Publications récentes
37 - Bonnamour G, Soret R, Pilon N. (2020). Dhh-expressing Schwann cell precursors contribute to skin and cochlear melanocytes, but not to vestibular melanocytes. Pigment Cell & Melanoma Research. (in press).
36 - Soret R, Schneider S, Bernas G, Christophers B, Souchkova O, Charrier B, Righini-Grunder F, Aspirot A, Landry M, Kembel SW, Faure C, Heuckeroth RO, Pilon N. (2020). Glial Cell Derived Neurotrophic Factor Induces Enteric Neurogenesis and Improves Colon Structure and Function in Mouse Models of Hirschsprung Disease. Gastroenterology. 17:S0016-5085(20)34944-1.
35 - Cardinal T, Bergeron KF, Soret R, Souchkova O, Faure C, Guillon A, Pilon N. (2020). Male-biased aganglionic megacolon in the TashT mouse model of Hirschsprung disease involves upregulation of p53 protein activity and Ddx3y gene expression. PLoS Genet, 8;16(9):e1009008.
34 - Bérubé-Simard, F. A., & Pilon, N. (2019). Molecular dissection of CHARGE syndrome highlights the vulnerability of neural crest cells to problems with alternative splicing and other transcription-related processes. Transcription, 10(1), 21-28.
33-Touré, A. M., Landry, M., Souchkova, O., Kembel, S. W., & Pilon, N. (2019). Gut microbiota-mediated Gene-Environment interaction in the TashT mouse model of Hirschsprung disease. Scientific reports, 9(1), 492.
32- Bélanger C*, Bérubé-Simard FA*, Leduc E, Bernas G, Campeau PM, Lalani SR, Martin DM, Bielas S, Moccia A, Srivastava A, Silversides DW and Pilon N. (2018) Dysregulation of co-transcriptional alternative splicing underlies CHARGE syndrome. Proceedings of the National Academy of Sciences USA 2018 Jan 8. pii: 201715378 (* contribution équivalente)
31- Farrell SA, Sodhi S, Marshall CR, Paton T, Guerin A, Scherer SW, Bérubé-Simard FA and Pilon N. (2017) HLX is a candidate gene for congenital diaphragmatic hernia, short bowel and asplenia in humans. American Journal of Medical Genetics, Part A 173(11):3070-3074.
30- Charrier B and Pilon N. (2017) Towards a better understanding of enteric gliogenesis. Neurogenesis 4(1): e1293958.
29- Soret R and Pilon N. (2016) Analysis of enteric neural crest cell migration using heterotopic grafts of embryonic guts. Bio-Protocols 6 (17) : e1924
28- Bergeron KF, Nguyen C, Cardinal T, Charrier B, Silversides DW and Pilon N. (2016) Upregulation of the Nr2f1-A830082K12Rik gene pair in murine neural crest cells results in a complex phenotype reminiscent of Waardenburg syndrome type 4. Disease Models and Mechanisms 9(11):1283-1293.
27- Touré AM, Charrier B and Pilon N. (2016) Male-specific colon motility dysfunction in the TashT mouse line. Neurogastroenterology and Motility 28(10):1494-507.
26- Pilon N. (2016) Pigmentation-based insertional mutagenesis is a simple and potent screening approach for identifying neurocristopathy-associated genes in mice. Rare Diseases 4 (1) : e1156287.
25- Sanchez-Ferras O*, Bernas G*, Farnos-Villar O, Touré AM, Souchkova O and Pilon N. (2016) A direct role for murine Caudal-related homeobox (Cdx) proteins in the trunk neural crest-gene regulatory network. Development 143(8):1363-74. (*contribution équivalente)
24- Soret R, Mennetrey M, Bergeron KF, Dariel A, Neunlist M, Grunder F, Faure C, Silversides DW and Pilon N. (2015) A collagen VI-dependent pathogenic mechanism for Hirschsprung’s disease. The Journal of Clinical Investigation 125(12):4483-96.
►Commentaires reliés:
Young HM and McKeown SJ (2015) Motility: Hirschsprung disease - laying down a suitable path. Nature Reviews in Gastroenterology and Hepatology (News and Views) 13(1):7-8.
Heuckeroth RO. (2015) Hirschsprung's disease, Down syndrome, and missing heritability: too much collagen slows migration. The Journal of Clinical Investigation (Commentary) 125(12):4323-6.
23- Bergeron KF*, Cardinal T*, Touré AM, Béland M, Raiwet DR, Silversides DW and Pilon N. (2015) Male-biased aganglionic megacolon in the TashT mouse line due to perturbation of silencer elements in a large gene desert of chromosome 10. PLoS Genetics 11(3):e1005093. (*contribution équivalente)
22- Sanchez-Ferras O, Bernas G, Laberge-Perrault E and Pilon N. (2014) Induction and dorsal restriction of Pax3 expression in the caudal neuroectoderm is mediated by integration of multiple pathways on a short neural crest enhancer. Bioch Biophys Acta-Gene regulatory Mechanisms 1839 (7):546-58.
21- Bergeron KF, Cardinal T and Pilon N (2013) A quantitative cell migration assay for murine enteric neural progenitors. Journal of Visualized Experiments (79) e50709, doi:10.3791/50709
20- Coutaud B, and Pilon N. (2013) Characterization of a novel transgenic mouse line expressing Cre recombinase under the control of the Cdx2 neural specific enhancer. Genesis 51(11):777-84
19-Bergeron K-F, Silversides DW and Pilon N. (2013) The developmental genetics of Hirschsprung’s disease. Clinical Genetics 83 (1):15-22.
18- Silversides DW, Raiwet D, Souchkova O, Viger RS and Pilon N. (2012) Transgenic mouse analysis of Sry expression during the pre- and peri-implantation stage. Developmental Dynamics 241(7): 1192-204.
17- Sanchez-Ferras O, Coutaud B, Djavanbakht-Samani T, Tremblay I, Souchkova O and Pilon N. (2012) Caudal-related homeobox (Cdx) protein-dependent integration of canonical Wnt signaling on Paired-box 3 (Pax3) neural crest enhancer. Journal of Biological Chemistry 287(20):16623-35.