نتایج جستجو برای: keratinization disorder

تعداد نتایج: 597575  

2016
Hideki Fukuoka Satoshi Kawasaki Norihiko Yokoi Kenta Yamasaki Shigeru Kinoshita

PURPOSE To report the cytopathological features of corneal intraepithelial neoplasia (CIN) through the investigation of cytokeratin expression pattern, keratinization, cell proliferation, apoptosis, and epithelial mesenchymal transition. PATIENT AND METHODS Corneal tissue excised from a CIN patient was examined in this study. Cryosections of the excised CIN epithelial tissue were examined by ...

Journal: :Experimental dermatology 2014
Aurélie Hayez Jérémy Malaisse Edith Roegiers Marie Reynier Chantal Renard Marek Haftek Vincent Geenen Guy Serre Michel Simon Catherine Lambert de Rouvroit Carine Michiels Yves Poumay

TMEM45A (DERP7, DNAPTP4 or FLJ10134) gene, belonging to the TMEM family encoding predicted transmembrane proteins, is highly expressed in epidermal keratinocytes. To investigate the potential involvement of TMEM45A during the differentiation and keratinization processes, its expression has been characterized in normal human keratinocytes and the protein subcellular localization has been studied...

2013
Geraint J. Parfitt Yilu Xie Mikhail Geyfman Donald J. Brown James V. Jester

Meibomian gland dysfunction (MGD) is frequent with aging and is the primary cause of dry eye disease, the most prevalent ocular complaint. We used a novel 3-D reconstruction technique, immunofluorescent computed tomography (ICT), to characterize meibomian gland keratinization and cell proliferation in a mouse model of age-related meibomian gland dysfunction (ARMGD). To visualize the changes ass...

Journal: :iranian journal of child neurology 0
abolfazl faraji genetic technician, special medical center, genetic diagnostic laboratory, tehran, iran maryam mobaraki genetic technician, special medical center, genetic diagnostic laboratory, tehran, iran amirreza yazdi resident of dermatology, special medical center, genetic diagnostic laboratory,tehran, iran seyyed mohammad seyyed hassani . genetic counselor, yazd genetic center, tehran, iran omid aryani genetic counselor, special medical center, genetic diagnostic laboratory, tehran, iran massoud houshmand assistant professor of human genetics, department of medical genetics, national institute of genetic engineering and biotechnology (nigeb), tehran, iran

objective autosomal recessive congenital ichthyosis (arci) is a rare, heterogenous keratinization disorder of the skin, classically divided into two clinical subtypes, lamellar ichthyosis (li) and nonbullous congenital ichthyosi-formis erythroderma (ncie). lamellar ichtyosis is caused by mutations in the tgm1 gene that encodes transglutaminase 1 enzyme, which is critical for the assembly of the...

2013
Marcius A. Peryassu Bernardo C. Peryassu Raphael C. Peryassu Juan Piñeiro-Maceira Marcia Ramos-e-Silva

The authors report a case of proliferating trichilemmal tumor on the tip of the nose of a man. This tumor is usually seen in women and on the scalp, and it shows trichilemmal keratinization on histopathology.

2004
R. Marks

The stratum corneum (SC) is the differentiated end product of the mammalian epidermis. It is vital to constancy of the milieu interieur (the environment within) because it prevents water loss and the penetration by potentially toxic xenobiotics, damaging radiation, and pathogenic microbes. The intercorneocyte space contains complex nonpolar lipids that constitute the water barrier. The formatio...

2012
Sunhee Chang Mee Joo Hanseong Kim

Carcinoma showing thymus-like differentiation (CASTLE) is a rare carcinoma of the thyroid or adjacent soft tissue of the neck with a histologic resemblance to thymic epithelial tumors. Although the fine-needle aspiration (FNA) plays a central role in the initial evaluation of thyroid nodules, few reports about the cytologic findings of CASTLE have been found according to a review of literatures...

Journal: :Australian Journal of Biological Sciences 1980

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