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 The cypriot and Iranian National Mutation Frequency Databases.
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The cypriot and Iranian National Mutation Frequency Databases.

Abstract The National Mutation Frequency Databases are continuously updated mutation depositories, which contain extensive information over the described genetic heterogeneity of an ethnic group or population. Here, we report the…

Continue ReadingThe cypriot and Iranian National Mutation Frequency Databases.
Read more about the article Visual cortical plasticity following unilateral sensorimotor cortical lesions in the neonatal rat.
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Visual cortical plasticity following unilateral sensorimotor cortical lesions in the neonatal rat.

Abstract Previous work has shown that unilateral sensorimotor cortex (SMC) lesions in newborn rats resulted in an apparent shift of the motor cortex map in the spared hemisphere, particularly of…

Continue ReadingVisual cortical plasticity following unilateral sensorimotor cortical lesions in the neonatal rat.
Read more about the article Novel germline mutations in the APC gene of Cypriot patients with familial and sporadic adenomatous polyposis.
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Novel germline mutations in the APC gene of Cypriot patients with familial and sporadic adenomatous polyposis.

Abstract Familial adenomatous polyposis (FAP) is one of the two commonest familial syndromes that predispose to colorectal cancer. FAP is caused by mutations in the adenomatous polyposis coli (APC) tumour…

Continue ReadingNovel germline mutations in the APC gene of Cypriot patients with familial and sporadic adenomatous polyposis.
Read more about the article Motor protein KIFC5A interacts with Nubp1 and Nubp2, and is implicated in the regulation of centrosome duplication.
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Motor protein KIFC5A interacts with Nubp1 and Nubp2, and is implicated in the regulation of centrosome duplication.

Abstract Inhibition of motor protein activity has been linked with defects in the formation of poles in the spindle of dividing cells. However, the molecular mechanisms underlying the functional relationship…

Continue ReadingMotor protein KIFC5A interacts with Nubp1 and Nubp2, and is implicated in the regulation of centrosome duplication.
Read more about the article The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues.
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The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues.

Abstract The interface between assisted reproductive technologies (ART) and genetics comprises several sensitive and important issues that affect infertile couples, families with severe genetic diseases, potential children, professionals in ART…

Continue ReadingThe interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues.
Read more about the article Neuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestations.
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Neuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestations.

Abstract Autoantibodies to Shaker-type (Kv1) K+ channels are now known to be associated with three syndromes. Peripheral nerve hyperexcitability is the chief manifestation of acquired neuromyotonia; the combination of neuromyotonia…

Continue ReadingNeuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestations.
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 Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.
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Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.

Abstract To determine the phenotypic and cellular expression of two novel connexin32 (Cx32) mutations causing X-linked Charcot-Marie-Tooth disease (CMT1X). The authors evaluated several members of two families with CMT1X clinically,…

Continue ReadingPhenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.