Read more about the article A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease.
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A novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease.

Abstract Charcot-Marie-Tooth (CMT) disease is the most common form of inherited motor and sensory neuropathy. Based on neurophysiological and neuropathological criteria CMT has been sub-classified into two main types: demyelinating…

Continue ReadingA novel GDAP1 mutation 439delA is associated with autosomal recessive CMT disease.
Read more about the article Differential expression of molecular motors in the motor cortex of sporadic ALS.
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Differential expression of molecular motors in the motor cortex of sporadic ALS.

Abstract The molecular mechanisms underlying the selective neurodegeneration of motor neurons in amyotrophic lateral sclerosis (ALS) are inadequately understood. Recent breakthroughs have implicated impaired axonal transport, mediated by molecular motors,…

Continue ReadingDifferential expression of molecular motors in the motor cortex of sporadic ALS.
Read more about the article Molecular homogeneity in diverse geographical populations of Phlebotomus papatasi (Diptera, Psychodidae) inferred from ND4 mtDNA and ITS2 rDNA Epidemiological consequences.
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Molecular homogeneity in diverse geographical populations of Phlebotomus papatasi (Diptera, Psychodidae) inferred from ND4 mtDNA and ITS2 rDNA Epidemiological consequences.

Abstract An intraspecific study on Phlebotomus papatasi, the main proven vector of Leishmania major among the members of the subgenus Phlebotomus, was performed. The internal transcribed spacer 2 (ITS 2)…

Continue ReadingMolecular homogeneity in diverse geographical populations of Phlebotomus papatasi (Diptera, Psychodidae) inferred from ND4 mtDNA and ITS2 rDNA Epidemiological consequences.
Read more about the article Introgression of Alectoris chukar genes into a Spanish wild Alectoris rufa population.
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Introgression of Alectoris chukar genes into a Spanish wild Alectoris rufa population.

Abstract In order to detect introgression of other Alectoris genus species into wild populations of Spanish Alectoris rufa, we studied a sample of 93 red-legged partridges (supposed to be A.…

Continue ReadingIntrogression of Alectoris chukar genes into a Spanish wild Alectoris rufa population.
Read more about the article Genetic polymorphisms in the DNA repair genes XRCC1, XRCC2 and XRCC3 and risk of breast cancer in Cyprus.
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Genetic polymorphisms in the DNA repair genes XRCC1, XRCC2 and XRCC3 and risk of breast cancer in Cyprus.

Abstract Population-based studies have reported significant associations between specific genetic polymorphisms and breast cancer susceptibility. A number of studies have demonstrated that common variants of genes involved in the DNA…

Continue ReadingGenetic polymorphisms in the DNA repair genes XRCC1, XRCC2 and XRCC3 and risk of breast cancer in Cyprus.
Read more about the article Amyotrophic lateral sclerosis–the tools of the trait.
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Amyotrophic lateral sclerosis–the tools of the trait.

Abstract The aim of this review is to analyze how our knowledge on the etiology, pathology, and treatment of amyotrophic lateral sclerosis (ALS) has profited from the application of biotechnology…

Continue ReadingAmyotrophic lateral sclerosis–the tools of the trait.
Read more about the article Recombinant Sabin environmental isolates in Greece and Cyprus.
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Recombinant Sabin environmental isolates in Greece and Cyprus.

Abstract Twenty-one polioviruses (PVs) Sabin strains were isolated from sewage treatment plants from Metamorphosis, Athens, Greece during the time period from May to October 1996, and from two other sites…

Continue ReadingRecombinant Sabin environmental isolates in Greece and Cyprus.
Read more about the article Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.
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Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations.

Abstract We studied 325 thalassemia intermedia patients from Iran, India, Pakistan, Thailand, Mauritius and Cyprus to examine factors which influence the phenotype. The beta-thalassemia (thal) mutations were determined for 219…

Continue ReadingMulticenter study of the molecular basis of thalassemia intermedia in different ethnic populations.
Read more about the article Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.
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Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.

Abstract The rapid advancement of high-resolution DNA copy number assessment methods revealed the significant contribution of submicroscopic genetic imbalances to abnormal phenotypes, including mental retardation. In order to detect submicroscopic…

Continue ReadingScreening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.