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Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

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

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A semi-automated system can effectively help choose emulsion ingredients, simplifying the creation of medicinal and cosmetic products.

Introducing the OTC gene improved symptoms in mice with OTC deficiency.

Defects in certain proteins cause major heart abnormalities during early development.

Higher CO2 levels help a cyanobacterium grow better by boosting photosynthesis and carbon uptake.

The Itpr3 gene causes a specific hair pattern in mice.

EFFC might be common but underreported.

Compound 6 is a promising candidate for better wound healing.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Cantú syndrome is caused by mutations in the ABCC9 gene.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

FFA can be mistaken for rosacea, requiring specific treatment for accurate diagnosis and management.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

A rare family case of multiple benign hair follicle tumors was identified, highlighting the need to distinguish them from similar conditions.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

miR-877-3p can improve cashmere quality by regulating hair growth in goats.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Uncombable hair is inherited dominantly with complete penetrance.

A family had a genetic condition causing hair loss on the scalp, passed down through four generations.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.