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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

Some men's prostate tissues have low enzyme levels due to genetic changes, possibly affecting treatment for prostate enlargement.

Gene variation affects prostate issues and hair loss.

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

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

No link found between specific genes and female pattern hair loss.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

PLA2R1 overexpression harms kidney cells by stopping their growth cycle.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

New genes linked to male pattern baldness were found on chromosome 20p11.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

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

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

ESR2 gene linked to female-pattern hair loss.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.