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Hair follicle bulge cells don't help skin regrow after glucocorticoid damage; interfollicular epidermis cells do.

Mutations in claudin-1 and claudin-3 cause hair loss in baby mice.

The skin can still regenerate and function well even with fewer fibroblasts.

Ceramide Synthase 4 is crucial for maintaining hair follicle stem cells and preventing hair loss.

Ubiquitination of the insulin receptor regulates collagen secretion in human skin.

New diabetes tech and therapies improve care for endocrine disorders.

Nanocarriers can improve skin treatments after cancer therapy by enhancing antioxidant delivery and effectiveness.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

Neural organoids show promise for future CNS disease treatments.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Keratins are crucial for hair strength, and mutations in certain keratin genes cause hair disorders.

Recessive X-linked ichthyosis involves a less efficient enzyme in hair follicles, suggesting two distinct enzymes.

Low selenium levels can extend lifespan but worsen health issues.

Localized ROS production is essential for cell growth and movement in plants and animals.

Brain-made chemicals can control nerve cell function differently in various parts of a mouse's brain, which may help us understand neurological conditions.

Exosomes show promise in treating acute kidney injury by protecting and repairing kidney cells.

Netherton syndrome causes specific skin and hair changes that help in early diagnosis.

The Kras mutation changes normal cell signals, leading to disrupted tissue structure and potential cancer.

Hair graying happens because certain cells aren't maintained properly.

Hearing decline in SAMP8 mice starts before outer hair cell loss and may be linked to other changes.

Disruptions in Wnt signaling can lead to skin and hair diseases.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Mice lacking a key DNA methylation enzyme in skin cells have a lower chance of activating stem cells necessary for hair growth, leading to progressive hair loss.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.