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The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

Using minoxidil for hair growth may cause skin lesions in some people, and taking breaks from nitrate patches for angina might worsen symptoms.

The document concludes that MGRN1 affects mouse fur color by interfering with a receptor's signaling, but its full role in the body is still unknown.

Alopecia areata is an autoimmune disease causing hair loss, treatable with immune-modulating drugs, and linked to genetics.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

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

Azathioprine can cause severe blood issues and hair loss, needing careful monitoring and possible discontinuation.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

Genetic factors and diet significantly increase the risk of male pattern baldness.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

RXRα is crucial for proper immune response and links diet to immune function.

Different fish use the same genes to regrow teeth.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

A specific gene mutation causes congenital hair loss.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

Finasteride dosages should be adjusted based on CYP3A5 genotype and liver function to avoid side effects.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Genetic discoveries are leading to new treatments for alopecia areata.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

The genetic variant studied does not affect PCOS symptoms in Kashmiri women.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.