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Jolly, Lachlan A, Nguyen, Lam Son, Domingo, Deepti, Sun, Ying, Barry, Simon, Hancarova, Miroslava, Plevova, Pavlina, Vlckova, Marketa, Havlovicova, Marketa, Kalscheuer, Vera M, Graziano, Claudio, Pippucci, Tommaso, Bonora, Elena, Sedlacek, Zdenek, Gecz, Jozef
Published in Human molecular genetics (15.06.2015)
Published in Human molecular genetics (15.06.2015)
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Mechanism and Genotype-Phenotype Correlation of Two Proximal 6q Deletions Characterized Using mBAND, FISH, Array CGH, and DNA Sequencing
Vlckova, M., Trkova, M., Zemanova, Z., Hancarova, M., Novotna, D., Raskova, D., Puchmajerova, A., Drabova, J., Zmitkova, Z., Tan, Y., Sedlacek, Z.
Published in Cytogenetic and genome research (01.01.2012)
Published in Cytogenetic and genome research (01.01.2012)
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A rare cause of mediastinal expansion with a massive pleural effusion
Šubrt, Z, Ferko, A, Papík, Z, Vacek, Z, Sedláček, Z
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Published in Postgraduate medical journal (01.11.2005)
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Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?
Trkova, Marie, Hladikova, Marie, Kasal, Pavel, Goetz, Petr, Sedlacek, Zdenek
Published in Journal of human genetics (01.08.2002)
Published in Journal of human genetics (01.08.2002)
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Two Li-Fraumeni syndrome families with novel germline p53 mutations : loss of the wild-type p53 allele in only 50% of tumours
SEDLACEK, Z, KODET, R, KRIZ, V, SEEMANOVA, E, VODVARKA, P, WILGENBUS, P, MARES, J, POUSTKA, A, GOETZ, P
Published in British journal of cancer (01.04.1998)
Published in British journal of cancer (01.04.1998)
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The expression of PAX5, p53 immunohistochemistry and p53 mutation analysis in superficial bladder carcinoma tissue. Correlation with pathological findings and clinical outcome
Babjuk, M, Soukup, V, Mares, J, Dusková, J, Sedlácek, Z, Trková, M, Pecen, L, Dvorácek, J, Hanus, T, Kocvara, R, Novák, J, Povýsil, C
Published in International urology and nephrology (2002)
Published in International urology and nephrology (2002)
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Methylation changes in promoter and enhancer regions of the WT1 gene in Wilms’ tumours
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Published in Cancer letters (26.05.2001)
Published in Cancer letters (26.05.2001)
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Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Geisheker, Madeleine R, Heymann, Gabriel, Wang, Tianyun, Coe, Bradley P, Turner, Tychele N, Stessman, Holly A F, Hoekzema, Kendra, Kvarnung, Malin, Shaw, Marie, Friend, Kathryn, Liebelt, Jan, Barnett, Christopher, Thompson, Elizabeth M, Haan, Eric, Guo, Hui, Anderlid, Britt-Marie, Nordgren, Ann, Lindstrand, Anna, Vandeweyer, Geert, Alberti, Antonino, Avola, Emanuela, Vinci, Mirella, Giusto, Stefania, Pramparo, Tiziano, Pierce, Karen, Nalabolu, Srinivasa, Michaelson, Jacob J, Sedlacek, Zdenek, Santen, Gijs W E, Peeters, Hilde, Hakonarson, Hakon, Courchesne, Eric, Romano, Corrado, Kooy, R Frank, Bernier, Raphael A, Nordenskjöld, Magnus, Gecz, Jozef, Xia, Kun, Zweifel, Larry S, Eichler, Evan E
Published in Nature neuroscience (01.08.2017)
Published in Nature neuroscience (01.08.2017)
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Oncogene amplification and expression in pediatric solid tumors
Mares, J, Polanská, V, Görgens, H, Sedlácek, Z, Maríková, T, Bocek, P, Kodet, R, Schackert, J, Goetz, P
Published in Neoplasma (1998)
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Published in Neoplasma (1998)
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A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene
BATES, G. P, MACDONALD, M. E, LEHRACH, H, BAXENDALE, S, SEDLACEK, Z, YOUNGMAN, S, ROMANO, D, WHALEY, W. L, ALLITTO, B. A, POUSTKA, A, GUSELLA, J. F
Published in American journal of human genetics (01.04.1990)
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Published in American journal of human genetics (01.04.1990)
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Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation
Bućan, M., Zimmer, M., Whaley, W.L., Poustka, A., Youngman, S., Allitto, B.A., Ormondroyd, E., Smith, B., Pohl, T.M., MacDonald, M., Bates, G.P., Richards, J., Volinia, S., Gilliam, T.C., Sedlacek, Z., Collins, F.S., Wasmuth, J.J., Shaw, D.J., Gusella, J.F., Frischauf, A-M., Lehrach, H.
Published in Genomics (San Diego, Calif.) (1990)
Published in Genomics (San Diego, Calif.) (1990)
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Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations
Krutilkova, Vera, Trkova, Marie, Fleitz, Julie, Gregor, Vladimir, Novotna, Kamila, Krepelova, Anna, Sumerauer, David, Kodet, Roman, Siruckova, Simona, Plevova, Pavlina, Bendova, Sarka, Hedvicakova, Petra, Foreman, Nicholas K., Sedlacek, Zdenek
Published in European journal of cancer (1990) (01.07.2005)
Published in European journal of cancer (1990) (01.07.2005)
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