Phenotypic and Biochemical Analyses of BACE1- and BACE2-deficient Mice von Dominguez, Diana, Tournoy, Jos, Hartmann, Dieter, Huth, Tobias, Cryns, Kim, Deforce, Siska, Serneels, Lutgarde, Camacho, Ira Espuny, Marjaux, Els, Craessaerts, Katleen, Roebroek, Anton J.M., Schwake, Michael, D'Hooge, Rudi, Bach, Patricia, Kalinke, Ulrich, Moechars, Dieder, Alzheimer, Christian, Reiss, Karina, Saftig, Paul, De Strooper, Bart

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IMPA1 is essential for embryonic development and lithium-like pilocarpine sensitivity von Cryns, Kim, Shamir, Alon, Van Acker, Nathalie, Levi, Itzhak, Daneels, Guy, Goris, Ilse, Bouwknecht, J Adriaan, Andries, Luc, Kass, Stefan, Agam, Galila, Belmaker, Haim, Bersudsky, Yuly, Steckler, Thomas, Moechars, Dieder

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Lack of lithium-like behavioral and molecular effects in IMPA2 knockout mice von CRYNS, Kim, SHAMIR, Alon, STECKLER, Thomas, SHAPIRO, Joseph, DANEELS, Gie, GORIS, Ilse, VAN CRAENENDONCK, Hansfried, STRAETEMANS, Roel, BELMAKER, Rh, AGAM, Galila, MOECHARS, Dieder

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Transgenic Mice Overexpressing Glycogen Synthase Kinase 3β: A Putative Model of Hyperactivity and Mania von Prickaerts, Jos, Moechars, Dieder, Cryns, Kim, Lenaerts, Ilse, van Craenendonck, Hansfried, Goris, Ilse, Daneels, Guy, Bouwknecht, J. Adriaan, Steckler, Thomas

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The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells von Cryns, Kim, Thys, Sofie, Van Laer, Lut, Oka, Yoshitomo, Pfister, Markus, Van Nassauw, Luc, Smith, Richard J. H., Timmermans, Jean-Pierre, Van Camp, Guy

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Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease von Cryns, Kim, Sivakumaran, Theru A., Van den Ouweland, Jody M.W., Pennings, Ronald J.E., Cremers, Cor W.R.J., Flothmann, Kris, Young, Terry-Lynn, Smith, Richard J.H., Lesperance, Marci M., Camp, Guy Van

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Mutational spectrum of theWFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease von Cryns, Kim, Sivakumaran, Theru A., Van den Ouweland, Jody M.W., Pennings, Ronald J.E., Cremers, Cor W.R.J., Flothmann, Kris, Young, Terry-Lynn, Smith, Richard J.H., Lesperance, Marci M., Camp, Guy Van

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Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss von Bespalova, I N, Van Camp, G, Bom, S J, Brown, D J, Cryns, K, DeWan, A T, Erson, A E, Flothmann, K, Kunst, H P, Kurnool, P, Sivakumaran, T A, Cremers, C W, Leal, S M, Burmeister, M, Lesperance, M M

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Deafness Genes and Their Diagnostic Applications von Cryns, Kim, van Camp, Guy

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Nonsyndromic Hearing Loss von Van Laer, Lut, Cryns, Kim, Smith, Richard J. H, Van Camp, Guy

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The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells von Cryns, Kim, Thys, Sofie, Van Laer, Lut, Oka, Yoshitomo, Pfister, Markus, Van Nassauw, Luc, Smith, Richard J H, Timmermans, Jean-Pierre, Van Camp, Guy

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Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations von CRYNS, Kim, PFISTER, Markus, KUPKA, Susan, BLIN, Nikolaus, NÜRNBERG, Peter, THIELE, Holger, DE HEYNING, Paul H, REARDON, William, STEPHENS, Dafydd, CREMERS, Cor W. R. J, SMITH, Richard J. H, VAN CAMP, Guy, PENNINGS, Ronald J. E, BOM, Steven J. H, FLOTHMANN, Kris, CAETHOVEN, Goele, KREMER, Hannie, SCHATTEMAN, Isabelle, KÖLN, Karen A, TOTH, Timea

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Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss von BESPALOVA, Irina N, VAN CAMP, Guy, SIVAKUMARAN, Theru A, CREMERS, Cor W. R. J, LEAL, Suzanne M, BURMEISTER, Margit, LESPERANCE, Marci M, BOM, Steven J. H, BROWN, David J, CRYNS, Kim, DEWAN, Andrew T, ERSON, Ayse E, FLOTHMANN, Kris, KUNST, Henricus P. M, KURNOOL, Purnima

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Circling behavior in the Ecl mouse is caused by lateral semicircular canal defects von Cryns, Kim, Van Alphen, Arjan M., Van Spaendonck, Michiel P., Van De Heyning, Paul H., Timmermans, Jean-Pierre, De Zeeuw, Chris I., Van Camp, Guy

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IMPAI is Essential for Embryonic Development and Lithium-Like Pilocarpine Sensitivity von CRYNS, Kim, SHAMIR, Alon, BELMAKER, Haim, BERSUDSKY, Yuly, STECKLER, Thomas, MOECHARS, Dieder, VAN ACKER, Nathalie, LEVI, Itzhak, DANEELS, Guy, GORIS, Ilse, ADRIAAN BOUWKNECHT, J, ANDRIES, Luc, KASS, Stefan, AGAM, Galila

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Transgenic Mice Overexpressing Glycogen Synthase Kinase 3beta: A Putative Model of Hyperactivity and Mania von Prickaerts, Jos, Moechars, Dieder, Cryns, Kim, Lenaerts, Ilse, van Craenendonck, Hansfried, Goris, Ilse, Daneels, Guy, Bouwknecht, J. Adriaan, Steckler, Thomas

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Molecular Characterization of WFS1 in Patients with Wolfram Syndrome von Van Den Ouweland, Johannes M.W., Cryns, Kim, Pennings, Ronald J.E., Walraven, Inge, Janssen, George M.C., Maassen, J. Antonie, Veldhuijzen, Bernard F.E., Arntzenius, Alexander B., Lindhout, Dick, Cremers, Cor W.R.J., Van Camp, Guy, Dikkeschei, Lambert D.

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Sex-Related Hearing Impairment in Wolfram Syndrome Patients Identified by Inactivating WFS1 Mutations von Pennings, Ronald J.E., Huygen, Patrick L.M., van den Ouweland, Jody M.W., Cryns, Kim, Dikkeschei, Lambert D., van Camp, Guy, Cremers, Cor W.R.J.

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Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genes von Cryns, Kim, Van Spaendonck, Michiel P, Flothmann, Kris, van Alphen, Arjan M, Van De Heyning, Paul H, Timmermans, Jean-Pierre, De Zeeuw, Chris I, Van Camp, Guy

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Phenotypic and biochemical analyses of BACE1- and BACE2-deficient mice von Dominguez, Diana Ines, Tournoy, Jos, Hartmann, Dieter, Huth, Tobias, Cryns, Kim, Deforce, Siska, Serneels, Lutgarde, Camacho, Ira Espuny, Marjaux, Els, Craessaerts, Kathleen, Roebroek, Anton, Schwake, Michael, D'Hooge, Rudi, Bach, Patricia, Kalinke, Ulrich, Moechars, Dieder, Alzheimer, Christian, Reiss, Karina, Saftig, Paul, De Strooper, Bart

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