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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

The Gsdma3 gene is essential for normal hair development in mice.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

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

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

Cantú syndrome is caused by mutations in the ABCC9 gene.

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

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

Retinoic acid affects skin and hair health by working with specific receptors, and its absence can lead to hair loss and skin changes.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

A specific gene variation is linked to a higher risk of polycystic ovary syndrome in Caucasian women.

A genetic variant in goats is linked to cashmere growth.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

Ruxolitinib helped a patient with alopecia areata regrow hair.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

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

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

Revertant cell therapy shows promise for treating type XVII collagen deficiency, but better cell selection methods are needed.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.