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Plos One|February 7, 2019
Deregulation of LRSAM1 expression impairs the levels of TSG101, UBE2N, VPS28, MDM2 and EGFRAnna Minaidou, Paschalis Nicolaou, Kyproula ChristodoulouCell Journal|May 31, 2018
LRSAM1 Depletion Affects Neuroblastoma SH-SY5Y Cell Growth and Morphology: The LRSAM1 c.2047-1G>A Loss-of-Function Variant Fails to Rescue The PhenotypeAnna Minaidou, Paschalis Nicolaou, Kyproula ChristodoulouCerebellum (London, England)|June 1, 2022
ANO10 Function in Health and DiseaseAndroniki Chrysanthou, Antonis Ververis, Kyproula ChristodoulouHuman Immunology|December 17, 2016
Genomic and genetic studies of systemic sclerosis: A systematic reviewParaskevi Chairta, Paschalis Nicolaou, Kyproula ChristodoulouNeurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 28, 2018
Quantification of dysarthrοphonia in a Cypriot family with autosomal recessive hereditary spastic paraplegia associated with a homozygous SPG11 mutationKostas Konstantopoulos, Eleni Zamba-Papanicolaou, Kyproula ChristodoulouScientific Reports|February 2, 2023
Enrichr in silico analysis of MS-based extracted candidate proteomic biomarkers highlights pathogenic pathways in systemic sclerosisParaskevi P Chairta, Paschalis Nicolaou, Kyproula ChristodoulouEuropean Journal of Medical Genetics|September 20, 2019
Early-onset presentation of a new subtype of β-Propeller protein-associated neurodegeneration (BPAN) caused by a de novo WDR45 deletion in a 6 year-old female patientStephanie Christoforou, Kyproula Christodoulou, Violetta Anastasiadou, et al.Computational and Structural Biotechnology Journal|January 9, 2023
PathIN: an integrated tool for the visualization of pathway interaction networksGeorge Minadakis, Kyproula Christodoulou, George Tsouloupas, et al.Neurology|January 6, 2009
A novel ALS2 splice-site mutation in a Cypriot juvenile-onset primary lateral sclerosis familyNikolay Mintchev, Eleni Zamba-Papanicolaou, Kleopas A Kleopa, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 21, 2007
Auditory nerve is affected in one of two different point mutations of the neurofilament light geneDusan Butinar, Arnold Starr, Janez Zidar, et al.Pageof 7