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Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

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.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Haplogroup X found in Altaian population supports Amerindian origin.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

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

ESR2 gene linked to female-pattern hair loss.

Finasteride doesn't affect omeprazole metabolism in Japanese people.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Removing part of the vitamin D receptor stops vitamin D from working properly.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

Gene therapy with the Math1 gene helped regenerate balance-related cells and improve balance in mice.

Applying a special compound can promote hair growth without harmful side effects.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Abnormal Hedgehog signaling in blood cancers may help tumors grow and resist chemotherapy, suggesting potential for targeted treatments.

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

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Distinct β-catenin patterns are linked to cell growth, not cell death, in lung cancer.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

A male with aromatase deficiency improved bone health with estradiol treatment.

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

Signaling pathways are crucial for hair growth in goats.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

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

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.