Search Results - "Obeidová, L"

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

“…Focal segmental glomerulosclerosis and minimal change disease represent frequent histological patterns of renal injury in patients with nephrotic syndrome. Few…”
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Mutational analysis of ACTN4, encoding α-actinin 4, in patients with focal segmental glomerulosclerosis using HRM method by Safaříková, M, Reiterová, J, Safránková, H, Stekrová, J, Zidková, A, Obeidová, L, Kohoutová, M, Tesař, V

“…α-Actinin 4, encoded by ACTN4, is an F-actin crosslinking protein which belongs to the spectrin gene superfamily. It has a head-to-tail homodimer structure…”
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Mutational Analysis of ACTN4, Encoding [alpha]-Actinin 4, in Patients with Focal Segmental Glomerulosclerosis Using HRM Method by Safaríková, M, Reiterová, J, Safránková, H, Stekrová, J, Zidková, A, Obeidová, L, Kohoutová, M, Tesar, V

“…α-Actinin 4, encoded by ACTN4, is an F-actin crosslinking protein which belongs to the spectrin gene superfamily. It has a head-to-tail homodimer structure…”
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TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease by Obeidová, L, Reiterová, J, Lněnička, P, Štekrová, J, Šafránková, H, Kohoutová, M, Tesař, V

“…Blood filtration and formation of primary urine in the kidney glomerulus is provided by a specialized membrane called slit diaphragm located between…”
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A suitable sequence of bioinformatics tools for NGS diagnosis of familial hypercholesterolemia by Horinek, A., Hirschfeldová, K., Obeidova, L., Pazourková, E., Todorovova, V., Vrablík, M., Satny, M.

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Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report by Elisakova, Veronika, Merta, Miroslav, Reiterova, Jana, Baxova, Alica, Kotlas, Jaroslav, Hirschfeldova, Katerina, Obeidova, Lena, Tesar, Vladimir, Stekrova, Jitka

“…Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disorder, leading to end stage renal failure and kidney…”
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Renal development and cystic diseases by 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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