Search Results - Kim Cryns
- Showing 1 - 7 results of 7
-
1
A genotype-phenotype correlation for GJB2 (connexin 26) deafness by Kim Cryns
Published 2004Artigo -
2
Transgenic Mice Overexpressing Glycogen Synthase Kinase 3β: A Putative Model of Hyperactivity and Mania by Jos Prickaerts, Dieder Moechars, Kim Cryns, Ilse Lenaerts, Hansfried Van Craenendonck, Ilse Goris, Guy Daneels, J. Adriaan Bouwknecht, Thomas Steckler
Published 2006Artigo -
3
IMPA1 is Essential for Embryonic Development and Lithium-Like Pilocarpine Sensitivity by Kim Cryns, Alon Shamir, Nathalie Van Acker, Itzhak Levi, Guy Daneels, Ilse Goris, J Adriaan Bouwknecht, Luc Andries, Stefan U. Kass, Galila Agam, H. Belmaker, Yuly Bersudsky, Thomas Steckler, Dieder Moechars
Published 2007Artigo -
4
Mutational spectrum of theWFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease by Kim Cryns, Theru A. Sivakumaran, Jody M.W. van den Ouweland, Ronald J. E. Pennings, Cor W. R. J. Cremers, Kris Flothmann, Terry‐Lynn Young, Richard J. Smith, Marci M. Lesperance, Guy Van Camp
Published 2003Revisão -
5
Phenotypic and Biochemical Analyses of BACE1- and BACE2-deficient Mice by Diana Dominguez, Jos Tournoy, Dieter Hartmann, Tobias Huth, Kim Cryns, Siska Deforce, Lutgarde Serneels, Ira Espuny-Camacho, Els Marjaux, Katleen Craessaerts, Anton Roebroek, Michael Schwake, Rudi D’Hooge, Patricia Bach, Ulrich Kalinke, Dieder Moechars, Christian Alzheimer, Karina Reiß, Paul Säftig, Bart De Strooper
Published 2005Artigo -
6
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss by Irina N. Bespalova, Guy Van Camp, Steven J. H. Bom, David J. Brown, Kim Cryns, Andrew T. DeWan, Ayse Elif Erson‐Bensan, Kris Flothmann, Henricus P. M. Kunst, Purnima Kurnool, Theru A. Sivakumaran, Cor W. R. J. Cremers, Suzanne M. Leal, Margit Burmeister, Marci M. Lesperance
Published 2001Artigo -
7
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study by Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann, Sandrine Marlin, Françoise Denoyelle, J Waligora, Małgorzata Mueller‐Malesińska, Agnieszka Pollak, Rafał Płoski, Alessandra Murgia, Eva Orzan, Pierangela Castorina, Umberto Ambrosetti, Ewa Nowakowska-Szyrwińska, Jerzy Bal, Wojciech Wiszniewski, Andreas Janecke, Doris Nekahm-Heis, Pavel Seeman, O. Bendová, Margaret A. Kenna, Anna Frangulov, Heidi L. Rehm, Mustafa Tekin, Armağan İncesulu, Hans‐Henrik M. Dahl, Desirée du Sart, Lucy Jenkins, Deirdre Lucas, Maria Bitner‐Glindzicz, Karen B. Avraham, Zippora Brownstein, Ignacio del Castillo, Felipe Moreno, Nikolaus Blin, Markus Pfister, István Sziklai, Tímea Tóth, Philip M. Kelley, Edward Cohn, Lionel Van Maldergem, Pascale Hilbert, Anne‐Françoise Roux, M. Mondain, Lies H. Hoefsloot, Cor W. R. J. Cremers, Tuija Löppönen, Heikki Löppönen, Agnete Parving, Karen Grønskov, Iris Schrijver, Joseph Roberson, Francesca Gualandi, Alessandro Martini, Geneviève Lina‐Granade, Nathalie Pallares‐Ruiz, Céu Correia, Graça Fialho, Kim Cryns, Nele Hilgert, Paul Van de Heyning, Carla Nishimura, Richard J. Smith, Guy Van Camp
Published 2005Artigo
Search Tools:
Related Subjects
Biology
Gene
Genetics
Medicine
Audiology
Hearing loss
Phenotype
Allele
Compound heterozygosity
Endocrinology
Internal medicine
Mutation
Atrophy
Genotype
Hippocampus
Lithium (medication)
Missense mutation
Neuroscience
Sensorineural hearing loss
Wolfram syndrome
Antidepressant
Behavioural despair test
Biochemistry
Cell biology
Chemistry
Diabetes insipidus
Diabetes mellitus
Disease
Embryonic stem cell
Epilepsy