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

New mutations in the DSG4 gene cause a rare hair condition.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Hoxd gene regulation in mammals and birds is robust despite differences in DNA sequences, due to 3D chromatin structures.

cDermo-1 causes dense skin, feathers, and scales in chickens.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

The marker 5-hmC changes in hair follicle stem cells when they start to grow.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

CD2 might be a new treatment target for patchy alopecia areata.

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

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A genetic marker linked to a type of hair loss was found in most patients studied.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

A specific gene mutation causes congenital hair loss.

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

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Over a third of women thought to have non-classical congenital adrenal hyperplasia didn't have it confirmed by genetic tests.

Mutations in claudin-1 and claudin-3 cause hair loss in baby mice.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

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

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

p120-catenin helps control skin inflammation by regulating cadherin levels.