Advanced search
Publication Cover
Rare Diseases Volume 4, 2016 - Issue 1
Journal homepage
1,254
Views
13
CrossRef citations to date
0
Altmetric
Addendum

Pigmentation-based insertional mutagenesis is a simple and potent screening approach for identifying neurocristopathy-associated genes in mice

Nicolas PilonMolecular Genetics of Development Laboratory, Department of Biological Sciences and BioMed Research Center, Faculty of Sciences, University of Quebec at Montreal (UQAM), Montreal, Quebec, Canada;UQAM Research Chair on Rare Genetic Diseases, Montreal, CanadaCorrespondence[email protected]
Article: e1156287 | Received 17 Dec 2015, Accepted 12 Feb 2016, Published online: 06 Apr 2016

Citations (13)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (2)

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.
Read now
Baptiste Charrier & Nicolas Pilon. (2017) Toward a better understanding of enteric gliogenesis. Neurogenesis 4:1.
Read now

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.
Crossref
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.
Crossref
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.
Crossref
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.
Crossref
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.
Crossref
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.
Crossref
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.
Crossref
Fjodor Merkuri & Jennifer L. Fish. (2018) Developmental processes regulate craniofacial variation in disease and evolution. genesis 57:1, pages e23249.
Crossref
Robert O. Heuckeroth. (2018) Hirschsprung disease — integrating basic science and clinical medicine to improve outcomes. Nature Reviews Gastroenterology & Hepatology 15:3, pages 152-167.
Crossref
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.
Crossref
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.
Crossref

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.