Read more about the article Number of embryos biopsied as a predictive indicator for the outcome of preimplantation genetic diagnosis by fluorescence in situ hybridisation in translocation cases.
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Number of embryos biopsied as a predictive indicator for the outcome of preimplantation genetic diagnosis by fluorescence in situ hybridisation in translocation cases.

Abstract This study aimed to investigate the optimum number of embryos to be biopsied in order to increase the likelihood of obtaining a balanced/normal embryo following preimplantation genetic diagnosis (PGD)…

Continue ReadingNumber of embryos biopsied as a predictive indicator for the outcome of preimplantation genetic diagnosis by fluorescence in situ hybridisation in translocation cases.
Read more about the article Altered metabolic pathways in clear cell renal cell carcinoma: A meta-analysis and validation study focused on the deregulated genes and their associated networks.
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Altered metabolic pathways in clear cell renal cell carcinoma: A meta-analysis and validation study focused on the deregulated genes and their associated networks.

Abstract Clear cell renal cell carcinoma (ccRCC) is the predominant subtype of renal cell carcinoma (RCC). It is one of the most therapy-resistant carcinomas, responding very poorly or not at…

Continue ReadingAltered metabolic pathways in clear cell renal cell carcinoma: A meta-analysis and validation study focused on the deregulated genes and their associated networks.
Read more about the article Validation of signalling pathways: Case study of the p16-mediated pathway.
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Validation of signalling pathways: Case study of the p16-mediated pathway.

Abstract p16 is recognized as a tumor suppressor gene due to the prevalence of its genetic inactivation in all types of human cancers. Additionally, p16 gene plays a critical role…

Continue ReadingValidation of signalling pathways: Case study of the p16-mediated pathway.
Read more about the article Gene expression changes in HLA mismatched mixed lymphocyte cultures reveal genes associated with allorecognition.
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Gene expression changes in HLA mismatched mixed lymphocyte cultures reveal genes associated with allorecognition.

Abstract Human leucocyte antigen (HLA) compatibility is the main factor determining the occurrence of graft-vs-host disease (GVHD) in patients. It has also been shown that minor histocompatibility antigen differences as…

Continue ReadingGene expression changes in HLA mismatched mixed lymphocyte cultures reveal genes associated with allorecognition.
Read more about the article Molecular characterization and phylogeny of Kalotermes populations from the Levant, and description of Kalotermes phoeniciae sp. nov.
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Molecular characterization and phylogeny of Kalotermes populations from the Levant, and description of Kalotermes phoeniciae sp. nov.

Abstract The presence of the yellow-necked drywood termite, Kalotermes flavicollis Fabr., has been reported along most of the Mediterranean coasts of Europe, Africa and Asia. While morphological and genetic data…

Continue ReadingMolecular characterization and phylogeny of Kalotermes populations from the Levant, and description of Kalotermes phoeniciae sp. nov.
Read more about the article MicroRNA responses to environmental liver carcinogens: Biological and clinical significance.
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MicroRNA responses to environmental liver carcinogens: Biological and clinical significance.

Abstract A large number of biological, chemical, and dietary factors have been implicated in the development of liver cancer. These involve complex and protracted interactions between genetic, epigenetic, and environmental…

Continue ReadingMicroRNA responses to environmental liver carcinogens: Biological and clinical significance.
Read more about the article A start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32.
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A start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32.

Abstract X-linked Charcot-Marie-Tooth disease (CMTX1) results from numerous mutations in the GJB1 gene encoding the gap junction protein connexin32 (Cx32) and is one of the commonest forms of inherited neuropathy.…

Continue ReadingA start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32.
Read more about the article Anti-inflammatory and cytoprotective properties of hydrogen sulfide.
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Anti-inflammatory and cytoprotective properties of hydrogen sulfide.

Abstract Hydrogen sulfide is an endogenous gaseous mediator that plays important roles in many physiological processes in microbes, plants, and animals. This chapter focuses on the important roles of hydrogen…

Continue ReadingAnti-inflammatory and cytoprotective properties of hydrogen sulfide.
Read more about the article In vivo allergenic activity of a hypoallergenic mutant of the major fish allergen Cyp c 1 evaluated by means of skin testing.
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In vivo allergenic activity of a hypoallergenic mutant of the major fish allergen Cyp c 1 evaluated by means of skin testing.

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Abstract

Continue ReadingIn vivo allergenic activity of a hypoallergenic mutant of the major fish allergen Cyp c 1 evaluated by means of skin testing.
Read more about the article Prediction of autism by translation and immune/inflammation coexpressed genes in toddlers from pediatric community practices.
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Prediction of autism by translation and immune/inflammation coexpressed genes in toddlers from pediatric community practices.

Abstract The identification of genomic signatures that aid early identification of individuals at risk for autism spectrum disorder (ASD) in the toddler period remains a major challenge because of the…

Continue ReadingPrediction of autism by translation and immune/inflammation coexpressed genes in toddlers from pediatric community practices.