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	1.	Emerging complexity of the HuD/ELAVl4 gene; implications for neuronal development, function, and dysfunction. [electronic resource] by Bronicki, Lucas M Jasmin, Bernard J Producer: 20130927 In: RNA (New York, N.Y.) vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Trans-acting factors governing acetylcholinesterase mRNA metabolism in neurons. [electronic resource] by Bronicki, Lucas M Jasmin, Bernard J Producer: 20121002 In: Frontiers in molecular neuroscience vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Characterization of multiple exon 1 variants in mammalian HuD mRNA and neuron-specific transcriptional control via neurogenin 2. [electronic resource] by Bronicki, Lucas M Bélanger, Guy Jasmin, Bernard J Producer: 20121102 In: The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Beyond osteogenesis imperfecta: Causes of fractures during infancy and childhood. [electronic resource] by Bronicki, Lucas M Stevenson, Roger E Spranger, Jürgen W Producer: 20161019 In: American journal of medical genetics. Part C, Seminars in medical genetics vol. 169 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Combinatorial therapeutic activation with heparin and AICAR stimulates additive effects on utrophin A expression in dystrophic muscles. [electronic resource] by Péladeau, Christine Ahmed, Aatika Amirouche, Adel Crawford Parks, Tara E Bronicki, Lucas M Ljubicic, Vladimir Renaud, Jean-Marc Jasmin, Bernard J Producer: 20160923 In: Human molecular genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A. [electronic resource] by Bronicki, Lucas M Redin, Claire Drunat, Severine Piton, Amélie Lyons, Michael Passemard, Sandrine Baumann, Clarisse Faivre, Laurence Thevenon, Julien Rivière, Jean-Baptiste Isidor, Bertrand Gan, Grace Francannet, Christine Willems, Marjolaine Gunel, Murat Jones, Julie R Gleeson, Joseph G Mandel, Jean-Louis Stevenson, Roger E Friez, Michael J Aylsworth, Arthur S Producer: 20160506 In: European journal of human genetics : EJHG vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)