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7. Keratin 8 and 18 hyperphosphorylation is a marker of progression of human liver disease. Toivola DM; Ku NO; Resurreccion EZ; Nelson DR; Wright TL; Omary MB Hepatology; 2004 Aug; 40(2):459-66. PubMed ID: 15368451 [TBL] [Abstract][Full Text] [Related]
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9. Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK). Reis A; Hennies HC; Langbein L; Digweed M; Mischke D; Drechsler M; Schröck E; Royer-Pokora B; Franke WW; Sperling K Nat Genet; 1994 Feb; 6(2):174-9. PubMed ID: 7512862 [TBL] [Abstract][Full Text] [Related]
10. Keratin mutation in transgenic mice predisposes to Fas but not TNF-induced apoptosis and massive liver injury. Ku NO; Soetikno RM; Omary MB Hepatology; 2003 May; 37(5):1006-14. PubMed ID: 12717381 [TBL] [Abstract][Full Text] [Related]
11. Denaturing temperature selection may underestimate keratin mutation detection by DHPLC. Strnad P; Lienau TC; Tao GZ; Ku NO; Magin TM; Omary MB Hum Mutat; 2006 May; 27(5):444-52. PubMed ID: 16575832 [TBL] [Abstract][Full Text] [Related]
12. Mutation of human keratin 18 in association with cryptogenic cirrhosis. Ku NO; Wright TL; Terrault NA; Gish R; Omary MB J Clin Invest; 1997 Jan; 99(1):19-23. PubMed ID: 9011570 [TBL] [Abstract][Full Text] [Related]
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14. The keratin cytoskeleton in liver diseases. Zatloukal K; Stumptner C; Fuchsbichler A; Fickert P; Lackner C; Trauner M; Denk H J Pathol; 2004 Nov; 204(4):367-76. PubMed ID: 15495250 [TBL] [Abstract][Full Text] [Related]
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16. Keratin 8 Y54H and G62C mutations are not associated with inflammatory bowel disease. Büning C; Halangk J; Dignass A; Ockenga J; Deindl P; Nickel R; Genschel J; Landt O; Lochs H; Schmidt H; Witt H Dig Liver Dis; 2004 Jun; 36(6):388-91. PubMed ID: 15248378 [TBL] [Abstract][Full Text] [Related]
17. Keratin-mediated resistance to stress and apoptosis in simple epithelial cells in relation to health and disease. Marceau N; Loranger A; Gilbert S; Daigle N; Champetier S Biochem Cell Biol; 2001; 79(5):543-55. PubMed ID: 11716296 [TBL] [Abstract][Full Text] [Related]
19. Concurrence between the molecular overlap regions in keratin intermediate filaments and the locations of keratin mutations in genodermatoses. Steinert PM; Yang JM; Bale SJ; Compton JG Biochem Biophys Res Commun; 1993 Dec; 197(2):840-8. PubMed ID: 7505575 [TBL] [Abstract][Full Text] [Related]
20. Mild recessive epidermolytic hyperkeratosis associated with a novel keratin 10 donor splice-site mutation in a family of Norfolk terrier dogs. Credille KM; Barnhart KF; Minor JS; Dunstan RW Br J Dermatol; 2005 Jul; 153(1):51-8. PubMed ID: 16029326 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]