-
1
-
-
33751085299
-
Dystrophia epithelialis corneae
-
Fuchs E. Dystrophia epithelialis corneae. Graefes. Arch. Clin. Exp. Ophthalmol. 76(3), 478-508 (1910).
-
(1910)
Graefes. Arch. Clin. Exp. Ophthalmol.
, vol.76
, Issue.3
, pp. 478-508
-
-
Fuchs, E.1
-
2
-
-
3242686589
-
Diseases of the cornea: Remarks on dystrophies of the cornea and glaucoma, with especial reference to a familial ariety of the former
-
Clegg JG. Diseases of the cornea: Remarks on dystrophies of the cornea and glaucoma, with especial reference to a familial ariety of the former. Trans. Ophthalmol. Soc. UK 35, 245-253 (1915).
-
(1915)
Trans. Ophthalmol. Soc. UK
, vol.35
, pp. 245-253
-
-
Clegg, J.G.1
-
7
-
-
34447488621
-
Epithelial dystrophy of he cornea
-
Graves B. Notes on microscopy of the living eye: Report of the Lang Clinical Research Scholarship, Royal London Ophthalmic Hospital. Br. J. Ophthalmol. 8(10), 467-472 (1924). 7 Friedenwald H, Friedenwald JS. Epithelial dystrophy of he cornea. Br. J. Ophthalmol. 9(1), 14-20 (1925).
-
(1925)
Br J Ophthalmol
, vol.9
, Issue.1
, pp. 14-20
-
-
Friedenwald, H.1
Friedenwald, J.S.2
-
8
-
-
0017895893
-
Corneal endothelial dystrophy. A study of 64 families
-
Krachmer JH, Purcell JJ Jr, Young CW, Bucher KD. Corneal endothelial dystrophy: A study of 64 families. Arch. Ophthalmol. 96(11), 2036-2039 (1978). (Pubitemid 8404086)
-
(1978)
Archives of Ophthalmology
, vol.96
, Issue.11
, pp. 2036-2039
-
-
Krachmer, J.H.1
Purcell Jr., J.J.2
Young, C.W.3
Bucher, K.D.4
-
9
-
-
0014186785
-
Central cornea guttata Incidence in the general population
-
Lorenzetti DW, Uotila MH, Parikh N, Kaufman HE. Central cornea guttata. Incidence in the general population. Am. J. Ophthalmol. 64(6), 1155-1158 (1967).
-
(1967)
Am. J. Ophthalmol.
, vol.64
, Issue.6
, pp. 1155-1158
-
-
Lorenzetti, D.W.1
Uotila, M.H.2
Parikh, N.3
Kaufman, H.E.4
-
10
-
-
33645353332
-
Prevalence and risk factors for cornea guttata in the Reykjavik Eye Study
-
Zoega GM, Fujisawa A, Sasaki H et al. Prevalence and risk factors for cornea guttata in the Reykjavik Eye Study. Ophthalmology 113(4), 565-569 (2006).
-
(2006)
Ophthalmology
, vol.113
, Issue.4
, pp. 565-569
-
-
Zoega, G.M.1
Fujisawa, A.2
Sasaki, H.3
-
11
-
-
84862808816
-
Prevalence and severity of Fuchs corneal dystrophy in tangier island
-
Eghrari AO, McGlumphy EJ, Iliff BW et al. Prevalence and severity of Fuchs corneal dystrophy in tangier island. Am. J. Ophthalmol. 153(6), 1067-1072 (2012).
-
(2012)
Am. J. Ophthalmol.
, vol.153
, Issue.6
, pp. 1067-1072
-
-
Eghrari, A.O.1
McGlumphy, E.J.2
Iliff, B.W.3
-
12
-
-
0036020401
-
Prevalence of primary cornea guttata and morphology of corneal endothelium in aging Japanese and Singaporean subjects
-
DOI 10.1159/000063656
-
Kitagawa K, Kojima M, Sasaki H et al. Prevalence of primary cornea guttata and morphology of corneal endothelium in aging Japanese and Singaporean subjects. Ophthalmic Res. 34(3), 135-138 (2002). (Pubitemid 34827813)
-
(2002)
Ophthalmic Research
, vol.34
, Issue.3
, pp. 135-138
-
-
Kitagawa, K.1
Kojima, M.2
Sasaki, H.3
Shui, Y.-B.4
Chew, S.J.5
Cheng, H.-M.6
Ono, M.7
Morikawa, Y.8
Sasaki, K.9
-
13
-
-
0000555262
-
The endothelium of the cornea and its clinical implications
-
Stocker FW. The endothelium of the cornea and its clinical implications. Trans. Am. Ophthalmol. Soc. 51, 669-786 (1953).
-
(1953)
Trans. Am. Ophthalmol. Soc.
, vol.51
, pp. 669-786
-
-
Stocker, F.W.1
-
14
-
-
3242720087
-
Fuchs's epithelial dystrophy of the cornea
-
Doggart JH. Fuchs's epithelial dystrophy of the cornea. Br. J. Ophthalmol. 41(9), 533-540 (1957).
-
(1957)
Br. J. Ophthalmol.
, vol.41
, Issue.9
, pp. 533-540
-
-
Doggart, J.H.1
-
15
-
-
84856494249
-
A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability
-
FECD Genetics Multi-Center Study Group.
-
Louttit MD, Kopplin LJ, Igo RP Jr et al.; FECD Genetics Multi-Center Study Group. A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability. Cornea 31(1), 26-35 (2012).
-
(2012)
Cornea
, vol.31
, Issue.1
, pp. 26-35
-
-
Louttit, M.D.1
Kopplin, L.J.2
Igo Jr., R.P.3
-
16
-
-
0014975542
-
Electron microscopic studies on Fuchs' combined dystrophy: I Posterior portion of the cornea
-
Iwamoto T, DeVoe AG. Electron microscopic studies on Fuchs' combined dystrophy: I. Posterior portion of the cornea. Invest. Ophthalmol. 10(1), 9-28 (1971).
-
(1971)
Invest. Ophthalmol.
, vol.10
, Issue.1
, pp. 9-28
-
-
Iwamoto, T.1
DeVoe, A.G.2
-
18
-
-
0023712886
-
Endothelial function and aqueous humor flow rate in patients with Fuchs' dystrophy
-
Wilson SE, Bourne WM, O'Brien PC, Brubaker RF. Endothelial function and aqueous humor flow rate in patients with Fuchs' dystrophy. Am. J. Ophthalmol. 106(3), 270-278 (1988).
-
(1988)
Am. J. Ophthalmol.
, vol.106
, Issue.3
, pp. 270-278
-
-
Wilson, S.E.1
Bourne, W.M.2
O'Brien, P.C.3
Brubaker, R.F.4
-
19
-
-
0021806620
-
Pump function of the human corneal endothelium. Effects of age and cornea guttata
-
Geroski DH, Matsuda M, Yee RW, Edelhauser HF. Pump function of the human corneal endothelium. Effects of age and cornea guttata. Ophthalmology 92(6), 759-763 (1985). (Pubitemid 15060003)
-
(1985)
Ophthalmology
, vol.92
, Issue.6
, pp. 759-763
-
-
Geroski, D.H.1
Matsuda, M.2
Yee, R.W.3
Edelhauser, H.F.4
-
20
-
-
0023553088
-
ATPase pump site density in human dysfunctional corneal endothelium
-
McCartney MD, Robertson DP, Wood TO, McLaughlin BJ. ATPase pump site density in human dysfunctional corneal endothelium. Invest. Ophthalmol. Vis. Sci. 28(12), 1955-1962 (1987). (Pubitemid 18019953)
-
(1987)
Investigative Ophthalmology and Visual Science
, vol.28
, Issue.12
, pp. 1955-1962
-
-
McCartney, M.D.1
Robertson, D.P.2
Wood, T.O.3
McLaughlin, B.J.4
-
22
-
-
84860009374
-
Relationship of Fuchs endothelial corneal dystrophy severity to central corneal thickness
-
Fuchs' Endothelial Corneal Dystrophy Genetics Multi-Center Study Group
-
Kopplin LJ, Przepyszny K, Schmotzer B et al.; Fuchs' Endothelial Corneal Dystrophy Genetics Multi-Center Study Group. Relationship of Fuchs endothelial corneal dystrophy severity to central corneal thickness. Arch. Ophthalmol. 130(4), 433-439 (2012).
-
(2012)
Arch. Ophthalmol.
, vol.130
, Issue.4
, pp. 433-439
-
-
Kopplin, L.J.1
Przepyszny, K.2
Schmotzer, B.3
-
23
-
-
0002266448
-
The fine structure of the cornea in Fuchs' endothelial dystrophy
-
Kayes J, Holmberg A. The fine structure of the cornea in Fuchs' endothelial dystrophy. Invest. Ophthalmol. 3, 47-67 (1964).
-
(1964)
Invest. Ophthalmol.
, vol.3
, pp. 47-67
-
-
Kayes, J.1
Holmberg, A.2
-
24
-
-
33644843021
-
Linkage of late-onset fuchs corneal dystrophy to a novel locus at 13pTel-13q12.13
-
DOI 10.1167/iovs.05-0578
-
Sundin OH, Jun AS, Broman KW et al. Linkage of late-onset Fuchs corneal dystrophy to a novel locus at 13pTel- 13q12.13. Invest. Ophthalmol. Vis. Sci. 47(1), 140-145 (2006). (Pubitemid 46780806)
-
(2006)
Investigative Ophthalmology and Visual Science
, vol.47
, Issue.1
, pp. 140-145
-
-
Sundin, O.H.1
Jun, A.S.2
Broman, K.W.3
Liu, S.H.4
Sheehan, S.E.5
Vito, E.C.L.6
Stark, W.J.7
Gottsch, J.D.8
-
25
-
-
33749148802
-
A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32
-
DOI 10.1167/iovs.05-1619
-
Sundin OH, Broman KW, Chang HH, Vito EC, Stark WJ, Gottsch JD. A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32. Invest. Ophthalmol. Vis. Sci. 47(9), 3919-3926 (2006). (Pubitemid 46044307)
-
(2006)
Investigative Ophthalmology and Visual Science
, vol.47
, Issue.9
, pp. 3919-3926
-
-
Sundin, O.H.1
Broman, K.W.2
Chang, H.H.3
Vito, E.C.L.4
Stark, W.J.5
Gottsch, J.D.6
-
26
-
-
79955968131
-
Age-severity relationships in families linked to FCD2 with retroillumination photography
-
McGlumphy EJ, Yeo WS, Riazuddin SA et al. Age-severity relationships in families linked to FCD2 with retroillumination photography. Invest. Ophthalmol. Vis. Sci. 51(12), 6298-6302 (2010).
-
(2010)
Invest. Ophthalmol. Vis. Sci.
, vol.51
, Issue.12
, pp. 6298-6302
-
-
McGlumphy, E.J.1
Yeo, W.S.2
Riazuddin, S.A.3
-
27
-
-
73149123913
-
Linkage of a mild late-onset phenotype of Fuchs corneal dystrophy to a novel locus at 5q33.1-q35.2
-
Riazuddin SA, Eghrari AO, Al-Saif A et al. Linkage of a mild late-onset phenotype of Fuchs corneal dystrophy to a novel locus at 5q33.1-q35.2. Invest. Ophthalmol. Vis. Sci. 50(12), 5667-5671 (2009).
-
(2009)
Invest. Ophthalmol. Vis. Sci.
, vol.50
, Issue.12
, pp. 5667-5671
-
-
Riazuddin, S.A.1
Eghrari, A.O.2
Al-Saif, A.3
-
28
-
-
73149085311
-
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p
-
Riazuddin SA, Zaghloul NA, Al-Saif A et al. Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. Am. J. Hum. Genet. 86(1), 45-53 (2010).
-
(2010)
Am. J. Hum. Genet.
, vol.86
, Issue.1
, pp. 45-53
-
-
Riazuddin, S.A.1
Zaghloul, N.A.2
Al-Saif, A.3
-
29
-
-
27244444742
-
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells
-
DOI 10.1086/497348
-
Krafchak CM, Pawar H, Moroi SE et al. Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells. Am. J. Hum. Genet. 77(5), 694-708 (2005). (Pubitemid 41513274)
-
(2005)
American Journal of Human Genetics
, vol.77
, Issue.5
, pp. 694-708
-
-
Krafchak, C.M.1
Pawar, H.2
Moroi, S.E.3
Sugar, A.4
Lichter, P.R.5
Mackey, D.A.6
Mian, S.7
Nairus, T.8
Elner, V.9
Schteingart, M.T.10
Downs, C.A.11
Kijek, T.G.12
Johnson, J.M.13
Trager, E.H.14
Rozsa, F.W.15
Mandal, N.A.16
Epstein, M.P.17
Vollrath, D.18
Ayyagari, R.19
Boehnke, M.20
Richards, J.E.21
more..
-
30
-
-
62649145581
-
Genomewide linkage scan in Fuchs endothelial corneal dystrophy
-
Afshari NA, Li YJ, Pericak-Vance MA, Gregory S, Klintworth GK. Genomewide linkage scan in Fuchs endothelial corneal dystrophy. Invest. Ophthalmol. Vis. Sci. 50(3), 1093-1097 (2009).
-
(2009)
Invest. Ophthalmol. Vis. Sci.
, vol.50
, Issue.3
, pp. 1093-1097
-
-
Afshari, N.A.1
Li, Y.J.2
Pericak-Vance, M.A.3
Gregory, S.4
Klintworth, G.K.5
-
31
-
-
79955454681
-
Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy
-
Li YJ, Minear MA, Rimmler J et al. Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. PLoS ONE 6(4), e18044 (2011).
-
(2011)
PLoS ONE
, vol.6
, Issue.4
-
-
Li, Y.J.1
Minear, M.A.2
Rimmler, J.3
-
32
-
-
39549098200
-
Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophy
-
Mehta JS, Vithana EN, Tan DT et al. Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophy. Invest. Ophthalmol. Vis. Sci. 49(1), 184-188 (2008).
-
(2008)
Invest. Ophthalmol. Vis. Sci.
, vol.49
, Issue.1
, pp. 184-188
-
-
Mehta, J.S.1
Vithana, E.N.2
Tan, D.T.3
-
33
-
-
73449124813
-
Phenotypic characterisation and ZEB1 mutational analysis in posterior polymorphous corneal dystrophy in a New Zealand population
-
Vincent AL, Niederer RL, Richards A, Karolyi B, Patel DV, McGhee CN. Phenotypic characterisation and ZEB1 mutational analysis in posterior polymorphous corneal dystrophy in a New Zealand population. Mol. Vis. 15, 2544-2553 (2009).
-
(2009)
Mol. Vis.
, vol.15
, pp. 2544-2553
-
-
Vincent, A.L.1
Niederer, R.L.2
Richards, A.3
Karolyi, B.4
Patel, D.V.5
McGhee, C.N.6
-
34
-
-
85047686830
-
Analysis of the role of ZEB1 in the pathogenesis of posterior polymorphous corneal dystrophy
-
Yellore VS, Rayner SA, Nguyen CK et al. Analysis of the role of ZEB1 in the pathogenesis of posterior polymorphous corneal dystrophy. Invest. Ophthalmol. Vis. Sci. 53(1), 273-278 (2012).
-
(2012)
Invest. Ophthalmol. Vis. Sci.
, vol.53
, Issue.1
, pp. 273-278
-
-
Yellore, V.S.1
Rayner, S.A.2
Nguyen, C.K.3
-
35
-
-
0037311473
-
Serial analysis of gene expression in the corneal endothelium of Fuchs' dystrophy
-
DOI 10.1167/iovs.02-0300
-
Gottsch JD, Bowers AL, Margulies EH et al. Serial analysis of gene expression in the corneal endothelium of Fuchs' dystrophy. Invest. Ophthalmol. Vis. Sci. 44(2), 594-599 (2003). (Pubitemid 36159704)
-
(2003)
Investigative Ophthalmology and Visual Science
, vol.44
, Issue.2
, pp. 594-599
-
-
Gottsch, J.D.1
Bowers, A.L.2
Margulies, E.H.3
Seitzman, G.D.4
Kim, S.W.5
Saba, S.6
Jun, A.S.7
Stark, W.J.8
Liu, S.H.9
-
36
-
-
33745544253
-
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
-
DOI 10.1038/ng1824, PII N1824
-
Vithana EN, Morgan P, Sundaresan P et al. Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2). Nat. Genet. 38(7), 755-757 (2006). (Pubitemid 43980595)
-
(2006)
Nature Genetics
, vol.38
, Issue.7
, pp. 755-757
-
-
Vithana, E.N.1
Morgan, P.2
Sundaresan, P.3
Ebenezer, N.D.4
Tan, D.T.H.5
Mohamed, M.D.6
Anand, S.7
Khine, K.O.8
Venkataraman, D.9
Yong, V.H.K.10
Salto-Tellez, M.11
Venkatraman, A.12
Guo, K.13
Hemadevi, B.14
Srinivasan, M.15
Prajna, V.16
Khine, M.17
Casey, J.R.18
Inglehearn, C.F.19
Aung, T.20
more..
-
37
-
-
34248332574
-
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy
-
DOI 10.1136/jmg.2006.046904
-
Desir J, Moya G, Reish O et al. Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy. J. Med. Genet. 44(5), 322-326 (2007). (Pubitemid 46732626)
-
(2007)
Journal of Medical Genetics
, vol.44
, Issue.5
, pp. 322-326
-
-
Desir, J.1
Moya, G.2
Reish, O.3
Van Regemorter, N.4
Deconinck, H.5
David, K.L.6
Meire, F.M.7
Abramowicz, M.J.8
-
38
-
-
39749109494
-
SLC4A11 mutations in Fuchs endothelial corneal dystrophy
-
DOI 10.1093/hmg/ddm337
-
Vithana EN, Morgan PE, Ramprasad V et al. SLC4A11 mutations in Fuchs endothelial corneal dystrophy. Hum. Mol. Genet. 17(5), 656-666 (2008). (Pubitemid 351292255)
-
(2008)
Human Molecular Genetics
, vol.17
, Issue.5
, pp. 656-666
-
-
Vithana, E.N.1
Morgan, P.E.2
Ramprasad, V.3
Tan, D.T.H.4
Yong, V.H.K.5
Venkataraman, D.6
Venkatraman, A.7
Yam, G.H.F.8
Nagasamy, S.9
Law, R.W.K.10
Rajagopal, R.11
Pang, C.P.12
Kumaramanickevel, G.13
Casey, J.R.14
Aung, T.15
-
39
-
-
78049435712
-
Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy
-
Riazuddin SA, Vithana EN, Seet LF et al. Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy. Hum. Mutat. 31(11), 1261-1268 (2010).
-
(2010)
Hum. Mutat.
, vol.31
, Issue.11
, pp. 1261-1268
-
-
Riazuddin, S.A.1
Vithana, E.N.2
Seet, L.F.3
-
40
-
-
84861974117
-
Depletion of SLC4A11 causes cell death by apoptosis in an immortalized human corneal endothelial cell line
-
Liu J, Seet LF, Koh LW et al. Depletion of SLC4A11 causes cell death by apoptosis in an immortalized human corneal endothelial cell line. Invest. Ophthalmol. Vis. Sci. 53(7), 3270-3279 (2012).
-
(2012)
Invest. Ophthalmol. Vis. Sci.
, vol.53
, Issue.7
, pp. 3270-3279
-
-
Liu, J.1
Seet, L.F.2
Koh, L.W.3
-
41
-
-
84858080556
-
Mutations in LOXHD1, a recessivedeafness locus, cause dominant late-onset Fuchs corneal dystrophy
-
Riazuddin SA, Parker DS, McGlumphy EJ et al. Mutations in LOXHD1, a recessivedeafness locus, cause dominant late-onset Fuchs corneal dystrophy. Am. J. Hum. Genet. 90(3), 533-539 (2012).
-
(2012)
Am. J. Hum. Genet.
, vol.90
, Issue.3
, pp. 533-539
-
-
Riazuddin, S.A.1
Parker, D.S.2
McGlumphy, E.J.3
-
42
-
-
77956521660
-
E2-2 protein and Fuchs's corneal dystrophy
-
Baratz KH, Tosakulwong N, Ryu E et al. E2-2 protein and Fuchs's corneal dystrophy. N. Engl. J. Med. 363(11), 1016-1024 (2010).
-
(2010)
N. Engl. J. Med.
, vol.363
, Issue.11
, pp. 1016-1024
-
-
Baratz, K.H.1
Tosakulwong, N.2
Ryu, E.3
-
43
-
-
79955437761
-
Replication of the TCF4 intronic variant in late-onset Fuchs corneal dystrophy and evidence of independence from the FCD2 locus
-
Riazuddin SA, McGlumphy EJ, Yeo WS, Wang J, Katsanis N, Gottsch JD. Replication of the TCF4 intronic variant in late-onset Fuchs corneal dystrophy and evidence of independence from the FCD2 locus. Invest. Ophthalmol. Vis. Sci. 52(5), 2825-2829 (2011).
-
(2011)
Invest. Ophthalmol. Vis. Sci.
, vol.52
, Issue.5
, pp. 2825-2829
-
-
Riazuddin, S.A.1
McGlumphy, E.J.2
Yeo, W.S.3
Wang, J.4
Katsanis, N.5
Gottsch, J.D.6
-
44
-
-
84863411278
-
Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process
-
Kuot A, Hewitt AW, Griggs K et al. Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process. Eur. J. Hum. Genet. 20(6), 632-638 (2012).
-
(2012)
Eur. J. Hum. Genet.
, vol.20
, Issue.6
, pp. 632-638
-
-
Kuot, A.1
Hewitt, A.W.2
Griggs, K.3
-
45
-
-
80053302726
-
Association of TCF4 gene polymorphisms with Fuchs' corneal dystrophy in the Chinese
-
Thalamuthu A, Khor CC, Venkataraman D et al. Association of TCF4 gene polymorphisms with Fuchs' corneal dystrophy in the Chinese. Invest. Ophthalmol. Vis. Sci. 52(8), 5573-5578 (2011).
-
(2011)
Invest. Ophthalmol. Vis. Sci.
, vol.52
, Issue.8
, pp. 5573-5578
-
-
Thalamuthu, A.1
Khor, C.C.2
Venkataraman, D.3
-
46
-
-
0026650896
-
Competition between cell-substratum interactions and cell-cell interactions
-
Tung PS, Burdzy K, Wong K, Fritz IB. Competition between cell-substratum interactions and cell-cell interactions. J. Cell. Physiol. 152(2), 410-421 (1992).
-
(1992)
J. Cell. Physiol.
, vol.152
, Issue.2
, pp. 410-421
-
-
Tung, P.S.1
Burdzy, K.2
Wong, K.3
Fritz, I.B.4
-
47
-
-
48249126412
-
Increased clusterin expression in Fuchs' endothelial dystrophy
-
Jurkunas UV, Bitar MS, Rawe I, Harris DL, Colby K, Joyce NC. Increased clusterin expression in Fuchs' endothelial dystrophy. Invest. Ophthalmol. Vis. Sci. 49(7), 2946-2955 (2008).
-
(2008)
Invest. Ophthalmol. Vis. Sci.
, vol.49
, Issue.7
, pp. 2946-2955
-
-
Jurkunas, U.V.1
Bitar, M.S.2
Rawe, I.3
Harris, D.L.4
Colby, K.5
Joyce, N.C.6
-
48
-
-
0029762295
-
βig-h3 is synthesized by corneal epithelium and perhaps endothelium in Fuchs' dystrophic corneas
-
Hirano K, Klintworth GK, Zhan Q, Bennett K, Cintron C. β Ig-h3 is synthesized by corneal epithelium and perhaps endotheliumin Fuchs' dystrophic corneas. Curr. Eye Res. 15(9), 965-972 (1996). (Pubitemid 26332236)
-
(1996)
Current Eye Research
, vol.15
, Issue.9
, pp. 965-972
-
-
Hirano, K.1
Klintworth, G.K.2
Zhan, Q.3
Bennett, K.4
Cintron, C.5
-
49
-
-
0031020733
-
Kerato-epithelin mutations in four 5q31-linked corneal dystrophies
-
DOI 10.1038/ng0397-247
-
Munier FL, Korvatska E, Djemai A et al. Kerato-epithelin mutations in four 5q31-linked corneal dystrophies. Nat. Genet. 15(3), 247-251 (1997). (Pubitemid 27098716)
-
(1997)
Nature Genetics
, vol.15
, Issue.3
, pp. 247-251
-
-
Munier, F.L.1
Korvatska, E.2
Djemai, A.3
Le Paslier, D.4
Zografos, L.5
Pescia, G.6
Schorderet, D.F.7
-
50
-
-
62649086642
-
Colocalization of increased transforming growth factor-β-induced protein (TGFBIp) and Clusterin in Fuchs endothelial corneal dystrophy
-
Jurkunas UV, Bitar M, Rawe I. Colocalization of increased transforming growth factor-β-induced protein (TGFBIp) and Clusterin in Fuchs endothelial corneal dystrophy. Invest. Ophthalmol. Vis. Sci. 50(3), 1129-1136 (2009).
-
(2009)
Invest. Ophthalmol. Vis. Sci.
, vol.50
, Issue.3
, pp. 1129-1136
-
-
Jurkunas, U.V.1
Bitar, M.2
Rawe, I.3
-
51
-
-
73349102508
-
Progression of Fuchs corneal dystrophy in a family linked to the FCD1 locus
-
Meadows DN, Eghrari AO, Riazuddin SA, Emmert DG, Katsanis N, Gottsch JD. Progression of Fuchs corneal dystrophy in a family linked to the FCD1 locus. Invest. Ophthalmol. Vis. Sci. 50(12), 5662-5666 (2009).
-
(2009)
Invest. Ophthalmol. Vis. Sci.
, vol.50
, Issue.12
, pp. 5662-5666
-
-
Meadows, D.N.1
Eghrari, A.O.2
Riazuddin, S.A.3
Emmert, D.G.4
Katsanis, N.5
Gottsch, J.D.6
-
52
-
-
0035504694
-
Missense mutations in COL8A2, the gene encoding the α2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy
-
Biswas S, Munier FL, Yardley J et al. Missense mutations in COL8A2, the gene encoding the a2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy. Hum. Mol. Genet. 10(21), 2415-2423 (2001). (Pubitemid 33069547)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.21
, pp. 2415-2423
-
-
Biswas, S.1
Munier, F.L.2
Yardley, J.3
Hart-Holden, N.4
Perveen, R.5
Cousin, P.6
Sutphin, J.E.7
Noble, B.8
Batterbury, M.9
Kielty, C.10
Hackett, A.11
Bonshek, R.12
Ridgway, A.13
McLeod, D.14
Sheffield, V.C.15
Stone, E.M.16
Schorderet, D.F.17
Black, G.C.M.18
-
53
-
-
2542462332
-
Analysis of COL8A2 gene mutation in Japanese patients with Fuchs' endothelial dystrophy and posterior polymorphous dystrophy
-
DOI 10.1007/s10384-003-0063-6
-
Kobayashi A, Fujiki K, Murakami A et al. Analysis of COL8A2 gene mutation in Japanese patients with Fuchs' endothelial dystrophy and posterior polymorphous dystrophy. Jpn. J. Ophthalmol. 48(3), 195-198 (2004). (Pubitemid 38691425)
-
(2004)
Japanese Journal of Ophthalmology
, vol.48
, Issue.3
, pp. 195-198
-
-
Kobayashi, A.1
Fujiki, K.2
Murakami, A.3
Kato, T.4
Chen, L.-Z.5
Onoe, H.6
Nakayasu, K.7
Sakurai, M.8
Takahashi, M.9
Sugiyama, K.10
Kanai, A.11
-
54
-
-
65349126473
-
Q455V mutation in COL8A2 is associated with Fuchs' corneal dystrophy in Korean patients
-
Mok JW, Kim HS, Joo CK. Q455V mutation in COL8A2 is associated with Fuchs' corneal dystrophy in Korean patients. Eye (Lond.) 23(4), 895-903 (2009).
-
(2009)
Eye (Lond.
, vol.23
, Issue.4
, pp. 895-903
-
-
Mok, J.W.1
Kim, H.S.2
Joo, C.K.3
-
55
-
-
22144445323
-
Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of Fuchs corneal dystrophy
-
Gottsch JD, Sundin OH, Liu SH et al. Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of Fuchs corneal dystrophy. Invest. Ophthalmol. Vis. Sci. 46(6), 1934-1939 (2005).
-
(2005)
Invest. Ophthalmol. Vis. Sci.
, vol.46
, Issue.6
, pp. 1934-1939
-
-
Gottsch, J.D.1
Sundin, O.H.2
Liu, S.H.3
-
56
-
-
0018606624
-
Inheritance of Fuchs' combined dystrophy
-
Magovern M, Beauchamp GR, McTigue JW, Fine BS, Baumiller RC. Inheritance of Fuchs' combined dystrophy. Ophthalmology 86(10), 1897-1923 (1979).
-
(1979)
Ophthalmology
, vol.86
, Issue.10
, pp. 1897-1923
-
-
Magovern, M.1
Beauchamp, G.R.2
McTigue, J.W.3
Fine, B.S.4
Baumiller, R.C.5
-
57
-
-
36749018104
-
British family with early-onset Fuchs' endothelial corneal dystrophy associated with p.L450W mutation in the COL8A2 gene [8]
-
DOI 10.1136/bjo.2007.115154
-
Liskova P, Prescott Q, Bhattacharya SS, Tuft SJ. British family with early-onset Fuchs' endothelial corneal dystrophy associated with p.L450W mutation in the COL8A2 gene. Br. J. Ophthalmol. 91(12), 1717-1718 (2007). (Pubitemid 350207412)
-
(2007)
British Journal of Ophthalmology
, vol.91
, Issue.12
, pp. 1717-1718
-
-
Liskova, P.1
Prescott, Q.2
Bhattacharya, S.S.3
Tuft, S.J.4
-
58
-
-
33644815534
-
Fuchs corneal dystrophy: Aberrant collagen distribution in an L450W Mutant of the COL8A2 gene
-
DOI 10.1167/iovs.05-0497
-
Gottsch JD, Zhang C, Sundin OH, Bell WR, Stark WJ, Green WR. Fuchs corneal dystrophy: Aberrant collagen distribution in an L450W mutant of the COL8A2 gene. Invest. Ophthalmol. Vis. Sci. 46(12), 4504-4511 (2005). (Pubitemid 44264546)
-
(2005)
Investigative Ophthalmology and Visual Science
, vol.46
, Issue.12
, pp. 4504-4511
-
-
Gottsch, J.D.1
Zhang, C.2
Sundin, O.H.3
Bell, W.R.4
Stark, W.J.5
Green, W.R.6
-
59
-
-
33947708852
-
Immunohistochemistry and electron microscopy of early-onset Fuchs corneal dystrophy in three cases with the same L450W COL8A2 mutation
-
Zhang C, Bell WR, Sundin OH et al. Immunohistochemistry and electron microscopy of early-onset Fuchs corneal dystrophy in three cases with the same L450W COL8A2 mutation. Trans. Am. Ophthalmol. Soc. 104, 85-97 (2006).
-
(2006)
Trans. Am. Ophthalmol. Soc.
, vol.104
, pp. 85-97
-
-
Zhang, C.1
Bell, W.R.2
Sundin, O.H.3
-
60
-
-
0036321733
-
Endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning (EDICT) syndrome maps to chromosome 15q22.1-q25.3
-
DOI 10.1016/S0002-9394(02)01401-0, PII S0002939402014010
-
Jun AS, Broman KW, Do DV, Akpek EK, Stark WJ, Gottsch JD. Endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning (EDICT) syndrome maps to chromosome 15q22.1-q25.3. Am. J. Ophthalmol. 134(2), 172-176 (2002). (Pubitemid 34831819)
-
(2002)
American Journal of Ophthalmology
, vol.134
, Issue.2
, pp. 172-176
-
-
Jun, A.S.1
Broman, K.W.2
Do, D.V.3
Akpek, E.K.4
Stark, W.J.5
Gottsch, J.D.6
-
61
-
-
0036188164
-
Clinical and ultrastructural features of a novel hereditary anterior segment dysgenesis
-
DOI 10.1016/S0161-6420(01)00975-7, PII S0161642001009757
-
Akpek EK, Jun AS, Goodman DF, Green WR, Gottsch JD. Clinical and ultrastructural features of a novel hereditary anterior segment dysgenesis. Ophthalmology 109(3), 513-519 (2002). (Pubitemid 34184918)
-
(2002)
Ophthalmology
, vol.109
, Issue.3
, pp. 513-519
-
-
Karamursel Akpek, E.1
Jun, A.S.2
Goodman, D.F.3
Green W.Richard4
Gottsch, J.D.5
-
62
-
-
84859241050
-
A single-base substitution in the seed region of miR-184 causes EDICT syndrome
-
Iliff BW, Riazuddin SA, Gottsch JD. A single-base substitution in the seed region of miR-184 causes EDICT syndrome. Invest. Ophthalmol. Vis. Sci. 53(1), 348-353 (2012).
-
(2012)
Invest. Ophthalmol. Vis. Sci.
, vol.53
, Issue.1
, pp. 348-353
-
-
Iliff, B.W.1
Riazuddin, S.A.2
Gottsch, J.D.3
-
63
-
-
0344442775
-
Snowflake Vitreoretinal Degeneration: Follow-up of the Original Family
-
DOI 10.1016/S0161-6420(03)00828-5
-
Lee MM, Ritter R 3rd, Hirose T, Vu CD, Edwards AO. Snowflake vitreoretinal degeneration: Follow-up of the original family. Ophthalmology 110(12), 2418-2426 (2003). (Pubitemid 37485175)
-
(2003)
Ophthalmology
, vol.110
, Issue.12
, pp. 2418-2426
-
-
Lee, M.M.1
Ritter III, R.2
Hirose, T.3
Vu, C.D.4
Edwards, A.O.5
-
64
-
-
38749087988
-
Mutations in KCNJ13 Cause Autosomal-Dominant Snowflake Vitreoretinal Degeneration
-
DOI 10.1016/j.ajhg.2007.08.002, PII S0002929707000031
-
Hejtmancik JF, Jiao X, Li A et al. Mutations in KCNJ13 cause autosomaldominant snowflake vitreoretinal degeneration. Am. J. Hum. Genet. 82(1), 174-180 (2008). (Pubitemid 351726076)
-
(2008)
American Journal of Human Genetics
, vol.82
, Issue.1
, pp. 174-180
-
-
Hejtmancik, J.F.1
Jiao, X.2
Li, A.3
Sergeev, Y.V.4
Ding, X.5
Sharma, A.K.6
Chan, C.-C.7
Medina, I.8
Edwards, A.O.9
-
65
-
-
0022653913
-
Family cases of Harboyan syndrome
-
Nemoto S. Family cases of Harboyan syndrome. Jibiinkoka 58, 161-165 (1986). (Pubitemid 16164810)
-
(1986)
Otolaryngology
, vol.58
, Issue.3
, pp. 161-165
-
-
Nemoto, S.1
-
66
-
-
0030872290
-
A further observation of corneal dystrophy and perceptive deafness in two siblings
-
Magli A, Capasso L, Foa T, Maurino V, Ventruto V. A further observation of corneal dystrophy and perceptive deafness in two siblings. Ophthalmic Genet. 18(2), 87-91 (1997). (Pubitemid 27338829)
-
(1997)
Ophthalmic Genetics
, vol.18
, Issue.2
, pp. 87-91
-
-
Magli, A.1
Capasso, L.2
Foa, T.3
Maurino, V.4
Ventruto, V.5
-
67
-
-
0031762371
-
Congenital corneal dystrophy and progressive sensorineural hearing loss (Harboyan syndrome) [1]
-
DOI 10.1002/(SICI)1096-8628(19981102)80:2<177::AID-AJMG17>3.0.CO;2- D
-
Puga AC, Nogueira AH, Felix TM, Kwitko S. Congenital corneal dystrophy and progressive sensorineural hearing loss (Harboyan syndrome). Am. J. Med. Genet. 80(2), 177-179 (1998). (Pubitemid 28485701)
-
(1998)
American Journal of Medical Genetics
, vol.80
, Issue.2
, pp. 177-179
-
-
Puga, A.C.S.1
Nogueira, A.H.H.2
Felix, T.M.3
Kwitko, S.4
-
68
-
-
0036166254
-
Corneal dystrophy and perceptive deafness (Harboyan syndrome): CDPD 1 maps to 20p13
-
Abramowicz MJ, Albuquerque-Silva J, Zanen A. Corneal dystrophy and perceptive deafness (Harboyan syndrome): CDPD1 maps to 20p13. J. Med. Genet. 39(2), 110-112 (2002). (Pubitemid 34146379)
-
(2002)
Journal of Medical Genetics
, vol.39
, Issue.2
, pp. 110-112
-
-
Abramowicz, M.J.1
Albuquerque-Silva, J.2
Zanen, A.3
-
69
-
-
8644251840
-
+-coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation
-
DOI 10.1016/j.molcel.2004.09.030, PII S1097276504005829
-
Park M, Li Q, Shcheynikov N, Zeng W, Muallem S. NaBC1 is a ubiquitous electrogenic Na+-coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation. Mol. Cell 16(3), 331-341 (2004). (Pubitemid 39504788)
-
(2004)
Molecular Cell
, vol.16
, Issue.3
, pp. 331-341
-
-
Park, M.1
Li, Q.2
Shcheynikov, N.3
Zeng, W.4
Muallem, S.5
-
70
-
-
0034049278
-
The development of the stria vascularis in the human foetus
-
DOI 10.1046/j.1365-2273.2000.00340.x
-
Bibas A, Liang J, Michaels L, Wright A. The development of the stria vascularis in the human foetus. Clin. Otolaryngol. Allied Sci. 25(2), 126-129 (2000). (Pubitemid 30216125)
-
(2000)
Clinical Otolaryngology and Allied Sciences
, vol.25
, Issue.2
, pp. 126-129
-
-
Bibas, A.1
Liang, J.2
Michaels, L.3
Wright, A.4
-
72
-
-
18144366547
-
Differential expression of genes within the cochlea as defined by a custom mouse inner ear microarray
-
DOI 10.1007/s10162-004-5046-x
-
Morris KA, Snir E, Pompeia C et al. Differential expression of genes within the cochlea as defined by a custom mouse inner ear microarray. J. Assoc. Res. Otolaryngol. 6(1), 75-89 (2005). (Pubitemid 40616506)
-
(2005)
JARO - Journal of the Association for Research in Otolaryngology
, vol.6
, Issue.1
, pp. 75-89
-
-
Morris, K.A.1
Snir, E.2
Pompeia, C.3
Koroleva, I.V.4
Kachar, B.5
Hayashizaki, Y.6
Carninci, P.7
Soares, M.B.8
Beisel, K.W.9
-
73
-
-
77957785425
-
Ion homeostasis in the ear: mechanisms, maladies, and management
-
Trune DR. Ion homeostasis in the ear: mechanisms, maladies, and management. Curr. Opin. Otolaryngol. Head Neck Surg. 18(5), 413-419 (2010).
-
(2010)
Curr. Opin. Otolaryngol. Head Neck Surg.
, vol.18
, Issue.5
, pp. 413-419
-
-
Trune, D.R.1
-
74
-
-
33748910482
-
Supporting sensory transduction: Cochlear fluid homeostasis and the endocochlear potential
-
Wangemann P. Supporting sensory transduction: Cochlear fluid homeostasis and the endocochlear potential. J. Physiol. (Lond.) 576(Pt 1), 11-21 (2006).
-
(2006)
J. Physiol. (Lond.
, vol.PART 1
, pp. 11-21
-
-
Wangemann, P.1
-
75
-
-
70350357319
-
Slc4a11 gene disruption in mice: Cellular targets of sensorineuronal abnormalities
-
Lopez IA, Rosenblatt MI, Kim C et al. Slc4a11 gene disruption in mice: Cellular targets of sensorineuronal abnormalities. J Biol. Chem. 284(39), 26882-26896 (2009).
-
(2009)
J Biol. Chem.
, vol.284
, Issue.39
, pp. 26882-26896
-
-
Lopez, I.A.1
Rosenblatt, M.I.2
Kim, C.3
-
76
-
-
69449086147
-
Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans
-
Grillet N, Schwander M, Hildebrand MS et al. Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans. Am. J. Hum. Genet. 85(3), 328-337 (2009).
-
(2009)
Am. J. Hum. Genet.
, vol.85
, Issue.3
, pp. 328-337
-
-
Grillet, N.1
Schwander, M.2
Hildebrand, M.S.3
-
77
-
-
79955038896
-
A deleterious mutation in the LOXHD1 gene causes autosomal recessive hearing loss in Ashkenazi Jews
-
Edvardson S, Jalas C, Shaag A et al. A deleterious mutation in the LOXHD1 gene causes autosomal recessive hearing loss in Ashkenazi Jews. Am. J. Med. Genet. A 155A(5), 1170-1172 (2011).
-
(2011)
Am. J. Med. Genet. A 155A
, vol.5
, pp. 1170-1172
-
-
Edvardson, S.1
Jalas, C.2
Shaag, A.3
-
78
-
-
0031895167
-
Fuch's corneal dystrophy in a patient with mitochondrial DNA mutations
-
Albin RL. Fuchs corneal dystrophy in a patient with mitochondrial DNA mutations. J. Med. Genet. 35(3), 258-259 (1998). (Pubitemid 28159936)
-
(1998)
Journal of Medical Genetics
, vol.35
, Issue.3
, pp. 258-259
-
-
Albin, R.L.1
-
79
-
-
81055144789
-
Hearing disability in patients with Fuchs' endothelial corneal dystrophy: unrecognized co-pathology?
-
Stehouwer M, Bijlsma WR, Van der Lelij A. Hearing disability in patients with Fuchs' endothelial corneal dystrophy: unrecognized co-pathology? Clin. Ophthalmol. 5, 1297-1301 (2011).
-
(2011)
Clin. Ophthalmol.
, vol.5
, pp. 1297-1301
-
-
Stehouwer, M.1
Bijlsma, W.R.2
Van Der Lelij, A.3
-
80
-
-
35548971958
-
Stem cell markers in the human posterior limbus and corneal endothelium of unwounded and wounded corneas
-
McGowan SL, Edelhauser HF, Pfister RR, Whikehart DR. Stem cell markers in the human posterior limbus and corneal endothelium of unwounded and wounded corneas. Mol. Vis. 13, 1984-2000 (2007). (Pubitemid 350001954)
-
(2007)
Molecular Vision
, vol.13
, pp. 1984-2000
-
-
McGowan, S.L.1
Edelhauser, H.F.2
Pfister, R.R.3
Whikehart, D.R.4
-
81
-
-
20144388095
-
DeltaEF1 is a transcriptional repressor of E-cadherin and regulates epithelial plasticity in breast cancer cells
-
DOI 10.1038/sj.onc.1208429
-
Eger A, Aigner K, Sonderegger S et al.ΔEF1 is a transcriptional repressor of E-cadherin and regulates epithelial plasticity in breast cancer cells. Oncogene 24(14), 2375-2385 (2005). (Pubitemid 40546696)
-
(2005)
Oncogene
, vol.24
, Issue.14
, pp. 2375-2385
-
-
Eger, A.1
Aigner, K.2
Sonderegger, S.3
Dampier, B.4
Oehler, S.5
Schreiber, M.6
Berx, G.7
Cano, A.8
Beug, H.9
Foisner, R.10
-
82
-
-
66849104147
-
The class I bHLH factors E2-2A and E2-2B regulate EMT
-
Sobrado VR, Moreno-Bueno G, Cubillo E et al. The class I bHLH factors E2-2A and E2-2B regulate EMT. J. Cell. Sci. 122(Pt 7), 1014-1024 (2009).
-
(2009)
J. Cell. Sci.
, vol.122
, Issue.PART 7
, pp. 1014-1024
-
-
Sobrado, V.R.1
Moreno-Bueno, G.2
Cubillo, E.3
-
83
-
-
38949174649
-
Extracellular matrix protein βig-h3/TGFBI promotes metastasis of colon cancer by enhancing cell extravasation
-
DOI 10.1101/gad.1632008
-
Ma C, Rong Y, Radiloff DR et al. Extracellular matrix protein βig-h3/TGFBI promotes metastasis of colon cancer by enhancing cell extravasation. Genes Dev. 22(3), 308-321 (2008). (Pubitemid 351214273)
-
(2008)
Genes and Development
, vol.22
, Issue.3
, pp. 308-321
-
-
Ma, C.1
Rong, Y.2
Radiloff, D.R.3
Datto, M.B.4
Centeno, B.5
Bao, S.6
Cheng, A.W.M.7
Lin, F.8
Jiang, S.9
Yeatman, T.J.10
Wang, X.-F.11
-
84
-
-
60549108144
-
Clusterin silencing in human lung adenocarcinoma cells induces a mesenchymal-to-epithelial transition through modulating the ERK/Slug pathway
-
Chou TY, Chen WC, Lee AC, Hung SM, Shih NY, Chen MY. Clusterin silencing in human lung adenocarcinoma cells induces a mesenchymal-to-epithelial transition through modulating the ERK/Slug pathway. Cell. Signal. 21(5), 704-711 (2009).
-
(2009)
Cell. Signal.
, vol.21
, Issue.5
, pp. 704-711
-
-
Chou, T.Y.1
Chen, W.C.2
Lee, A.C.3
Hung, S.M.4
Shih, N.Y.5
Chen, M.Y.6
-
85
-
-
0038179723
-
Cost of migration: Invasion of malignant gliomas and implications for treatment
-
DOI 10.1200/JCO.2003.05.063
-
Giese A, Bjerkvig R, Berens ME, Westphal M. Cost of migration: Invasion of malignant gliomas and implications for treatment. J. Clin. Oncol. 21(8), 1624-1636 (2003). (Pubitemid 46594118)
-
(2003)
Journal of Clinical Oncology
, vol.21
, Issue.8
, pp. 1624-1636
-
-
Giese, A.1
Bjerkvig, R.2
Berens, M.E.3
Westphal, M.4
-
86
-
-
0037728809
-
The protein kinase Akt induces epithelial mesenchymal transition and promotes enhanced motility and invasiveness of squamous cell carcinoma lines
-
Grille SJ, Bellacosa A, Upson J et al. The protein kinase Akt induces epithelial-mesenchymal transition and promotes enhanced motility and invasiveness of squamous cell carcinoma lines. Cancer Res. 63(9), 2172-2178 (2003). (Pubitemid 36538623)
-
(2003)
Cancer Research
, vol.63
, Issue.9
, pp. 2172-2178
-
-
Grille, S.J.1
Bellacosa, A.2
Upson, J.3
Klein-Szanto, A.J.4
Van Roy, F.5
Lee-Kwon, W.6
Donowitz, M.7
Tsichlis, P.N.8
Larue, L.9
-
87
-
-
67651160305
-
PTEN and SHIP2 regulates PI3K/Akt pathway through focal adhesion kinase
-
Gupta A, Dey CS. PTEN and SHIP2 regulates PI3K/Akt pathway through focal adhesion kinase. Mol. Cell. Endocrinol. 309(1-2), 55-62 (2009).
-
(2009)
Mol. Cell. Endocrinol.
, vol.309
, Issue.1-2
, pp. 55-62
-
-
Gupta, A.1
Dey, C.S.2
-
88
-
-
77957853315
-
MicroRNA-205 promotes keratinocyte migration via the lipid phosphatase SHIP2
-
Yu J, Peng H, Ruan Q, Fatima A, Getsios S, Lavker RM. MicroRNA-205 promotes keratinocyte migration via the lipid phosphatase SHIP2. FASEB J. 24(10), 3950-3959 (2010).
-
(2010)
FASEB J.
, vol.24
, Issue.10
, pp. 3950-3959
-
-
Yu, J.1
Peng, H.2
Ruan, Q.3
Fatima, A.4
Getsios, S.5
Lavker, R.M.6
-
89
-
-
43049103824
-
The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1
-
DOI 10.1038/ncb1722, PII NCB1722
-
Gregory PA, Bert AG, Paterson EL et al. The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1. Nat. Cell Biol. 10(5), 593-601 (2008). (Pubitemid 351627379)
-
(2008)
Nature Cell Biology
, vol.10
, Issue.5
, pp. 593-601
-
-
Gregory, P.A.1
Bert, A.G.2
Paterson, E.L.3
Barry, S.C.4
Tsykin, A.5
Farshid, G.6
Vadas, M.A.7
Khew-Goodall, Y.8
Goodall, G.J.9
-
90
-
-
47249091921
-
The miR-200 family inhibits epithelial- mesenchymal transition and cancer cell migration by direct targeting of E-cadherin transcriptional repressors ZEB1 and ZEB2
-
Korpal M, Lee ES, Hu G, Kang Y. The miR-200 family inhibits epithelial- mesenchymal transition and cancer cell migration by direct targeting of E-cadherin transcriptional repressors ZEB1 and ZEB2. J. Biol. Chem. 283(22), 14910-14914 (2008).
-
(2008)
J. Biol. Chem.
, vol.283
, Issue.22
, pp. 14910-14914
-
-
Korpal, M.1
Lee, E.S.2
Hu, G.3
Kang, Y.4
-
91
-
-
0033854047
-
Corneal endothelial cell apoptosis in patients with Fuchs' dystrophy
-
Borderie VM, Baudrimont M, Vallee A, Ereau TL, Gray F, Laroche L. Corneal endothelial cell apoptosis in patients with Fuchs' dystrophy. Invest. Ophthalmol. Vis. Sci. 41(9), 2501-2505 (2000). (Pubitemid 30624376)
-
(2000)
Investigative Ophthalmology and Visual Science
, vol.41
, Issue.9
, pp. 2501-2505
-
-
Borderie, V.M.1
Baudrimont, M.2
Vallee, A.3
Ereau, T.L.4
Gray, F.5
Laroche, L.6
-
92
-
-
0034765687
-
The role of apoptosis in the pathogenesis of Fuchs endothelial dystrophy of the cornea
-
Li Q J, Ashraf MF, Shen DF et al. The role of apoptosis in the pathogenesis of Fuchs endothelial dystrophy of the cornea. Arch. Ophthalmol. 119(11), 1597-1604 (2001). (Pubitemid 33035700)
-
(2001)
Archives of Ophthalmology
, vol.119
, Issue.11
, pp. 1597-1604
-
-
Li, Q.J.1
Ashraf, M.F.2
Shen, D.3
Green, W.R.4
Stark, W.J.5
Chan, C.-C.6
O'Brien, T.P.7
-
93
-
-
34547167873
-
Advanced Glycation End Products and Receptors in Fuchs' Dystrophy Corneas Undergoing Descemet's Stripping with Endothelial Keratoplasty
-
DOI 10.1016/j.ophtha.2006.10.049, PII S0161642006015557
-
Wang Z, Handa JT, Green WR, Stark WJ, Weinberg RS, Jun AS. Advanced glycation end products and receptors in Fuchs' dystrophy corneas undergoing Descemet's stripping with endothelial keratoplasty. Ophthalmology 114(8), 1453-1460 (2007). (Pubitemid 47126573)
-
(2007)
Ophthalmology
, vol.114
, Issue.8
, pp. 1453-1460
-
-
Wang, Z.1
Handa, J.T.2
Green, W.R.3
Stark, W.J.4
Weinberg, R.S.5
Jun, A.S.6
-
94
-
-
0036182862
-
Evidence of oxidative stress in human corneal diseases
-
Buddi R, Lin B, Atilano SR, Zorapapel NC, Kenney MC, Brown DJ. Evidence of oxidative stress in human corneal diseases. J. Histochem. Cytochem. 50(3), 341-351 (2002). (Pubitemid 34173022)
-
(2002)
Journal of Histochemistry and Cytochemistry
, vol.50
, Issue.3
, pp. 341-351
-
-
Buddi, R.1
Lin, B.2
Atilano, S.R.3
Zorapapel, N.C.4
Kenney, M.C.5
Brown, D.J.6
-
95
-
-
78149321314
-
Evidence of oxidative stress in the pathogenesis of Fuchs endothelial corneal dystrophy
-
Jurkunas UV, Bitar MS, Funaki T, Azizi B. Evidence of oxidative stress in the pathogenesis of Fuchs endothelial corneal dystrophy. Am. J. Pathol. 177(5), 2278-2289 (2010).
-
(2010)
Am. J. Pathol.
, vol.177
, Issue.5
, pp. 2278-2289
-
-
Jurkunas, U.V.1
Bitar, M.S.2
Funaki, T.3
Azizi, B.4
-
96
-
-
0033796250
-
Mitochondrial free radical generation, oxidative stress, and aging
-
Cadenas E, Davies KJ. Mitochondrial free radical generation, oxidative stress, and aging. Free Radic. Biol. Med. 29(3-4), 222-230 (2000).
-
(2000)
Free Radic. Biol. Med.
, vol.29
, Issue.3-4
, pp. 222-230
-
-
Cadenas, E.1
Davies, K.J.2
-
97
-
-
0015291670
-
The metabolic basis to the fluid pump in the cornea
-
Dikstein S, Maurice DM. The metabolic basis to the fluid pump in the cornea. J. Physiol. (Lond.) 221(1), 29-41 (1972).
-
(1972)
J. Physiol. (Lond.
, vol.221
, Issue.1
, pp. 29-41
-
-
Dikstein, S.1
Maurice, D.M.2
-
98
-
-
48249084528
-
Decreased expression of peroxiredoxins in Fuchs' endothelial dystrophy
-
Jurkunas UV, Rawe I, Bitar MS et al. Decreased expression of peroxiredoxins in Fuchs' endothelial dystrophy. Invest. Ophthalmol. Vis. Sci. 49(7), 2956-2963 (2008).
-
(2008)
Invest. Ophthalmol. Vis. Sci.
, vol.49
, Issue.7
, pp. 2956-2963
-
-
Jurkunas, U.V.1
Rawe, I.2
Bitar, M.S.3
-
99
-
-
82955194742
-
P53-regulated increase in oxidative-stress-induced apoptosis in Fuchs endothelial corneal dystrophy: A native tissue model
-
Azizi B, Ziaei A, Fuchsluger T, Schmedt T, Chen Y, Jurkunas UV. p53-regulated increase in oxidative-stress-induced apoptosis in Fuchs endothelial corneal dystrophy: A native tissue model. Invest. Ophthalmol. Vis. Sci. 52(13), 9291-9297 (2011).
-
(2011)
Invest. Ophthalmol. Vis. Sci.
, vol.52
, Issue.13
, pp. 9291-9297
-
-
Azizi, B.1
Ziaei, A.2
Fuchsluger, T.3
Schmedt, T.4
Chen, Y.5
Jurkunas, U.V.6
-
100
-
-
73549119975
-
Unfolded protein response in Fuchs endothelial corneal dystrophy: A unifying pathogenic pathway?
-
Engler C, Kelliher C, Spitze AR, Speck CL, Eberhart CG, Jun AS. Unfolded protein response in Fuchs endothelial corneal dystrophy: A unifying pathogenic pathway? Am. J. Ophthalmol. 149(2), 194.e2-202.e2 (2010).
-
(2010)
Am. J. Ophthalmol.
, vol.149
, Issue.2
-
-
Engler, C.1
Kelliher, C.2
Spitze, A.R.3
Speck, C.L.4
Eberhart, C.G.5
Jun, A.S.6
|