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Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

Overexpression of FGF5s makes Chinese Merino sheep grow longer and heavier wool.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

Genetic profiling can improve androgenetic alopecia treatment by predicting drug response and minimizing side effects.

Researchers found a genetic region that influences the number of coat layers in dogs.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

Gene differences affect finasteride side effects in men with hair loss.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Blocking certain immune signals can reduce skin damage from radiation therapy.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

Suppressing ODC activity reduces tumor growth in hair follicles.

Increasing type 17 collagen reduces aging signs in skin cells caused by UV light.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

HPV16 oncogenes disrupt the normal activity of hair follicle stem cells.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

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

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.

Methylation in specific gene region causes finasteride resistance in some BPH patients.

Mice hair follicles take in the amino acid cystine.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.