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The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

CDK4/6 inhibitors may cause hair loss in breast cancer patients.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Keratin-associated proteins may have roles in various mouse tissues, not just hair.

New genetic mutations linked to rare skin disorders were found in three newborns.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

Nilotinib can cause generalized keratosis pilaris.

A new method, iSiMPRe, effectively identifies key protein regions in cancer genes, highlighting potential drug targets.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Mutations in the KRT85 gene cause hair and nail problems.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.