The influence of endothelin-A receptor gene polymorphism on the progression of autosomal dominant polycystic kidney disease and IgA nephropathy von Reiterová, J, Merta, M, Stekrová, J, Maixnerová, D, Obeidová, H, Kebrdlová, V, Viklický, O, Tesar, V

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Genetic basis of nephrotic syndrome--review von Obeidová, H, Merta, M, Reiterová, J, Maixnerová, D, Stekrová, J, Rysavá, R, Tesar, V

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The pathogenetic aspects and gene polymorphisms of IgA nephropathy von Maixnerová, D, Merta, M, Reiterová, J, Stekrová, J, Rysavá, R, Obeidová, H, Tesar, V

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Influence of VEGF Polymorphism on Progression of Autosomal Dominant Polycystic Kidney Disease von Reiterová, J., Obeidová, H., Leníček, M., Štekrová, J., Merta, M., Maixnerová, D., Vítek, L., Viklický, O., Tesař, V.

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The influence of three endothelin-1 polymorphisms on the progression of IgA nephropathy von Maixnerová, D, Merta, M, Reiterová, J, Stekrová, J, Rysavá, R, Obeidová, H, Viklický, O, Potmĕsil, P, Tesar, V

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Does electron microscopy change the view of the diagnosis of IgA nephropathy? von Maixnerová, D, Honsová, E, Merta, M, Reiterová, J, Rysavá, R, Tesar, V, Obeidová, H, Motan, J

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The influence of two megsin polymorphisms on the progression of IgA nephropathy von Maixnerová, D, Merta, M, Reiterová, J, Stekrová, J, Rysavá, R, Viklický, O, Obeidová, H, Tesar, V

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The Influence of Endothelin-A Receptor Gene Polymorphism on the Progression of Autosomal Dominant Poly cystic Kidney Disease and IgA Nephropathy von Reiterova, J, Merta, M, Stekrova, J, Maexnerova, D, Obeidova, H, Kebrdlova, V, Viklicky, O, Tesar, V

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The Influence of Three Endothelin-1 Polymorphisms on the Progression of IgA Nephropathy von Maixnerova, D, Merta, M, Reiterova, J, Stekrova, J, Rysava, R, Obeidova, H, Viklicky, O, Potmesil, P, Tesar, V

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Mutational Analysis of ACTN4, Encoding [alpha]-Actinin 4, in Patients with Focal Segmental Glomerulosclerosis Using HRM Method von Safaríková, M, Reiterová, J, Safránková, H, Stekrová, J, Zidková, A, Obeidová, L, Kohoutová, M, Tesar, V

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TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease von Obeidová, L, Reiterová, J, Lněnička, P, Štekrová, J, Šafránková, H, Kohoutová, M, Tesař, V

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Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome von Reiterová, J, Safránková, H, Obeidová, L, Stěkrová, J, Maixnerová, D, Merta, M, Tesař, V

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Mutational analysis of ACTN4, encoding α-actinin 4, in patients with focal segmental glomerulosclerosis using HRM method von Safaříková, M, Reiterová, J, Safránková, H, Stekrová, J, Zidková, A, Obeidová, L, Kohoutová, M, Tesař, V

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Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease von Claus, Laura R., Chen, Chuan, Stallworth, Jennifer, Turner, Joshua L., Slaats, Gisela G., Mabillard, Holly, Senum, Sarah R., Srikanth, Sujata, Flanagan-Steet, Heather, Louie, Raymond J., Silver, Josh, Lerner-Ellis, Jordan, Morel, Chantal, Mighton, Chloe, Sleutels, Frank, van Slegtenhorst, Marjon, van Ham, Tjakko, Brooks, Alice S., Dorresteijn, Eiske M., Barakat, Tahsin Stefan, Dahan, Karin, Demoulin, Nathalie, Goffin, Eric Jean, Olinger, Eric, Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R., Brittain, Helen, Caulfield, Mark J., Chan, Georgia C., Elgar, Greg, Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jackson, Rob, Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E.A., Leong, Ivonne U.S., Lopez, Javier F., Maleady-Crowe, Fiona, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Need, Anna C., O’Donovan, Peter, Odhams, Chris A., Patch, Christine, Pereira, Mariana Buongermino, Perez-Gil, Daniel, Pullinger, John, Rahim, Tahrima, Rendon, Augusto, Rogers, Tim, Savage, Kevin, Sawant, Kushmita, Scott, Richard H., Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Thompson, Simon R., Tucci, Arianna, Welland, Matthew J., Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M., Larsen, Martin, Hertz, Jens Michael, Lilien, Marc R., Obeidová, Lena, Stone, Hillarey K., Kerecuk, Larissa, Gurgu, Mihai, Yousef Yengej, Fjodor A., Ammerlaan, Carola M.E., Rookmaaker, Maarten B., Hanna, Christian, Rogers, R. Curtis, Duran, Karen, Peters, Edith, Sayer, John A., van Haaften, Gijs, Harris, Peter C., Ling, Kun, Mason, Jennifer M., van Eerde, Albertien M., Steet, Richard

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Heterozygous Variants in NEK8 Kinase Domain Cause an Autosomal-Dominant Ciliopathy: PO1246 von Claus, Laura R., Stallworth, Jennifer, van Jaarsveld, Richard H., Louie, Raymond, Silver, Josh, Lerner-Ellis, Jordan, Morel, Chantal F., Mighton, Chloe, Ziegler, Alban, Barakat, Tahsin Stefan, Dahan, Karin, Demoulin, Nathalie, Goffin, Eric, Larsen, Martin J., Hertz, Jens Michael, Lilien, Marc, Olinger, Eric G., Sayer, John A., Obeidova, Lena, Seeman, Tomas, Rogers, Richard C., Duran, Karen J., van Haaften, Gijs W., Steet, Richard, van Eerde, Albertien M.

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Renal development and cystic diseases von Cornec-Le Gall, E., Treguer, L., Sawadogo, T., Benarbia, S., Le Meur, Y., Zittema, D., van den Berg, E., Meijer, E., Boertien, W. E., Muller Kobold, A. C., Franssen, C. F. M., de Jong, P. E., Bakker, S. J. L., Navis, G. J., Gansevoort, R. T., Melemadathil, S., Kamal, M., Tuta, L., Botea, F., Sciarrone Alibrandi, M. T., Nuzzo, M., Delli Carpini, S., Merlino, L., Brioni, E., Zagato, L., Simonini, M., Rivera, R., Manunta, P., Park, H. C., Kim, H., Koo, T. Y., Han, M., Park, Y. J., Oh, K.-H., Noh, J. W., Ha, I. S., Cheong, H. I., Hwang, Y.-H., Ahn, C., Lacquaniti, A., Buemi, M., Lupica, R., Lucisano, S., Chirico, V., Ozucer, B., KazancIoglu, R., Ozturk, B., Alay, M., Veyseller, B., Ozturan, O., Erkoc, R., Obeidova, L., Stekrova, J., Reiterova, J., Elisakova, V., Merta, M., Kohoutova, M., Tesar, V., Gul, B., Cekic, S., Asiltas, B., Dogan, S., Aktas, N., Oruc, A., Dogan, I., Ersoy, A., Gullulu, M., Yurtkuran, M., Yildiz, A.

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