Recent advances in congenital ichthyoses.
Madrid, Spain. In Curr Opin Pediatr, Aug 2015
Mutations in keratin 10 have been identified as the cause of ichthyosis with confetti, a rare form of ichthyosis characterized by severe erythroderma in which healthy spots gradually develop since childhood.
Comparative study of cytokeratin and langerin expression in keratinized cystic lesions of the oral and maxillofacial regions.
Oral, Kazakhstan. In J Oral Sci, 2014
Seven DMCs, 30 EDMCs, 11 OOCs, and 28 KCOTs were examined immunohistochemically using antibodies against CK10, 13, 14, 16, 17, 19, and langerin.
Benign mucinous metaplasia of the genital mucosa: histomorphological and immunohistochemical features and criteria for differentiation from extramammary Paget disease.
Hamburg, Germany. In Br J Dermatol, 2011
METHODS: Eight biopsy specimens of BMM were stained with haematoxylin and eosin, periodic acid-Schiff and alcian blue, and for cytokeratin (CK) 7, CK10, CK14, CK20, carcinoembryonic antigen (CEA), epithelial membrane antigen (EMA), S100, gross cystic disease fluid protein-15 (GCDFP-15), lysozyme and Ki67 and compared with PD.
Cytogenic Behavior of a Knobbed Chromosome 10 in Maize.
In Science, 1961
Unlike maize plants heterozygous the abnormal chromosome 10 (K10) and the normal chromosome 10 (k10), those heterozygous for a knobbed chromosome 10 (K(T)10/k10) do not undergo preferential segregation or "meiotic drive."