Defective class II transactivator expression in a B lymphoma cell line
PROD'HOMME, T, DRENOU, B, DE RUYFFELAERE, C, BARBIERI, G, WISZNIEWSKI, W, BASTARD, C, CHARRON, D, ALCAIDE-LORIDAN, C
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Published in Leukemia (01.04.2004)
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Mutation in the Class II trans-Activator Leading to a Mild Immunodeficiency
Wiszniewski, Wojciech, Fondaneche, Marie-Claude, Le Deist, Francoise, Kanariou, Maria, Selz, Francoise, Brousse, Nicole, Steimle, Viktor, Barbieri, Giovanna, Alcaide-Loridan, Catherine, Charron, Dominique, Fischer, Alain, Lisowska-Grospierre, Barbara
Published in The Journal of immunology (1950) (01.08.2001)
Published in The Journal of immunology (1950) (01.08.2001)
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Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B
Wiszniewski, W, Fondaneche, M C, Lambert, N, Masternak, K, Picard, C, Notarangelo, L, Schwartz, K, Bal, J, Reith, W, Alcaide, C, de Saint Basile, G, Fischer, A, Lisowska-Grospierre, B
Published in Immunogenetics (New York) (01.04.2000)
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GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Snoeckx, Rikkert L., Huygen, Patrick L.M., Feldmann, Delphine, Marlin, Sandrine, Denoyelle, Françoise, Waligora, Jaroslaw, Mueller-Malesinska, Malgorzata, Pollak, Agneszka, Ploski, Rafal, Murgia, Alessandra, Orzan, Eva, Castorina, Pierangela, Ambrosetti, Umberto, Nowakowska-Szyrwinska, Ewa, Bal, Jerzy, Wiszniewski, Wojciech, Janecke, Andreas R., Nekahm-Heis, Doris, Seeman, Pavel, Bendova, Olga, Kenna, Margaret A., Frangulov, Anna, Rehm, Heidi L., Tekin, Mustafa, Incesulu, Armagan, Dahl, Hans-Henrik M., du Sart, Desirée, Jenkins, Lucy, Lucas, Deirdre, Bitner-Glindzicz, Maria, Avraham, Karen B., Brownstein, Zippora, del Castillo, Ignacio, Moreno, Felipe, Blin, Nikolaus, Pfister, Markus, Sziklai, Istvan, Toth, Timea, Kelley, Philip M., Cohn, Edward S., Van Maldergem, Lionel, Hilbert, Pascale, Roux, Anne-Françoise, Mondain, Michel, Hoefsloot, Lies H., Cremers, Cor W.R.J., Löppönen, Tuija, Löppönen, Heikki, Parving, Agnete, Gronskov, Karen, Schrijver, Iris, Roberson, Joseph, Gualandi, Francesca, Martini, Alessandro, Lina-Granade, Geneviève, Pallares-Ruiz, Nathalie, Correia, Céu, Fialho, Graça, Cryns, Kim, Hilgert, Nele, Van de Heyning, Paul, Nishimura, Carla J., Smith, Richard J.H., Van Camp, Guy
Published in American journal of human genetics (01.12.2005)
Published in American journal of human genetics (01.12.2005)
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Curcumin Treatment Abrogates Endoplasmic Reticulum Retention and Aggregation-Induced Apoptosis Associated with Neuropathy-Causing Myelin Protein Zero–Truncating Mutants
Khajavi, Mehrdad, Inoue, Ken, Wiszniewski, Wojciech, Ohyama, Tomoko, Snipes, G. Jackson, Lupski, James R.
Published in American journal of human genetics (01.11.2005)
Published in American journal of human genetics (01.11.2005)
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ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies
Wiszniewski, Wojciech, Zaremba, Charles M., Yatsenko, Alexander N., Jamrich, Milan, Wensel, Theodore G., Lewis, Richard Alan, Lupski, James R.
Published in Human molecular genetics (01.10.2005)
Published in Human molecular genetics (01.10.2005)
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Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond–Blackfan anaemia
Wat, Margaret J, Enciso, Victoria B, Wiszniewski, Wojciech, Resnick, Trevor, Bader, Patricia, Roeder, Elizabeth R, Freedenberg, Debra, Brown, Chester, Stankiewicz, Pawel, Cheung, Sau-Wai, Scott, Daryl A
Published in Journal of medical genetics (01.11.2010)
Published in Journal of medical genetics (01.11.2010)
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SIMPLE mutations in Charcot‐Marie‐Tooth disease and the potential role of its protein product in protein degradation
Saifi, Gulam Mustafa, Szigeti, Kinga, Wiszniewski, Wojciech, Shy, Michael E., Krajewski, Karen, Hausmanowa‐Petrusewicz, Irena, Kochanski, Andrzej, Reeser, Suzanne, Mancias, Pedro, Butler, Ian, Lupski, James R.
Published in Human mutation (01.04.2005)
Published in Human mutation (01.04.2005)
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Evolution of ABCA4 proteins in vertebrates
Yatsenko, Alexander N, Wiszniewski, Wojciech, Zaremba, Charles M, Jamrich, Milan, Lupski, James R
Published in Journal of molecular evolution (01.01.2005)
Published in Journal of molecular evolution (01.01.2005)
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Novel mutations in the RFXANK gene: RFX complex containing in-vitro-generated RFXANK mutant binds the promoter without transactivating MHC II
Wiszniewski, Wojciech, Fondaneche, Marie-Claude, Louise-Plence, Pascale, Prochnicka-Chalufour, Ada, Selz, Françoise, Picard, Cappucine, Le Deist, Françoise, Eliaou, Jean-François, Fischer, Alain, Lisowska-Grospierre, Barbara
Published in Immunogenetics (New York) (01.02.2003)
Published in Immunogenetics (New York) (01.02.2003)
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Three novel mutations of the CIITA gene in MHC class II-deficient patients with a severe immunodeficiency
Dziembowska, Magda, Fondaneche, Marie-Claude, Vedrenne, Jocelyn, Barbieri, Giovanna, Wiszniewski, Wojciech, Picard, Capucine, Cant, Andrew J, Steimle, Viktor, Charron, Dominique, Alca-Loridan, Catherine, Fischer, Alain, Lisowska-Grospierre, Barbara
Published in Immunogenetics (New York) (01.02.2002)
Published in Immunogenetics (New York) (01.02.2002)
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Refined Genetic and Physical Localization of the Wagner Disease (WGN1) Locus and the Genes CRTL1 and CSPG2 to a 2- to 2.5-cM Region of Chromosome 5q14.3
Perveen, Rahat, Hart-Holden, Niki, Dixon, Michael J., Wiszniewski, Wojtek, Fryer, Alan E., Brunner, Han G., Pinkners, Alfred J.L.H., van Beersum, Sylvie E.C., Black, Graeme C.M.
Published in Genomics (San Diego, Calif.) (15.04.1999)
Published in Genomics (San Diego, Calif.) (15.04.1999)
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A novel hereditary developmental vitreoretinopathy with multiple ocular abnormalities localizing to a 5-cM region of chromosome 5q13-q14
Black, Graeme C.M, Perveen, Rahat, Wiszniewski, Wojtek, Dodd, Christopher L, Donnai, Dian, McLeod, David
Published in Ophthalmology (Rochester, Minn.) (01.11.1999)
Published in Ophthalmology (Rochester, Minn.) (01.11.1999)
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Mutation in the Class II trans -Activator Leading to a Mild Immunodeficiency
Wiszniewski, Wojciech, Fondaneche, Marie-Claude, Le Deist, Françoise, Kanariou, Maria, Selz, Françoise, Brousse, Nicole, Steimle, Viktor, Barbieri, Giovanna, Alcaide-Loridan, Catherine, Charron, Dominique, Fischer, Alain, Lisowska-Grospierre, Barbara
Published in The Journal of immunology (1950) (01.07.2002)
Published in The Journal of immunology (1950) (01.07.2002)
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