Search

everythinglearnresearchcommunity

for

Search:↓

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

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

A mutation in the KRT25 gene causes woolly hair and hair loss.

A KRT32 gene variant causes loose anagen hair syndrome.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

A truncated protein linked to breast cancer may change cell adhesion.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

The 4C32 gene may help in mouse skin development and differentiation.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

KLF4 is important for keeping hair follicle stem cells inactive.

Mutations in the KRT85 gene cause hair and nail problems.

Researchers found a new mutation causing total hair loss from birth.

A new gene mutation is linked to monilethrix in the studied family.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Most mouse hair keratin genes are on chromosomes 11 and 15.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Mutations in the KRT16 gene can cause skin and nail disorders.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.