Read more about the article Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy.
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Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy.

Abstract Although there is good experimental data that utrophin, the autosomal analog of dystrophin, can ameliorate the phenotype in dystrophinopathies, there is scant evidence from human data to support this…

Continue ReadingNaturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy.
Read more about the article Sandfly fever virus outbreak in Cyprus.
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Sandfly fever virus outbreak in Cyprus.

Abstract A major outbreak of febrile syndrome occurred during 2002 among the Greek Army forces in Cyprus. Serological and molecular investigations revealed that the causative agent was a Sicilian-like phlebovirus.…

Continue ReadingSandfly fever virus outbreak in Cyprus.
Read more about the article Gathered Mediterranean food plants–ethnobotanical investigations and historical development.
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Gathered Mediterranean food plants–ethnobotanical investigations and historical development.

Abstract The diversity of local Mediterranean food elements is not known in detail, but offers itself to search for new vegetables, salads, fruits and spices which could be used in…

Continue ReadingGathered Mediterranean food plants–ethnobotanical investigations and historical development.
Read more about the article Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis.
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Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis.

Abstract To evaluate clinical disease expression, non-invasive diagnosis, and prognosis in families with dominant vs. recessive arrhythmogenic right ventricular cardiomyopathy (ARVC) due to mutations in related desmosomal proteins plakophilin-2 (PKP2)…

Continue ReadingArrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis.
Read more about the article Molecular genetics of X-linked Charcot-Marie-Tooth disease.
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Molecular genetics of X-linked Charcot-Marie-Tooth disease.

Abstract The X-linked form of Charcot-Marie-Tooth disease (CMT1X) is the second most common molecularly designated form of hereditary motor and sensory neuropathy. The clinical phenotype is characterized by progressive distal…

Continue ReadingMolecular genetics of X-linked Charcot-Marie-Tooth disease.
Read more about the article Possible therapy of male infertility by reproductive cloning: one cloned human 4-cell embryo.
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Possible therapy of male infertility by reproductive cloning: one cloned human 4-cell embryo.

Abstract This study was conducted to evaluate the preimplantation embryonic potential of adult somatic cells from an infertile man using an interspecies bioassay for quality control and also to create…

Continue ReadingPossible therapy of male infertility by reproductive cloning: one cloned human 4-cell embryo.
Read more about the article Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Greek Cypriot population.
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Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Greek Cypriot population.

Abstract Mutations in the GJB2 (connexin-26) gene are responsible for more than half of all cases of prelingual recessive inherited non-syndromic deafness in Europe. One specific mutation 35delG, accounts for…

Continue ReadingDetermination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Greek Cypriot population.
Read more about the article High frequency of 35delG GJB2 mutation and absence of del(GJB6-D13S1830) in Greek Cypriot patients with nonsyndromic hearing loss.
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High frequency of 35delG GJB2 mutation and absence of del(GJB6-D13S1830) in Greek Cypriot patients with nonsyndromic hearing loss.

Abstract Mutations in the GJB2 (Connexin 26) gene are responsible for more than half of all cases of prelingual, recessive, inherited, nonsyndromic deafness in Europe. This paper presents a mutation…

Continue ReadingHigh frequency of 35delG GJB2 mutation and absence of del(GJB6-D13S1830) in Greek Cypriot patients with nonsyndromic hearing loss.
Read more about the article Contribution of BRCA1 and BRCA2 germline mutations to the incidence of early-onset breast cancer in Cyprus.
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Contribution of BRCA1 and BRCA2 germline mutations to the incidence of early-onset breast cancer in Cyprus.

Abstract In Cyprus, the prevalence of breast cancer associated with BRCA1 and BRCA2 mutations in young women is unknown. In this study, we present the results of mutational analysis of…

Continue ReadingContribution of BRCA1 and BRCA2 germline mutations to the incidence of early-onset breast cancer in Cyprus.