The hyaluronan receptor for RHAMM in noradrenergic fibers contributes to axon growth capacity of locus coeruleus neurons in an intraocular transplant model
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W. Staines | B. D. Lynn | J. Nagy | A. Granholm | M. L. Price | B. Lynn
[1] I. Zachary,et al. Focal adhesion kinase. , 1997, The international journal of biochemistry & cell biology.
[2] A. Granholm,et al. Collateral Sprouting of Central Noradrenergic Neurons during Aging: Histochemical and Neurochemical Studies in Intraocular Triple Transplants , 1997, Experimental Neurology.
[3] J. Nagy,et al. Subcellular localization of ryanodine receptors in rat brain. , 1996, European journal of pharmacology.
[4] E. Arenas,et al. GDNF prevents degeneration and promotes the phenotype of brain noradrenergic neurons in vivo , 1995, Neuron.
[5] E. Turley,et al. Characterization of the murine gene encoding the hyaluronan receptor RHAMM. , 1995, Gene.
[6] R. Savani,et al. Overexpression of the hyaluronan receptor RHAMM is transforming and is also required for H-ras transformation , 1995, Cell.
[7] D. Nance,et al. Migration of bovine aortic smooth muscle cells after wounding injury. The role of hyaluronan and RHAMM. , 1995, The Journal of clinical investigation.
[8] J. Nagy,et al. Requirement of the hyaluronan receptor RHAMM in neurite extension and motility as demonstrated in primary neurons and neuronal cell lines , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[9] J F Pujol,et al. Postnatal development of the tyrosine hydroxylase-containing cell population within the rat locus coeruleus: topological organization andphenotypic plasticity , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[10] R. Mize. Quantitative image analysis for immunocytochemistry and in situ hybridization , 1994, Journal of Neuroscience Methods.
[11] J. Sleeman,et al. Hyaluronate receptors: key players in growth, differentiation, migration and tumor progression. , 1994, Current opinion in cell biology.
[12] L. Jordan,et al. Astrocyte and microglial motility in vitro is functionally dependent on the hyaluronan receptor RHAMM , 1994, Glia.
[13] E. Turley,et al. Hyaluronan and the hyaluronan receptor RHAMM promote focal adhesion turnover and transient tyrosine kinase activity , 1994, The Journal of cell biology.
[14] S. Hockfield,et al. BEHAB, a new member of the proteoglycan tandem repeat family of hyaluronan-binding proteins that is restricted to the brain [published erratum appears in J Cell Biol 1997 Apr 21;137(2):521] , 1994, The Journal of cell biology.
[15] W. Staines,et al. Neurons derived from P19 embryonal carcinoma cells have varied morphologies and neurotransmitters , 1994, Neuroscience.
[16] E. Arenas,et al. Neurotrophin-3 prevents the death of adult central noradrenergic neurons in vivo , 1994, Nature.
[17] R. Savani,et al. Identification of a common hyaluronan binding motif in the hyaluronan binding proteins RHAMM, CD44 and link protein. , 1994, The EMBO journal.
[18] E. Turley,et al. TGF-beta 1 stimulation of cell locomotion utilizes the hyaluronan receptor RHAMM and hyaluronan , 1993, The Journal of cell biology.
[19] E. Turley,et al. Ras-transformed cells express both CD44 and RHAMM hyaluronan receptors: only RHAMM is essential for hyaluronan-promoted locomotion. , 1993, Experimental cell research.
[20] E. Turley,et al. Identification of two hyaluronan-binding domains in the hyaluronan receptor RHAMM. , 1993, The Journal of biological chemistry.
[21] I. Black,et al. Differential Actions of Neurotrophins in the Locus Coeruleus and Basal Forebrain , 1993, Experimental Neurology.
[22] M. Becker‐André,et al. Expression of an N-terminally truncated form of human focal adhesion kinase in brain. , 1993, Biochemical and biophysical research communications.
[23] A. Bignami,et al. The astrocyte-extracellular matrix complex in CNS myelinated tracts: a comparative study on the distribution of hyaluronate in rat, goldfish and lamprey , 1992, Journal of neurocytology.
[24] J. Fritschy,et al. Restoration of ascending noradrenergic projections by residual locus coeruleus neurons: Compensatory response to neurotoxin‐induced cell death in the adult rat brain , 1992, The Journal of comparative neurology.
[25] D. Nance,et al. Molecular cloning of a novel hyaluronan receptor that mediates tumor cell motility [published erratum appears in J Cell Biol 1992 Aug;118(3):753] , 1992, The Journal of cell biology.
[26] E. Zypen,et al. Ultrastructural localization of hyaluronan in myelin sheaths of the rat central and rat and human peripheral nervous systems using hyaluronan-binding protein-gold and link protein-gold , 1992, Neuroscience.
[27] J. Pujol,et al. Somatotopic organization of tyrosine hydroxylase expression in the rat locus coeruleus: long term effect of RU24722 , 1992, Brain Research.
[28] A. Bignami,et al. Some observations on the localization of hyaluronic acid in adult, newborn and embryonal rat brain , 1992, International Journal of Developmental Neuroscience.
[29] E. Turley. Hyaluronan-binding proteins and receptors , 1991 .
[30] Paul C. Letourneau,et al. Identification of cytoskeletal, focal adhesion, and cell adhesion proteins in growth cone particles isolated from developing chick brain , 1991, Journal of neuroscience research.
[31] Shoji Nakamura,et al. The mode of axonal regeneration of locus coeruleus neurons in the lateral geniculate nucleus following neonatal 6-hydroxydopamine treatment , 1991, Experimental Neurology.
[32] E. Turley,et al. Hyaluronan and a cell-associated hyaluronan binding protein regulate the locomotion of ras-transformed cells , 1991, The Journal of cell biology.
[33] M. Geffard,et al. The response of noradrenergic axons to systemically administered DSP-4 in the rat: an immunohistochemical study using antibodies to noradrenaline and dopamine-beta-hydroxylase. , 1990, Journal of chemical neuroanatomy.
[34] J. Fritschy,et al. Immunohistochemical analysis of the neurotoxic effects of DSP-4 identifies two populations of noradrenergic axon terminals , 1989, Neuroscience.
[35] D. Price,et al. Innervation of human hippocampus by noradrenergic systems: Normal anatomy and structural abnormalities in aging and in Alzheimer's disease , 1988, Neuroscience.
[36] R. U. Margolis,et al. Light and electron microscopic studies on the localization of hyaluronic acid in developing rat cerebellum , 1988, The Journal of cell biology.
[37] E. Turley,et al. Characterization of hyaluronate binding proteins isolated from 3T3 and murine sarcoma virus transformed 3T3 cells. , 1987, Biochemistry.
[38] J. D. McGaugh,et al. Noradrenergic changes and memory loss in aged mice , 1985, Brain Research.
[39] S. Zornetzer. Catecholamine System Involvement in Age‐related Memory Dysfunction , 1985, Annals of the New York Academy of Sciences.
[40] F. E. Bloom,et al. Loss of pigmented dopamine-β-hydroxylase positive cells from locus coeruleus in senile dementia of alzheimer's type , 1983, Neuroscience Letters.
[41] James N. Davis,et al. Sprouting of noradrenergic fibers in hippocampus after medial septal lesions: Contributions of the central and peripheral nervous systems , 1983, Experimental Neurology.
[42] H. Olpe,et al. Age-related decline in the activity of noradrenergic neurons of the rat locus coeruleus , 1982, Brain Research.
[43] A. Bjo¨rklund,et al. In vivo evidence for a hippocampal adrenergic neuronotrophic factor specifically released on septal deafferentation , 1981, Brain Research.
[44] Eugene M. Johnson,et al. Effects of exposure to nerve growth factor antibodies on the developing nervous system of the rat: an experimental autoimmune approach. , 1980, Developmental biology.
[45] A. Björklund,et al. Regeneration of normal terminal innervation patterns by central noradrenergic neurons after 5,7-dihydroxytryptamine-induced axotomy in the adult rat , 1979, Brain Research.
[46] C. Cotman,et al. Decrease in adrenergic axon sprouting in the senescent rat. , 1978, Science.
[47] F. Bloom,et al. Axonal proliferation following lesions of cerebellar peduncles. A combined fluorescence microscopic and radioautographic study , 1974, The Journal of comparative neurology.
[48] Sigurdur Thor Jonsson,et al. MATERIAL AND METHODS , 1973 .
[49] F. Bloom,et al. Proliferation of norepinephrine-containing axons in rat cerebellar cortex after peduncle lesions. , 1973, Brain research.
[50] A. Pastor,et al. Influence of the postsynaptic target on the functional properties of neurons in the adult mammalian central nervous system. , 1996 .
[51] A. Granholm,et al. Synapsin I in intraocular hippocampal transplants during maturation and aging: effects of brainstem cografts. , 1995, Cell transplantation.
[52] A. Granholm. 22 – Hippocampal Transplants in Oculo: A Model for Establishment of Isolated Circuits , 1991 .
[53] A. Björklund,et al. Morphological plasticity of central adrenergic neurons. , 1973, Brain, behavior and evolution.