Polyductin undergoes notch-like processing and regulated release from primary cilia (English)
- New search for: Kaimori, J. y.
- New search for: Nagasawa, Y.
- New search for: Menezes, L. F.
- New search for: Garcia-Gonzalez, M. A.
- New search for: Deng, J.
- New search for: Imai, E.
- New search for: Onuchic, L. F.
- New search for: Guay-Woodford, L. M.
- New search for: Germino, G. G.
- New search for: Kaimori, J. y.
- New search for: Nagasawa, Y.
- New search for: Menezes, L. F.
- New search for: Garcia-Gonzalez, M. A.
- New search for: Deng, J.
- New search for: Imai, E.
- New search for: Onuchic, L. F.
- New search for: Guay-Woodford, L. M.
- New search for: Germino, G. G.
In:
HUMAN MOLECULAR GENETICS
;
16
, 8
;
942-956
;
2007
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ISSN:
- Article (Journal) / Print
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Title:Polyductin undergoes notch-like processing and regulated release from primary cilia
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Contributors:Kaimori, J. y. ( author ) / Nagasawa, Y. ( author ) / Menezes, L. F. ( author ) / Garcia-Gonzalez, M. A. ( author ) / Deng, J. ( author ) / Imai, E. ( author ) / Onuchic, L. F. ( author ) / Guay-Woodford, L. M. ( author ) / Germino, G. G. ( author )
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Published in:HUMAN MOLECULAR GENETICS ; 16, 8 ; 942-956
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Publisher:
- New search for: Oxford University Press
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Publication date:2007-01-01
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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 16, Issue 8
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.
- 865
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Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variantsGrupe, Andrew / Abraham, Richard / Li, Yonghong / Rowland, Charles / Hollingworth, Paul / Morgan, Angharad / Jehu, Luke / Segurado, Ricardo / Stone, David / Schadt, Eric et al. | 2007
- 874
-
Multiple roles for neurofibromin in skeletal development and growthKolanczyk, Mateusz / Kossler, Nadine / Kühnisch, Jirko / Lavitas, Liron / Stricker, Sigmar / Wilkening, Ulrich / Manjubala, Inderchand / Fratzl, Peter / Spörle, Ralf / Herrmann, Bernhard G. et al. | 2007
- 887
-
Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery diseaseBaessler, Andrea / Fischer, Marcus / Mayer, Bjoern / Koehler, Martina / Wiedmann, Silke / Stark, Klaus / Doering, Angela / Erdmann, Jeanette / Riegger, Guenter / Schunkert, Heribert et al. | 2007
- 900
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Corticosteroid-exacerbated symptoms in an Andersen's syndrome kindredBendahhou, Saïd / Fournier, Emmanuel / Gallet, Serge / Ménard, Dominique / Larroque, Marie-Madeleine / Barhanin, Jacques et al. | 2007
- 907
-
Cellular and molecular studies of Marfan syndrome mutations identify co-operative protein folding in the cbEGF12-13 region of fibrillin-1Whiteman, Pat / Willis, Antony C. / Warner, Andrew / Brown, James / Redfield, Christina / Handford, Penny A. et al. | 2007
- 919
-
Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in miceWeihl, Conrad C. / Miller, Sara E. / Hanson, Phyllis I. / Pestronk, Alan et al. | 2007
- 929
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Mitochondrial frataxin interacts with ISD11 of the NFS1/ISCU complex and multiple mitochondrial chaperonesShan, Yuxi / Napoli, Eleonora / Cortopassi, Gino et al. | 2007
- 942
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Polyductin undergoes notch-like processing and regulated release from primary ciliaKaimori, Jun-ya / Nagasawa, Yasuyuki / Menezes, Luis F. / Garcia-Gonzalez, Miguel A. / Deng, Jie / Imai, Enyu / Onuchic, Luiz F. / Guay-Woodford, Lisa M. / Germino, Gregory G. et al. | 2007
- 957
-
Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and a-hydroxy ceramide accumulation, and altered prosaposin traffickingSun, Y. / Witte, D. P. / Zamzow, M. / Ran, H. / Quinn, B. / Matsuda, J. / Grabowski, G. A. et al. | 2007
- 957
-
Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and {alpha}-hydroxy ceramide accumulation, and altered prosaposin traffickingSun, Ying / Witte, David P. / Zamzow, Matt / Ran, Huimin / Quinn, Brian / Matsuda, Junko / Grabowski, Gregory A. et al. | 2007
- 972
-
Tissue-specific imprinting of the ZAC/PLAGL1 tumour suppressor gene results from variable utilization of monoallelic and biallelic promotersValleley, Elizabeth M. / Cordery, Sarah F. / Bonthron, David T. et al. | 2007
- 982
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The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivoMonet, Marie / Domenga, Valérie / Lemaire, Barbara / Souilhol, Céline / Langa, Francina / Babinet, Charles / Gridley, Thomas / Tournier-Lasserve, Elisabeth / Cohen-Tannoudji, Michel / Joutel, Anne et al. | 2007
- 993
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PGC-1a/b upregulation is associated with improved oxidative phosphorylation in cells harboring nonsense mtDNA mutationsSrivastava, S. / Barrett, J. N. / Moraes, C. T. et al. | 2007
- 993
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PGC-1{alpha}/{beta} upregulation is associated with improved oxidative phosphorylation in cells harboring nonsense mtDNA mutationsSrivastava, Sarika / Barrett, John N. / Moraes, Carlos T. et al. | 2007
- 1006
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Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathwayKramerova, I. / Kudryashova, E. / Venkatraman, G. / Spencer, M.J. et al. | 2007