The PCP genes Celsr1 and Vangl2 are required for normal lung branching morphogenesis (English)
- New search for: Yates, L. L.
- New search for: Schnatwinkel, C.
- New search for: Murdoch, J. N.
- New search for: Bogani, D.
- New search for: Formstone, C. J.
- New search for: Townsend, S.
- New search for: Greenfield, A.
- New search for: Niswander, L. A.
- New search for: Dean, C. H.
- New search for: Yates, L. L.
- New search for: Schnatwinkel, C.
- New search for: Murdoch, J. N.
- New search for: Bogani, D.
- New search for: Formstone, C. J.
- New search for: Townsend, S.
- New search for: Greenfield, A.
- New search for: Niswander, L. A.
- New search for: Dean, C. H.
In:
HUMAN MOLECULAR GENETICS
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19
, 11
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2251-2267
;
2010
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ISSN:
- Article (Journal) / Print
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Title:The PCP genes Celsr1 and Vangl2 are required for normal lung branching morphogenesis
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Contributors:Yates, L. L. ( author ) / Schnatwinkel, C. ( author ) / Murdoch, J. N. ( author ) / Bogani, D. ( author ) / Formstone, C. J. ( author ) / Townsend, S. ( author ) / Greenfield, A. ( author ) / Niswander, L. A. ( author ) / Dean, C. H. ( author )
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Published in:HUMAN MOLECULAR GENETICS ; 19, 11 ; 2251-2267
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Publisher:
- New search for: Oxford University Press
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Publication date:2010-01-01
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Size:17 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 19, Issue 11
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.
- 2087
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Synphilin-1 attenuates neuronal degeneration in the A53T a-synuclein transgenic mouse modelSmith, W. W. / Liu, Z. / Liang, Y. / Masuda, N. / Swing, D. A. / Jenkins, N. A. / Copeland, N. G. / Troncoso, J. C. / Pletnikov, M. / Dawson, T. M. et al. | 2010
- 2099
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Mutant huntingtin fragment selectively suppresses Brn-2 POU domain transcription factor to mediate hypothalamic cell dysfunctionYamanaka, T. / Tosaki, A. / Miyazaki, H. / Kurosawa, M. / Furukawa, Y. / Yamada, M. / Nukina, N. et al. | 2010
- 2113
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OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulationBan, T. / Heymann, J. A. / Song, Z. / Hinshaw, J. E. / Chan, D. C. et al. | 2010
- 2123
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mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiaeStumpf, J. D. / Bailey, C. M. / Spell, D. / Stillwagon, M. / Anderson, K. S. / Copeland, W. C. et al. | 2010
- 2134
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The multiple sclerosis whole blood mRNA transcriptome and genetic associations indicate dysregulation of specific T cell pathways in pathogenesisGandhi, K. S. / McKay, F. C. / Cox, M. / Riveros, C. / Armstrong, N. / Heard, R. N. / Vucic, S. / Williams, D. W. / Stankovich, J. / Brown, M. et al. | 2010
- 2144
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Rilmenidine attenuates toxicity of polyglutamine expansions in a mouse model of Huntingtons diseaseRose, C. / Menzies, F. M. / Renna, M. / Acevedo-Arozena, A. / Corrochano, S. / Sadiq, O. / Brown, S. D. / Rubinsztein, D. C. et al. | 2010
- 2154
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Deficiency of the splicing factor Sfrs10 results in early embryonic lethality in mice and has no impact on full-length SMN/Smn splicingMende, Y. / Jakubik, M. / Riessland, M. / Schoenen, F. / Robach, K. / Kleinridders, A. / Kohler, C. / Buch, T. / Wirth, B. et al. | 2010
- 2168
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Epigenetic maturation in colonic mucosa continues beyond infancy in miceKellermayer, R. / Balasa, A. / Zhang, W. / Lee, S. / Mirza, S. / Chakravarty, A. / Szigeti, R. / Laritsky, E. / Tatevian, N. / Smith, C. W. et al. | 2010
- 2177
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Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal developmentAlvarez-Saavedra, M. / Carrasco, L. / Sura-Trueba, S. / Demarchi Aiello, V. / Walz, K. / Neto, J. X. / Young, J. I. et al. | 2010
- 2191
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Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibresTrollet, C. / Anvar, S. Y. / Venema, A. / Hargreaves, I. P. / Foster, K. / Vignaud, A. / Ferry, A. / Negroni, E. / Hourde, C. / Baraibar, M. A. et al. | 2010
- 2208
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Widespread enzymatic correction of CNS tissues by a single intracerebral injection of therapeutic lentiviral vector in leukodystrophy mouse modelsLattanzi, A. / Neri, M. / Maderna, C. / di Girolamo, I. / Martino, S. / Orlacchio, A. / Amendola, M. / Naldini, L. / Gritti, A. et al. | 2010
- 2228
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Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutationsUrwin, H. / Authier, A. / Nielsen, J. E. / Metcalf, D. / Powell, C. / Froud, K. / Malcolm, D. S. / Holm, I. / Johannsen, P. / Brown, J. et al. | 2010
- 2239
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Trafficking defects and loss of ligand binding are the underlying causes of all reported DDR2 missense mutations found in SMED-SL patientsAli, B. R. / Xu, H. / Akawi, N. A. / John, A. / Karuvantevida, N. S. / Langer, R. / Al-Gazali, L. / Leitinger, B. et al. | 2010
- 2251
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The PCP genes Celsr1 and Vangl2 are required for normal lung branching morphogenesisYates, L. L. / Schnatwinkel, C. / Murdoch, J. N. / Bogani, D. / Formstone, C. J. / Townsend, S. / Greenfield, A. / Niswander, L. A. / Dean, C. H. et al. | 2010
- 2268
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Functional muscle analysis of the Tcap knockout mouseMarkert, C. D. / Meaney, M. P. / Voelker, K. A. / Grange, R. W. / Dalley, H. W. / Cann, J. K. / Ahmed, M. / Bishwokarma, B. / Walker, S. J. / Yu, S. X. et al. | 2010
- 2284
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Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic miceWong, M. / Martin, L. J. et al. | 2010
- 2303
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A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height lociOkada, Y. / Kamatani, Y. / Takahashi, A. / Matsuda, K. / Hosono, N. / Ohmiya, H. / Daigo, Y. / Yamamoto, K. / Kubo, M. / Nakamura, Y. et al. | 2010
- 2313
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Regulatory polymorphisms in EGR2 are associated with susceptibility to systemic lupus erythematosusMyouzen, K. / Kochi, Y. / Shimane, K. / Fujio, K. / Okamura, T. / Okada, Y. / Suzuki, A. / Atsumi, T. / Ito, S. / Takada, K. et al. | 2010
- 2321
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Variation in the uric acid transporter gene (SLC2A9) and memory performanceHoulihan, L. M. / Wyatt, N. D. / Harris, S. E. / Hayward, C. / Gow, A. J. / Marioni, R. E. / Strachan, M. W. / Price, J. F. / Starr, J. M. / Wright, A. F. et al. | 2010
- 2331
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CIITA variation in the presence of HLA-DRB11501 increases risk for multiple sclerosisBronson, P. G. / Caillier, S. / Ramsay, P. P. / McCauley, J. L. / Zuvich, R. L. / De Jager, P. L. / Rioux, J. D. / Ivinson, A. J. / Compston, A. / Hafler, D. A. et al. | 2010
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Cover Page| 2010