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The antibody 005-C04 blocks prolactin receptors, causing reversible infertility, impaired lactation, and hair regrowth in female mice.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Differences in androgen receptor expression and tissue properties may lead to higher cryptorchidism risk in certain rats.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

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

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

Mice with more Flightless I protein grew back their claws better after amputation.

TCDD changes skin cell growth and keratin production in mice.

Ovariectomized mice mimic postmenopausal hair loss, and estradiol helps maintain hair density.

Certain gene variations are found in people with polycystic ovary syndrome.

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

Scientists found a gene in mice that causes early hearing loss.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

The research mapped diverse cell types in mouse lacrimal glands, aiding understanding of gland biology and diseases.

The mutation helps mice handle heat better without affecting hair growth.

A zinc-deficient diet stunted growth and affected organs in mice, with C57BL/6J mice showing more severe symptoms.

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

Researchers found 15 new genetic links to skin traits in Japanese women.

Human basal cell carcinomas and squamous cell carcinomas have unique gene expression patterns not fully mirrored in mouse models.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Corneal health relies on cell migration and cooperation with the lacrimal gland, not Bmi1+ cells, and Eda gene mutations can cause dry eye disease.

Mice without the IL-6 gene had more hair growth after injury due to higher activity of a related protein, Stat3.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Removing certain brain receptors in mice worsens seizure severity and response to treatment during hormone withdrawal.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.