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About 38% of patients at a dermatology clinic had oral lesions, with coated tongue, fissured tongue, and Fordyce granules being most common.

Abnormal keratin expression in mice causes severe oral issues, affecting feeding.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Dermoscopy can non-invasively detect eruptive vellus hair cysts on the labia majora.

Different bovine tissues show varying types of cytokeratins.

Basal cell carcinoma may start from parts of tiny hair follicles.

Tongue cancer cells show more plectin-1 than non-cancer cells, but both have similar levels of trichohyalin.

Retinoic acid changes skin cells to mucosal cells with goblet cells, needing TG2/Gh, Gbx1, and TGF-beta.

Children with Epidermolysis Bullosa need better access to specialized dental care.

Basal cell epithelioma-like changes are most similar to normal basal cells.

Oncogenic K-ras causes rapid cancerous changes in the mouth's lining.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

People with palmoplantar pustulosis, especially with bone issues, have different mouth bacteria compared to healthy people.

Different tissues in cows have different types of cytokeratins.

The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

Hyper-keratinisation in Meibomian glands contributes to gland dysfunction.

A 68-year-old woman with benign mucous membrane pemphigoid has eye, mouth, and skin issues, including thick plaques and nail changes.

A man had a large, rare cyst in his mouth removed after 10 years, which fixed his swallowing and breathing problems.

Trichocytic cytokeratins are found in hair, nails, tongue, and thymus cells, showing complex regulation in tissue development.

Fish teeth and taste bud densities are linked and can change between types due to shared genetic and molecular factors.

HBCs in the olfactory epithelium can self-renew or differentiate into other cell types, with specific patterns during regeneration.

A 29-year-old man had a jaw plaque diagnosed as follicular mucinosis, linked to nestin-positive hair follicle stem cells.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

Fatty acid composition in human skin, mouth, and hair cells varies with keratinization, and cultured cells show essential fatty acid deficiency.

Skin tumors and normal skin structures have different lectin-binding patterns.

Basal cell epithelioma resembles fetal hair follicles, not adult or fetal skin.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Most patients with blistering skin disorders in South India had bullous pemphigoid and often had other conditions like hypertension and diabetes.