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Matriptase is crucial for skin barrier, hair growth, and may contribute to skin cancer.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

Transglutaminase-3 is often reduced in esophageal cancer.

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

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Gsdma3 affects hair growth by controlling Wnt5a, which influences hair cell development.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

Mutations in hKAP1 genes may cause hereditary hair disorders.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

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

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

The K5 promoter controls gene expression in skin cells, with specific DNA segments crucial for targeting and regulation.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

TR3 is mainly found in hair follicle stem cells and may be involved in hair loss.

S100A3 protein is crucial for hair shaft formation in mice.

Decreasing MIG6 can increase the movement and invasiveness of MEK-inhibited mutant NRAS melanoma, particularly when stimulated by EGF.

Antizyme reduces tumor growth and normalizes skin cell development affected by MEK.

PKM2 is a promising target for heart repair and regeneration.

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

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

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

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

Removing MCPIP1 from myeloid cells in mice leads to hair loss and prevents skin tumors but causes pigmented spots.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.