Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

A new gene variant causes curly coats in some dog breeds.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

AgK114 protein helps in hamster skin injury recovery.

Keratin-associated proteins are crucial for hair strength and structure.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

DermaCult™ Keratinocyte Expansion Medium allows human skin cells to grow longer while keeping their ability to develop properly.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

The study found nine new hair protein genes in human hair follicles.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The new keratin film without KAPs stains better and could help study keratin functions.

Activating Kras in mouse skin causes excess skin and hair loss.

K31 can identify clear secretory cells in human sweat glands.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

Keratin-associated proteins help link filaments and affect keratin's strength.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

KRT17 may be a new target for endometrial cancer treatment because it helps cancer cells move and form new blood vessels.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Blocking mTORC1 reduces skin tumor growth in mice.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.