Blood Volatile Organic Compounds as Potential Biomarkers for Amyotrophic Lateral Sclerosis: an Animal Study in the SOD1 G93A Mouse
暂无分享,去创建一个
Xiang Yin | Enyou Li | Hongquan Jiang | Changsong Wang | M. Ren | Chaofu Ke | Ming Ren | Changsong Wang | C. Chi | Lei Guo | E. Li | Hongquan Jiang | Xiang Yin | H. Feng | Chaofu Ke | Lei Guo | Chunjie Chi | Honglin Feng
[1] S. W. Lin,et al. Protein damage and degradation by oxygen radicals. II. Modification of amino acids. , 1987, The Journal of biological chemistry.
[2] W. Bradley,et al. Amyotrophc Lateral Sclerosis: Part 1. Clinical Features, Pathology, and E h c d Issues in Management* , 2004 .
[3] S. Rozen,et al. Metabolomic analysis and signatures in motor neuron disease , 2005, Metabolomics.
[4] Barry Halliwell,et al. Oxidative stress and neurodegeneration: where are we now? , 2006, Journal of neurochemistry.
[5] W. Matson,et al. Increased oxidative damage to DNA in an animal model of amyotrophic lateral sclerosis , 2005, Free radical research.
[6] J. Haines,et al. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis , 1993, Nature.
[7] P. Massion,et al. The State of Molecular Biomarkers for the Early Detection of Lung Cancer , 2012, Cancer Prevention Research.
[8] P. J. Callahan,et al. Volatile organic compounds as breath biomarkers for active and passive smoking. , 2002, Environmental health perspectives.
[9] Matthew C Kiernan,et al. Biomarkers in amyotrophic lateral sclerosis , 2009, The Lancet Neurology.
[10] J. Ciriza,et al. Optimal methods to characterize the G93A mouse model of ALS , 2005, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.
[11] O. Hardiman,et al. Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria: A population-based study. , 2000, Archives of neurology.
[12] M. Beal,et al. Increased oxidative damage to DNA in ALS patients. , 2000, Free radical biology & medicine.
[13] P. Shaw,et al. Molecular and cellular pathways of neurodegeneration in motor neurone disease , 2005, Journal of Neurology, Neurosurgery & Psychiatry.
[14] M. Bogdanov,et al. Oxidative stress biomarkers in sporadic ALS , 2008, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[15] R. Miller,et al. Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND). , 2003, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.
[16] J. Kinsella,et al. Initiation of lipid peroxidation in biological systems. , 1987, Critical reviews in food science and nutrition.
[17] L. Fuentes-Broto,et al. Monitoring systemic oxidative stress in an animal model of amyotrophic lateral sclerosis , 2011, Journal of Neurology.
[18] J. Knight. Free radicals: their history and current status in aging and disease. , 1998, Annals of clinical and laboratory science.
[19] S. Appel,et al. Increased lipid peroxidation in sera of ALS patients , 2004, Neurology.
[20] H. Haick,et al. Detection of lung, breast, colorectal, and prostate cancers from exhaled breath using a single array of nanosensors , 2010, British Journal of Cancer.
[21] W. Robberecht,et al. The neurobiology of amyotrophic lateral sclerosis , 2010, The European journal of neuroscience.
[22] H. Haick,et al. Detection of Alzheimer's and Parkinson's disease from exhaled breath using nanomaterial-based sensors. , 2013, Nanomedicine.
[23] Albert Ludolph,et al. Mechanisms, models and biomarkers in amyotrophic lateral sclerosis , 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.
[24] Bruce L. Miller,et al. Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis , 2006, Science.
[25] J. Andersen,et al. Oxidative stress in neurodegeneration: cause or consequence? , 2004, Nature Reviews Neuroscience.
[26] M. Gurney,et al. Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation. , 1994, Science.
[27] M. Kuźma,et al. Activity and expression of glutathione S-transferase pi in patients with amyotrophic lateral sclerosis. , 2006, Clinica chimica acta; international journal of clinical chemistry.
[28] R. Bowser,et al. Applying proteomics to the diagnosis and treatment of ALS and related diseases , 2009, Muscle and Nerve.
[29] D. Burke,et al. Riluzole therapy for motor neurone disease: An early Australian experience (1996–2002) , 2006, Journal of Clinical Neuroscience.
[30] L. Trizio,et al. Exhaled volatile organic compounds identify patients with colorectal cancer , 2013, The British journal of surgery.
[31] M. Gurney,et al. Relationship of oxygen radical‐induced lipid peroxidative damage to disease onset and progression in a transgenic model of familial ALS , 1998, Journal of neuroscience research.
[32] R. Bowser,et al. The application of biomarkers in clinical trials for motor neuron disease. , 2010, Biomarkers in medicine.
[33] Patrick Emond,et al. Metabolomics in cerebrospinal fluid of patients with amyotrophic lateral sclerosis: an untargeted approach via high-resolution mass spectrometry. , 2013, Journal of proteome research.
[34] M. Swash,et al. El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis , 2000, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.