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Odontogenic keratocysts are caused by abnormal Hedgehog signaling and can lead to tooth and bone issues.

The KAP8-1 gene affects skin, hair follicle development, and wool quality in different sheep varieties.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Certain CD8+ T cells attack hair follicles in alopecia areata, suggesting they could be targeted for treatment.

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

Changing CDK4 levels affects the number of stem cells in mouse hair follicles.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Cysteines in wool fibers are accessible and form important disulfide bonds.

The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

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

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

T cell subsets are crucial in kidney cancer, and a new model predicts patient outcomes using key genes.

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

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

A new mouse mutation causes skin and hair defects due to a gene change.

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

CIPK13 and CIPK18 genes are crucial for root hair growth in plants.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

CCC1 is essential for ion balance and proper plant cell function.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.