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1. Full Text Expression of microRNAs, miR‐21, miR‐31, miR‐122, miR‐145, miR‐146a, miR‐200c, miR‐221, miR‐222, and miR‐223 in patients with hepatocellular carcinoma or intrahepatic cholangiocarcinoma and its prognostic significance
by Karakatsanis, Andreas and Papaconstantinou, Ioannis and Gazouli, Maria and Lyberopoulou, Anna and Polymeneas, George and Voros, Dionysios
Molecular Carcinogenesis, ISSN 0899-1987, 04/2013, Volume 52, Issue 4, pp. 297 - 303
MicroRNAs are a class of non‐coding molecules found to regulate a variety of cellular functions in health and disease. Dysregulation of microRNAs is involved... 
miRNA | hepatocellular carcinoma | intrahepatic cholangiocarcinoma | Hepatocellular carcinoma | Intrahepatic cholangiocarcinoma | MiRNA | DIAGNOSIS | SUPPRESSOR GENE | BIOCHEMISTRY & MOLECULAR BIOLOGY | RNAS | PROLIFERATION | HUMAN BREAST-CANCER | LIVER-DISEASE | CELL-LINES | FEATURES | PATHOGENESIS | BIOMARKERS | ONCOLOGY | Prognosis | Cholangiocarcinoma - diagnosis | Liver Neoplasms - genetics | Carcinoma, Hepatocellular - diagnosis | Humans | Liver - metabolism | Middle Aged | Gene Expression Regulation, Neoplastic | Male | Gene Expression Profiling | Liver Neoplasms - diagnosis | Carcinoma, Hepatocellular - genetics | Bile Duct Neoplasms | Cholangiocarcinoma - genetics | Bile Ducts, Intrahepatic | Female | Aged | Biomarkers, Tumor - genetics | MicroRNAs - genetics | Care and treatment | MicroRNA | Analysis | Adjuvant treatment | Genetic transcription | Hepatoma | Liver cirrhosis | Cancer | Liver cancer | Pathology | Oncology | Gene expression | MicroRNAs | Index Medicus
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2. Full Text Digestive System Diseases
: Stem Cell Mechanisms and Therapies
by Gazouli, Maria and Theodoropoulos, George E
03/2019, Stem cell biology and regenerative medicine, ISBN 3030119645, 194
Digestive organs | Stem cells-Therapeutic use | Digestive organs-Diseases-Treatment | Digestive organs-Diseases
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3. Full Text Gallium-68 labeled iron oxide nanoparticles coated with 2,3-dicarboxypropane-1,1-diphosphonic acid as a potential PET/MR imaging agent: A proof-of-concept study
by Karageorgou, Maria-Argyro and Vranješ-Djurić, Sanja and Radović, Magdalena and Lyberopoulou, Anna and Antić, Bratislav and Rouchota, Maritina and Gazouli, Maria and Loudos, George and Xanthopoulos, Stavros and Sideratou, Zili and Stamopoulos, Dimosthenis and Bouziotis, Penelope and Tsoukalas, Charalampos
Contrast Media and Molecular Imaging, ISSN 1555-4309, 2017, Volume 2017, pp. 6951240 - 13
The aim of this study was to develop a dual-modality PET/MR imaging probe by radiolabeling iron oxide magnetic nanoparticles (IONPs), surface functionalized... 
CELLS | BIOCOMPATIBILITY | SUPERPARAMAGNETIC NANOPARTICLES | SENTINEL LYMPH-NODES | CONTRAST AGENTS | IN-VIVO | BIOMEDICAL APPLICATIONS | BIODISTRIBUTION | MAGNETIC NANOPARTICLES | INORGANIC NANOPARTICLES | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Ethylenediaminetetraacetic acid | Nanoparticles | Magnetite | Iron compounds | Ferric oxide | Research | Comparative analysis | Magnetic properties | Nuclear medicine | Gallium | Nuclear magnetic resonance--NMR | Toxicity | Liver | Cytotoxicity | Image acquisition | Radiochemistry | Tomography | Biocompatibility | Emitters | Spleen | Surface charge | Medical imaging | Positron emission | Magnetic resonance imaging | Acids | Diagnostic software | Diagnostic systems | Iron oxides | Hyperthermia | Cancer | Index Medicus
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4. Full Text Tu1788 - Baff, April, Baff-R and Infliximab Therapy in Inflammatory Bowel Disease Patients
by Gazouli, Maria and Karamanolis, Georgios and Sechi, Leonardo
Gastroenterology, ISSN 0016-5085, 05/2018, Volume 154, Issue 6, pp. S-1019 - S-1019
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5. Full Text Association of the clock genes polymorphisms with colorectal cancer susceptibility
by Karantanos, Theodoros and Theodoropoulos, George and Gazouli, Maria and Vaiopoulou, Anna and Karantanou, Christina and Stravopodis, Dimitrios J and Bramis, Konstantinos and Lymperi, Maria and Pektasidis, Dimitrios
Journal of Surgical Oncology, ISSN 0022-4790, 12/2013, Volume 108, Issue 8, pp. 563 - 567
Background and ObjectivesThe circadian rhythm regulates the cell cycle progression and DNA damage response. The aim of our study was to investigate the... 
polymorphisms | circadian genes | colorectal cancer | SYSTEM | SURGERY | TUMOR SUPPRESSION | CIRCADIAN CLOCK | BREAST-CANCER | PER3 | ONCOLOGY | PLAYS | EXPRESSION | CARCINOMA | Genetic Predisposition to Disease | Colorectal Neoplasms - genetics | Gene Frequency | Humans | Middle Aged | Genotype | Male | CLOCK Proteins - genetics | Case-Control Studies | Period Circadian Proteins - genetics | Polymorphism, Restriction Fragment Length | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Colorectal Neoplasms - pathology | Neoplasm Staging | Genetic research | Disease susceptibility | Genetic aspects | Genes | Colorectal cancer | Cancer | Index Medicus
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6. Full Text NOD2/CARD15,ATG16L1andIL23Rgene polymorphisms and childhood-onset of Crohn’s disease
by Gazouli, Maria
World Journal of Gastroenterology, ISSN 1007-9327, 2010, Volume 16, Issue 14, p. 1753
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7. Full Text OCT4 spliced variant OCT4B1 is expressed in human colorectal cancer
by Gazouli, Maria and Roubelakis, Maria G and Theodoropoulos, George E and Papailiou, Joanna and Vaiopoulou, Anna and I. Pappa, Kalliopi and Nikiteas, Nikolaos and Anagnou, Nicholas P
Molecular Carcinogenesis, ISSN 0899-1987, 02/2012, Volume 51, Issue 2, pp. 165 - 173
OCT4 , a POU‐domain transcription factor is considered to be a key factor in maintaining the pluripotency of stem cells. Several OCT4 isoforms are... 
OCT4 | stem cells | colorectal cancer | cancer stem cells | Sox‐2 | Sox-2 | Cancer stem cells | Colorectal cancer | Stem cells | BLADDER-CANCER | STEM-CELLS | MARKER | BIOCHEMISTRY & MOLECULAR BIOLOGY | GERM-CELL TUMORS | SELF-RENEWAL | POU5F1 | PLURIPOTENT | MAMMALIAN EMBRYO | ONCOLOGY | TRANSCRIPTION FACTOR OCT4 | TISSUES | Colorectal Neoplasms - genetics | Humans | Middle Aged | Male | DNA Primers | Reverse Transcriptase Polymerase Chain Reaction | Octamer Transcription Factor-3 - genetics | RNA Splicing | Base Sequence | Aged, 80 and over | Adult | Female | Aged | Real-Time Polymerase Chain Reaction | Index Medicus
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8. Full Text Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
by Anderson, Carl A and Boucher, Gabrielle and Lees, Charlie W and Franke, Ane and D'Amato, Mauro and Taylor, Kent D and Lee, James C and Goyette, Philippe and Imielinski, Marcin and Latiano, Anna and Lagacé, Caroline and Scott, Regan and Amininejad, Leila and Bumpstead, Suzannah and Baidoo, Leonard and Baldassano, Robert N and Barclay, Murray and Bayless, Theodore M and Brand, Stephan and Büning, Carsten and Colombel, Jean-Frédéric and Denson, Lee A and de Vos, Martine and Dubinsky, Marla and Edwards, Cathryn and Ellinghaus, David and Fehrmann, Rudolf S. N and Floyd, James A. B and Florin, Timothy and Franchimont, Denis and Franke, Lude and Georges, Michel and Glas, Jürgen and Glazer, Nicole L and Guthery, Stephen L and Haritunians, Talin and Hayward, Nicholas K and Hugot, Jean-Pierre and Jobin, Gilles and Laukens, Debby and Lawrance, Ian and Lémann, Marc and Levine, Arie and Libioulle, Cecile and Louis, Edouard and McGovern, Dermot P and Milla, Monica and Montgomery, Grant W and Morley, Katherine I and Mowat, Craig and Ng, Aylwin and Newman, William and Ophoff, Roel A and Papi, Laura and Palmieri, Orazio and Peyrin-Biroulet, Laurent and Panés, Julián and Phillips, Anne and Prescott, Natalie J and Proctor, Deborah D and Roberts, Rebecca and Russell, Richard and Rutgeerts, Paul and Sanderson, Jeremy and Sans, Miquel and Schumm, Philip and Seibold, Frank and Sharma, Yashoda and Simms, Lisa A and Seielstad, Mark and Steinhart, A. Hillary and Targan, Stephan R and van den Berg, Leonard H and Vatn, Morten and Verspaget, Hein and Walters, Thomas and Wijmenga, Cisca and Wilson, David C and Westra, Harm-Jan and Xavier, Ramnik J and Zhao, Zhen Z and Ponsioen, Cyriel Y and Andersen, Vibeke and Torkvist, Leif and Gazouli, Maria and Anagnou, Nicholas P and Karlsen, Tom H and Kupcinskas, Limas and Sventoraityte, Jurgita and Mansfield, John C and Kugathasan, Subra and Silverberg, Mark S and Halfvarson, Jonas and Rotter, Jerome I and Mathew, Christopher G and Griffiths, Anne M and Gearry, Richard and Ahmad, Tariq and Brant, Steven R and Chamaillard, Mathias and ... and Hälsoakademin and Örebro universitet
Nature genetics, ISSN 1061-4036, 2011, Volume 43, Issue 3, pp. 246 - 252
Genome-wide association studies and candidate gene studies in ulcerative colitis have identified 18 susceptibility loci. We conducted a meta-analysis of six... 
COMMON VARIANTS | CELLS | INFLAMMATORY-BOWEL-DISEASE | PROTEIN | CROHNS-DISEASE | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | GENE-EXPRESSION | ENRICHMENT | MULTIPLE | GENOME-WIDE ASSOCIATION | Crohn Disease - genetics | Risk | Genome-Wide Association Study | Humans | Colitis, Ulcerative - genetics | Genetic aspects | Disease susceptibility | Research | Risk factors | Ulcerative colitis | Meta-analysis | Studies | Inflammatory bowel disease | Celiac disease | Genetics | Genomics | Genes | Index Medicus | Medicine | Medicin | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
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9. Full Text Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility
by Franke, Ane and Balschun, Tobias and Karlsen, Tom H and Sventoraityte, Jurgita and Nikolaus, Susanna and Mayr, Gabriele and Domingues, Francisco S and Albrecht, Mario and Nothnagel, Michael and Ellinghaus, David and Sina, Christian and Onnie, Clive M and Weersma, Rinse K and Stokkers, Pieter C. F and Wijmenga, Cisca and Gazouli, Maria and Strachan, David and McArdle, Wendy L and Vermeire, Séverine and Rutgeerts, Paul and Rosenstiel, Philip and Krawczak, Michael and Vatn, Morten H and Mathew, Christopher G and Schreiber, Stefan and Moum, Bjørn and Jahnsen, Jørgen and Solberg, Camilla and Stray, Njål and Henriksen, Magne and Sauar, Jostein and Høie, Ole and IBSEN Study Grp and IBSEN study group and the IBSEN study group
Nature genetics, ISSN 1061-4036, 2008, Volume 40, Issue 11, pp. 1319 - 1323
Inflammatory bowel disease (IBD) typically manifests as either ulcerative colitis (UC) or Crohn's disease (CD). Systematic identification of susceptibility... 
INFLAMMATORY-BOWEL-DISEASE | METAANALYSIS | CROHNS-DISEASE | GENETICS & HEREDITY | PHENOTYPE | IL-10 GENE | IBD | TNF-ALPHA | INTERLEUKIN-10 | CYTOKINE GENE POLYMORPHISMS | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Base Sequence | Humans | Interleukin-10 - genetics | Colitis, Ulcerative - genetics | Actin-Related Protein 2-3 Complex - genetics | Mutation - genetics | Case-Control Studies | Interleukin-10 | Genetic aspects | Research | Single nucleotide polymorphisms | Health aspects | Risk factors | Ulcerative colitis | Data analysis | Statistical analysis | Genes | Risk | Histology | Information management | Crohns disease | Inflammatory bowel disease | Genotype & phenotype | Software packages | Bowel disease | Quality control | Genetics | Index Medicus
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10. Full Text Intestinal bacteria composition and translocation of bacteria in inflammatory bowel disease
by Vrakas, Spyros and Mountzouris, Konstantinos C and Michalopoulos, George and Karamanolis, George and Papatheodoridis, George and Tzathas, Charalampos and Gazouli, Maria
PLoS ONE, ISSN 1932-6203, 01/2017, Volume 12, Issue 1, pp. e0170034 - e0170034
Background Live commensal intestinal bacteria are present in the peripheral blood where they can induce inflammation. Objective To evaluate the intestinal... 
CROHNS-DISEASE | DYSBIOSIS | MULTIDISCIPLINARY SCIENCES | ULCERATIVE-COLITIS | RISK | FAECALIBACTERIUM-PRAUSNITZII | MUCOSAL FLORA | DIVERSITY | GUT MICROBIOTA | ASSOCIATION | BLOOD | Humans | Middle Aged | Male | Nod2 Signaling Adaptor Protein - genetics | Blood - microbiology | Clostridium - isolation & purification | Dysbiosis | Gastrointestinal Microbiome - genetics | Case-Control Studies | Polymorphism, Genetic | Colitis, Ulcerative - microbiology | Escherichia coli - isolation & purification | DNA, Bacterial - blood | Adult | Crohn Disease - microbiology | DNA, Bacterial - analysis | Female | Inflammatory Bowel Diseases - microbiology | Aged | Bacteroides - isolation & purification | Bacteria | Inflammatory bowel diseases | Research | Microbiota (Symbiotic organisms) | Comparative analysis | Salmonella | Dysbacteriosis | Reverse transcription | Blood | Microbiota | Intestine | Colonoscopy | Gastroenterology | Peripheral blood | Colon | Active control | Deoxyribonucleic acid--DNA | NOD2 protein | Translocation | Inflammation | Patients | Inflammatory bowel disease | Hospitals | Antibiotics | Genotyping | Biopsy | Diabetes | Mutation | Ulcerative colitis | Index Medicus | Deoxyribonucleic acid | DNA
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11. Full Text Common germline variants within the CDKN2A/2B region affect risk of pancreatic neuroendocrine tumors
by Campa, Daniele and Capurso, Gabriele and Pastore, Manuela and Talar-Wojnarowska, Renata and Milanetto, Anna Caterina and Landoni, Luca and Maiello, Evaristo and Lawlor, Rita T and Malecka-Panas, Ewa and Funel, Niccola and Gazouli, Maria and De Bonis, Antonio and Klüter, Harald and Rinzivillo, Maria and Delle Fave, Gianfranco and Hackert, Thilo and Landi, Stefano and Bugert, Peter and Bambi, Franco and Archibugi, Livia and Scarpa, Aldo and Katzke, Verena and Dervenis, Christos and Liço, Valbona and Furlanello, Sara and Strobel, Oliver and Tavano, Francesca and Basso, Daniela and Kaaks, Rudolf and Pasquali, Claudio and Gentiluomo, Manuel and Rizzato, Cosmeri and Canzian, Federico
Scientific Reports, ISSN 2045-2322, 12/2016, Volume 6, Issue 1, pp. 39565 - 39565
Pancreatic neuroendocrine tumors (PNETs) are heterogeneous neoplasms which represent only 2% of all pancreatic neoplasms by incidence, but 10% by prevalence.... 
POLYMORPHISMS | METAANALYSIS | P14(ARF) | ANNOTATION | MULTIDISCIPLINARY SCIENCES | ACUTE LYMPHOBLASTIC-LEUKEMIA | SUSCEPTIBILITY LOCI | MDM2 | REGULATORY MOTIF | CANCER | GENOME-WIDE ASSOCIATION | Homozygotes | Statistical analysis | Linkage disequilibrium | Alleles | Single-nucleotide polymorphism | Regulatory sequences | Pancreas | Health risk assessment | Risk factors | Neuroendocrine tumors | Tumors | Cancer | Index Medicus
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12. Full Text Mutational analysis of circulating tumor cells from colorectal cancer patients and correlation with primary tumor tissue
by Lyberopoulou, Anna and Aravantinos, Gerasimos and Efstathopoulos, Efstathios P and Nikiteas, Nikolaos and Bouziotis, Penelope and Isaakidou, Athina and Papalois, Apostolos and Marinos, Evangelos and Gazouli, Maria
PLoS ONE, ISSN 1932-6203, 04/2015, Volume 10, Issue 4, pp. e0123902 - e0123902
Circulating tumor cells (CTCs) provide a non-invasive accessible source of tumor material from patients with cancer. The cellular heterogeneity within CTC... 
BREAST-CANCER | LUNG-CANCER | STEM-CELLS | THERAPY | MULTIDISCIPLINARY SCIENCES | PERIPHERAL-BLOOD | KRAS | BRAF | MESENCHYMAL TRANSITION | CARCINOMA | CHEMOTHERAPY | Epithelial Cells - metabolism | Neoplastic Cells, Circulating - pathology | Colorectal Neoplasms - genetics | Humans | Middle Aged | Neoplastic Cells, Circulating - metabolism | Epithelial Cells - pathology | Male | Epithelial-Mesenchymal Transition - genetics | Feasibility Studies | Neoplastic Stem Cells - metabolism | DNA Mutational Analysis | Aged, 80 and over | Neoplastic Stem Cells - pathology | Adult | Female | Aged | Biomarkers, Tumor - genetics | Colorectal Neoplasms - pathology | Development and progression | Genetic aspects | Metastasis | Health aspects | Colorectal cancer | Immunoassay | Carcinoma | Profiling | Disease | Laboratories | Genomics | Colorectal carcinoma | Genomes | Biology | Kinases | Medical diagnosis | Cancer therapies | Metastases | Heterogeneity | Bioindicators | Growth factors | Deoxyribonucleic acid--DNA | Subpopulations | Tumor cells | Quantum dots | Invasiveness | Discordance | Feasibility studies | Patients | Medicine | Polymerase chain reaction | Chemotherapy | Hospitals | Restriction fragment length polymorphism | Biopsy | Stem cells | Biomarkers | Mutation | Tumors | Cancer | Index Medicus | Deoxyribonucleic acid | DNA
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