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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.

DORN1 receptor affects eATP-induced stomatal changes but not eADP in Arabidopsis thaliana.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

Dapagliflozin improved blood sugar control in a man with Werner syndrome without side effects.

The scraggly mutation causes hair loss and skin defects in mice.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

MsPG3 protein gathers at root hair tips, aiding growth.

AGD1's PH domain is essential for its role in root hair growth and polarity.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

Deleting the scd1 gene in mice prevents obesity by disrupting skin lipids and improving heat regulation.

cDermo-1 causes dense skin, feathers, and scales in chickens.

New genes and pathways are important for testosterone production and male sexual development.

In STSD patients, the body compensates for low androgen levels by increasing another enzyme's activity.

RSPO1 could help create new diabetes treatments by increasing pancreatic β cells.

A mutation in the Sgkl gene causes defective hair growth in mice.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

The gene GJA1 is important for regulating coarse hair density in goats.

Androgens and estrogens are crucial for insulin secretion in males.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

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