cached image

Gordon K. Klintworth, MD PhD - Publications

Pathology Duke University, Durham, NC 
Ophthalmic Pathology (angiogenesis, eye pathology, cornea dystrophies)

68 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2014 Poulsen ET, Runager K, Risør MW, Dyrlund TF, Scavenius C, Karring H, Praetorius J, Vorum H, Otzen DE, Klintworth GK, Enghild JJ. 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. PMID 24302499 DOI: 10.1002/Prca.201300058  0.4
2013 Minear MA, Li YJ, Rimmler J, Balajonda E, Watson S, Allingham RR, Hauser MA, Klintworth GK, Afshari NA, Gregory SG. Genetic screen of African Americans with Fuchs endothelial corneal dystrophy. Molecular Vision. 19: 2508-16. PMID 24348007  0.4
2013 Karring H, Poulsen ET, Runager K, Thøgersen IB, Klintworth GK, Højrup P, Enghild JJ. Serine protease HtrA1 accumulates in corneal transforming growth factor beta induced protein (TGFBIp) amyloid deposits. Molecular Vision. 19: 861-76. PMID 23592924  0.4
2011 Li YJ, Minear MA, Rimmler J, Zhao B, Balajonda E, Hauser MA, Allingham RR, Eghrari AO, Riazuddin SA, Katsanis N, Gottsch JD, Gregory SG, Klintworth GK, Afshari NA. Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. Plos One. 6: e18044. PMID 21533127 DOI: 10.1371/Journal.Pone.0018044  0.4
2011 Basaiawmoit RV, Oliveira CL, Runager K, Sørensen CS, Behrens MA, Jonsson BH, Kristensen T, Klintworth GK, Enghild JJ, Pedersen JS, Otzen DE. 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. PMID 21371477 DOI: 10.1016/J.Jmb.2011.02.052  0.4
2011 Runager K, Basaiawmoit RV, Deva T, Andreasen M, Valnickova Z, Sørensen CS, Karring H, Thøgersen IB, Christiansen G, Underhaug J, Kristensen T, Nielsen NC, Klintworth GK, Otzen DE, Enghild JJ. 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. PMID 21135107 DOI: 10.1074/Jbc.M110.181099  0.4
2010 Riazuddin SA, Zaghloul NA, Al-Saif A, Davey L, Diplas BH, Meadows DN, Eghrari AO, Minear MA, Li YJ, Klintworth GK, Afshari N, Gregory SG, Gottsch JD, Katsanis N. 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. PMID 20036349 DOI: 10.1016/J.Ajhg.2009.12.001  0.4
2010 Klintworth GK, Jester JV. Genetic basis of corneal diseases and the role of keratocytes in corneal transparency - a review Clinical and Experimental Ophthalmology. 38: 23-33. DOI: 10.1111/J.1442-9071.2010.02365.X  0.4
2009 Runager K, García-Castellanos R, Valnickova Z, Kristensen T, Nielsen NC, Klintworth GK, Gomis-Rüth FX, Enghild JJ. 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. PMID 19255489 DOI: 10.1107/S1744309109005016  0.4
2009 Afshari NA, Li YJ, Pericak-Vance MA, Gregory S, Klintworth GK. Genome-wide linkage scan in fuchs endothelial corneal dystrophy. Investigative Ophthalmology & Visual Science. 50: 1093-7. PMID 18502986 DOI: 10.1167/Iovs.08-1839  0.4
2008 Lagoo AS, Haggerty C, Kim Y, Hammons M, Neufeld K, Redher C, Woodward J, Klintworth GK. 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. PMID 18788851 DOI: 10.1043/1543-2165(2008)132[1405:Mfolot]2.0.Co;2  0.4
2008 Cummings TJ, Dodd LG, Eedes CR, Klintworth GK. Hereditary benign intraepithelial dyskeratosis: an evaluation of diagnostic cytology. Archives of Pathology & Laboratory Medicine. 132: 1325-8. PMID 18684035 DOI: 10.1043/1543-2165(2008)132[1325:Hbidae]2.0.Co;2  0.4
2008 Afshari NA, Bahadur RP, Eifrig DE, Thogersen IB, Enghild JJ, Klintworth GK. Atypical asymmetric lattice corneal dystrophy associated with a novel homozygous mutation (Val624Met) in the TGFBI gene. Molecular Vision. 14: 495-9. PMID 18385782  0.4
2008 Liskova P, Klintworth GK, Bowling BL, Filipec M, Jirsova K, Tuft SJ, Bhattacharya SS, Hardcastle AJ, Ebenezer ND. Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families. Ophthalmic Research. 40: 105-8. PMID 18259096 DOI: 10.1159/000115325  0.4
2007 Karring H, Valnickova Z, Thøgersen IB, Hedegaard CJ, Møller-Pedersen T, Kristensen T, Klintworth GK, Enghild JJ. Evidence against a blood derived origin for transforming growth factor beta induced protein in corneal disorders caused by mutations in the TGFBI gene. Molecular Vision. 13: 997-1004. PMID 17653042  0.4
2006 Liu NP, Smith CF, Bowling BL, Jonasson F, Klintworth GK. Macular corneal dystrophy types I and II are caused by distinct mutations in the CHST6 gene in Iceland. Molecular Vision. 12: 1148-52. PMID 17093400  0.4
2006 Klintworth GK, Smith CF, Bowling BL. CHST6 mutations in North American subjects with macular corneal dystrophy: a comprehensive molecular genetic review. Molecular Vision. 12: 159-76. PMID 16568029  0.4
2005 Sultana A, Sridhar MS, Klintworth GK, Balasubramanian D, Kannabiran C. Allelic heterogeneity of the carbohydrate sulfotransferase-6 gene in patients with macular corneal dystrophy. Clinical Genetics. 68: 454-60. PMID 16207214 DOI: 10.1111/J.1399-0004.2005.00517.X  0.4
2005 Cummings TJ, Stenzel TT, Klintworth G, Jaffe GJ. Primary intraocular T-cell-rich large B-cell lymphoma. Archives of Pathology & Laboratory Medicine. 129: 1050-3. PMID 16048400 DOI: 10.1043/1543-2165(2005)129[1050:Pitlbl]2.0.Co;2  0.4
2005 Liu NP, Bao W, Smith CF, Vance JM, Klintworth GK. Different mutations in carbohydrate sulfotransferase 6 (CHST6) gene cause macular corneal dystrophy types I and II in a single sibship. American Journal of Ophthalmology. 139: 1118-20. PMID 15953452 DOI: 10.1016/J.Ajo.2004.11.054  0.4
2004 Andersen RB, Karring H, Møller-Pedersen T, Valnickova Z, Thøgersen IB, Hedegaard CJ, Kristensen T, Klintworth GK, Enghild JJ. Purification and structural characterization of transforming growth factor beta induced protein (TGFBIp) from porcine and human corneas. Biochemistry. 43: 16374-84. PMID 15610032 DOI: 10.1021/Bi048589S  0.4
2004 Eifrig DE, Afshari NA, Buchanan HW, Bowling BL, Klintworth GK. Polymorphic corneal amyloidosis: a disorder due to a novel mutation in the transforming growth factor beta-induced (BIGH3) gene. Ophthalmology. 111: 1108-14. PMID 15177960 DOI: 10.1016/J.Ophtha.2003.09.043  0.4
2003 Sultana A, Sridhar MS, Jagannathan A, Balasubramanian D, Kannabiran C, Klintworth GK. Novel mutations of the carbohydrate sulfotransferase-6 (CHST6) gene causing macular corneal dystrophy in India. Molecular Vision. 9: 730-4. PMID 14735064  0.4
2001 Borrás T, Gabelt BT, Klintworth GK, Peterson JC, Kaufman PL. Non-invasive observation of repeated adenoviral GFP gene delivery to the anterior segment of the monkey eye in vivo. The Journal of Gene Medicine. 3: 437-49. PMID 11601757 DOI: 10.1002/Jgm.210  0.4
2001 Allingham RR, Seo B, Rampersaud E, Bembe M, Challa P, Liu N, Parrish T, Karolak L, Gilbert J, Pericak-Vance MA, Klintworth GK, Vance JM. A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis. American Journal of Human Genetics. 68: 491-4. PMID 11170897 DOI: 10.1086/318194  0.4
2000 Holck DE, Klintworth GK, Dutton JJ, Foulks GN, Manning FJ. Localized conjunctival argyrosis: a late sequela of strabismus surgery. Ophthalmic Surgery and Lasers. 31: 495-8. PMID 11095129 DOI: 10.3928/1542-8877-20001101-12  0.4
2000 Cummings TJ, Provenzale JM, Hunter SB, Friedman AH, Klintworth GK, Bigner SH, McLendon RE. Gliomas of the optic nerve: histological, immunohistochemical (MIB-1 and p53), and MRI analysis. Acta Neuropathologica. 99: 563-70. PMID 10805102 DOI: 10.1007/S004010051161  0.4
1997 Klintworth GK, Oshima E, al-Rajhi A, al-Saif A, Thonar EJ, Karcioglu ZA. Macular corneal dystrophy in Saudi Arabia: a study of 56 cases and recognition of a new immunophenotype. American Journal of Ophthalmology. 124: 9-18. PMID 9222226 DOI: 10.1016/S0002-9394(14)71637-X  0.4
1995 Provenzale JM, Weber AL, Klintworth GK, McLendon RE. Radiologic-pathologic correlation. Bilateral retinoblastoma with coexistent pinealoblastoma (trilateral retinoblastoma). Ajnr. American Journal of Neuroradiology. 16: 157-65. PMID 7900586  0.4
1994 Conrad TJ, Chandler DB, Corless JM, Klintworth GK. In vivo measurement of corneal angiogenesis with video data acquisition and computerized image analysis. Laboratory Investigation; a Journal of Technical Methods and Pathology. 70: 426-34. PMID 7511717  0.4
1992 Small KW, Scheinman J, Klintworth GK. A clinicopathological study of ocular involvement in primary hyperoxaluria type I. The British Journal of Ophthalmology. 76: 54-7. PMID 1739695 DOI: 10.1136/bjo.76.1.54  0.4
1992 Klein KL, Klintworth GK, Bernstein A, Breitman ML. Embryology and morphology of microphthalmia in transgenic mice expressing a gamma F-crystallin/diphtheria toxin A hybrid gene. Laboratory Investigation; a Journal of Technical Methods and Pathology. 67: 31-41. PMID 1625446  0.4
1992 Green JE, Baird AM, Hinrichs SH, Klintworth GK, Jay G. Adrenal medullary tumors and iris proliferation in a transgenic mouse model of neurofibromatosis. The American Journal of Pathology. 140: 1401-10. PMID 1605307  0.4
1992 Balkan W, Klintworth GK, Bock CB, Linney E. Transgenic mice expressing a constitutively active retinoic acid receptor in the lens exhibit ocular defects. Developmental Biology. 151: 622-5. PMID 1318236 DOI: 10.1016/0012-1606(92)90200-Z  0.4
1991 Harrington L, Klintworth GK, Secor TE, Breitman ML. Developmental analysis of ocular morphogenesis in alpha A-crystallin/diphtheria toxin transgenic mice undergoing ablation of the lens. Developmental Biology. 148: 508-16. PMID 1743399 DOI: 10.1016/0012-1606(91)90269-9  0.4
1990 Breitman ML, Rombola H, Maxwell IH, Klintworth GK, Bernstein A. Genetic ablation in transgenic mice with an attenuated diphtheria toxin A gene. Molecular and Cellular Biology. 10: 474-9. PMID 2300048 DOI: 10.1128/Mcb.10.2.474  0.4
1989 Breitman ML, Bryce DM, Giddens E, Clapoff S, Goring D, Tsui LC, Klintworth GK, Bernstein A. Analysis of lens cell fate and eye morphogenesis in transgenic mice ablated for cells of the lens lineage. Development (Cambridge, England). 106: 457-63. PMID 2598819  0.4
1988 Newton C, Hatchell DL, Klintworth GK, Brown CF. Topical fibronectin and corneal epithelial wound healing in the rabbit. Archives of Ophthalmology (Chicago, Ill. : 1960). 106: 1277-9. PMID 3415553 DOI: 10.1001/Archopht.1988.01060140437048  0.4
1988 Morris PB, Hida T, Blackshear PJ, Klintworth GK, Swain JL. Tumor-promoting phorbol esters induce angiogenesis in vivo. The American Journal of Physiology. 254: C318-22. PMID 2450466 DOI: 10.1152/Ajpcell.1988.254.2.C318  0.4
1987 Lang RA, Metcalf D, Cuthbertson RA, Lyons I, Stanley E, Kelso A, Kannourakis G, Williamson DJ, Klintworth GK, Gonda TJ. Transgenic mice expressing a hemopoietic growth factor gene (GM-CSF) develop accumulations of macrophages, blindness, and a fatal syndrome of tissue damage. Cell. 51: 675-86. PMID 3499986 DOI: 10.1016/0092-8674(87)90136-X  0.4
1986 Klintworth GK, Meyer R, Dennis R, Hewitt AT, Stock EL, Lenz ME, Hassell JR, Stark WJ, Kuettner KE, Thonar EJ. Macular corneal dystrophy. Lack of keratan sulfate in serum and cornea. Ophthalmic Paediatrics and Genetics. 7: 139-43. PMID 2951638 DOI: 10.3109/13816818609004130  0.4
1986 Thonar EJ, Meyer RF, Dennis RF, Lenz ME, Maldonado B, Hassell JR, Hewitt AT, Stark WJ, Stock EL, Kuettner KE. Absence of normal keratan sulfate in the blood of patients with macular corneal dystrophy. American Journal of Ophthalmology. 102: 561-9. PMID 2946233 DOI: 10.1016/0002-9394(86)90525-8  0.4
1986 Klintworth GK, Meyer R, Dennis R, Hewitt AT, Stock EL, Lenz ME, Hassell JR, Stark WJ, Kuettner KE, Thonar EJMA. Macular corneal dystrophy lack of keratan sulfate in serum and cornea Ophthalmic Genetics. 7: 139-143. DOI: 10.3109/13816818609004130  0.4
1985 Shields MB, Chandler DB, Hickingbotham D, Klintworth GK. Intraocular cyclophotocoagulation. Histopathologic evaluation in primates. Archives of Ophthalmology (Chicago, Ill. : 1960). 103: 1731-5. PMID 4062642 DOI: 10.1001/Archopht.1985.01050110127040  0.4
1985 Leonardy NJ, Smith CF, Brown CF, Klintworth GK. Intercellular relationships in the synthesis of macromolecules by organ cultures of corneas. Investigative Ophthalmology & Visual Science. 26: 1216-22. PMID 3928521  0.4
1985 Shields MB, Buckley E, Klintworth GK, Thresher R. Axenfeld-Rieger syndrome. A spectrum of developmental disorders. Survey of Ophthalmology. 29: 387-409. PMID 3892740 DOI: 10.1016/0039-6257(85)90205-X  0.4
1985 Chung SM, Proia AD, Klintworth GK, Watson SP, Lapetina EG. Deoxycholate induces the preferential hydrolysis of polyphosphoinositides by human platelet and rat corneal phospholipase C. Biochemical and Biophysical Research Communications. 129: 411-6. PMID 2990455 DOI: 10.1016/0006-291X(85)90166-4  0.4
1985 Thonar EJ, Lenz ME, Klintworth GK, Caterson B, Pachman LM, Glickman P, Katz R, Huff J, Kuettner KE. Quantification of keratan sulfate in blood as a marker of cartilage catabolism. Arthritis and Rheumatism. 28: 1367-76. PMID 2935158 DOI: 10.1002/Art.1780281209  0.4
1985 Glatt HJ, Vu MT, Burger PC, Klintworth GK. Effect of irradiation on vascularization of corneas grafted onto chorioallantoic membranes. Investigative Ophthalmology & Visual Science. 26: 1533-42. PMID 2414249  0.4
1985 Vu MT, Smith CF, Burger PC, Klintworth GK. An evaluation of methods to quantitate the chick chorioallantoic membrane assay in angiogenesis. Laboratory Investigation; a Journal of Technical Methods and Pathology. 53: 499-508. PMID 2413278  0.4
1985 Vu MT, Burger PC, Klintworth GK. Angiogenic activity in injured rat corneas as assayed on the chick chorioallantoic membrane. Laboratory Investigation; a Journal of Technical Methods and Pathology. 53: 311-9. PMID 2412000  0.4
1983 Klintworth GK, Smith CF. Abnormalities of proteoglycans and glycoproteins synthesized by corneal organ cultures derived from patients with macular corneal dystrophy. Laboratory Investigation; a Journal of Technical Methods and Pathology. 48: 603-12. PMID 6601743  0.4
1983 Lane JC, Klintworth GK. A study of astrocytes in retinoblastomas using the immunoperoxidase technique and antibodies to glial fibrillary acidic protein. American Journal of Ophthalmology. 95: 197-207. PMID 6337496 DOI: 10.1016/0002-9394(83)90014-4  0.4
1982 Hamilton CW, Chandler D, Klintworth GK, Machemer R. A transmission and scanning electron microscopic study of surgically excised preretinal membrane proliferations in diabetes mellitus. American Journal of Ophthalmology. 94: 473-88. PMID 7137272 DOI: 10.1016/0002-9394(82)90241-0  0.4
1981 Spector B, Klintworth GK, Wells SA. Histologic study of the ocular lesions in multiple endocrine neoplasia syndrome type IIb. American Journal of Ophthalmology. 91: 204-15. PMID 7468736 DOI: 10.1016/0002-9394(81)90175-6  0.4
1981 Klintworth GK, Smith CF. Difference between the glycosaminoglycans synthetized by corneal and cutaneous fibroblasts in culture. Laboratory Investigation; a Journal of Technical Methods and Pathology. 44: 553-9. PMID 7230738  0.4
1980 Shields MB, Klintworth GK. Anterior uveal melanomas and intraocular pressure. Ophthalmology. 87: 503-17. PMID 7413139 DOI: 10.1016/S0161-6420(80)35202-0  0.4
1980 Klintworth GK, Smith CF. Abnormal product of corneal explants from patients with macular corneal dystrophy. The American Journal of Pathology. 101: 143-58. PMID 6969547  0.4
1979 Shields MB, McCracken JS, Klintworth GK, Campbell DG. Corneal edema in essential iris atrophy. Ophthalmology. 86: 1533-50. PMID 396496  0.4
1979 Klintworth GK, Hawkins HK, Smith CF. Acridine orange particles in cultured fibroblasts. A comparative study of macular corneal dystrophy, systemic mucopolysaccharidoses types I-H and II, and normal controls. Archives of Pathology & Laboratory Medicine. 103: 297-9. PMID 88211  0.4
1977 Schwartz JN, Donnelly EH, Klintworth GK. Ocular and orbital phycomycosis. Survey of Ophthalmology. 22: 3-28. PMID 333648 DOI: 10.1016/0039-6257(77)90025-X  0.4
1977 Klintworth GK, Smith CF. Macular corneal dystrophy. Studies of sulfated glycosaminoglycans in corneal explant and confluent stromal cell cultures. The American Journal of Pathology. 89: 167-82. PMID 143892  0.4
1976 Schwartz JN, Cashwell F, Hawkins HK, Klintworth GK. Necrotizing retinopathy with herpes zoster ophthalmicus: a light and electron microscopical study. Archives of Pathology & Laboratory Medicine. 100: 386-91. PMID 180930  0.4
1976 Klintworth GK, Smith CF. A comparative study of extracellular sulfated glycosaminoglycans synthesized by rabbit corneal fibroblasts in organ and confluent cultures. Laboratory Investigation; a Journal of Technical Methods and Pathology. 35: 258-63. PMID 134175  0.4
1975 Schwartz JN, Daniels CA, Klintworth GK. Lymphoid cell necrosis, thymic atrophy, and growth retardation in newborn mice inoculated with murine cytomegalovirus. The American Journal of Pathology. 79: 509-22. PMID 166564  0.4
1974 Schwartz JN, Daniels CA, Shivers JC, Klintworth GK. Experimental cytomegalovirus ophthalmitis. The American Journal of Pathology. 77: 477-92. PMID 4372891  0.4
1965 Heinz HJ, Klintworth GK. Cysticercosis in the aetiology of epilepsy. The South African Journal of Medical Sciences. 30: 32-6. PMID 5856496  0.4
Show low-probability matches.