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Félix-Antoine Bérubé-Simard & Nicolas Pilon. (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, pages 21-28.
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Baptiste Charrier & Nicolas Pilon. (2017) Toward a better understanding of enteric gliogenesis. Neurogenesis 4:1.
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Articles from other publishers (11)
Sephora Sallis, Félix-Antoine Bérubé-Simard, Benoit Grondin, Elizabeth Leduc, Fatiha Azouz, Catherine Bélanger & Nicolas Pilon. (2023) The CHARGE syndrome-associated protein FAM172A controls AGO2 nuclear import. Life Science Alliance 6:8, pages e202302133.
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Mahum Nadeem, Lewis A Hassell, Hussein Bitar & Ijlal Akbar Ali. (2022) True Colonic Melanosis: An Interesting Phenotypic Variation of Neurocristopathy. Journal of the Canadian Association of Gastroenterology 5:5, pages 201-202.
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Grégoire Bonnamour, Baptiste Charrier, Sephora Sallis, Elizabeth Leduc & Nicolas Pilon. (2022)
NR2F1
regulates a Schwann cell precursor‐vs‐melanocyte cell fate switch in a mouse model of Waardenburg syndrome type
IV
. Pigment Cell & Melanoma Research 35:5, pages 506-516.
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Rodolphe Soret, Nejia Lassoued, Grégoire Bonnamour, Guillaume Bernas, Aurélie Barbe, Mélanie Pelletier, Manon Aichi & Nicolas Pilon. (2021) Genetic Background Influences Severity of Colonic Aganglionosis and Response to GDNF Enemas in the Holstein Mouse Model of Hirschsprung Disease. International Journal of Molecular Sciences 22:23, pages 13140.
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Grégoire Bonnamour, Rodolphe Soret & Nicolas Pilon. (2020)
Dhh
‐expressing Schwann cell precursors contribute to skin and cochlear melanocytes, but not to vestibular melanocytes
. Pigment Cell & Melanoma Research 34:3, pages 648-654.
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Tatiana Cardinal, Karl-Frédérik Bergeron, Rodolphe Soret, Ouliana Souchkova, Christophe Faure, Amélina Guillon & Nicolas Pilon. (2020) Male-biased aganglionic megacolon in the TashT mouse model of Hirschsprung disease involves upregulation of p53 protein activity and Ddx3y gene expression. PLOS Genetics 16:9, pages e1009008.
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Aboubacrine Mahamane Touré, Mathieu Landry, Ouliana Souchkova, Steven W. Kembel & Nicolas Pilon. (2019) Gut microbiota-mediated Gene-Environment interaction in the TashT mouse model of Hirschsprung disease. Scientific Reports 9:1.
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Fjodor Merkuri & Jennifer L. Fish. (2018) Developmental processes regulate craniofacial variation in disease and evolution. genesis 57:1, pages e23249.
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Robert O. Heuckeroth. (2018) Hirschsprung disease — integrating basic science and clinical medicine to improve outcomes. Nature Reviews Gastroenterology & Hepatology 15:3, pages 152-167.
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Catherine BélangerFélix-Antoine Bérubé-SimardElizabeth LeducGuillaume BernasPhilippe M. CampeauSeema R. LalaniDonna M. MartinStephanie BielasAmanda MocciaAnshika SrivastavaDavid W. Silversides & Nicolas Pilon. (2018) Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome. Proceedings of the National Academy of Sciences 115:4.
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Karl-F. Bergeron, Chloé M. A. Nguyen, Tatiana Cardinal, Baptiste Charrier, David W. Silversides & Nicolas Pilon. (2016)
Upregulation of
Nr2f1
-
A830082K12Rik
gene pair in murine neural crest cells results in a complex phenotype reminiscent of waardenburg syndrome type 4
. Disease Models & Mechanisms.
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