Zebrafish in-vivo study reveals deleterious activity of human TBC1D24 genetic variants linked with autosomal dominant hearing loss by Sarosiak, A., Jędrychowska, J., Oziębło, D., Gan, N.S., Bałdyga, N., Leja, M.L., Węgierski, T., Cruz, I.A., Raible, D.W., Skarżyński, H., Tylzanowski, P., Korzh, V., Ołdak, M.

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Association of MYH9 rs3752462 and rs5756168 Polymorphisms With Transplanted Kidney Artery Stenosis by Pazik, J, Lewandowski, Z, Oldak, M, Oziębło, D, Perkowska Ptasinska, A, Sadowska, A, Nowacka-Cieciura, E, Nowaczyk, M, Malejczyk, J, Kwiatkowski, A, Durlik, M

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CTG 18.1 trinucleotide repeat expansion in Polish patients with Fuchs endothelial corneal dystrophy by Udziela, M., Oziębło, D., Sarosiak, A., Ołdak, M., Szaflik, J.P.

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CTG18.1 trinucleotide repeat expansion in Polish patients with Fuchs endothelial corneal dystrophy by Udziela, M., Oziębło, D., Sarosiak, A., Ołdak, M., Szaflik, J.P.

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Search for electromagnetic super-preshowers using gamma-ray telescopes by K Almeida Cheminant, Gora, D, Dhital, N, Homola, P, Poznanski, P, Bratek, L, Bretz, T, Jagoda, P, Jalocha, J, Jarvis, J F, Kopanski, K, Krupinski, M, Lemanski, D, Nazari, V, Niedzwiedzki, J, Nocun, M, Noga, W, Ozieblo, A, Smelcerz, K, Smolek, K, Stasielak, J, Stuglik, S, Sulek, M, Sushchov, O, Zamora-Saa, J

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We are all the Cosmic-Ray Extremely Distributed Observatory by Dhital, N, Homola, P, Jarvis, J F, Poznanski, P, K Almeida Cheminant, Bratek, Ł, Bretz, T, Gora, D, Jagoda, P, Jałocha, J, Kopanski, K, Lemanski, D, Magrys, M, Nazari, V, Niedzwiedzki, J, Nocun, M, Noga, W, Ozieblo, A, Smelcerz, K, Smolek, K, Stasielak, J, Stuglik, S, Sułek, M, Sushchov, O, Zamora-Saa, J

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