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Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocolIdentification and chromosomal localisation by fluorescence in situ hybridisation of human gene of phosphoinositide-specific phospholipase C beta(1)A restricted spectrum of NRAS mutations causes Noonan syndromeIdentification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assayChromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genesAcute effects of modafinil on brain resting state networks in young healthy subjectsMK-954 (losartan potassium) exerts endothelial protective effects against reperfusion injury: evidence of an e-NOS mRNA overexpression after global ischemia.Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion.Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrumInfluence of novel nano-titanium implant surface on human osteoblast behavior and growth.Associations between the antioxidant network and emotional intelligence: a preliminary studySpectrum of phenotypic anomalies in four families with deletion of the SHOX enhancer region.Age-Dependent Modifications of AMPA Receptor Subunit Expression Levels and Related Cognitive Effects in 3xTg-AD Mice.Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome.The distribution of genes on chromosomes: a cytological approach.Intravenous grafts of amniotic fluid-derived stem cells induce endogenous cell proliferation and attenuate behavioral deficits in ischemic stroke rats.MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic setting.Gene expression modifications in Wharton's Jelly mesenchymal stem cells promoted by prolonged in vitro culturingDeregulation of sertoli and leydig cells function in patients with Klinefelter syndrome as evidenced by testis transcriptome analysis.Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseases.Epidermal growth factor promotes a neural phenotype in thymic epithelial cells and enhances neuropoietic cytokine expression.Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols.Wnt signaling behaves as a "master regulator" in the osteogenic and adipogenic commitment of human amniotic fluid mesenchymal stem cells.Early and sustained altered expression of aging-related genes in young 3xTg-AD mice.Genetics of syndromic and nonsyndromic cleft lip and palate.An epigenetic approach to pancreatic cancer treatment: the prospective role of histone deacetylase inhibitors.Amniotic fluid stem cells: a promising therapeutic resource for cell-based regenerative therapy.Human height genes and cancer.Genetic testing in couples undergoing assisted reproduction technique protocols.Gene expression profiles of cumulus cells obtained from women treated with recombinant human luteinizing hormone + recombinant human follicle-stimulating hormone or highly purified human menopausal gonadotropin versus recombinant human follicle-stimFISH analysis in detecting 9p duplication (p22p24).Complex translocations of the Ph chromosome and Ph negative CML arise from similar mechanisms, as evidenced by FISH analysis.A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man.TNF-alpha-induced apoptosis in Daudi cells: multiparametric analysis.Y-chromosome haplogroups and susceptibility to azoospermia factor c microdeletion in an Italian populationMolecular studies in three patients with isodicentric Y chromosome.Human immunodeficiency virus type 1 tat protein modulates fibronectin expression in thymic epithelial cells and impairs in vitro thymocyte development.Nuclear translocation of beta II PKC isoenzyme in phorbol ester-stimulated KM-3 pre-B human leukemic cells.Difficulty describing feelings and post-traumatic symptoms after a collective trauma in survivors of L'Aquila earthquake.Human second trimester amniotic fluid cells are able to create embryoid body-like structures in vitro and to show typical expression profiles of embryonic and primordial germ cells.
P50
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P50
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