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Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

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

HLA-DRB5 and other genes may be linked to alopecia universalis.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

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

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Alopecia areata involves complex immune and genetic factors, with potential treatment targets identified, but more research is needed.

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

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

A gene mutation causes woolly hair in a Syrian patient.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

Mutations in specific llama genes may affect fiber quality for textiles.

A specific genetic deletion in goats affects cashmere yield and thickness.

The document explains the genetic causes and characteristics of inherited hair disorders.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

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

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.

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

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

No significant link between male pattern baldness and COVID-19 severity was found.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.