about
Sequence, "subtle" alternative splicing and expression of the CYYR1 (cysteine/tyrosine-rich 1) mRNA in human neuroendocrine tumorsA new gene family including DSCR1 (Down Syndrome Candidate Region 1) and ZAKI-4: characterization from yeast to human and identification of DSCR1-like 2, a novel human member (DSCR1L2)Proteins encoded by human Down syndrome critical region gene 1-like 2 (DSCR1L2) mRNA and by a novel DSCR1L2 mRNA isoform interact with cardiac troponin I (TNNI3)Uncertainty principle of genetic information in a living cell.Identification of minimal eukaryotic introns through GeneBase, a user-friendly tool for parsing the NCBI Gene databankDiamond-Blackfan anemia: report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian populationCompound heterozygosity for two different amino-acid substitution mutations in the thrombopoietin receptor (c-mpl gene) in congenital amegakaryocytic thrombocytopenia (CAMT)Cysteine and tyrosine-rich 1 (CYYR1), a novel unpredicted gene on human chromosome 21 (21q21.2), encodes a cysteine and tyrosine-rich protein and defines a new family of highly conserved vertebrate-specific genesMicroarray-based identification and RT-PCR test screening for epithelial-specific mRNAs in peripheral blood of patients with colon cancerDisplayed correlation between gene expression profiles and submicroscopic alterations in response to cetuximab, gefitinib and EGF in human colon cancer cell lines.Clinical implications of the heterogeneity of hematopoietic progenitors elicited in peripheral blood by anticancer therapy with cyclophosphamide and cytokine(s).Mutational screening of thrombopoietin receptor gene (c-mpl) in patients with congenital thrombocytopenia and absent radii (TAR).TRAM (Transcriptome Mapper): database-driven creation and analysis of transcriptome maps from multiple sources.Complexity of bidirectional transcription and alternative splicing at human RCAN3 locus.An estimation of the number of cells in the human body.Segmental paralogy in the human genome: a large-scale triplication on 1p, 6p, and 21q.Identification and analysis of human RCAN3 (DSCR1L2) mRNA and protein isoforms.Integrated differential transcriptome maps of Acute Megakaryoblastic Leukemia (AMKL) in children with or without Down Syndrome (DS)Systematic large-scale meta-analysis identifies a panel of two mRNAs as blood biomarkers for colorectal cancer detection.Systematic identification of human housekeeping genes possibly useful as references in gene expression studies.Expression of T cell receptor alpha gene (TCRA) in human rhabdomyosarcoma and other musculo-skeletal sarcomas.Identification of candidate genes involved in the reversal of malignant phenotype of osteosarcoma cells transfected with the liver/bone/kidney alkaline phosphatase gene.A quantitative transcriptome reference map of the normal human hippocampus.Regioselective synthesis and biological profiling of butyric and phenylalkylcarboxylic esters derivated from D-mannose and xylitol: influence of alkyl chain length on acute toxicity.Epithelial cells are the major source of biologically active granulocyte macrophage colony-stimulating factor in human endometrium.A molecular view of the normal human thyroid structure and function reconstructed from its reference transcriptome map.Systematic analysis of mRNA 5' coding sequence incompleteness in Danio rerio: an automated EST-based approach.Hemopoiesis in healthy old people and centenarians: well-maintained responsiveness of CD34+ cells to hemopoietic growth factors and remodeling of cytokine network.Improving mRNA 5' coding sequence determination in the mouse genome.Genome-scale analysis of human mRNA 5' coding sequences based on expressed sequence tag (EST) database.A quantitative transcriptome reference map of the normal human brain.Renaming the DSCR1/Adapt78 gene family as RCAN: regulators of calcineurin.Characterization of human gene locus CYYR1: a complex multi-transcript system.Letter to the Editor: On osteocytes density in the human body.The murine DSCR1-like (Down syndrome candidate region 1) gene family: conserved synteny with the human orthologous genes.Universal tight correlation of codon bias and pool of RNA codons (codonome): The genome is optimized to allow any distribution of gene expression values in the transcriptome from bacteria to humans.Sequence and expression analysis of the beta-2-microglobulin gene in dialysis patients.UniGene Tabulator: a full parser for the UniGene format.LGALS4, CEACAM6, TSPAN8, and COL1A2: Blood Markers for Colorectal Cancer-Validation in a Cohort of Subjects With Positive Fecal Immunochemical Test Result.Plasma and urinary metabolomic profiles of Down syndrome correlate with alteration of mitochondrial metabolism.
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Pierluigi Strippoli
@ast
Pierluigi Strippoli
@en
Pierluigi Strippoli
@es
Pierluigi Strippoli
@nl
type
label
Pierluigi Strippoli
@ast
Pierluigi Strippoli
@en
Pierluigi Strippoli
@es
Pierluigi Strippoli
@nl
prefLabel
Pierluigi Strippoli
@ast
Pierluigi Strippoli
@en
Pierluigi Strippoli
@es
Pierluigi Strippoli
@nl
P106
P1153
57192320139
P31
P496
0000-0001-8769-8832