Huylebroeck D - Search Results

1

Involvement of SIP1 in positioning of somite boundaries in the mouse embryo.

Maruhashi M, Van De Putte T, Huylebroeck D, Kondoh H, Higashi Y. Maruhashi M, et al. Among authors: huylebroeck d. Dev Dyn. 2005 Oct;234(2):332-8. doi: 10.1002/dvdy.20546. Dev Dyn. 2005. PMID: 16127714 Free article.

2

Complementary expression pattern of Zfhx1 genes Sip1 and deltaEF1 in the mouse embryo and their genetic interaction revealed by compound mutants.

Miyoshi T, Maruhashi M, Van De Putte T, Kondoh H, Huylebroeck D, Higashi Y. Miyoshi T, et al. Among authors: huylebroeck d. Dev Dyn. 2006 Jul;235(7):1941-52. doi: 10.1002/dvdy.20799. Dev Dyn. 2006. PMID: 16598713 Free article.

3

Generation of the floxed allele of the SIP1 (Smad-interacting protein 1) gene for Cre-mediated conditional knockout in the mouse.

Higashi Y, Maruhashi M, Nelles L, Van de Putte T, Verschueren K, Miyoshi T, Yoshimoto A, Kondoh H, Huylebroeck D. Higashi Y, et al. Among authors: huylebroeck d. Genesis. 2002 Feb;32(2):82-4. doi: 10.1002/gene.10048. Genesis. 2002. PMID: 11857784 No abstract available.

4

Deletion of MgcRacGAP in the male germ cells impairs spermatogenesis and causes male sterility in the mouse.

Lorès P, Vernet N, Kurosaki T, Van de Putte T, Huylebroeck D, Hikida M, Gacon G, Touré A. Lorès P, et al. Among authors: huylebroeck d. Dev Biol. 2014 Feb 15;386(2):419-27. doi: 10.1016/j.ydbio.2013.12.006. Epub 2013 Dec 16. Dev Biol. 2014. PMID: 24355749 Free article.

5

Sip1 regulates the generation of the inner nuclear layer retinal cell lineages in mammals.

Menuchin-Lasowski Y, Oren-Giladi P, Xie Q, Ezra-Elia R, Ofri R, Peled-Hajaj S, Farhy C, Higashi Y, Van de Putte T, Kondoh H, Huylebroeck D, Cvekl A, Ashery-Padan R. Menuchin-Lasowski Y, et al. Among authors: huylebroeck d. Development. 2016 Aug 1;143(15):2829-41. doi: 10.1242/dev.136101. Epub 2016 Jul 6. Development. 2016. PMID: 27385012 Free PMC article.

6

Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome.

Van de Putte T, Maruhashi M, Francis A, Nelles L, Kondoh H, Huylebroeck D, Higashi Y. Van de Putte T, et al. Among authors: huylebroeck d. Am J Hum Genet. 2003 Feb;72(2):465-70. doi: 10.1086/346092. Epub 2003 Jan 9. Am J Hum Genet. 2003. PMID: 12522767 Free PMC article.

7

Smad-interacting protein-1 (Zfhx1b) acts upstream of Wnt signaling in the mouse hippocampus and controls its formation.

Miquelajauregui A, Van de Putte T, Polyakov A, Nityanandam A, Boppana S, Seuntjens E, Karabinos A, Higashi Y, Huylebroeck D, Tarabykin V. Miquelajauregui A, et al. Among authors: huylebroeck d. Proc Natl Acad Sci U S A. 2007 Jul 31;104(31):12919-24. doi: 10.1073/pnas.0609863104. Epub 2007 Jul 20. Proc Natl Acad Sci U S A. 2007. PMID: 17644613 Free PMC article.

8

Genetic interaction between Sox10 and Zfhx1b during enteric nervous system development.

Stanchina L, Van de Putte T, Goossens M, Huylebroeck D, Bondurand N. Stanchina L, et al. Among authors: huylebroeck d. Dev Biol. 2010 May 15;341(2):416-28. doi: 10.1016/j.ydbio.2010.02.036. Epub 2010 Mar 4. Dev Biol. 2010. PMID: 20206619 Free article.

9

Dual-mode modulation of Smad signaling by Smad-interacting protein Sip1 is required for myelination in the central nervous system.

Weng Q, Chen Y, Wang H, Xu X, Yang B, He Q, Shou W, Chen Y, Higashi Y, van den Berghe V, Seuntjens E, Kernie SG, Bukshpun P, Sherr EH, Huylebroeck D, Lu QR. Weng Q, et al. Among authors: huylebroeck d. Neuron. 2012 Feb 23;73(4):713-28. doi: 10.1016/j.neuron.2011.12.021. Neuron. 2012. PMID: 22365546 Free PMC article.

10

Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex.

Verstappen G, van Grunsven LA, Michiels C, Van de Putte T, Souopgui J, Van Damme J, Bellefroid E, Vandekerckhove J, Huylebroeck D. Verstappen G, et al. Among authors: huylebroeck d. Hum Mol Genet. 2008 Apr 15;17(8):1175-83. doi: 10.1093/hmg/ddn007. Epub 2008 Jan 8. Hum Mol Genet. 2008. PMID: 18182442 Free article.

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