Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Cynthia Soderblom"'
Autor:
Do-Hun Lee, Kara L. Spiller, Cynthia Soderblom, Vance Lemmon, Yunjiao Zhu, Kirill A. Lyapichev, John R. Bethea, Y. Zhang, J. Zha, Nicole M. Ferraro, Jae K. Lee, Stephanie L. Yahn, Dario Motti
Publikováno v:
The Journal of Neuroscience. 37:2362-2376
Although infiltrating macrophages influence many pathological processes after spinal cord injury (SCI), the intrinsic molecular mechanisms that regulate their function are poorly understood. A major hurdle has been dissecting macrophage-specific func
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::823f6bae29435e7145fe93e69aecb5bd
https://doi.org/10.1523/jneurosci.2751-16.2017
https://doi.org/10.1523/jneurosci.2751-16.2017
Publikováno v:
Neurobiology of Disease, Vol 74, Iss, Pp 114-125 (2015)
Spinal cord injury (SCI) leads to formation of a fibrotic scar that is inhibitory to axon regeneration. Recent evidence indicates that the fibrotic scar is formed by perivascular fibroblasts, but the mechanism by which they are recruited to the injur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50e9781c1f5dab991268fb67bf16b314
https://doi.org/10.1016/j.nbd.2014.10.024
https://doi.org/10.1016/j.nbd.2014.10.024
Autor:
José Geraldo Lopes Ramos, Pantelis Tsoulfas, Jae K. Lee, Ezra Blumenthal, Xueting Luo, Catherine Lai-Hsu, Kirill A. Lyapichev, Cynthia Soderblom, Eric R. Bray, Kevin K. Park, Vidhya Krishnan
Publikováno v:
The Journal of Neuroscience. 33:13882-13887
Injury to the CNS leads to formation of scar tissue, which is important in sealing the lesion and inhibiting axon regeneration. The fibrotic scar that comprises a dense extracellular matrix is thought to originate from meningeal cells surrounding the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d3acd0301974b51e6c39b230fff8f23
https://doi.org/10.1523/jneurosci.2524-13.2013
https://doi.org/10.1523/jneurosci.2524-13.2013
Autor:
Olga Vorontsova, Jenny E. Hinshaw, Anna Sundborger, Cynthia Soderblom, Oleg Shupliakov, Emma Evergren
Publikováno v:
Journal of Cell Science. 124:133-143
Clathrin-mediated vesicle recycling in synapses is maintained by a unique set of endocytic proteins and interactions. We show that endophilin localizes in the vesicle pool at rest and in spirals at the necks of clathrin-coated pits (CCPs) during acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27ea9bc2ac684e9d82e88b98139a30de
https://doi.org/10.1242/jcs.072686
https://doi.org/10.1242/jcs.072686
Autor:
Michael C. Hanna, Henri J. Jupille, Cynthia Soderblom, Oleg Shupliakov, Julia Stadler, Craig Blackstone
Publikováno v:
neurogenetics. 11:369-378
Mast syndrome (SPG21) is a childhood-onset, autosomal recessive, complicated form of hereditary spastic paraplegia (HSP) characterized by dementia, thin corpus callosum, white matter abnormalities, and cerebellar and extrapyramidal signs in addition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0f75348022a846a53b6aa0c6e105749
https://doi.org/10.1007/s10048-010-0252-7
https://doi.org/10.1007/s10048-010-0252-7
Autor:
Annie Levert, Patrick A. Dion, Cynthia Soderblom, Craig Blackstone, Guy A. Rouleau, Nicolas Dupré, Inge A. Meijer, Peng-Peng Zhu, Sandra Laurent, Michel Sylvain, Jacques Puymirat, Bernard Brais, Julia Stadler
Publikováno v:
Annals of Neurology. 61:599-603
Hereditary spastic paraplegias (HSPs) are characterized by progressive lower limb spasticity and weakness. Mutations in the SPG3A gene, which encodes the large guanosine triphosphatase atlastin, are the second most common cause of autosomal dominant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc30b1f64c9d6508b94ca4d47a3b0475
https://doi.org/10.1002/ana.21114
https://doi.org/10.1002/ana.21114
Autor:
Cynthia Soderblom, Craig Blackstone
Publikováno v:
Pharmacology & Therapeutics. 109:42-56
The hereditary spastic paraplegias (HSPs) comprise a clinically and genetically diverse group of inherited neurological disorders in which the primary manifestation is progressive spasticity and weakness of the lower limbs. The identification of over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3b87c3aafa375e6faa87996949535f1
https://doi.org/10.1016/j.pharmthera.2005.06.001
https://doi.org/10.1016/j.pharmthera.2005.06.001
Publikováno v:
Journal of neurotrauma. 32(15)
After spinal cord injury (SCI), a fibrotic scar forms at the injury site that is best characterized by the accumulation of perivascular fibroblasts and deposition of the extracellular matrix protein fibronectin. While fibronectin is a growth-permissi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a9c70efbcb3d4bb1a848a1d841d562e
https://pubmed.ncbi.nlm.nih.gov/25492623
https://pubmed.ncbi.nlm.nih.gov/25492623
Publikováno v:
Human molecular genetics. 17(11)
The hereditary spastic paraplegias (SPG1-33) comprise a cluster of inherited neurological disorders characterized principally by lower extremity spasticity and weakness due to a length-dependent, retrograde axonopathy of corticospinal motor neurons.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c419f1e90e77d9a72dba138cb399f80f
https://pubmed.ncbi.nlm.nih.gov/18270207
https://pubmed.ncbi.nlm.nih.gov/18270207
Autor:
Inge A, Meijer, Patrick, Dion, Sandra, Laurent, Nicolas, Dupré, Bernard, Brais, Annie, Levert, Jacques, Puymirat, Marie France, Rioux, Michel, Sylvain, Peng-Peng, Zhu, Cynthia, Soderblom, Julia, Stadler, Craig, Blackstone, Guy A, Rouleau
Publikováno v:
Annals of neurology. 61(6)
Hereditary spastic paraplegias (HSPs) are characterized by progressive lower limb spasticity and weakness. Mutations in the SPG3A gene, which encodes the large guanosine triphosphatase atlastin, are the second most common cause of autosomal dominant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::689e383cfe985a50c7bb0d39ef3847dc
https://pubmed.ncbi.nlm.nih.gov/17427918
https://pubmed.ncbi.nlm.nih.gov/17427918