siRNA Silencing of the Mutant Keratin 12 Allele in Corneal Limbal Epithelial Cells Grown From Patients With Meesmann's Epithelial Corneal Dystrophy

2014 ◽  
Vol 55 (5) ◽  
pp. 3352 ◽  
Author(s):  
David G. Courtney ◽  
Sarah D. Atkinson ◽  
Edwin H. A. Allen ◽  
Johnny E. Moore ◽  
Colum P. Walsh ◽  
...  
Keyword(s):  
Epithelial Cells ◽  
Corneal Dystrophy ◽  
Sirna Silencing ◽  
Keratin 12

scholarly journals Allele-Specific siRNA Silencing for the Common Keratin 12 Founder Mutation in Meesmann Epithelial Corneal Dystrophy

2013 ◽  
Vol 54 (1) ◽  
pp. 494 ◽  
Author(s):  
Edwin H. A. Allen ◽  
Sarah D. Atkinson ◽  
Haihui Liao ◽  
Jonathan E. Moore ◽  
Deena M. Leslie Pedrioli ◽  
...  
Keyword(s):  
Founder Mutation ◽  
Corneal Dystrophy ◽  
Allele Specific ◽  
The Common ◽  
Sirna Silencing ◽  
Keratin 12

scholarly journals Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy

2016 ◽  
Vol 25 (6) ◽  
pp. 1176-1191 ◽  
Author(s):  
Edwin H.A. Allen ◽  
David G. Courtney ◽  
Sarah D. Atkinson ◽  
Johnny E. Moore ◽  
Laura Mairs ◽  
...  
Keyword(s):  
Unfolded Protein Response ◽  
Missense Mutation ◽  
Corneal Dystrophy ◽  
Unfolded Protein ◽  
The Unfolded Protein Response ◽  
Protein Response ◽  
Keratin 12

scholarly journals Autosomal-dominant Meesmann epithelial corneal dystrophy without an exon mutation in the keratin-3 or keratin-12 gene in a Chinese family

2013 ◽  
Vol 41 (2) ◽  
pp. 511-518 ◽  
Author(s):  
Wei Cao ◽  
Ming Yan ◽  
QianYun Hao ◽  
ShuLin Wang ◽  
LiHua Wu ◽  
...  
Keyword(s):  
Autosomal Dominant ◽  
Corneal Dystrophy ◽  
Chinese Family ◽  
Keratin 12

scholarly journals A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy

2000 ◽  
Vol 84 (5) ◽  
pp. 527-530 ◽  
Author(s):  
L D Corden
Keyword(s):  
Corneal Dystrophy ◽  
Keratin 12

Novel Mutations in the Helix Termination Motif of Keratin 3 and Keratin 12 in 2 Taiwanese Families with Meesmann Corneal Dystrophy

Cornea ◽  
2005 ◽  
Vol 24 (8) ◽  
pp. 928-932 ◽  
Author(s):  
Ying-Ting Chen ◽  
Sung-Huei Tseng ◽  
Sheau-Chiou Chao
Keyword(s):  
Corneal Dystrophy ◽  
Novel Mutations ◽  
Keratin 12

scholarly journals Severe Meesmann’s epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12

Eye ◽  
2012 ◽  
Vol 27 (3) ◽  
pp. 367-373 ◽  
Author(s):  
H Hassan ◽  
C Thaung ◽  
N D Ebenezer ◽  
G Larkin ◽  
A J Hardcastle ◽  
...  
Keyword(s):  
Missense Mutation ◽  
Corneal Dystrophy ◽  
Keratin 12

Molecular Genetics of Meesmann's Corneal Dystrophy: Ancestral and Novel Mutations in Keratin 12 (K12) and Complete Sequence of the Human KRT12 Gene

2000 ◽  
Vol 70 (1) ◽  
pp. 41-49 ◽  
Author(s):  
LAURA D. CORDEN ◽  
OLE SWENSSON ◽  
BEATE SWENSSON ◽  
FRANCES J.D. SMITH ◽  
RAINER ROCHELS ◽  
...  
Keyword(s):  
Molecular Genetics ◽  
Corneal Dystrophy ◽  
Complete Sequence ◽  
Novel Mutations ◽  
Keratin 12

Conjunctival epithelial cells can resurface denuded cornea, but do not transdifferentiate to express cornea-specific keratin 12 following removal of limbal epithelium in mouse

1996 ◽  
Vol 60 (1) ◽  
pp. 31-38 ◽  
Author(s):  
Paul D. Moyer ◽  
Adam H. Kaufman ◽  
Zhong Zhang ◽  
Candace W.-C. Kao ◽  
Abbot G. Spaulding ◽  
...  
Keyword(s):  
Epithelial Cells ◽  
Limbal Epithelium ◽  
Keratin 12 ◽  
Conjunctival Epithelial Cells
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