Collin C - Search Results

1

Cortical Layer Inversion and Deregulation of Reelin Signaling in the Absence of SOCS6 and SOCS7.

Lawrenson ID, Krebs DL, Linossi EM, Zhang JG, McLennan TJ, Collin C, McRae HM, Kolesnik TB, Koh K, Britto JM, Kueh AJ, Sheikh BN, El-Saafin F, Nicola NA, Tan SS, Babon JJ, Nicholson SE, Alexander WS, Thomas T, Voss AK. Lawrenson ID, et al. Among authors: collin c. Cereb Cortex. 2017 Jan 1;27(1):576-588. doi: 10.1093/cercor/bhv253. Cereb Cortex. 2017. PMID: 26503265

2

C3G regulates cortical neuron migration, preplate splitting and radial glial cell attachment.

Voss AK, Britto JM, Dixon MP, Sheikh BN, Collin C, Tan SS, Thomas T. Voss AK, et al. Among authors: collin c. Development. 2008 Jun;135(12):2139-49. doi: 10.1242/dev.016725. Development. 2008. PMID: 18506028

3

MOZ directs the distal-less homeobox gene expression program during craniofacial development.

Vanyai HK, Garnham A, May RE, McRae HM, Collin C, Wilcox S, Smyth GK, Thomas T, Voss AK. Vanyai HK, et al. Among authors: collin c. Development. 2019 Jul 24;146(14):dev175042. doi: 10.1242/dev.175042. Development. 2019. PMID: 31340933

4

MOZ regulates the Tbx1 locus, and Moz mutation partially phenocopies DiGeorge syndrome.

Voss AK, Vanyai HK, Collin C, Dixon MP, McLennan TJ, Sheikh BN, Scambler P, Thomas T. Voss AK, et al. Among authors: collin c. Dev Cell. 2012 Sep 11;23(3):652-63. doi: 10.1016/j.devcel.2012.07.010. Epub 2012 Aug 23. Dev Cell. 2012. PMID: 22921202 Free PMC article.

5

The transcriptional coactivator Querkopf controls adult neurogenesis.

Merson TD, Dixon MP, Collin C, Rietze RL, Bartlett PF, Thomas T, Voss AK. Merson TD, et al. Among authors: collin c. J Neurosci. 2006 Nov 1;26(44):11359-70. doi: 10.1523/JNEUROSCI.2247-06.2006. J Neurosci. 2006. PMID: 17079664 Free PMC article.

6

Moz and retinoic acid coordinately regulate H3K9 acetylation, Hox gene expression, and segment identity.

Voss AK, Collin C, Dixon MP, Thomas T. Voss AK, et al. Among authors: collin c. Dev Cell. 2009 Nov;17(5):674-86. doi: 10.1016/j.devcel.2009.10.006. Dev Cell. 2009. PMID: 19922872 Free article.

7

Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity.

Voss AK, Gamble R, Collin C, Shoubridge C, Corbett M, Gécz J, Thomas T. Voss AK, et al. Among authors: collin c. Gene Expr Patterns. 2007 Oct;7(8):858-71. doi: 10.1016/j.modgep.2007.06.007. Epub 2007 Jul 6. Gene Expr Patterns. 2007. PMID: 17698420

8

ERG dependence distinguishes developmental control of hematopoietic stem cell maintenance from hematopoietic specification.

Taoudi S, Bee T, Hilton A, Knezevic K, Scott J, Willson TA, Collin C, Thomas T, Voss AK, Kile BT, Alexander WS, Pimanda JE, Hilton DJ. Taoudi S, et al. Among authors: collin c. Genes Dev. 2011 Feb 1;25(3):251-62. doi: 10.1101/gad.2009211. Epub 2011 Jan 18. Genes Dev. 2011. PMID: 21245161 Free PMC article.

9

NHS-A isoform of the NHS gene is a novel interactor of ZO-1.

Sharma S, Koh KS, Collin C, Dave A, McMellon A, Sugiyama Y, McAvoy JW, Voss AK, Gécz J, Craig JE. Sharma S, et al. Among authors: collin c. Exp Cell Res. 2009 Aug 15;315(14):2358-72. doi: 10.1016/j.yexcr.2009.05.008. Epub 2009 May 15. Exp Cell Res. 2009. PMID: 19447104

10

Neurog3-dependent pancreas dysgenesis causes ectopic pancreas in Hes1 mutant mice.

Jørgensen MC, de Lichtenberg KH, Collin CA, Klinck R, Ekberg JH, Engelstoft MS, Lickert H, Serup P. Jørgensen MC, et al. Among authors: collin ca. Development. 2018 Sep 3;145(17):dev163568. doi: 10.1242/dev.163568. Development. 2018. PMID: 30093553

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