Phenotypic and Biochemical Analyses of BACE1- and BACE2-deficient Mice
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
Published in The Journal of biological chemistry (02.09.2005)
Published in The Journal of biological chemistry (02.09.2005)
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Journal Article
IMPA1 is essential for embryonic development and lithium-like pilocarpine sensitivity
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
Published in Neuropsychopharmacology (New York, N.Y.) (01.02.2008)
Published in Neuropsychopharmacology (New York, N.Y.) (01.02.2008)
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Journal Article
Lack of lithium-like behavioral and molecular effects in IMPA2 knockout mice
CRYNS, Kim, SHAMIR, Alon, STECKLER, Thomas, SHAPIRO, Joseph, DANEELS, Gie, GORIS, Ilse, VAN CRAENENDONCK, Hansfried, STRAETEMANS, Roel, BELMAKER, Rh, AGAM, Galila, MOECHARS, Dieder
Published in Neuropsychopharmacology (New York, N.Y.) (01.04.2007)
Published in Neuropsychopharmacology (New York, N.Y.) (01.04.2007)
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Journal Article
The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells
Cryns, Kim, Thys, Sofie, Van Laer, Lut, Oka, Yoshitomo, Pfister, Markus, Van Nassauw, Luc, Smith, Richard J. H., Timmermans, Jean-Pierre, Van Camp, Guy
Published in Histochemistry and cell biology (01.03.2003)
Published in Histochemistry and cell biology (01.03.2003)
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Journal Article
Transgenic Mice Overexpressing Glycogen Synthase Kinase 3β: A Putative Model of Hyperactivity and Mania
Prickaerts, Jos, Moechars, Dieder, Cryns, Kim, Lenaerts, Ilse, van Craenendonck, Hansfried, Goris, Ilse, Daneels, Guy, Bouwknecht, J. Adriaan, Steckler, Thomas
Published in The Journal of neuroscience (30.08.2006)
Published in The Journal of neuroscience (30.08.2006)
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Journal Article
Mutational spectrum of theWFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease
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
Published in Human mutation (01.10.2003)
Published in Human mutation (01.10.2003)
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Journal Article
Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease
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
Published in Human mutation (01.10.2003)
Published in Human mutation (01.10.2003)
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Journal Article
Progression of Low-Frequency Sensorineural Hearing Loss (DFNA6/14-WFS1)
Pennings, Ronald J. E, Bom, Steven J. H, Cryns, Kim, Flothmann, Kris, Huygen, Patrick L. M, Kremer, Hannie, Van Camp, Guy, Cremers, Cor W. R. J
Published in Archives of otolaryngology--head & neck surgery (01.04.2003)
Published in Archives of otolaryngology--head & neck surgery (01.04.2003)
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Journal Article
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss
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
Published in Human molecular genetics (15.10.2001)
Published in Human molecular genetics (15.10.2001)
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Journal Article
Nonsyndromic hearing loss
Van Laer, Lut, Cryns, Kim, Smith, Richard J H, Van Camp, Guy
Published in Ear and hearing (01.08.2003)
Published in Ear and hearing (01.08.2003)
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Journal Article
The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells
Cryns, Kim, Thys, Sofie, Van Laer, Lut, Oka, Yoshitomo, Pfister, Markus, Van Nassauw, Luc, Smith, Richard J H, Timmermans, Jean-Pierre, Van Camp, Guy
Published in Histochemistry and cell biology (01.03.2003)
Published in Histochemistry and cell biology (01.03.2003)
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Journal Article
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss
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
Published in Human molecular genetics (01.10.2001)
Published in Human molecular genetics (01.10.2001)
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Journal Article
IMPAI is Essential for Embryonic Development and Lithium-Like Pilocarpine Sensitivity
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
Published in Neuropsychopharmacology (New York, N.Y.) (2008)
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Published in Neuropsychopharmacology (New York, N.Y.) (2008)
Journal Article
Transgenic Mice Overexpressing Glycogen Synthase Kinase 3beta: A Putative Model of Hyperactivity and Mania
Prickaerts, Jos, Moechars, Dieder, Cryns, Kim, Lenaerts, Ilse, van Craenendonck, Hansfried, Goris, Ilse, Daneels, Guy, Bouwknecht, J. Adriaan, Steckler, Thomas
Published in The Journal of neuroscience (30.08.2006)
Published in The Journal of neuroscience (30.08.2006)
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Journal Article
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations
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
Published in Human genetics (01.05.2002)
Published in Human genetics (01.05.2002)
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Journal Article
Circling behavior in the Ecl mouse is caused by lateral semicircular canal defects
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
Published in Journal of comparative neurology (1911) (19.01.2004)
Published in Journal of comparative neurology (1911) (19.01.2004)
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Journal Article
Molecular Characterization of WFS1 in Patients with Wolfram Syndrome
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.
Published in The Journal of molecular diagnostics : JMD (01.05.2003)
Published in The Journal of molecular diagnostics : JMD (01.05.2003)
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Journal Article
Sex-Related Hearing Impairment in Wolfram Syndrome Patients Identified by Inactivating WFS1 Mutations
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.
Published in Audiology & neurotology (01.01.2004)
Published in Audiology & neurotology (01.01.2004)
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Journal Article
Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genes
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
Published in Genome research (01.04.2002)
Published in Genome research (01.04.2002)
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Journal Article