LRSAM1 Depletion Affects Neuroblastoma SH-SY5Y Cell Growth and Morphology: The LRSAM1 c.2047-1G>A Loss-of-Function Variant Fails to Rescue The Phenotype

od Minaidou, Anna, Nicolaou, Paschalis, Christodoulou, Kyproula
Izdano u Cell J (2018)

Deregulation of LRSAM1 expression impairs the levels of TSG101, UBE2N, VPS28, MDM2 and EGFR

od Minaidou, Anna, Nicolaou, Paschalis, Christodoulou, Kyproula
Izdano u PLoS One (2019)

Greek Sage Exhibits Neuroprotective Activity against Amyloid Beta-Induced Toxicity

od Ververis, Antonis, Savvidou, Georgia, Ioannou, Kristia, Nicolaou, Paschalis, Christodoulou, Kyproula, Plioukas, Michael
Izdano u Evid Based Complement Alternat Med (2020)

A novel c.5308_5311delGAGA mutation in Senataxin in a Cypriot family with an autosomal recessive cerebellar ataxia

od Nicolaou, Paschalis, Georghiou, Anthi, Votsi, Christina, Middleton, Lefkos T, Zamba-Papanicolaou, Eleni, Christodoulou, Kyproula
Izdano 2008

Down-Regulation of Myogenin Can Reverse Terminal Muscle Cell Differentiation

od Mastroyiannopoulos, Nikolaos P., Nicolaou, Paschalis, Anayasa, Mustafa, Uney, James B., Phylactou, Leonidas A.
Izdano 2012

Genetic Susceptibility to Systemic Sclerosis in the Greek-Cypriot Population: A Pilot Study

od Chairta, Paraskevi, Psarelis, Savvas, Michailidou, Kyriaki, Demetriou, Christiana, Symeonidou, Sofia, Nicolaou, Paschalis, Christodoulou, Kyproula
Izdano u Genet Test Mol Biomarkers (2020)

A novel LRSAM1 mutation is associated with autosomal dominant axonal Charcot-Marie-Tooth disease

od Nicolaou, Paschalis, Cianchetti, Carlo, Minaidou, Anna, Marrosu, Giovanni, Zamba-Papanicolaou, Eleni, Middleton, Lefkos, Christodoulou, Kyproula
Izdano 2013

Comparative analysis of affected and unaffected areas of systemic sclerosis skin biopsies by high-throughput proteomic approaches

od Chairta, Paraskevi, Nicolaou, Paschalis, Sokratous, Kleitos, Galant, Christine, Houssiau, Frédéric, Oulas, Anastasis, Spyrou, George M., Alarcon-Riquelme, Marta E., Lauwerys, Bernard R., Christodoulou, Kyproula
Izdano u Arthritis Res Ther (2020)

PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation

od Chelban, Viorica, Wilson, Matthew P., Warman Chardon, Jodi, Vandrovcova, Jana, Zanetti, M. Natalia, Zamba‐Papanicolaou, Eleni, Efthymiou, Stephanie, Pope, Simon, Conte, Maria R., Abis, Giancarlo, Liu, Yo‐Tsen, Tribollet, Eloise, Haridy, Nourelhoda A., Botía, Juan A., Ryten, Mina, Nicolaou, Paschalis, Minaidou, Anna, Christodoulou, Kyproula, Kernohan, Kristin D., Eaton, Alison, Osmond, Matthew, Ito, Yoko, Bourque, Pierre, Jepson, James E. C., Bello, Oscar, Bremner, Fion, Cordivari, Carla, Reilly, Mary M., Foiani, Martha, Heslegrave, Amanda, Zetterberg, Henrik, Heales, Simon J. R., Wood, Nicholas W., Rothman, James E., Boycott, Kym M., Mills, Philippa B., Clayton, Peter T., Houlden, Henry
Izdano u Ann Neurol (2019)