Clinico-pathologic findings in medullary cystic kidney disease type 2 von Bleyer, Anthony J, Hart, Thomas C, Willingham, Mark C, Iskandar, Samy S, Gorry, Michael C, Trachtman, Howard

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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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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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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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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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Phosphorylation of the prolyl isomerase Cyclophilin A regulates its localisation and release from the centrosome during mitosis von Gorry, Rebecca, Brennan, Kieran, Lavin, Paul TM, Sheridan, Rebecca, Mc Gee, Margaret M

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Clinical characterization of a family with a mutation in the uromodulin (Tamm-Horsfall glycoprotein) gene von Bleyer, Anthony J., Woodard, Arch S., Shihabi, Zak, Sandhu, Jaspreet, Zhu, Honping, Satko, Scott G., Weller, Nelson, Deterding, Elizabeth, Mcbride, Debra, Gorry, Michael C., Xu, Linda, Ganier, Deann, Hart, Thomas C.

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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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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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Renal manifestations of a mutation in the uromodulin (Tamm Horsfall protein) gene von Bleyer, Anthony J, Trachtman, Howard, Sandhu, Jaspreet, Gorry, Michael C, Hart, Thomas C

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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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Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta von Hart, P. Suzanne, Wright, J. Timothy, Savage, Mathew, Kang, George, Bensen, Jeannette T., Gorry, Michael C., Hart, Thomas C.

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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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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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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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Toy-Making von Hionruaidh, S. Ó, Gorry, Kate Mc

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Farm Animals von Hionruaidh, S. Ó, Gorry, Lizzie Mc

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