The molecular anatomy and functions of the choroid plexus in healthy and diseased brain.
暂无分享,去创建一个
H. Stolp | J. Ek | I. Kratzer
[1] A. C. Duarte,et al. The senses of the choroid plexus , 2019, Progress in Neurobiology.
[2] M. Prinz,et al. Macrophages at CNS interfaces: ontogeny and function in health and disease , 2019, Nature Reviews Neuroscience.
[3] Liqun He,et al. Publisher Correction: Claudin-3-deficient C57BL/6J mice display intact brain barriers , 2019, Scientific Reports.
[4] M. Kiebler,et al. Choroid plexus‐derived miR‐204 regulates the number of quiescent neural stem cells in the adult brain , 2019, The EMBO journal.
[5] H. Hagberg,et al. Choroid plexus transcriptome and ultrastructure analysis reveals a TLR2-specific chemotaxis signature and cytoskeleton remodeling in leukocyte trafficking , 2019, Brain, Behavior, and Immunity.
[6] D. Janigro,et al. Cerebrospinal fluid dynamics and intracranial pressure elevation in neurological diseases , 2019, Fluids and barriers of the CNS.
[7] B. Snow,et al. A phase IIb, randomised, double-blind, placebo-controlled, dose-ranging investigation of the safety and efficacy of NTCELL® [immunoprotected (alginate-encapsulated) porcine choroid plexus cells for xenotransplantation] in patients with Parkinson's disease. , 2019, Parkinsonism & related disorders.
[8] J. Nathans,et al. Beta-catenin signaling regulates barrier-specific gene expression in circumventricular organ and ocular vasculatures , 2019, eLife.
[9] F. Alvarez-Leefmans,et al. Genetic and pharmacological inactivation of apical Na+-K+-2Cl- cotransporter 1 in choroid plexus epithelial cells reveals the physiological function of the cotransporter. , 2019, American journal of physiology. Cell physiology.
[10] C. D. Fowler,et al. Nicotine Acts on Cholinergic Signaling Mechanisms to Directly Modulate Choroid Plexus Function , 2019, eNeuro.
[11] C. Weber,et al. ApoE attenuates unresolvable inflammation by complex formation with activated C1q , 2019, Nature Medicine.
[12] E. Stopa,et al. Choroid plexus genes for CSF production and brain homeostasis are altered in Alzheimer’s disease , 2018, Fluids and Barriers of the CNS.
[13] L. Mucke,et al. Klotho controls the brain–immune system interface in the choroid plexus , 2018, Proceedings of the National Academy of Sciences.
[14] A. C. Duarte,et al. Choroid plexus is an additional source of melatonin in the brain , 2018, Journal of pineal research.
[15] N. Saunders,et al. Physiology and molecular biology of barrier mechanisms in the fetal and neonatal brain , 2018, The Journal of physiology.
[16] T. Lane,et al. Strong Circadian Rhythms in the Choroid Plexus: Implications for Sleep-Independent Brain Metabolite Clearance , 2018, Journal of experimental neuroscience.
[17] J. Ghersi-Egea,et al. Choroid plexus glutathione peroxidases are instrumental in protecting the brain fluid environment from hydroperoxides during postnatal development. , 2018, American journal of physiology. Cell physiology.
[18] Ying Sun,et al. A Comparative Proteomics Analysis of Five Body Fluids: Plasma, Urine, Cerebrospinal Fluid, Amniotic Fluid, and Saliva , 2018, Proteomics. Clinical applications.
[19] C. Rose,et al. Cotransporter-mediated water transport underlying cerebrospinal fluid formation , 2018, Nature Communications.
[20] K. Barszcz,et al. Lymphatic drainage of cerebrospinal fluid in mammals – are arachnoid granulations the main route of cerebrospinal fluid outflow? , 2018, Biologia.
[21] Miles C. Miller,et al. Comparative transcriptomics of choroid plexus in Alzheimer’s disease, frontotemporal dementia and Huntington’s disease: implications for CSF homeostasis , 2018, Fluids and Barriers of the CNS.
[22] T. Nakada,et al. Fluid Dynamics Inside the Brain Barrier: Current Concept of Interstitial Flow, Glymphatic Flow, and Cerebrospinal Fluid Circulation in the Brain , 2018, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.
[23] A. Nemirovsky,et al. The Choroid Plexus Functions as a Niche for T-Cell Stimulation Within the Central Nervous System , 2018, Front. Immunol..
[24] J. Praetorius,et al. Choroid plexus epithelial cells express the adhesion protein P-cadherin at cell-cell contacts and syntaxin-4 in the luminal membrane domain. , 2018, American journal of physiology. Cell physiology.
[25] J. Ghersi-Egea,et al. Glutathione Conjugation at the Blood–CSF Barrier Efficiently Prevents Exposure of the Developing Brain Fluid Environment to Blood-Borne Reactive Electrophilic Substances , 2018, The Journal of Neuroscience.
[26] Clare Baecher-Allan,et al. Multiple Sclerosis: Mechanisms and Immunotherapy , 2018, Neuron.
[27] Hanspeter Herzel,et al. The choroid plexus is an important circadian clock component , 2018, Nature Communications.
[28] D. Janigro,et al. The role of brain barriers in fluid movement in the CNS: is there a ‘glymphatic’ system? , 2018, Acta Neuropathologica.
[29] J. Ghersi-Egea,et al. Molecular anatomy and functions of the choroidal blood-cerebrospinal fluid barrier in health and disease , 2018, Acta Neuropathologica.
[30] A. Prochiantz,et al. OTX2 Signals from the Choroid Plexus to Regulate Adult Neurogenesis , 2018, eNeuro.
[31] S. Lipton,et al. Recent advances in understanding NRF2 as a druggable target: development of pro-electrophilic and non-covalent NRF2 activators to overcome systemic side effects of electrophilic drugs like dimethyl fumarate , 2017, F1000Research.
[32] M. Detmar,et al. Outflow of cerebrospinal fluid is predominantly through lymphatic vessels and is reduced in aged mice , 2017, Nature Communications.
[33] J. Palha,et al. The choroid plexus in health and in disease: dialogues into and out of the brain , 2017, Neurobiology of Disease.
[34] N. Bulakbaşı,et al. Diffusion-weighted magnetic resonance imaging in the assessment of choroid plexus aging , 2017, The neuroradiology journal.
[35] J. Praetorius,et al. Transport across the choroid plexus epithelium. , 2017, American journal of physiology. Cell physiology.
[36] H. Hagberg,et al. TLR2‐mediated leukocyte trafficking to the developing brain , 2017, Journal of leukocyte biology.
[37] S. Hladky,et al. Fluid and ion transfer across the blood–brain and blood–cerebrospinal fluid barriers; a comparative account of mechanisms and roles , 2016, Fluids and Barriers of the CNS.
[38] M. Schwartz,et al. Neurological Disease as a Failure of Brain-Immune Crosstalk: The Multiple Faces of Neuroinflammation. , 2016, Trends in immunology.
[39] G. Eichele,et al. Cilia-based flow network in the brain ventricles , 2016, Science.
[40] S. Frase,et al. Alix-mediated assembly of the actomyosin–tight junction polarity complex preserves epithelial polarity and epithelial barrier , 2016, Nature Communications.
[41] J. Ghersi-Egea,et al. T-Lymphocytes Traffic into the Brain across the Blood-CSF Barrier: Evidence Using a Reconstituted Choroid Plexus Epithelium , 2016, PloS one.
[42] R. Bowser,et al. Amyotrophic lateral sclerosis: Is the spinal fluid pathway involved in seeding and spread? , 2015, Medical hypotheses.
[43] M. Siebes,et al. Clearance from the mouse brain by convection of interstitial fluid towards the ventricular system , 2015, Fluids and Barriers of the CNS.
[44] T. Terasaki,et al. Quantitative targeted absolute proteomics of rat blood–cerebrospinal fluid barrier transporters: comparison with a human specimen , 2015, Journal of neurochemistry.
[45] P. Nathanielsz,et al. Expression of tight junction proteins and transporters for xenobiotic metabolism at the blood-CSF barrier during development in the nonhuman primate (P. hamadryas). , 2015, Reproductive toxicology.
[46] M. Coughtrie. Ontogeny of Human Conjugating Enzymes. , 2015, Drug metabolism letters.
[47] Maria K. Lehtinen,et al. Development and functions of the choroid plexus–cerebrospinal fluid system , 2015, Nature Reviews Neuroscience.
[48] A. Pisoschi,et al. The role of antioxidants in the chemistry of oxidative stress: A review. , 2015, European journal of medicinal chemistry.
[49] M. Schwartz,et al. Immunization with a Myelin-Derived Antigen Activates the Brain's Choroid Plexus for Recruitment of Immunoregulatory Cells to the CNS and Attenuates Disease Progression in a Mouse Model of ALS , 2015, The Journal of Neuroscience.
[50] P. Ferretti,et al. The neural milieu of the developing choroid plexus: neural stem cells, neurons and innervation , 2015, Front. Neurosci..
[51] Maria K. Lehtinen,et al. Spatially Heterogeneous Choroid Plexus Transcriptomes Encode Positional Identity and Contribute to Regional CSF Production , 2015, The Journal of Neuroscience.
[52] P. Nathanielsz,et al. Transcriptomal changes and functional annotation of the developing non-human primate choroid plexus , 2015, Front. Neurosci..
[53] A. Castañeyra-Perdomo,et al. Choroid plexus dysfunction impairs beta-amyloid clearance in a triple transgenic mouse model of Alzheimer’s disease , 2015, Front. Cell. Neurosci..
[54] J. Ghersi-Egea,et al. Efflux transporters in blood-brain interfaces of the developing brain , 2015, Front. Neurosci..
[55] A. Traweger,et al. “You Shall Not Pass”—tight junctions of the blood brain barrier , 2014, Front. Neurosci..
[56] B. Warf,et al. Combined endoscopic third ventriculostomy and choroid plexus cauterization as primary treatment for infant hydrocephalus: a prospective North American series. , 2014, Journal of neurosurgery. Pediatrics.
[57] J. Garcia-Fernández,et al. Embryonic blood-cerebrospinal fluid barrier formation and function , 2014, Front. Neurosci..
[58] P. Johansson. The choroid plexuses and their impact on developmental neurogenesis , 2014, Front. Neurosci..
[59] I. Amit,et al. Aging-induced type I interferon response at the choroid plexus negatively affects brain function , 2014, Science.
[60] F. Oesch,et al. Extrahepatic metabolism at the body's internal–external interfaces , 2014, Drug metabolism reviews.
[61] M. Gollasch,et al. Disturbed function of the blood–cerebrospinal fluid barrier aggravates neuro-inflammation , 2014, Acta Neuropathologica.
[62] Z. Molnár,et al. STAT1-induced ASPP2 transcription identifies a link between neuroinflammation, cell polarity, and tumor suppression , 2014, Proceedings of the National Academy of Sciences.
[63] Thomas Brinker,et al. A new look at cerebrospinal fluid circulation , 2014, Fluids and Barriers of the CNS.
[64] Chuan Wu,et al. EncephalomyelitisPlexus in Murine Experimental Autoimmune Recruitment to the Brain across the Choroid Negatively Regulates Initial Leukocyte Syndecan-1, a Cell Surface Proteoglycan, , 2013 .
[65] J. Praetorius,et al. Cerebrospinal fluid secretion by the choroid plexus. , 2013, Physiological reviews.
[66] C. Johanson,et al. Sustained choroid plexus function in human elderly and Alzheimer’s disease patients , 2013, Fluids and Barriers of the CNS.
[67] J. Ghersi-Egea,et al. Developmental changes in the transcriptome of the rat choroid plexus in relation to neuroprotection , 2013, Fluids and Barriers of the CNS.
[68] J. Ghersi-Egea,et al. Mechanisms That Determine the Internal Environment of the Developing Brain: A Transcriptomic, Functional and Ultrastructural Approach , 2013, PloS one.
[69] Manuel A. S. Santos,et al. Analysis of the Effects of Sex Hormone Background on the Rat Choroid Plexus Transcriptome by cDNA Microarrays , 2013, PloS one.
[70] S. Liddelow,et al. Transporters of the blood-brain and blood-CSF interfaces in development and in the adult. , 2013, Molecular aspects of medicine.
[71] Magdalena Götz,et al. The transcription factor Otx2 regulates choroid plexus development and function , 2013, Development.
[72] J. Ghersi-Egea,et al. Complexity and developmental changes in the expression pattern of claudins at the blood–CSF barrier , 2012, Histochemistry and Cell Biology.
[73] A. Pisani,et al. Increased blood-cerebrospinal fluid transfer of albumin in advanced Parkinson’s disease , 2012, Journal of Neuroinflammation.
[74] J. Ghersi-Egea,et al. Brain leukocyte infiltration initiated by peripheral inflammation or experimental autoimmune encephalomyelitis occurs through pathways connected to the CSF-filled compartments of the forebrain and midbrain , 2012, Journal of Neuroinflammation.
[75] J. Ghersi-Egea,et al. Transport and Metabolism at Blood–Brain Interfaces and in Neural Cells: Relevance to Bilirubin-Induced Encephalopathy , 2012, Front. Pharmacol..
[76] S. Oi. Classification of hydrocephalus: critical analysis of classification categories and advantages of “Multi-categorical Hydrocephalus Classification” (Mc HC) , 2011, Child's Nervous System.
[77] B. Engelhardt,et al. Tight junctions in brain barriers during central nervous system inflammation. , 2011, Antioxidants & redox signaling.
[78] Maria K. Lehtinen,et al. The Cerebrospinal Fluid Provides a Proliferative Niche for Neural Progenitor Cells , 2011, Neuron.
[79] S. Liddelow,et al. Modification of protein transfer across blood/cerebrospinal fluid barrier in response to altered plasma protein composition during development , 2011, The European journal of neuroscience.
[80] R. Wennberg,et al. Modulation of Mrp1 (ABCc1) and Pgp (ABCb1) by Bilirubin at the Blood-CSF and Blood-Brain Barriers in the Gunn Rat , 2011, PloS one.
[81] R. Keep,et al. Distribution of Glycylsarcosine and Cefadroxil among Cerebrospinal Fluid, Choroid Plexus, and Brain Parenchyma after Intracerebroventricular Injection is Markedly Different between Wild-Type and Pept2 Null Mice , 2011, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[82] Steffen Hamann,et al. Cotransport of water by the Na+–K+–2Cl− cotransporter NKCC1 in mammalian epithelial cells , 2010, The Journal of physiology.
[83] S. Liddelow,et al. Development of the lateral ventricular choroid plexus in a marsupial, Monodelphis domestica , 2010, Cerebrospinal Fluid Research.
[84] Miles C. Miller,et al. Amyloid Efflux Transporter Expression at the Blood-Brain Barrier Declines in Normal Aging , 2010, Journal of neuropathology and experimental neurology.
[85] S. Liddelow,et al. Efflux mechanisms at the developing brain barriers: ABC-transporters in the fetal and postnatal rat. , 2010, Toxicology letters.
[86] N. MacAulay,et al. Water transport between CNS compartments: contributions of aquaporins and cotransporters , 2010, Neuroscience.
[87] Xin Lu,et al. ASPP2 binds Par-3 and controls the polarity and proliferation of neural progenitors during CNS development. , 2010, Developmental cell.
[88] H. Togari,et al. High cerebrospinal fluid antioxidants and interleukin 8 are protective of hypoxic brain damage in newborns , 2010, Free radical research.
[89] J. Falck,et al. Distribution of soluble and microsomal epoxide hydrolase in the mouse brain and its contribution to cerebral epoxyeicosatrienoic acid metabolism , 2009, Neuroscience.
[90] S. Dey,et al. Sonic hedgehog signaling regulates a novel epithelial progenitor domain of the hindbrain choroid plexus , 2009, Development.
[91] B. Engelhardt,et al. C-C chemokine receptor 6–regulated entry of TH-17 cells into the CNS through the choroid plexus is required for the initiation of EAE , 2009, Nature Immunology.
[92] J. Preston,et al. Age-related changes in choroid plexus and blood–cerebrospinal fluid barrier function in the sheep , 2009, Experimental Gerontology.
[93] J. Ghersi-Egea,et al. Differential expression of the multidrug resistance‐related proteins ABCb1 and ABCc1 between blood‐brain interfaces , 2008, The Journal of comparative neurology.
[94] Alberto Romagnolo,et al. Involvement of the choroid plexus in multiple sclerosis autoimmune inflammation: A neuropathological study , 2008, Journal of Neuroimmunology.
[95] M. Dietrich,et al. Megalin mediates the transport of leptin across the blood-CSF barrier , 2008, Neurobiology of Aging.
[96] Thomas Brinker,et al. Multiplicity of cerebrospinal fluid functions: New challenges in health and disease , 2008, Cerebrospinal Fluid Research.
[97] C. Walsh,et al. A comparative proteomic analysis of human and rat embryonic cerebrospinal fluid. , 2007, Journal of proteome research.
[98] H. Stolp,et al. Blood–CSF barrier function in the rat embryo , 2006, The European journal of neuroscience.
[99] J. Ghersi-Egea,et al. Brain Protection at the Blood–Cerebrospinal Fluid Interface Involves a Glutathione-Dependent Metabolic Barrier Mechanism , 2006, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[100] J. Verbavatz,et al. Aging affects choroidal proteins involved in CSF production in Sprague-Dawley rats , 2005, Neurobiology of Aging.
[101] J. Ghersi-Egea,et al. Detoxification systems, passive and specific transport for drugs at the blood-CSF barrier in normal and pathological situations. , 2004, Advanced drug delivery reviews.
[102] H. Kusuhara,et al. Efflux transport systems for organic anions and cations at the blood-CSF barrier. , 2004, Advanced drug delivery reviews.
[103] P. Wielinga,et al. Mrp4 Confers Resistance to Topotecan and Protects the Brain from Chemotherapy , 2004, Molecular and Cellular Biology.
[104] I. Phillips,et al. Cell-, tissue-, sex- and developmental stage-specific expression of mouse flavin-containing monooxygenases (Fmos). , 2004, Biochemical pharmacology.
[105] M. Kameyama,et al. Hydrocephalus due to cerebrospinal fluid overproduction by bilateral choroid plexus papillomas , 2004, Child's Nervous System.
[106] M. Béné,et al. Normal-pressure hydrocephalus and Alzheimer disease. , 2003, Journal of neurosurgery.
[107] R. Ransohoff,et al. Human cerebrospinal fluid central memory CD4+ T cells: Evidence for trafficking through choroid plexus and meninges via P-selectin , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[108] N. Saunders,et al. Structural characteristics and barrier properties of the choroid plexuses in developing brain of the opossum (Monodelphis Domestica) , 2003, The Journal of comparative neurology.
[109] H. Kusuhara,et al. Expression and functional characterization of rat organic anion transporter 3 (rOat3) in the choroid plexus. , 2002, Molecular pharmacology.
[110] M. Béné,et al. Choroid plexus and ageing in rats: a morphometric and ultrastructural study , 2001, The European journal of neuroscience.
[111] B. Engelhardt,et al. Claudin-1, claudin-2 and claudin-11 are present in tight junctions of choroid plexus epithelium of the mouse , 2001, Neuroscience Letters.
[112] T. Visser,et al. Sulfation of thyroid hormone and dopamine during human development: ontogeny of phenol sulfotransferases and arylsulfatase in liver, lung, and brain. , 2001, The Journal of clinical endocrinology and metabolism.
[113] S. Tsukita,et al. Conversion of Zonulae Occludentes from Tight to Leaky Strand Type by Introducing Claudin-2 into Madin-Darby Canine Kidney I Cells , 2001, The Journal of cell biology.
[114] K. Fuxe,et al. Organization of choroid plexus epithelial and endothelial cell tight junctions and regulation of claudin‐1, ‐2 and ‐5 expression by protein kinase C , 2000, Neuroreport.
[115] K. Fuxe,et al. Phorbol ester induced changes in tight and adherens junctions in the choroid plexus epithelium and in the ependyma , 2000, Brain Research.
[116] P. Meier,et al. Localization of the Organic Anion Transporting Polypeptide 2 (Oatp2) in Capillary Endothelium and Choroid Plexus Epithelium of Rat Brain , 1999, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.
[117] J. Ghersi-Egea,et al. Demonstration of a Coupled Metabolism–Efflux Process at the Choroid Plexus as a Mechanism of Brain Protection Toward Xenobiotics , 1999, The Journal of Neuroscience.
[118] B. Engelhardt,et al. Ultrastructural localization of adhesion molecules in the healthy , 1999, Cell and Tissue Research.
[119] J. Varesi,et al. Mitochondrial content of choroid plexus epithelium , 1997, Experimental Brain Research.
[120] M. Catala,et al. Carbonic anhydrase activity during development of the choroid plexus in the human fetus , 1997, Child's Nervous System.
[121] F. Ståhlberg,et al. Cerebrospinal fluid production and dynamics in normal aging: a MRI phase‐mapping study , 1994, Acta neurologica Scandinavica.
[122] G. Siest,et al. Localization of Drug‐Metabolizing Enzyme Activities to Blood‐Brain Interfaces and Circumventricular Organs , 1994, Journal of neurochemistry.
[123] K. Dziegielewska,et al. A developmentally regulated blood‐cerebrospinal fluid transfer mechanism for albumin in immature rats. , 1992, The Journal of physiology.
[124] V. Perry,et al. Stromal macrophages of the choroid plexus situated at an interface between the brain and peripheral immune system constitutively express major histocompatibility class II antigens , 1992, Journal of Neuroimmunology.
[125] R. Keep,et al. Cortical microvessels during brain development: a morphometric study in the rat. , 1990, Microvascular research.
[126] R. Keep,et al. A morphometric study on the development of the lateral ventricle choroid plexus, choroid plexus capillaries and ventricular ependyma in the rat. , 1990, Brain research. Developmental brain research.
[127] P. Carder,et al. Glutathione S‐transferase in human brain , 1990, Neuropathology and applied neurobiology.
[128] J. Kaye,et al. Cerebrospinal fluid production is reduced in healthy aging , 1990, Neurology.
[129] A. Meister,et al. Glutathione metabolism at the blood‐cerebrospinal fluid barrier , 1989, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[130] J. Bourre,et al. Antioxidant Enzymes and Related Trace Elements in Aging Brain Capillaries and Choroid Plexus , 1989, Journal of neurochemistry.
[131] Y. Inoue,et al. Successive appearance of glutathione S-transferase-positive cells in developing rat brain: Choroid plexus, pia mater, ventricular zone and astrocytes , 1986, Neuroscience Letters.
[132] M. Adinolfi,et al. THE DEVELOPMENT OF THE HUMAN BLOOD‐CSF‐BRAIN BARRIER , 1985, Developmental medicine and child neurology.
[133] K. Dziegielewska,et al. Proteins in cerebrospinal fluid and plasma of fetal sheep during development , 1980, The Journal of physiology.
[134] B. Lauritzen,et al. Double replica technique applied to choroid plexus from early foetal sheep: completeness and complexity of tight junctions , 1979, Journal of neurocytology.
[135] B. van Deurs,et al. Tight junctions in the choroid plexus epithelium. A freeze-fracture study including complementary replicas , 1979, The Journal of cell biology.
[136] L. Edvinsson,et al. Reduced cerebrospinal fluid formation through cholinergic mechanisms , 1978, Neuroscience Letters.
[137] L. Edvinsson,et al. Sympathetic nervous control of cerebrospinal fluid production from the choroid plexus. , 1978, Science.
[138] B. Christ,et al. Experimental analysis of the origin of the wing musculature in avian embryos , 1977, Anatomy and Embryology.
[139] N. Saunders,et al. Lack of correlation between tight junction morphology and permeability properties in developing choroid plexus , 1976, Nature.
[140] D. J. Reed,et al. Active transport of sodium and potassium by the choroid plexus of the rat , 1974, The Journal of physiology.
[141] N. Saunders,et al. The development of a blood‐brain barrier mechanism in foetal sheep , 1974, The Journal of physiology.
[142] P. Claude,et al. FRACTURE FACES OF ZONULAE OCCLUDENTES FROM "TIGHT" AND "LEAKY" EPITHELIA , 1973, The Journal of cell biology.
[143] P. Lundborg,et al. Postnatal development of mechanisms for the elimination of organic acids from the brain and cerebrospinal fluid system of the rat: rapid efflux of ( 3 H)para-aminohippuric acid following intrathecal infusion. , 1973, Brain research.
[144] W. B. Quay,et al. Twenty‐four‐hour rhythmicity in carbonic anhydrase activities of choroid plexuses and pineal gland , 1972, The Anatomical record.
[145] H. Tumani,et al. The cerebrospinal fluid and barriers - anatomic and physiologic considerations. , 2017, Handbook of clinical neurology.
[146] T. Quintela,et al. Gender associated circadian oscillations of the clock genes in rat choroid plexus , 2014, Brain Structure and Function.
[147] R. Brigelius-Flohé,et al. Glutathione peroxidases. , 2013, Biochimica et biophysica acta.
[148] J. Sérot,et al. A possible role for CSF turnover and choroid plexus in the pathogenesis of late onset Alzheimer's disease. , 2012, Journal of Alzheimer's disease : JAD.
[149] C. Parada,et al. Proteome analysis of chick embryonic cerebrospinal fluid , 2006, Proteomics.
[150] G. Manley,et al. Aquaporin-1 deletion reduces osmotic water permeability and cerebrospinal fluid production. , 2003, Acta neurochirurgica. Supplement.
[151] J. Wijnholds. Drug resistance caused by multidrug resistance-associated proteins. , 2002, Novartis Foundation symposium.
[152] K. Dziegielewska,et al. Development of the choroid plexus , 2001, Microscopy research and technique.
[153] J. Preston. Ageing choroid plexus‐cerebrospinal fluid system , 2001, Microscopy research and technique.