Read more about the article Phylogenetic analysis of European encephalomyocarditis viruses: comparison of two genomic regions.
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Phylogenetic analysis of European encephalomyocarditis viruses: comparison of two genomic regions.

Abstract The phylogenetic relationships of encephalomyocarditis (EMC) viruses isolated from pigs and rodents in Europe were determined by comparison of nucleotide sequences from two different regions of the virus genome,…

Continue ReadingPhylogenetic analysis of European encephalomyocarditis viruses: comparison of two genomic regions.
Read more about the article Typing of sandflies from Greece and Cyprus by DNA polymorphism of 18S rRNA gene.
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Typing of sandflies from Greece and Cyprus by DNA polymorphism of 18S rRNA gene.

Abstract A simple and reliable technique was developed to distinguish Phlebotomine sandflies by restriction fragment length polymorphism of PCR-amplified (PCR-RFLP) 18S rDNAs. Seven morphologically identified sandflies species from several localities…

Continue ReadingTyping of sandflies from Greece and Cyprus by DNA polymorphism of 18S rRNA gene.
Read more about the article Molecular analysis of the full-length genome of HIV type 1 subtype I: evidence of A/G/I recombination.
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Molecular analysis of the full-length genome of HIV type 1 subtype I: evidence of A/G/I recombination.

Abstract Phylogenetic analysis of partial env sequences of HIV-1 isolates from Cyprus and Greece suggested the existence of a distinct subtype of the virus, designated as I. We examined whether…

Continue ReadingMolecular analysis of the full-length genome of HIV type 1 subtype I: evidence of A/G/I recombination.
Read more about the article Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population.
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Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population.

Abstract In order to identify genetic factors governing expansion of the CGG repeat in the FMR1 gene and to determine what predisposes or causes a normal stable allele to change…

Continue ReadingGenetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population.
Read more about the article Frequencies of "grey-zone" and premutation-size FMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada.
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Frequencies of "grey-zone" and premutation-size FMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada.

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Abstract

Continue ReadingFrequencies of "grey-zone" and premutation-size FMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada.
Read more about the article Binding free energies and free energy components from molecular dynamics and Poisson-Boltzmann calculations. Application to amino acid recognition by aspartyl-tRNA synthetase.
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Binding free energies and free energy components from molecular dynamics and Poisson-Boltzmann calculations. Application to amino acid recognition by aspartyl-tRNA synthetase.

Abstract Specific amino acid binding by aminoacyl-tRNA synthetases (aaRS) is necessary for correct translation of the genetic code. Engineering a modified specificity into aminoacyl-tRNA synthetases has been proposed as a…

Continue ReadingBinding free energies and free energy components from molecular dynamics and Poisson-Boltzmann calculations. Application to amino acid recognition by aspartyl-tRNA synthetase.
Read more about the article RT-PCR for the identification of developmentally regulated novel members of the kinesin-like superfamily.
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RT-PCR for the identification of developmentally regulated novel members of the kinesin-like superfamily.

Abstract

Continue ReadingRT-PCR for the identification of developmentally regulated novel members of the kinesin-like superfamily.
Read more about the article Identification of a novel beta0-thalassemia mutation, codons 80/81 (-C), in an Iranian family.
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Identification of a novel beta0-thalassemia mutation, codons 80/81 (-C), in an Iranian family.

Abstract

Continue ReadingIdentification of a novel beta0-thalassemia mutation, codons 80/81 (-C), in an Iranian family.
Read more about the article Cytochrome b sequences reveal Acomys minous (Rodentia, Muridae) paraphyly and answer the question about the ancestral karyotype of Acomys dimidiatus.
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Cytochrome b sequences reveal Acomys minous (Rodentia, Muridae) paraphyly and answer the question about the ancestral karyotype of Acomys dimidiatus.

Abstract Sequences of the cytochrome b (cyt b) mitochondrial gene show that the spiny mouse Acomys from Crete, known as the endemic species A. minous, is composed of two distinct…

Continue ReadingCytochrome b sequences reveal Acomys minous (Rodentia, Muridae) paraphyly and answer the question about the ancestral karyotype of Acomys dimidiatus.
Read more about the article A novel arginine vasopressin-neurophysin II mutation causes autosomal dominant neurohypophyseal diabetes insipidus and morphologic pituitary changes.
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A novel arginine vasopressin-neurophysin II mutation causes autosomal dominant neurohypophyseal diabetes insipidus and morphologic pituitary changes.

Abstract To determine the genetic basis of autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) in a Cypriot family, we ascertained and studied a large, four-generation kindred in which all participating family…

Continue ReadingA novel arginine vasopressin-neurophysin II mutation causes autosomal dominant neurohypophyseal diabetes insipidus and morphologic pituitary changes.