Blood-spinal cord barrier leakage is not caused by neurodegeneration in amyotrophic lateral sclerosis Running head title: Blood-spinal cord barrier leakage in ALS
暂无分享,去创建一个
M. Dragunow | R. Bowser | Emma L. Scotter | M. Curtis | R. Faull | H. Waldvogel | B. Dieriks | S. Waters | Jiyan An | M. Swanson | Yibin Zhang | C. Turner | Helen C. Murray | L. Natasha | Grimsey
[1] John X. Morris,et al. Blood-brain barrier breakdown is an early biomarker of human cognitive dysfunction , 2018, Nature Medicine.
[2] P. Sanberg,et al. Reduction of microhemorrhages in the spinal cord of symptomatic ALS mice after intravenous human bone marrow stem cell transplantation accompanies repair of the blood-spinal cord barrier , 2018, Oncotarget.
[3] D. Pizzo,et al. Mutant TDP-43 within motor neurons drives disease onset but not progression in amyotrophic lateral sclerosis , 2017, Acta Neuropathologica.
[4] A. Frostell,et al. A Review of the Segmental Diameter of the Healthy Human Spinal Cord , 2016, Front. Neurol..
[5] S. Sasaki. Alterations of the blood‐spinal cord barrier in sporadic amyotrophic lateral sclerosis , 2015, Neuropathology : official journal of the Japanese Society of Neuropathology.
[6] G. Sobue,et al. Alterations in the blood–spinal cord barrier in TDP-43 conditional knockout mice , 2015, Neuroscience Letters.
[7] C. Shaw,et al. Dipeptide repeat protein inclusions are rare in the spinal cord and almost absent from motor neurons in C9ORF72 mutant amyotrophic lateral sclerosis and are unlikely to cause their degeneration , 2015, Acta neuropathologica communications.
[8] C. Shaw,et al. Erratum to: TDP-43 Proteinopathy and ALS: Insights into Disease Mechanisms and Therapeutic Targets , 2015, Neurotherapeutics.
[9] Sidney Strickland,et al. Fibrin deposited in the Alzheimer's disease brain promotes neuronal degeneration , 2015, Neurobiology of Aging.
[10] John L. Robinson,et al. TDP-43 pathology and neuronal loss in amyotrophic lateral sclerosis spinal cord , 2014, Acta Neuropathologica.
[11] Jesse D. Sengillo,et al. Blood–spinal cord barrier disruption contributes to early motor-neuron degeneration in ALS-model mice , 2014, Proceedings of the National Academy of Sciences.
[12] E. Kremmer,et al. Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins , 2013, Acta Neuropathologica.
[13] S. Lorenzl,et al. Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations , 2013, Acta Neuropathologica.
[14] D. Cleveland,et al. Converging Mechanisms in ALS and FTD: Disrupted RNA and Protein Homeostasis , 2013, Neuron.
[15] Murray Grossman,et al. Stages of pTDP‐43 pathology in amyotrophic lateral sclerosis , 2013, Annals of neurology.
[16] Y. Li,et al. Degeneration and impaired regeneration of gray matter oligodendrocytes in amyotrophic lateral sclerosis , 2013, Nature Neuroscience.
[17] Jesse D. Sengillo,et al. Blood–spinal cord barrier breakdown and pericyte reductions in amyotrophic lateral sclerosis , 2012, Acta Neuropathologica.
[18] Paul R. Sanberg,et al. Impaired blood–brain/spinal cord barrier in ALS patients , 2012, Brain Research.
[19] Jesse D. Sengillo,et al. Blood–spinal cord barrier pericyte reductions contribute to increased capillary permeability , 2012, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[20] J. Trojanowski,et al. Gains or losses: molecular mechanisms of TDP43-mediated neurodegeneration , 2011, Nature Reviews Neuroscience.
[21] D. Jezova,et al. The blood–spinal cord barrier: Morphology and Clinical Implications , 2011, Annals of neurology.
[22] K. Abe,et al. Disruption of neurovascular unit prior to motor neuron degeneration in amyotrophic lateral sclerosis , 2011, Journal of neuroscience research.
[23] B. Zlokovic,et al. Microhemorrhages: Undetectable but clinically meaningful the question persists , 2011, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[24] W. Le,et al. Prevention of Motor Neuron Degeneration by Novel Iron Chelators in SOD1G93A Transgenic Mice of Amyotrophic Lateral Sclerosis , 2011, Neurodegenerative Diseases.
[25] M. P. van den Heuvel,et al. No evidence of microbleeds in ALS patients at 7 Tesla MRI , 2010, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
[26] F. Sörgel,et al. Penetration of Drugs through the Blood-Cerebrospinal Fluid/Blood-Brain Barrier for Treatment of Central Nervous System Infections , 2010, Clinical Microbiology Reviews.
[27] P. Demetter,et al. Impaired blood–brain and blood–spinal cord barriers in mutant SOD1-linked ALS rat , 2009, Brain Research.
[28] B. Engelhardt,et al. The blood–brain and the blood–cerebrospinal fluid barriers: function and dysfunction , 2009, Seminars in Immunopathology.
[29] R. Bowser,et al. DECREASED mRNA EXPRESSION OF TIGHT JUNCTION PROTEINS IN LUMBAR SPINAL CORDS OF PATIENTS WITH ALS , 2009, Neurology.
[30] R. Deane,et al. ALS-causing SOD1 mutants generate vascular changes prior to motor neuron degeneration , 2008, Nature Neuroscience.
[31] Xun Hu,et al. TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis , 2008, Science.
[32] B. Zlokovic. The Blood-Brain Barrier in Health and Chronic Neurodegenerative Disorders , 2008, Neuron.
[33] Catherine lomen-Hoerth. The Motor Neurone Disease Handbook , 2007 .
[34] J. Ravits,et al. Focality of upper and lower motor neuron degeneration at the clinical onset of ALS , 2007, Neurology.
[35] R. Keep,et al. Brain Injury After Intracerebral Hemorrhage: The Role of Thrombin and Iron , 2007, Stroke.
[36] Bruce L. Miller,et al. Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis , 2006, Science.
[37] M. Nedergaard,et al. The blood–brain barrier: an overview Structure, regulation, and clinical implications , 2004, Neurobiology of Disease.
[38] R. Regan,et al. Toxic effect of hemoglobin on spinal cord neurons in culture. , 1998, Journal of neurotrauma.
[39] H. Davson. Blood–brain barrier , 1977, Nature.
[40] A. Ludolph,et al. Amyotrophic lateral sclerosis. , 2012, Current opinion in neurology.
[41] R. Orrell,et al. Passive transfer of purified IgG from patients with amyotrophic lateral sclerosis to mice results in degeneration of motor neurons accompanied by Ca2+ enhancement , 2003, Acta Neuropathologica.
[42] FLUIDS AND BARRIERS OF THE CNS REVIEW Open Access , 2022 .