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	681.	Therapeutics development for spinal muscular atrophy. [electronic resource] by Sumner, Charlotte J Producer: 20060503 In: NeuroRx : the journal of the American Society for Experimental NeuroTherapeutics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	682.	Preservation of VGLUT1 synapses on ventral calbindin-immunoreactive interneurons and normal locomotor function in a mouse model of spinal muscular atrophy. [electronic resource] by Thirumalai, Vatsala Behrend, Rachel M Birineni, Swetha Liu, Wenfang Blivis, Dvir O'Donovan, Michael J Producer: 20130716 In: Journal of neurophysiology vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	683.	Dilysine motifs in exon 2b of SMN protein mediate binding to the COPI vesicle protein α-COP and neurite outgrowth in a cell culture model of spinal muscular atrophy. [electronic resource] by Custer, Sara K Todd, Adrian G Singh, Natalia N Androphy, Elliot J Producer: 20140422 In: Human molecular genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	684.	The SMN Tudor SIM-like domain is key to SmD1 and coilin interactions and to Cajal body biogenesis. [electronic resource] by Tapia, Olga Lafarga, Vanesa Bengoechea, Rocio Palanca, Ana Lafarga, Miguel Berciano, María T Producer: 20141104 In: Journal of cell science vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	685.	An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN. [electronic resource] by Lorson, C L Androphy, E J Producer: 20000228 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	686.	High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients. [electronic resource] by Bouhouche, A Benomar, A Birouk, N Bouslam, N Ouazzani, R Yahyaoui, M Chkili, T Producer: 20031212 In: Journal of neurology vol. 250 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	687.	Embryonic motor axon development in the severe SMA mouse. [electronic resource] by McGovern, Vicki L Gavrilina, Tatiana O Beattie, Christine E Burghes, Arthur H M Producer: 20081016 In: Human molecular genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	688.	Spinal muscular atrophy: clinical validation of a single-tube multiplex real time PCR assay for determination of SMN1 and SMN2 copy numbers. [electronic resource] by Maranda, Bruno Fan, Li Soucy, Jean-François Simard, Louise Mitchell, Grant A Producer: 20120628 In: Clinical biochemistry vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	689.	Bioenergetic status modulates motor neuron vulnerability and pathogenesis in a zebrafish model of spinal muscular atrophy. [electronic resource] by Boyd, Penelope J Tu, Wen-Yo Shorrock, Hannah K Groen, Ewout J N Carter, Roderick N Powis, Rachael A Thomson, Sophie R Thomson, Derek Graham, Laura C Motyl, Anna A L Wishart, Thomas M Highley, J Robin Morton, Nicholas M Becker, Thomas Becker, Catherina G Heath, Paul R Gillingwater, Thomas H Producer: 20170601 In: PLoS genetics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	690.	Targeted sequencing with expanded gene profile enables high diagnostic yield in non-5q-spinal muscular atrophies. [electronic resource] by Karakaya, Mert Storbeck, Markus Strathmann, Eike A Delle Vedove, Andrea Hölker, Irmgard Altmueller, Janine Naghiyeva, Leyla Schmitz-Steinkrüger, Lea Vezyroglou, Katharina Motameny, Susanne Alawbathani, Salem Thiele, Holger Polat, Ayse Ipek Okur, Derya Boostani, Reza Karimiani, Ehsan Ghayoor Wunderlich, Gilbert Ardicli, Didem Topaloglu, Haluk Kirschner, Janbernd Schrank, Bertold Maroofian, Reza Magnusson, Olafur Yis, Uluc Nürnberg, Peter Heller, Raoul Wirth, Brunhilde Producer: 20190726 In: Human mutation vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	691.	SMN protein analysis in fibroblast, amniocyte and CVS cultures from spinal muscular atrophy patients and its relevance for diagnosis. [electronic resource] by Patrizi, A L Tiziano, F Zappata, S Donati, M A Neri, G Brahe, C Producer: 19990628 In: European journal of human genetics : EJHG vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	692.	Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling. [electronic resource] by Cusin, V Clermont, O Gérard, B Chantereau, D Elion, J Producer: 20030417 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	693.	Spinal muscular atrophy: recent advances and future prospects. [electronic resource] by Nicole, Sophie Diaz, Carmen Cifuentes Frugier, Tony Melki, Judith Producer: 20020805 In: Muscle & nerve vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	694.	Subcutaneous administration of TC007 reduces disease severity in an animal model of SMA. [electronic resource] by Mattis, Virginia B Fosso, Marina Y Chang, Cheng-Wei Lorson, Christian L Producer: 20100114 In: BMC neuroscience vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	695.	A new splice site mutation in the SMN1 gene causes discrepant results in SMN1 deletion screening approaches. [electronic resource] by Eggermann, Thomas Eggermann, Katja Elbracht, Miriam Zerres, Klaus Rudnik-Schöneborn, Sabine Producer: 20080609 In: Neuromuscular disorders : NMD vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	696.	Rapid diagnosis of spinal muscular atrophy using tetra-primer ARMS PCR assay: simultaneous detection of SMN1 and SMN2 deletion. [electronic resource] by Baris, Ibrahim Etlik, Ozdal Koksal, Vedat Arican-Baris, S Tugba Producer: 20100810 In: Molecular and cellular probes vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	697.	[Point mutation analysis of SMN1 gene in patients with spinal muscular atrophy]. [electronic resource] by QU, Yu-jin DU, Juan LI, Er-zhen YANG, Yan-ling ZOU, Li-ping BAI, Jin-li WANG, Hong JIN, Yu-wei SONG, Fang Producer: 20110531 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	698.	The neuroprotective drug riluzole acts via small conductance Ca2+-activated K+ channels to ameliorate defects in spinal muscular atrophy models. [electronic resource] by Dimitriadi, Maria Kye, Min Jeong Kalloo, Geetika Yersak, Jill M Sahin, Mustafa Hart, Anne C Producer: 20130605 In: The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	699.	Aggregation of ALS-linked FUS mutant sequesters RNA binding proteins and impairs RNA granules formation. [electronic resource] by Takanashi, Keisuke Yamaguchi, Atsushi Producer: 20150225 In: Biochemical and biophysical research communications vol. 452 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	700.	[Spinal muscular atrophy : Time for newborn screening?] [electronic resource] by Vill, K Blaschek, A Schara, U Kölbel, H Hohenfellner, K Harms, E Olgemöller, B Walter, Maggie C Müller-Felber, W Producer: 20190327 In: Der Nervenarzt vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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