Citations for
1KRT12
Monoallelic expression of Krt12 gene during corneal-type epithelium differentiation of limbal stem cells
Hayashi Y, Call MK, Liu CY, Hayashi M, Babcock G, Ohashi Y, Kao WW.
Invest Ophthalmol Vis Sci. 51(9):4562-8. 2010
2CDM1, CDM2, KRT12, KRT13, KRT14, KRT3, KRT5, KTRT4, WHSN1, WHSN2
The molecular basis of human keratin disorders.
Arin MJ.
Hum Genet 125(4):355-73. Epub 2009 Feb 27. Review. 2009
3KRT12, KRT14, KRT15, KRT19
Cytokeratin 15 can be used to identify the limbal phenotype in normal and diseased ocular surfaces.
Yoshida S, Shimmura S, Kawakita T, Miyashita H, Den S, Shimazaki J, Tsubota K.
Invest Ophthalmol Vis Sci. 47(11):4780-6. 2006
4KRT1, KRT10, KRT12, KRT13, KRT14, KRT14P, KRT15, KRT16, KRT17, KRT17P3, KRT18, KRT18P12, KRT18P16, KRT18P17, KRT18P18, KRT18P19, KRT18P20, KRT18P21, KRT18P22, KRT18P23, KRT18P24, KRT18P25, KRT18P26, KRT18P27, KRT18P28, KRT18P29, KRT18P30, KRT18P31, KRT18P32, KRT18P33, KRT18P34, KRT18P35, KRT18P36, KRT18P37, KRT18P38, KRT18P39, KRT18P40, KRT18P41, KRT18P42, KRT18P43, KRT18P44, KRT18P45, KRT18P46, KRT18P47, KRT18P48, KRT18P49, KRT18P5, KRT18P50, KRT18P8, KRT19, KRT19P1, KRT19P2, KRT19P3, KRT2, KRT20, KRT222, KRT23, KRT24, KRT25, KRT26, KRT27, KRT28, KRT3, KRT31, KRT32, KRT33, KRT33A, KRT34, KRT35, KRT36, KRT37, KRT38, KRT39, KRT4, KRT40, KRT5, KRT6A, KRT6B, KRT6C, KRT7, KRT71, KRT72, KRT73, KRT74, KRT75, KRT76, KRT77, KRT78, KRT79, KRT8, KRT80, KRT81, KRT82, KRT83, KRT84, KRT85, KRT86, KRT8P10, KRT8P13, KRT8P15, KRT8P17, KRT8P18, KRT8P19, KRT8P20, KRT8P21, KRT8P22, KRT8P23, KRT8P24, KRT8P25, KRT8P26, KRT8P27, KRT8P28, KRT8P29, KRT8P30, KRT8P5, KRT8P6, KRT8P7, KRT8P8, KRT8P9, KRT9, KRTAP19-8, KRTAP20-4
New consensus nomenclature for mammalian keratins.
Schweizer J, Bowden PE, Coulombe PA, Langbein L, Lane EB, Magin TM, Maltais L, Omary MB, Parry DA, Rogers MA, Wright MW.
J Cell Biol 174(2):169-74. Epub 2006 Jul 10. 2006
5CDM2, KRT12
Meesmann corneal dystrophy (MECD): report of 2 families and a novel mutation in the cornea specific keratin 12 (KRT12) gene.
Nichini O, Manzi V, Munier FL, Schorderet DF.
Ophthalmic Genet 26(4):169-73. 2005
6CHST6, COL8A2, GLA, GSN, KRT12, KRT3, M1S1, STS, TGFBI
The molecular genetics of the corneal dystrophies--current status.
Klintworth GK.
Front Biosci 8:d687-713. Review. 2003
7KRT12, CDM2
A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy.
Irvine AD, Coleman CM, Moore JE, Swensson O, Morgan SJ, McCarthy JH, Smith FJ, Black GC, McLean WH.
Br J Ophthalmol 86(7):729-32. 2002
8CDM2, KRT12
Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.
Corden LD, Swensson O, Swensson B, Smith FJ, Rochels R, Uitto J, McLEAN WH.
Exp Eye Res 70(1):41-9. 2000
9CDM2, KRT12
A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy.
Coleman CM, Hannush S, Covello SP, Smith FJ, Uitto J, McLean WH.
Am J Ophthalmol 128(6):687-91. 1999
10CDM1, CDM2, KRT3, KRT12
Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy.
Irvine AD, Corden LD, Swensson O, Swensson B, Moore JE, Frazer DG, Smith FJ, Knowlton RG, Christophers E, Rochels R, Uitto J, McLean WH.
Nat Genet 16(2):184-7. 1997
11CDM2, KRT12
Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy.
Nishida K, Honma Y, Dota A, Kawasaki S, Adachi W, Nakamura T, Quantock AJ, Hosotani H, Yamamoto S, Okada M, Shimomura Y, Kinoshita S.
Am J Hum Genet 61(6):1268-75. 1997
12KRT12
A gene expression profile of human corneal epithelium and the isolation of human keratin 12 cDNA.
Nishida K, Adachi W, Shimizu-Matsumoto A, Kinoshita S, Mizuno K, Matsubara K, Okubo K.
Invest Ophthalmol Vis Sci 37(9):1800-9. 1996