The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1 (English)
- New search for: van Wijk, E.
- New search for: van der Zwaag, B.
- New search for: Peters, T.
- New search for: Zimmermann, U.
- New search for: te Brinke, H.
- New search for: Kersten, F. F.
- New search for: Marker, T.
- New search for: Aller, E.
- New search for: Hoefsloot, L. H.
- New search for: Cremers, C. W.
- New search for: van Wijk, E.
- New search for: van der Zwaag, B.
- New search for: Peters, T.
- New search for: Zimmermann, U.
- New search for: te Brinke, H.
- New search for: Kersten, F. F.
- New search for: Marker, T.
- New search for: Aller, E.
- New search for: Hoefsloot, L. H.
- New search for: Cremers, C. W.
In:
HUMAN MOLECULAR GENETICS
;
15
, 5
;
751-765
;
2006
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ISSN:
- Article (Journal) / Print
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Title:The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1
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Contributors:van Wijk, E. ( author ) / van der Zwaag, B. ( author ) / Peters, T. ( author ) / Zimmermann, U. ( author ) / te Brinke, H. ( author ) / Kersten, F. F. ( author ) / Marker, T. ( author ) / Aller, E. ( author ) / Hoefsloot, L. H. ( author ) / Cremers, C. W. ( author )
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Published in:HUMAN MOLECULAR GENETICS ; 15, 5 ; 751-765
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Publisher:
- New search for: Oxford University Press
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Publication date:2006-01-01
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Size:15 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 572.8
- Further information on Dewey Decimal Classification
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Classification:
DDC: 572.8 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 15, Issue 5
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 667
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Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia functionYen, Hsan-Jan / Tayeh, Marwan K. / Mullins, Robert F. / Stone, Edwin M. / Sheffield, Val C. / Slusarski, Diane C. et al. | 2006
- 679
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Mild Nijmegen breakage syndrome phenotype due to alternative splicingVaron, Raymonda / Dutrannoy, Véronique / Weikert, Georg / Tanzarella, Caterina / Antoccia, Antonio / Stöckl, Lars / Spadoni, Emanuela / Krüger, Lars-Arne / Masi, Alessandra di / Sperling, Karl et al. | 2006
- 691
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Polyglutamine expansion causes neurodegeneration by altering the neuronal differentiation programAbou-Sleymane, Gretta / Chalmel, Frédéric / Helmlinger, Dominique / Lardenois, Aurélie / Thibault, Christelle / Weber, Chantal / Mérienne, Karine / Mandel, Jean-Louis / Poch, Olivier / Devys, Didier et al. | 2006
- 705
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Post-weaning diet affects genomic imprinting at the insulin-like growth factor 2 (Igf2) locusWaterland, Robert A. / Lin, Juan-Ru / Smith, Charlotte A. / Jirtle, Randy L. et al. | 2006
- 717
-
Allele-specific deposition of macroH2A1 in imprinting control regionsChoo, Jung Ha / Kim, Jeong Do / Chung, Jae Hoon / Stubbs, Lisa / Kim, Joomyeong et al. | 2006
- 725
-
Structural stability and chromosome-specific telomere length is governed by cis-acting determinants in humansBritt-Compton, Bethan / Rowson, Jan / Locke, Matthew / Mackenzie, Ian / Kipling, David / Baird, Duncan M. et al. | 2006
- 735
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Podocalyxin variants and risk of prostate cancer and tumor aggressivenessCasey, Graham / Neville, Phillippa J. / Liu, Xin / Plummer, Sarah J. / Cicek, Mine S. / Krumroy, Lisa M. / Curran, Anthony P. / McGreevy, Michelle R. / Catalona, William J. / Klein, Eric A. et al. | 2006
- 743
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DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signalingWilson, Gary M. / Flibotte, Stephane / Chopra, Vikramjit / Melnyk, Brianna L. / Honer, William G. / Holt, Robert A. et al. | 2006
- 751
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The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1van Wijk, Erwin / van der Zwaag, Bert / Peters, Theo / Zimmermann, Ulrike / te Brinke, Heleen / Kersten, Ferry F.J. / Märker, Tina / Aller, Elena / Hoefsloot, Lies H. / Cremers, Cor W.R.J. et al. | 2006
- 767
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Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3Lefèvre, Caroline / Bouadjar, Bakar / Ferrand, Véronique / Tadini, Gianluca / Mégarbané, André / Lathrop, Mark / Prud'homme, Jean-François / Fischer, Judith et al. | 2006
- 777
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Differential expression of novel naturally occurring splice variants of PTEN and their functional consequences in Cowden syndrome and sporadic breast cancerAgrawal, Shipra / Eng, Charis et al. | 2006
- 789
-
Extended tracts of homozygosity in outbred human populationsGibson, Jane / Morton, Newton E. / Collins, Andrew et al. | 2006
- 797
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ABCB1/MDR1 gene determines susceptibility and phenotype in ulcerative colitis: discrimination of critical variants using a gene-wide haplotype tagging approachHo, G.-T. / Soranzo, N. / Nimmo, E.R. / Tenesa, A. / Goldstein, D.B. / Satsangi, J. et al. | 2006