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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 ChristodoulouJournal of Clinical Medicine|November 14, 2019
Genetic Modifiers at the Crossroads of Personalised Medicine for HaemoglobinopathiesCoralea Stephanou, Stella Tamana, Anna Minaidou, et al.European Journal of Human Genetics : EJHG|July 12, 2012
A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth diseasePaschalis Nicolaou, Carlo Cianchetti, Anna Minaidou, et al.International Journal of Molecular Sciences|December 23, 2022
A Novel Tool for the Analysis and Detection of Copy Number Variants Associated with HaemoglobinopathiesAnna Minaidou, Stella Tamana, Coralea Stephanou, et al.Elife|December 1, 2022
Evaluation of in silico predictors on short nucleotide variants in <i>HBA1</i>, <i>HBA2</i>, and <i>HBB</i> associated with haemoglobinopathiesStella Tamana, Maria Xenophontos, Anna Minaidou, et al.Annals of Neurology|June 13, 2019
PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementationViorica Chelban, Matthew P Wilson, Jodi Warman Chardon, et al.Pageof 1