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Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

LIPH mutations cause woolly hair in some Chinese people.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Progerin affects cell shape but not hair or skin in mice.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

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

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.

The same gene mutation can cause different symptoms in family members.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

A new gene mutation causes a rare type of hair loss.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

Genetic marker rs12558842 strongly linked to male hair loss.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

Aromatase gene variation may increase female hair loss risk.

Early-onset hair loss is linked to Parkinson's disease and decreased fertility.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

LRIG1 is linked to better survival in Merkel cell carcinoma.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

AR polyglycine repeat doesn't cause baldness.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.