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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

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

The document concludes that treatment for excessive hair growth depends on the cause, with options including hair removal methods and medications like anti-androgens or insulin-sensitizing drugs.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Golden oyster mushroom extract may protect skin cells from aging by its antioxidant properties.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Dietary essential fatty acids improved skin and hair conditions and partially corrected fat composition in diabetic mice.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Modified stem cells that overexpress a specific protein can improve hair growth and reduce hair abnormalities in mice.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Finasteride doesn't affect omeprazole metabolism in Japanese people.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.