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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 TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

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

Ethanol boosts brain steroid production by activating NMDA receptors, affecting memory formation.

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

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

Human hair cells can change based on their environment, especially interactions with certain skin cells.

Removing the p75 gene in mouse skin cells didn't affect their skin or hair growth.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

A gene mutation in mice causes severe skin disorder similar to a human condition.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Blocking EGFR in mice causes hair loss and skin changes.

DNA phenotyping can predict physical traits like eye, hair, and skin color, improving forensic investigations.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Lambs' skin showed similar but more severe responses to a second orf virus infection, involving immune cells and new skin formation.

Mice with human fetal thymic tissue and stem cells developed symptoms similar to chronic graft-versus-host disease.

Quiescent cells have increased mitochondrial activity and ECM gene expression, but reduced glycolysis.

Dual TCR Treg cells are common in mouse tissues and vary by location.

Fatp4 is crucial for healthy skin development and function.

TPA strongly increases ODC activity in certain skin cells, potentially aiding tumor growth.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Mouse touch-sensitive nerve cells adjust their connections based on competition with other similar cells.

Vitamin D receptor knockout mice have significant motor impairments but no cognitive deficits.

Blocking autophagy worsens lipid buildup and dysfunction in brain cells after injury.

Myc changes chromatin in stem cells, causing them to leave their niche.

Lack of Evi in skin causes psoriasis-like symptoms in mice.

Increased ornithine decarboxylase makes normally tumor-resistant mice more sensitive to tumors.