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

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.

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 genetic variant in the KRT25 gene causes tightly curled hair.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

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

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

Lack of KSR1 stops certain skin tumors in mice.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

Runx1 helps control the KAP5 gene in human hair follicles.

A mutation in the KRTHB5 gene causes hair and nail issues.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Using special RNA to target a mutant gene fixed hair problems in mice.

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

TRPS1 is crucial for bone, kidney, and hair follicle development.

Different keratins have unique expression patterns in mouse skin cells.