Search Results - "ZUCCHELLI, Marco"
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Expression analysis of the NLRP gene family suggests a role in human preimplantation development
Published in PloS one (23-07-2008)“…The NLRP (Nucleotide-binding oligomerization domain, Leucine rich Repeat and Pyrin domain containing) family, also referred to as NALP family, is well known…”
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Transcriptome profiling of human pre-implantation development
Published in PloS one (16-11-2009)“…Preimplantation development is a crucial step in early human development. However, the molecular basis of human preimplantation development is not well known…”
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3
Characterization of a Common Susceptibility Locus for Asthma-Related Traits
Published in Science (American Association for the Advancement of Science) (09-04-2004)“…Susceptibility to asthma depends on variation at an unknown number of genetic loci. To identify susceptibility genes on chromosome 7p, we adopted a…”
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Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia
Published in American journal of human genetics (01-01-2006)“…We searched for linkage disequilibrium (LD) in 137 triads with dyslexia, using markers that span the most-replicated dyslexia susceptibility region on…”
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Evidence for Genetic Association and Interaction Between the TYK2 and IRF5 Genes in Systemic Lupus Erythematosus
Published in Journal of rheumatology (01-08-2009)“…Objective. Several candidate genes have been implicated in susceptibility for systemic lupus erythematosus (SLE), a complex autoimmune disease. The proposed…”
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Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1)
Published in PloS one (21-12-2011)“…neuropeptide S (NPS) and its receptor NPSR1 act along the hypothalamic-pituitary-adrenal axis to modulate anxiety, fear responses, nociception and…”
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A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia
Published in Human molecular genetics (15-03-2007)“…DYX3, a locus for dyslexia, resides on chromosome 2p11-p15. We have refined its location on 2p12 to a 157 kb region in two rounds of linkage disequilibrium…”
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Large-Scale Zygosity Testing Using Single Nucleotide Polymorphisms
Published in Twin research and human genetics (01-08-2007)“…A requirement for performing robust genetic and statistical analyses on twins is correctly assigned zygosities. In order to increase the power to detect small…”
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Analysis of neuropeptide S receptor gene (NPSR1) polymorphism in rheumatoid arthritis
Published in PloS one (22-02-2010)“…Polymorphism in the neuropeptide S receptor gene NPSR1 is associated with asthma and inflammatory bowel disease. NPSR1 is expressed in the brain, where it…”
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A teratocarcinoma-like human embryonic stem cell (hESC) line and four hESC lines reveal potentially oncogenic genomic changes
Published in PloS one (23-04-2010)“…The first Swiss human embryonic stem cell (hESC) line, CH-ES1, has shown features of a malignant cell line. It originated from the only single blastomere that…”
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Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE)
Published in PloS one (07-12-2009)“…Systemic lupus erythematosus (SLE) is a complex autoimmune disorder with multiple susceptibility genes. We have previously reported suggestive linkage to the…”
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Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts
Published in Gut (2015)“…IBS shows genetic predisposition, but adequately powered gene-hunting efforts have been scarce so far. We sought to identify true IBS genetic risk factors by…”
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Germline Genetic Contributions to Risk for Esophageal Adenocarcinoma, Barrett's Esophagus, and Gastroesophageal Reflux
Published in JNCI : Journal of the National Cancer Institute (20-11-2013)“…Esophageal adenocarcinoma (EA) is an increasingly common cancer with poor survival. Barrett's esophagus (BE) is the main precursor to EA, and every year 0.12%…”
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Association of TNFSF15 polymorphism with irritable bowel syndrome
Published in Gut (01-12-2011)“…Irritable bowel syndrome (IBS) is the most common gastrointestinal disorder, affecting more than 10% of the general population worldwide. Although a genetic…”
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Interactions between Glutathione S-Transferase P1, Tumor Necrosis Factor, and Traffic-Related Air Pollution for Development of Childhood Allergic Disease
Published in Environmental health perspectives (01-08-2008)“…Background: Air pollutants may induce airway inflammation and sensitization due to generation of reactive oxygen species. The genetic background to these…”
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Perturbations of Heart Development and Function in Cardiomyocytes from Human Embryonic Stem Cells with Trisomy 21
Published in Stem cells (Dayton, Ohio) (01-05-2015)“…Congenital heart defects (CHD) occur in approximately 50% of patients with Down syndrome (DS); the mechanisms for this occurrence however remain unknown. In…”
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Replication of GWAS-identified systemic lupus erythematosus susceptibility genes affirms B-cell receptor pathway signalling and strengthens the role of IRF5 in disease susceptibility in a Northern European population
Published in Rheumatology (Oxford, England) (01-01-2012)“…Objective. A large number of genes, including several not previously implicated in SLE susceptibility, have recently been identified or confirmed by…”
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Neuropeptide S Receptor Induces Neuropeptide Expression and Associates With Intermediate Phenotypes of Functional Gastrointestinal Disorders
Published in Gastroenterology (New York, N.Y. 1943) (01-01-2010)“…Background & Aims NPSR1, the receptor for neuropeptide S (NPS), is expressed by gastrointestinal (GI) enteroendocrine cells, and is involved in inflammation,…”
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Assessment of the Neuropeptide S System in Anxiety Disorders
Published in Biological psychiatry (1969) (01-09-2010)“…Background The G protein-coupled receptor neuropeptide S receptor 1 (NPSR1) and its ligand neuropeptide S (NPS) form a signaling system mainly implicated in…”
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Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
Published in European journal of human genetics : EJHG (01-05-2014)“…Dyslexia is one of the most common childhood disorders with a prevalence of around 5-10% in school-age children. Although an important genetic component is…”
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