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The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

Tcf3 helps cells move and heal wounds by controlling lipocalin 2.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

SGK1 is important in cancer growth and treatment resistance, and targeting it could improve therapies.

Neurokinin B levels are higher in the placentas of women with PCOS who have female babies.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

Basal cell carcinoma shows keratin patterns similar to undifferentiated hair follicle cells.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Radiation therapy in breast cancer patients changes gene expression related to DNA damage, fibroblast growth, and hair follicle development, which could help improve treatment for radiation-induced fibrosis.

Keratin 16 delays skin maturation and affects skin and hair development in mice.

circRNA-1926 helps goat stem cells turn into hair follicles by affecting miR-148a/b-3p and CDK19.

ILC1-like cells can cause alopecia areata by themselves.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

AKN might be a skin marker for metabolic syndrome.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

A specific gene mutation causes complete hair loss without other health issues.

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

A new gene mutation causes insulin resistance in a girl and her mother.

A mutation in the KRT25 gene causes woolly hair and hair loss.

Baricitinib successfully regrew hair in an 8-year-old boy with alopecia totalis linked to a KRT74 gene variant.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

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

New genetic mutations causing hair loss were found in a Chinese family.

Suppressing ODC activity reduces tumor growth in hair follicles.

Nerve growth factor helps cashmere goat hair cells grow by activating a specific protein.