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Slowed conduction and thin myelination of peripheral nerves associated with mutant rho Guanine-nucleotide exchange factor 10.
Verhoeven K, De Jonghe P, Van de Putte T, Nelis E, Zwijsen A, Verpoorten N, De Vriendt E, Jacobs A, Van Gerwen V, Francis A, Ceuterick C, Huylebroeck D, Timmerman V. Verhoeven K, et al. Among authors: huylebroeck d. Am J Hum Genet. 2003 Oct;73(4):926-32. doi: 10.1086/378159. Epub 2003 Aug 19. Am J Hum Genet. 2003. PMID: 14508709 Free PMC article.
Transforming growth factor beta signalling in vitro and in vivo: activin ligand-receptor interaction, Smad5 in vasculogenesis, and repression of target genes by the deltaEF1/ZEB-related SIP1 in the vertebrate embryo.
Zwijsen A, van Grunsven LA, Bosman EA, Collart C, Nelles L, Umans L, Van de Putte T, Wuytens G, Huylebroeck D, Verschueren K. Zwijsen A, et al. Among authors: huylebroeck d. Mol Cell Endocrinol. 2001 Jun 30;180(1-2):13-24. doi: 10.1016/s0303-7207(01)00505-6. Mol Cell Endocrinol. 2001. PMID: 11451567 Review.
Endocardial cushion and myocardial defects after cardiac myocyte-specific conditional deletion of the bone morphogenetic protein receptor ALK3.
Gaussin V, Van de Putte T, Mishina Y, Hanks MC, Zwijsen A, Huylebroeck D, Behringer RR, Schneider MD. Gaussin V, et al. Among authors: huylebroeck d. Proc Natl Acad Sci U S A. 2002 Mar 5;99(5):2878-83. doi: 10.1073/pnas.042390499. Epub 2002 Feb 19. Proc Natl Acad Sci U S A. 2002. PMID: 11854453 Free PMC article.
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.
170 results