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Irene Sargiannidou
Irene Sargiannidou
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The role of thrombospondin-1 in tumor progression
I Sargiannidou, J Zhou, GP Tuszynski
Experimental biology and medicine 226 (8), 726-733, 2001
1632001
Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects
I Sargiannidou, N Vavlitou, S Aristodemou, A Hadjisavvas, K Kyriacou, ...
Journal of Neuroscience 29 (15), 4736-4749, 2009
1342009
Gap junction pathology in multiple sclerosis lesions and normal-appearing white matter
K Markoullis, I Sargiannidou, N Schiza, A Hadjisavvas, F Roncaroli, ...
Acta neuropathologica 123, 873-886, 2012
892012
Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy
A Kagiava, I Sargiannidou, G Theophilidis, C Karaiskos, J Richter, ...
Proceedings of the National Academy of Sciences 113 (17), E2421-E2429, 2016
812016
Disruption of oligodendrocyte gap junctions in experimental autoimmune encephalomyelitis
K Markoullis, I Sargiannidou, C Gardner, A Hadjisavvas, R Reynolds, ...
Glia 60 (7), 1053-1066, 2012
812012
Axonal pathology precedes demyelination in a mouse model of X-linked demyelinating/type I Charcot-Marie Tooth neuropathy
N Vavlitou, I Sargiannidou, K Markoullis, K Kyriacou, SS Scherer, ...
Journal of Neuropathology & Experimental Neurology 69 (9), 945-958, 2010
802010
Impairment of learning and memory in TAG-1 deficient mice associated with shorter CNS internodes and disrupted juxtaparanodes
M Savvaki, T Panagiotaropoulos, A Stamatakis, I Sargiannidou, ...
Molecular and Cellular Neuroscience 39 (3), 478-490, 2008
762008
Oligodendrocyte gap junction loss and disconnection from reactive astrocytes in multiple sclerosis gray matter
K Markoullis, I Sargiannidou, N Schiza, F Roncaroli, R Reynolds, ...
Journal of Neuropathology & Experimental Neurology 73 (9), 865-879, 2014
612014
Gene replacement therapy in a model of Charcot-Marie-Tooth 4C neuropathy
N Schiza, E Georgiou, A Kagiava, JJ Medard, J Richter, C Tryfonos, ...
Brain 142 (5), 1227-1241, 2019
582019
Emerging therapies for Charcot-Marie-Tooth inherited neuropathies
M Stavrou, I Sargiannidou, E Georgiou, A Kagiava, KA Kleopa
International Journal of Molecular Sciences 22 (11), 6048, 2021
492021
Connexins, gap junctions and peripheral neuropathy
KA Kleopa, I Sargiannidou
Neuroscience letters 596, 27-32, 2015
492015
Intraneural GJB1 gene delivery improves nerve pathology in a model of X‐linked Charcot–Marie–Tooth disease
I Sargiannidou, A Kagiava, S Bashiardes, J Richter, C Christodoulou, ...
Annals of neurology 78 (2), 303-316, 2015
482015
Gene therapy targeting oligodendrocytes provides therapeutic benefit in a leukodystrophy model
E Georgiou, K Sidiropoulou, J Richter, C Papaneophytou, I Sargiannidou, ...
Brain 140 (3), 599-616, 2017
472017
AAV9-mediated Schwann cell-targeted gene therapy rescues a model of demyelinating neuropathy
A Kagiava, C Karaiskos, J Richter, C Tryfonos, MJ Jennings, ...
Gene therapy 28 (10), 659-675, 2021
442021
Intrathecal gene therapy in mouse models expressing CMT1X mutations
A Kagiava, C Karaiskos, J Richter, C Tryfonos, G Lapathitis, ...
Human molecular genetics 27 (8), 1460-1473, 2018
442018
Mechanisms of thrombospondin-1-mediated metastasis and angiogenesis
I Sargiannidou, C Qiu, GP Tuszynski
Seminars in thrombosis and hemostasis 30 (01), 127-136, 2004
442004
Human oligodendrocytes express Cx31. 3: function and interactions with Cx32 mutants
I Sargiannidou, M Ahn, AD Enriquez, A Peinado, R Reynolds, C Abrams, ...
Neurobiology of disease 30 (2), 221-233, 2008
402008
Genetic mechanisms of peripheral nerve disease
M Stavrou, I Sargiannidou, T Christofi, KA Kleopa
neuroscience letters 742, 135357, 2021
382021
Cloning and characterization of angiocidin, a tumor cell binding protein for thrombospondin‐1
J Zhou, VL Rothman, I Sargiannidou, S Dimitrov, C Qiu, E Smith, ...
Journal of cellular biochemistry 92 (1), 125-146, 2004
352004
Gene replacement therapy after neuropathy onset provides therapeutic benefit in a model of CMT1X
A Kagiava, J Richter, C Tryfonos, C Karaiskos, AJ Heslegrave, ...
Human molecular genetics 28 (21), 3528-3542, 2019
342019
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