Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy von Hart, T C, Gorry, M C, Hart, P S, Woodard, A S, Shihabi, Z, Sandhu, J, Shirts, B, Xu, L, Zhu, H, Barmada, M M, Bleyer, A J

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Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects von Hart, T C, Hart, P S, Gorry, M C, Michalec, M D, Ryu, O H, Uygur, C, Ozdemir, D, Firatli, S, Aren, G, Firatli, E

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Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene von Whitcomb, David C, Gorry, Michael C, Preston, Robert A, Furey, William, Sossenheimer, Michael J, Ulrich, Charles D, Martin, Stephen P, Gates, Lawrence K, Amann, Stephen T, Toskes, Phillip P, Liddle, Roger, McGrath, Kevin, Uomo, G, Post, J. C, Ehrlich, Garth D

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Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis von Gorry, MC, Gabbaizedeh, D, Furey, W, Gates, LK, Preston, RA, Aston, CE, Zhang, Y, Ulrich, C, Ehrlich, GD, Whitcomb, DC

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Evidence of Bacterial Metabolic Activity in Culture-Negative Otitis Media With Effusion von Rayner, Mark G, Zhang, Yingze, Gorry, Michael C, Chen, Yiping, Post, J. Christopher, Ehrlich, Garth D

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Oncolytic virotherapy for ovarian carcinomatosis using a replication-selective vaccinia virus armed with a yeast cytosine deaminase gene von Chalikonda, S, Kivlen, M H, O'Malley, M E, (Eric) Dong, X D, McCart, J A, Gorry, M C, Yin, X-Y, Brown, C K, Zeh, H J, Guo, Z S, Bartlett, D L

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Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patients von Zhang, Y, Syed, R, Uygar, C, Pallos, D, Gorry, M C, Firatli, E, Cortelli, J R, VanDyke, T E, Hart, P S, Feingold, E, Hart, T C

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Caution Ahead: Traffic Accidents in Cuba von Gorry, Conner

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Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patients von Zhang, Y, Lundgren, T, Renvert, S, Tatakis, D N, Firatli, E, Uygur, C, Hart, P S, Gorry, M C, Marks, J J, Hart, T C

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Aquaporin expression in developing human teeth and selected orofacial tissues von Wang, W, Hart, P S, Piesco, N P, Lu, X, Gorry, M C, Hart, T C

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Lack of R117H mutation in the cationic trypsinogen gene in patients with tropical pancreatitis from Bangladesh von ROSSI, L, WHITCOMB, D. C, EHRLICH, G. D, GORRY, M. C, PARVIN, S, SATTAR, S, ALI, L, AZAD KHAN, A. K, GYR, N

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A Mutation in the SOS1 Gene Causes Hereditary Gingival Fibromatosis Type 1 von Hart, Thomas C., Zhang, Yingze, Gorry, Michael C., Hart, P. Suzanne, Cooper, Margaret, Marazita, Mary L., Marks, Jared M., Cortelli, Jose R., Pallos, Debora

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Structure and sequence of human FGF8 von GEMEL, J, GORRY, M, EHRLICH, G. D, MACARTHUR, C. A

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Targeting α-synuclein for treatment of Parkinson's disease: mechanistic and therapeutic considerations von Dehay, Benjamin, PhD, Bourdenx, Mathieu, MS, Gorry, Philippe, MD, Przedborski, Serge, Prof, Vila, Miquel, MD, Hunot, Stéphane, PhD, Singleton, Andrew, PhD, Olanow, C Warren, Prof, Merchant, Kalpana M, PhD, Bezard, Erwan, Prof, Petsko, Gregory A, Prof, Meissner, Wassilios G, Prof

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Genomic organization of the human fibroblast growth factor receptor 2 ( FGFR2) gene and comparative analysis of the human FGFR gene family von Zhang, Yingze, Gorry, Michael C., Post, J.Christopher, Ehrlich, Garth D.

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Evolution of Human Immunodeficiency Virus Type 1 Envelope Sequences in Infected Individuals with Differing Disease Progression Profiles von Shankarappa, Raj, Gupta, Phalguni, Learn, Gerald H., Rodrigo, Allen G., Rinaldo, Charles R., Gorry, Michael C., Mullins, James I., Nara, Peter L., Ehrlich, Garth D.

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RNA differential display of scarless wound healing in fetal rabbit indicates downregulation of a CCT chaperonin subunit and upregulation of a glycophorin-like gene transcript von Darden, Daryle L., Hu, Fen Ze, Ehrlich, Miles D., Gorry, Michael C., Dressman, Devin, Li, Ha-Sheng, Whitcomb, David C., Hebda, Patricia A., Dohar, Joseph E., Ehrlich, Garth D.

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Localization, genomic organization, and alternative transcription of a novel human SAM-dependent methyltransferase gene on chromosome 2p22→p21 von Zhang, Y., Gorry, M.C., Hart, P.S., Pettenati, M.J., Wang, L., Marks, J.J., Lu, X., Hart, T.C.

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Cuba's Latin American Medical School: can socially-accountable medical education make a difference? von Gorry, Conner

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CKDu ravages the Salvadoran countryside von Gorry, Conner

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