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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.

RACB in barley is crucial for cell polarity and nucleus positioning, aiding fungal infection.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

UT-018 speeds up wound healing and boosts hair growth in mice.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

Retinoic acid causes gland formation instead of hair in mouse skin by altering epidermal and dermal interactions.

Rab5c is crucial for blood stem cell development by regulating Notch and AKT signals.

Basonuclin helps identify and track hair follicle development and cycling in mice.

Removing β-catenin in certain stem cells causes hair whitening and pigmentation issues.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Overexpression of ΔNLef1 in mouse skin leads to hair loss, cysts, and skin tumors.

Notch signaling is crucial for specifying niche cells in Drosophila testis.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Genetically modified rats help reveal how vitamin D affects bone and skin health.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Basonuclin is crucial for hair follicle development and cycling in mice.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

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

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Sostdc1 controls the size and number of hair and mammary gland structures.

Ptprq has multiple forms that change during inner ear development.