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Dog skin with hair loss, when transplanted to mice, regrew hair, suggesting the hair loss cause is likely body-wide, not skin-specific.

Androgen receptor inactivation delays skin cancer onset and reduces incidence in mice, with gender differences in susceptibility.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Removing UBE2N from skin cells causes inflammation and immune response, which can be lessened with specific inhibitors.

The SAM model helps understand aging and related diseases.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Both induced and spontaneous AA lymphocytes can cause alopecia areata in mice.

miRNA-24 affects goat coat color by controlling proteins involved in pigment production.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

Activating liver X receptors can reduce fibrosis by stopping certain immune cells from releasing harmful proteins.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

Proteomic analysis can identify genetic differences in mouse hair, helping understand hair defects and variations.

Loss of TET2 increases the risk of skin and oral cancer.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

FOXN1 gene variants cause low T cells and immune issues from birth.

GRK2 is essential for healthy hair follicle function, and its absence can lead to hair loss and cysts.

Injecting recipient splenocytes into donors' thymus can prevent graft-versus-host disease.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

A new laser method helps observe and understand how intestines heal and change over time.

15-lipoxygenase helps keep skin healthy by reducing inflammation.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

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