L. Psiouri

Thalassaemia mutations within the 5′UTR of the human β‐globin gene disrupt transcription

A. Sgourou, S. Routledge, M. Antoniou, 2004, British journal of haematology.

Isolated Ventricular Noncompaction: A Rare Type of Hereditary Cardiomyopathy with Poor Prognosis

S. Mantagos, A. Manolis, A. Karatza, 2004 .

The β‐globin C→G mutation at 6 bp 3′ to the termination codon causes β‐thalassaemia by decreasing the mRNA level

R. Gibbs, A. Sgourou, M. Antoniou, 2002 .

Lack of Fas (APO-1/CD95) gene structural alterations or transcript variant ratio changes in breast cancer.

G. Voutsinas, V. Gorgoulis, A. Kotsinas, 2003, Cancer letters.

Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein.

M. Polymeropoulos, G. Voutsinas, E. Leroy, 1999, American journal of human genetics.

LCR-mediated, long-term tissue-specific gene expression within replicating episomal plasmid and cosmid vectors

S. Raguz, F. Grosveld, L. Harland, 2002, Gene Therapy.