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	1.	[Analysis of mutation in KRT12 gene in a Chinese family with Meesmann's corneal dystrophy]. [electronic resource] by Wang, Le-Jin Tian, Xin Zhang, Qing-Sheng Liu, Liang Producer: 20101104 In: [Zhonghua yan ke za zhi] Chinese journal of ophthalmology vol. 43 Availability: No items available. Save to lists Add to cart (remove)
	2.	Culture of feline corneal epithelial cells and infection with feline herpesvirus-1 as an investigative tool. [electronic resource] by Sandmeyer, Lynne S Keller, Charlotte B Bienzle, Dorothee Producer: 20050408 In: American journal of veterinary research vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A case of bilateral corneal epithelial dysplasia characterized by laser confocal biomicroscopy and cytokeratin immunofluorescence. [electronic resource] by Wakuta, Makiko Chikama, Tai-Ichiro Takahashi, Norihisa Nishida, Teruo Producer: 20080311 In: Cornea vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Particle-mediated gene transfer to ocular surface epithelium. [electronic resource] by Kao, Winston W Y Producer: 20030527 In: Advances in experimental medicine and biology vol. 506 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Identification of a novel mutation in the cornea specific keratin 12 gene causing Meesmann's corneal dystrophy in a German family. [electronic resource] by Clausen, Ina Duncker, Gernot I W Grünauer-Kloevekorn, Claudia Producer: 20100825 In: Molecular vision vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	6.	Autosomal-dominant Meesmann epithelial corneal dystrophy without an exon mutation in the keratin-3 or keratin-12 gene in a Chinese family. [electronic resource] by Cao, Wei Yan, Ming Hao, QianYun Wang, ShuLin Wu, LiHua Liu, Qing Li, MingYan Biddle, Fred G Wu, Wei Producer: 20140115 In: The Journal of international medical research vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Development of the cornea of true moles (Talpidae): morphogenesis and expression of PAX6 and cytokeratins. [electronic resource] by Carmona, F David Ou, Jingxing Jiménez, Rafael Collinson, J Martin Producer: 20110203 In: Journal of anatomy vol. 217 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A novel arginine substitution mutation in 1A domain and a novel 27 bp insertion mutation in 2B domain of keratin 12 gene associated with Meesmann's corneal dystrophy. [electronic resource] by Yoon, M K Warren, J F Holsclaw, D S Gritz, D C Margolis, T P Producer: 20040622 In: The British journal of ophthalmology vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	The histological characteristics of cultured oral epithelium in different culture conditions. [electronic resource] by Hashemi, Hassan Salehnia, Mojdeh Kamali, Morvarid Beigi Boroujeni, Mandana Producer: 20091117 In: Iranian biomedical journal vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	10.	A novel mutation in the cornea-specific keratin 12 gene in Meesmann corneal dystrophy. [electronic resource] by Seto, Takahiko Fujiki, Keiko Kishishita, Hitoshi Fujimaki, Takuro Murakami, Akira Kanai, Atsushi Producer: 20081110 In: Japanese journal of ophthalmology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Meesmann corneal dystrophy (MECD): report of 2 families and a novel mutation in the cornea specific keratin 12 (KRT12) gene. [electronic resource] by Nichini, Olivia Manzi, Violaine d'Allèves Munier, Francis L Schorderet, Daniel F Producer: 20060223 In: Ophthalmic genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	The "replacement hypothesis": corneal stem cell origin epithelia are replaced by limbal stem cell origin epithelia in mouse cornea during maturation. [electronic resource] by Hayashi, Yasuhito Watanabe, Narumi Ohashi, Yuichi Producer: 20130122 In: Cornea vol. 31 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Remodeling of epithelial cells and basement membranes in a corneal deficiency model with long-term follow-up. [electronic resource] by Kameishi, Sumako Sugiyama, Hiroaki Yamato, Masayuki Sado, Yoshikazu Namiki, Hideo Kato, Takashi Okano, Teruo Producer: 20150329 In: Laboratory investigation; a journal of technical methods and pathology vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Expression of keratin 12 and maturation of corneal epithelium during development and postnatal growth. [electronic resource] by Tanifuji-Terai, Noriko Terai, Kazuto Hayashi, Yasuhito Chikama, Tai-ichiro Kao, Winston W-Y Producer: 20060227 In: Investigative ophthalmology & visual science vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Limbal Stem Cell Deficiency Secondary to Diffuse Non-necrotizing Anterior Scleritis: A Clinicopathological Report. [electronic resource] by Khoo, Lin Wei Attzs, Michelle Srinivasan, Sathish Roberts, Fiona Producer: 20180831 In: Cornea vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Cytokeratin 15 can be used to identify the limbal phenotype in normal and diseased ocular surfaces. [electronic resource] by Yoshida, Satoru Shimmura, Shigeto Kawakita, Tetsuya Miyashita, Hideyuki Den, Seika Shimazaki, Jun Tsubota, Kazuo Producer: 20061208 In: Investigative ophthalmology & visual science vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Allele-specific siRNA silencing for the common keratin 12 founder mutation in Meesmann epithelial corneal dystrophy. [electronic resource] by Allen, Edwin H A Atkinson, Sarah D Liao, Haihui Moore, Jonathan E Pedrioli, Deena M Leslie Smith, Frances J D McLean, W H Irwin Moore, C B Tara Producer: 20130319 In: Investigative ophthalmology & visual science vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Novel mutations in the helix termination motif of keratin 3 and keratin 12 in 2 Taiwanese families with Meesmann corneal dystrophy. [electronic resource] by Chen, Ying-Ting Tseng, Sung-Huei Chao, Sheau-Chiou Producer: 20060207 In: Cornea vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	A novel mutation as the basis for asymptomatic meesmann dystrophy in a Danish family. [electronic resource] by Nielsen, Kim Orntoft, Torben Hjortdal, Jesper Rasmussen, Tommy Ehlers, Niels Producer: 20080311 In: Cornea vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12. [electronic resource] by Hassan, H Thaung, C Ebenezer, N D Larkin, G Hardcastle, A J Tuft, S J Producer: 20130802 In: Eye (London, England) vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 84 results.