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The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

Fgfr2b helps maintain healthy skin and prevent cancer.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

New gene variants were found for rare skin and hair disorders, improving understanding and treatment.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Systemic sclerosis skin shows varied gene patterns, suggesting potential for personalized treatment.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

EREG therapy may help treat hair loss by promoting hair growth.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

A girl had rickets due to a gene mutation affecting vitamin D response.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

A mutation in the KRTHB5 gene causes hair and nail issues.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

A unique gene mutation was found in a family with monilethrix.

FERONIA and LRX proteins help control cell growth in plants by regulating vacuole expansion.

Id2 gene helps keep hair follicle stem cells inactive.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.