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New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

A new method, iSiMPRe, effectively identifies key protein regions in cancer genes, highlighting potential drug targets.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

BAP1 mutations are rare in pediatric melanocytic tumors and may develop later in life.

Certain genetic markers may increase or decrease prostate cancer risk.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

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

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Gene variation affects prostate issues and hair loss.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

Targeting the TNFRSF1B gene may help treat hair loss.

Mutation in hairless gene may increase hair loss risk.

Mutation in hairless gene may increase hair loss risk.

A genetic hair protein variant is more common in Japanese people and is inherited.

GABEB is a less severe skin condition caused by a gene mutation affecting collagen, leading to blisters and other symptoms.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

The GG genotype of the KRT71 gene leads to longer wool in Gansu alpine fine-wool sheep.

The Shaven mutation in mice affects hair growth and causes a greasy coat due to abnormal lipid content.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.