Gordon K. Klintworth, MD PhD

Affiliations: 
Pathology Duke University, Durham, NC 
Area:
Ophthalmic Pathology (angiogenesis, eye pathology, cornea dystrophies)
Website:
http://pathology.mc.duke.edu/neuropath/np_faculty_klint2.htm
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"Gordon Klintworth"
Mean distance: 106866
 

Children

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Alan Proia grad student (Neuropathology Tree)
Charleen T. Chu post-doc 1997-1998
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Publications

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Poulsen ET, Runager K, Risør MW, et al. (2014) Comparison of two phenotypically distinct lattice corneal dystrophies caused by mutations in the transforming growth factor beta induced (TGFBI) gene. Proteomics. Clinical Applications. 8: 168-77
Minear MA, Li YJ, Rimmler J, et al. (2013) Genetic screen of African Americans with Fuchs endothelial corneal dystrophy. Molecular Vision. 19: 2508-16
Karring H, Poulsen ET, Runager K, et al. (2013) Serine protease HtrA1 accumulates in corneal transforming growth factor beta induced protein (TGFBIp) amyloid deposits. Molecular Vision. 19: 861-76
Li YJ, Minear MA, Rimmler J, et al. (2011) Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. Plos One. 6: e18044
Basaiawmoit RV, Oliveira CL, Runager K, et al. (2011) SAXS models of TGFBIp reveal a trimeric structure and show that the overall shape is not affected by the Arg124His mutation. Journal of Molecular Biology. 408: 503-13
Runager K, Basaiawmoit RV, Deva T, et al. (2011) Human phenotypically distinct TGFBI corneal dystrophies are linked to the stability of the fourth FAS1 domain of TGFBIp. The Journal of Biological Chemistry. 286: 4951-8
Riazuddin SA, Zaghloul NA, Al-Saif A, et al. (2010) Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. American Journal of Human Genetics. 86: 45-53
Runager K, García-Castellanos R, Valnickova Z, et al. (2009) Purification, crystallization and preliminary X-ray diffraction of wild-type and mutant recombinant human transforming growth factor beta-induced protein (TGFBIp). Acta Crystallographica. Section F, Structural Biology and Crystallization Communications. 65: 299-303
Afshari NA, Li YJ, Pericak-Vance MA, et al. (2009) Genome-wide linkage scan in fuchs endothelial corneal dystrophy. Investigative Ophthalmology & Visual Science. 50: 1093-7
Lagoo AS, Haggerty C, Kim Y, et al. (2008) Morphologic features of 115 lymphomas of the orbit and ocular adnexa categorized according to the World Health Organization classification: are marginal zone lymphomas in the orbit mucosa-associated lymphoid tissue-type lymphomas? Archives of Pathology & Laboratory Medicine. 132: 1405-16
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