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Резултати

Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe   [2000]

Dork, T; Macek, M; Mekus, F; Tummler, B; Tzountzouris, J; Casals, T; Krebsova, A; Koudova, M; Sakmaryova, I; Macek, M;
Vavrova, V; Zemkova, D; Ginter, E; Petrova, NV; Ivaschenko, T; Baranov, V; Witt, M; Pogorzelski, A; Bal, J; Zekanowsky, C; Wagner, K; Stuhrmann, M; Bauer, I; Seydewitz, HH; Neumann, T; Jakubiczka, S; Kraus, C; Thamm, B; Nechiporenko, M; Livshits, L; Mosse, N; Tsukerman, G; Kadasi, L; Ravnik-Glavac, M; Glavac, D; Komel, R; Vouk, K; Kucinskas, V; Krumina, A; Teder, M; Kocheva, S; Efremov, GD; Onay, T; Kirdar, B; Malone, G; Schwarz, M; Zhou, ZQ; Friedman, KJ; Carles, S; Claustres, M; Bozon, D; Verlingue, C; Ferec, C; Tzetis, M; Kanavakis, E; Cuppens, H; Bombieri, C; Pignatti, PF; Sangiuolo, F; Jordanova, A; Kušić-Tišma, Jelena  ; Radojković, Dragica  ; Sertić, J; Richter, D; Rukavina, AS; Bjorck, E; Strandvik, B; Cardoso, H; Montgomery, M; Nakielna, B; Hughes, D; Estivill, X; Aznarez, I; Tullis, E; Tsui, LC; Zielenski, J;

The TNF alpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis   [2006]

Stanke, F.; Becker, T.; Cuppens, H.; Kumar, V.; Cassiman, J.J.; Jansen, S.; Radojković, Dragica  ; Siebert, B.; Yarden, J.; Ussery, D.W.;
Wienker, T.F.; Tummler, B.;

Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract   [2015]

Hwang, Daw-Yang; ...; Stajic, Natasa; Bogdanovic, Radovan M; ...; (broj, koautora 25)

COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans   [2019]

Kitzler, Thomas M; ...; Bogdanovic, Radovan M; Stajic, Natasa; ...; (broj, koautora 22)

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