Search

everythinglearnresearchcommunity

for

Search:↓

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

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

Mutations in the KRT85 gene cause hair and nail problems.

A rabbit gene important for hair development was identified and detailed.

The KDM1 gene helps Venus flytraps close by managing potassium ions.

Noncoding RNAs help determine cashmere quality in goats.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

ATP-sensitive potassium channels are important for hair growth.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Mutations in hKAP1 genes may cause hereditary hair disorders.

FLCN helps control iron levels in cells.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Cantú syndrome is caused by mutations in the ABCC9 gene.

HOXC13 is essential for hair and nail development by regulating Foxn1.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Only one K16 gene on chromosome 17 makes a functional keratin protein.

A KRT32 gene variant causes loose anagen hair syndrome.

Certain gene variations increase the risk of alopecia areata in Koreans.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

A unique gene mutation was found in a family with monilethrix.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

p21waf1/cip1 and p27kip1 help in hair follicle differentiation in rats.