Factors involved in inflammation-induced developmental white matter damage
暂无分享,去创建一个
A. Potter | K. Dziegielewska | Benjamin J Wheaton | N. Bethge | Helen B. Stolp | C. J. Ek | Norman R. Saunders | Pia A. Johansson
[1] P. de Backer,et al. Identification and validation of housekeeping genes as internal control for gene expression in an intravenous LPS inflammation model in chickens. , 2008, Veterinary immunology and immunopathology.
[2] H. Stolp,et al. Effect of minocycline on inflammation‐induced damage to the blood–brain barrier and white matter during development , 2007, The European journal of neuroscience.
[3] C. Ek,et al. Age‐related differences in the local cellular and molecular responses to injury in developing spinal cord of the opossum, Monodelphis domestica , 2007, The European journal of neuroscience.
[4] L. Fan,et al. Role of interleukin-6 in lipopolysaccharide-induced brain injury and behavioral dysfunction in neonatal rats , 2006, Neuroscience.
[5] Urs Meyer,et al. The Time of Prenatal Immune Challenge Determines the Specificity of Inflammation-Mediated Brain and Behavioral Pathology , 2006, The Journal of Neuroscience.
[6] L. Fan,et al. Minocycline attenuates lipopolysaccharide-induced white matter injury in the neonatal rat brain , 2005, Neuroscience.
[7] H. Stolp,et al. Long‐term changes in blood–brain barrier permeability and white matter following prolonged systemic inflammation in early development in the rat , 2005, The European journal of neuroscience.
[8] H. Stolp,et al. Breakdown of the blood–brain barrier to proteins in white matter of the developing brain following systemic inflammation , 2005, Cell and Tissue Research.
[9] H. Hagberg,et al. Effect of inflammation on central nervous system development and vulnerability: review , 2005, Current opinion in neurology.
[10] G. D. de Courten-Myers,et al. Plasma infusions into porcine cerebral white matter induce early edema, oxidative stress, pro-inflammatory cytokine gene expression and DNA fragmentation: implications for white matter injury with increased blood-brain-barrier permeability. , 2005, Current neurovascular research.
[11] Y. Pang,et al. Disturbance of oligodendrocyte development, hypomyelination and white matter injury in the neonatal rat brain after intracerebral injection of lipopolysaccharide. , 2003, Brain research. Developmental brain research.
[12] Pamela L. Follett,et al. The Toll-Like Receptor TLR4 Is Necessary for Lipopolysaccharide-Induced Oligodendrocyte Injury in the CNS , 2002, The Journal of Neuroscience.
[13] D. Holtzman,et al. Selective Vulnerability of Late Oligodendrocyte Progenitors to Hypoxia–Ischemia , 2002, The Journal of Neuroscience.
[14] H. Kinney,et al. Late Oligodendrocyte Progenitors Coincide with the Developmental Window of Vulnerability for Human Perinatal White Matter Injury , 2001, The Journal of Neuroscience.
[15] J. Chi,et al. Experimentally induced intrauterine infection causes fetal brain white matter lesions in rabbits. , 1997, American journal of obstetrics and gynecology.
[16] Alan Leviton,et al. Maternal Intrauterine Infection, Cytokines, and Brain Damage in the Preterm Newborn , 1997, Pediatric Research.
[17] A. Borit,et al. MYELIN BASIC PROTEIN AND GLIAL FIBRILLARY ACIDIC PROTEIN IN HUMAN FETAL BRAIN* , 1981, Neuropathology and applied neurobiology.
[18] N. Saunders,et al. Monodelphis domestica (grey short-tailed opossum): an accessible model for studies of early neocortical development , 2004, Anatomy and Embryology.
[19] C. Nordborg,et al. The relationship between plasma protein extravasation and remote tissue changes after experimental brain infarction , 2004, Acta Neuropathologica.
[20] K. Dziegielewska,et al. Proteins in cerebrospinal fluid and plasma of postnatal Monodelphis domestica (grey short-tailed opossum). , 1989, Comparative biochemistry and physiology. B, Comparative biochemistry.
[21] L. Becker,et al. Developmental changes of glial fibrillary acidic protein in cerebral white matter. , 1983, Archives of neurology.