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Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

Using Lasswell's model can make CSR communication more effective and trusted.

Global oil use will rise, US corn-to-ethanol policy is flawed, and various social and economic issues need attention.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

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

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

WNT10A gene mutations cause short anagen hair syndrome.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

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

Mutant mice help researchers understand hair growth and related genetic factors.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

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.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Mutations at Val-889 and Arg-752 disrupt key interactions in the androgen receptor, affecting its function.

Researchers found two new genetic variants linked to Alzheimer's disease.