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Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

The EDAR gene greatly affects hair thickness in Asian populations.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

No link found between specific genes and female pattern hair loss.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

Scientists found a gene in mice that causes early hearing loss.

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

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

Personalized treatments for hair loss are becoming more effective by using genetic information.

Hair loss in men treated best with early medication or transplant, new treatments researched.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

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

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.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Selective breeding can enhance immunity in dairy cattle.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

The document concludes that alopecia areata is an autoimmune disease without a definitive cure, but treatments like corticosteroids are commonly used.

Male pattern hair loss caused by follicular miniaturization; early diagnosis and treatment can reduce psychological burden.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

ESR2 gene variations may be linked to female pattern hair loss.

Hair loss risk is influenced by multiple genes.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Gene linked to common hair loss found, may lead to new treatments.