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Small molecules KY19382 and KY19334 may help treat skin cancer by reducing CDK1 levels and blocking harmful cell signals.

Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

A specific DNA region controls skin cell gene expression by working with certain proteins.

Low m6Ascores in melanoma predict better survival and response to immunotherapy.

IL-1 blockade is effective for treating SURF, and personalized treatment is needed.

The document cannot be summarized as it is not provided or is unclear.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

Mouse skin has special cells in the epidermis that decrease with age and are linked to keratinocyte stem cells.

Schwann cell and M2 macrophage interactions contribute to keloid growth by increasing matrix deposition.

Selamectin spot-on effectively treats scabies in rabbits.

Keratin 15 cells from hair follicles help develop and maintain skin tumors in mice.

Blocking mTORC1 reduces skin tumor growth in mice.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

The Glu413Lys mutation in keratin affects hair stability, while Glu413Asp does not.

A new compound from Royoporus badius activates immune cells and induces inflammatory responses.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Activating PKM2 and Wnt/β-catenin signaling speeds up wound healing.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.