Expression of Taurine Transporter (TauT) is Modulated by Heat Shock Factor 1 (HSF1) in Motor Neurons of ALS
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N. Kowall | J. Sung | H. Ryu | Junghee Lee | Yunha Kim | Young-Sook Kang | Y. Hwang | Ki Yoon Kim | Na-young Lee | M. Jung | A. Mckee
[1] J. Mendell,et al. Astrocytes from Familial and Sporadic ALS Patients are Toxic to Motor Neurons , 2011, Nature Biotechnology.
[2] Jang-Yen Wu,et al. Taurine protection of PC12 cells against endoplasmic reticulum stress induced by oxidative stress , 2010, Journal of Biomedical Science.
[3] N. Kowall,et al. Differential regulation of neuronal and inducible nitric oxide synthase (NOS) in the spinal cord of mutant SOD1 (G93A) ALS mice. , 2009, Biochemical and biophysical research communications.
[4] N. Kowall,et al. Motor neuronal protection by L-arginine prolongs survival of mutant SOD1 (G93A) ALS mice. , 2009, Biochemical and biophysical research communications.
[5] J. Trojanowski,et al. Establishment of a cell model of ALS disease: Golgi apparatus disruption occurs independently from apoptosis , 2008, Biotechnology Letters.
[6] P. Altevogt,et al. Evidence for secretion of Cu,Zn superoxide dismutase via exosomes from a cell model of amyotrophic lateral sclerosis , 2007, Neuroscience Letters.
[7] R. Ferrante,et al. Antioxidants modulate mitochondrial PKA and increase CREB binding to D-loop DNA of the mitochondrial genome in neurons. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[8] G. Carter,et al. Current pharmacological management of amyotropic lateral sclerosis and a role for rational polypharmacy , 2004, Expert opinion on pharmacotherapy.
[9] J. Rothstein. Of mice and men: Reconciling preclinical ALS mouse studies and human clinical trials , 2003, Annals of neurology.
[10] Z. Stelmasiak,et al. Plasma amino acids concentration in amyotrophic lateral sclerosis patients , 2003, Amino Acids.
[11] R. Takahashi,et al. Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis , 2002, Journal of neurochemistry.
[12] H. Takanaga,et al. Regulation of taurine transport at the blood–brain barrier by tumor necrosis factor‐α, taurine and hypertonicity , 2002, Journal of neurochemistry.
[13] M. Bitoun,et al. Gene expression of the transporters and biosynthetic enzymes of the osmolytes in astrocyte primary cultures exposed to hyperosmotic conditions , 2000, Glia.
[14] M. Bitoun,et al. 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. , 2000, Brain research. Molecular brain research.
[15] Guoyao Wu,et al. Arginine metabolism: nitric oxide and beyond. , 1998, The Biochemical journal.
[16] L. Bruijn,et al. Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1. , 1998, Science.
[17] D. McMillan,et al. Stress (heat shock) proteins: molecular chaperones in cardiovascular biology and disease. , 1998, Circulation research.
[18] D. Borchelt,et al. ALS-Linked SOD1 Mutant G85R Mediates Damage to Astrocytes and Promotes Rapidly Progressive Disease with SOD1-Containing Inclusions , 1997, Neuron.
[19] A. Levey,et al. Selective loss of glial glutamate transporter GLT‐1 in amyotrophic lateral sclerosis , 1995, Annals of neurology.
[20] D. Borchelt,et al. An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria , 1995, Neuron.
[21] M. Aschner,et al. Potassium and Taurine Release Are Highly Correlated with Regulatory Volume Decrease in Neonatal Primary Rat Astrocyte Cultures , 1994, Journal of neurochemistry.
[22] M. Gurney,et al. Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation. , 1994, Science.
[23] J. Haines,et al. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis , 1993, Nature.
[24] T. Branchek,et al. Cloning and expression of a high affinity taurine transporter from rat brain. , 1992, Molecular pharmacology.
[25] G. P. Martin,et al. Bile Salt‐ and Lysophosphatidylcholine‐induced Membrane Damage in Human Erythrocytes , 1992, The Journal of pharmacy and pharmacology.
[26] T. Tabira,et al. Neuroblastoma × spinal cord (NSC) hybrid cell lines resemble developing motor neurons , 1992, Developmental dynamics : an official publication of the American Association of Anatomists.
[27] A. Plaitakis,et al. The neuroexcitotoxic amino acids glutamate and aspartate are altered in the spinal cord and brain in amyotrophic lateral sclerosis , 1988, Annals of neurology.
[28] S. Nelson,et al. A Possible Role for Taurine in Osmoregulation Within the Brain , 1988, Journal of neurochemistry.
[29] Jang-Yen Wu,et al. Is taurine a neurotransmitter in rabbit retina? , 1985, Brain Research.
[30] Y. Yoshino,et al. Free amino acids in motor cortex of amyotrophic lateral sclerosis , 1979, Experientia.
[31] P. Mcgeer,et al. Pharmacologic Approaches to the Treatment of Amyotrophic Lateral Sclerosis , 2012, BioDrugs.
[32] A. Ludolph,et al. Amyotrophic lateral sclerosis. , 2012, Current opinion in neurology.
[33] Guoyao Wu,et al. Analysis of citrulline, arginine, and methylarginines using high-performance liquid chromatography. , 2008, Methods in enzymology.
[34] M. Mozaffari,et al. Effects of dietary salt and fat on taurine excretion in healthy and diseased rats. , 2006, Advances in experimental medicine and biology.
[35] B. Citron,et al. Prospects for the Pharmacotherapy of Amyotrophic Lateral Sclerosis , 2003, CNS drugs.
[36] M. Bitoun,et al. 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. , 2000, Advances in experimental medicine and biology.
[37] M. Gurney,et al. Pathogenic mechanisms in familial amyotrophic lateral sclerosis due to mutation of Cu, Zn superoxide dismutase. , 1996, Pathologie-biologie.
[38] S. Dahrouge,et al. Evaluation of the spinal cord neuron X neuroblastoma hybrid cell line NSC-34 as a model for neurotoxicity testing. , 1993, Neurotoxicology.
[39] R J Huxtable,et al. Physiological actions of taurine. , 1992, Physiological reviews.
[40] Y. Yoshino,et al. [Free amino-acids in the human spinal cord--analysis of anterior, posterior columns and anterior, lateral and posterior funiculi]. , 1976, Rinshō shinkeigaku Clinical neurology.