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Arumanis mango rind extract and its fractions can kill breast cancer cells, especially the ethanol extract and ethyl acetate fraction.

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

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

Certain gene variations increase the risk of alopecia areata in Koreans.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

Mirvetuximab soravtansine improves quality of life and reduces symptoms more than standard chemotherapy in ovarian cancer patients.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

Two new gene mutations cause a rare hair disorder.

Certain genetic markers may increase or decrease prostate cancer risk.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

CAG repeat numbers in the AR gene likely don't affect male pattern baldness in Korean men.

Increased TEMRA cells can predict treatment outcomes in rapidly progressive alopecia areata.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Ritlecitinib may be more effective for severe alopecia areata than conventional treatments.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

A mutation in the IL2RA gene increases the risk of alopecia areata.

Vitamin D receptor FokI gene variation is not linked to alopecia areata.

CAR is a useful marker for assessing alopecia areata severity.

Certain changes to the B-ring of androgen receptor ligands can increase their effectiveness for potential treatments of muscle and bone conditions.

High CRP levels could indicate vitamin D deficiency in people with alopecia areata.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.