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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.

Lethal-milk mice produce zinc-deficient milk, causing health issues in pups unless supplemented with zinc.

The mouse model helps study and develop treatments for radiation-induced saliva reduction.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Skin grafts on mice can cause an immune response leading to hair loss, useful for studying human hair loss conditions.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.

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

The ACTH/MC2R system is crucial for controlling hair growth cycles in mice.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Gender-affirming hormone therapy affects metabolism differently based on treatment type.

Mice with human skin protein K8 had more skin problems and cancer.

Restoring mitochondrial function in mice reversed their skin wrinkling and hair loss.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

Alopecia Areata can develop without perforin-mediated cytolysis.

Targeting TCR-Vβ2 in cutaneous T cell lymphoma shows promise for safer, more specific treatment.

The angora mouse mutation causes long hair and hair defects due to a gene deletion.

Controlling Tslp can improve health in AEC syndrome patients.

Injecting specific cells into the skin can help improve skin structure and reduce blisters in a genetic skin disorder.

Vitamin C deficiency changes gene expression, affecting skin and hair health.

Copper injections improved symptoms and prevented brain damage in brindled mice.

Obese mice with a leptin gene mutation have a longer resting phase in their hair cycle, which may help understand certain hair loss conditions.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

Prenatal retinoic acid exposure did not affect mouse vibrissal follicle development.