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Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

The research identified new skin traits in mice, some linked to human skin conditions.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.

Modified rat hair follicle stem cells can help create artificial hair follicles, blood vessels, and skin.

Trps1 is essential for proper hair follicle development.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Heat shock proteins help basal cell carcinoma grow by responding to inflammation signals.

StemMACS media is better for growing therapeutic stem cells.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Antizyme reduces tumor growth and normalizes skin cell development affected by MEK.

The hairless mutant gene causes early hair loss and affects skin and thymus development in mice.

Hair-follicle stem cells can become neurons.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

Peptide nanoparticles can effectively deliver CRISPR-Cas9 to target KRAS mutations in cancer.

Boosting certain cell signals can prevent hair loss from cancer treatments.

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

Human thymus has stem cells that can self-renew and maintain their identity.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Hair follicle cells can become bone-like cells, useful for bone repair.

Oncogenic melanocyte stem cells can develop into melanoma similar to human cases.

Melanoma cells lose their ability to form tumors when placed in a zebrafish embryo environment.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

The new Hairless R/J mice model improves imaging for tumor monitoring and cancer therapy evaluation.