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Genome-wide Pathway Analysis Using Gene Expression Data of Colonic Mucosa in Patients with Inflammatory Bowel Disease.Thrombocytopenia-absent-radius syndrome in a child showing a larger 1q21.1 deletion than the one in his healthy mother, and a significant downregulation of the commonly deleted genes.Decreased free d-aspartate levels are linked to enhanced d-aspartate oxidase activity in the dorsolateral prefrontal cortex of schizophrenia patientsEvaluation of genome-wide expression profiles of blood and sputum neutrophils in cystic fibrosis patients before and after antibiotic therapy.Genomic organization and evolution of double minutes/homogeneously staining regions with MYC amplification in human cancer.Mirna expression profiles identify drivers in colorectal and pancreatic cancers.BEAT: Bioinformatics Exon Array Tool to store, analyze and visualize Affymetrix GeneChip Human Exon Array data from disease experimentsA miRNA signature for defining aggressive phenotype and prognosis in gliomas.Multifaceted enrichment analysis of RNA-RNA crosstalk reveals cooperating micro-societies in human colorectal cancerCombined microRNA and ER expression: a new classifier for familial and sporadic breast cancer patients.Differences in gene expression and cytokine release profiles highlight the heterogeneity of distinct subsets of adipose tissue-derived stem cells in the subcutaneous and visceral adipose tissue in humansMicroRNA expression profiling in male and female familial breast cancer.Genome-wide analysis of differentially expressed genes and splicing isoforms in clear cell renal cell carcinoma.Rhodobacter sphaeroides adaptation to high concentrations of cobalt ions requires energetic metabolism changes.MiR-578 and miR-573 as potential players in BRCA-related breast cancer angiogenesisThe KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome casesA novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial featuresNeurological features of 14q24-q32 interstitial deletion: report of a new case.Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1.Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3.Whole exome sequencing and single nucleotide polymorphism array analyses to identify germline alterations in genes associated with testosterone metabolism in a patient with androgen insensitivity syndrome and early-onset colorectal cancerTwo maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypes.Gene expression of muscular and neuronal pathways is cooperatively dysregulated in patients with idiopathic achalasia.Analysis of clock gene-miRNA correlation networks reveals candidate drivers in colorectal cancer.miR-151-5p, targeting chromatin remodeler SMARCA5, as a marker for the BRCAness phenotype.8q12.1q12.3 de novo microdeletion involving the CHD7 gene in a patient without the major features of CHARGE syndrome: case report and critical review of the literature.Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cells.Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome.Establishment and genetic characterization of ANGM-CSS, a novel, immortal cell line derived from a human glioblastoma multiforme.Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure.miRNA profiling in serum and tissue samples to assess noninvasive biomarkers for NSCLC clinical outcome.Functional Implications of MicroRNAs in Crohn's Disease Revealed by Integrating MicroRNA and Messenger RNA Expression Profiling.Large intragenic deletion of CDC73 (exons 4-10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family.Erratum to: Large intragenic deletion of CDC73 (exons 4-10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family.t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders.Large rearrangements detected by MLPA, point mutations, and survey of the frequency of mutations within the SLC3A1 and SLC7A9 genes in a cohort of 172 cystinuric Italian patients.On the reproducibility of results of pathway analysis in genome-wide expression studies of colorectal cancers.Wnt5a Drives an Invasive Phenotype in Human Glioblastoma Stem-like Cells.A primary tumor gene expression signature identifies a crucial role played by tumor stroma myofibroblasts in lymph node involvement in oral squamous cell carcinoma.MEN1 gene mutation with parathyroid carcinoma: first report of a familial case.
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Orazio Palumbo
@ast
Orazio Palumbo
@en
Orazio Palumbo
@es
Orazio Palumbo
@nl
Orazio Palumbo
@sl
type
label
Orazio Palumbo
@ast
Orazio Palumbo
@en
Orazio Palumbo
@es
Orazio Palumbo
@nl
Orazio Palumbo
@sl
altLabel
ORAZIO PALUMBO
@en
prefLabel
Orazio Palumbo
@ast
Orazio Palumbo
@en
Orazio Palumbo
@es
Orazio Palumbo
@nl
Orazio Palumbo
@sl
P1053
C-1133-2014
P106
P1153
24174899600
P2038
Orazio_Palumbo
P21
P2798
P31
P3829
P496
0000-0001-6583-3482