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	1.	Gene expression of taurine transporter and taurine biosynthetic enzymes in hyperosmotic states: a comparative study with the expression of the genes involved in the accumulation of other osmolytes. [electronic resource] by Bitoun, M Tappaz, M Producer: 20020129 In: Advances in experimental medicine and biology vol. 483 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Gene expression of the transporters and biosynthetic enzymes of the osmolytes in astrocyte primary cultures exposed to hyperosmotic conditions. [electronic resource] by Bitoun, M Tappaz, M Producer: 20001121 In: Glia vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	3.	Taurine down-regulates basal and osmolarity-induced gene expression of its transporter, but not the gene expression of its biosynthetic enzymes, in astrocyte primary cultures. [electronic resource] by Bitoun, M Tappaz, M Producer: 20000912 In: Journal of neurochemistry vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Gene expression of taurine transporter and taurine biosynthetic enzymes in brain of rats with acute or chronic hyperosmotic plasma. A comparative study with gene expression of myo-inositol transporter, betaine transporter and sorbitol biosynthetic enzyme. [electronic resource] by Bitoun, M Tappaz, M Producer: 20000727 In: Brain research. Molecular brain research vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Gene expression of the taurine transporter and taurine biosynthetic enzymes in rat kidney after antidiuresis and salt loading. [electronic resource] by Bitoun, M Levillain, O Tappaz, M Producer: 20011101 In: Pflugers Archiv : European journal of physiology vol. 442 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Cysteine sulfinate decarboxylase (CSD): molecular cloning, sequence and genomic expression in brain. [electronic resource] by Tappaz, M Reymond, I Bitoun, M Sergeant, A Producer: 19980903 In: Advances in experimental medicine and biology vol. 442 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Regional expression and histological localization of cysteine sulfinate decarboxylase mRNA in the rat kidney. [electronic resource] by Reymond, I Bitoun, M Levillain, O Tappaz, M Producer: 20001130 In: The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Characterization of the cDNA coding for rat brain cysteine sulfinate decarboxylase: brain and liver enzymes are identical proteins encoded by two distinct mRNAs. [electronic resource] by Tappaz, M Bitoun, M Reymond, I Sergeant, A Producer: 19990914 In: Journal of neurochemistry vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A new centronuclear myopathy phenotype due to a novel dynamin 2 mutation. [electronic resource] by Bitoun, M Bevilacqua, J A Eymard, B Prudhon, B Fardeau, M Guicheney, P Romero, N B Producer: 20090408 In: Neurology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations. [electronic resource] by Hanisch, F Müller, T Dietz, A Bitoun, M Kress, W Weis, J Stoltenburg, G Zierz, S Producer: 20110923 In: Journal of neurology vol. 258 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Dynamin 2-related centronuclear myopathy: clinical, histological and genetic aspects of further patients and review of the literature. [electronic resource] by Jeub, M Bitoun, M Guicheney, P Kappes-Horn, K Strach, K Druschky, K F Weis, J Fischer, D Producer: 20090210 In: Clinical neuropathology vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutation. [electronic resource] by Claeys, K G Maisonobe, T Böhm, J Laporte, J Hezode, M Romero, N B Brochier, G Bitoun, M Carlier, R Y Stojkovic, T Producer: 20100305 In: Neurology vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization. [electronic resource] by Bevilacqua, J A Monnier, N Bitoun, M Eymard, B Ferreiro, A Monges, S Lubieniecki, F Taratuto, A L Laquerrière, A Claeys, K G Marty, I Fardeau, M Guicheney, P Lunardi, J Romero, N B Producer: 20110620 In: Neuropathology and applied neurobiology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)