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Keratin 19 helps identify skin stem cells, with its presence varying by body location, age, and culture stage.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

A new keratin 6 type in mice explains why some mice without certain keratin genes still have normal hair and nails.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

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

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

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

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

A new mutation in mice causes crooked whiskers and messy hair.

The drug showed promise in treating renal cell carcinoma with manageable side effects.

Keratin 79 cells help form and regenerate hair canals.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

IL-26 has antimicrobial and pro-inflammatory effects in the chronic skin condition Hidradenitis Suppurativa.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

Keratin patterns in hair follicles help understand hair growth and potential hair and nail disorders.

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

A protein called IL-36γ causes skin side effects from certain cancer treatments when combined with a common skin bacteria.

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

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

Keratin 79 marks a new group of cells that are key for creating and repairing the hair follicle's structure.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

Kremen is crucial for proper development and preventing tumors by regulating Wnt signaling.

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

KAP-depleted hair causes less immune response and is more biocompatible for implants.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

KAP6 genes are conserved across species and active in hair follicles.