogs with dermatomyositis, especially Collies and Shetland Sheepdogs, need better treatments for their skin and muscle inflammation.