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Synovial Fibroblast Extracellular Vesicles Induce Inflammation via Delivering miR-21-5p in Osteoarthritis
Author / Creator:Konteles, Vasileios ; Papathanasiou, Ioanna ; Tzetis, Maria ; Kriebardis, Anastasios ; Tsezou, Aspasia
Publisher:Switzerland: MDPI AG
Journal title:Cells (Basel, Switzerland), 2025-03, Vol.14 (7), p.519
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Severe Hemophilia A and Moyamoya Syndrome in a 19-Year-Old Boy Caused by Xq28 Microdeletion
Author / Creator:Tzeravini, Evangelia ; Samara, Stamatia ; Kouramba, Anna ; Vakrinos, Georgios ; Efthimiou, Athina ; Tzetis, Maria ; Androutsakos, Theodoros
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Case reports in neurology, 2022-05, Vol.14 (2), p.261-267
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Integration of Transcriptome and MicroRNA Profile Analysis of iMSCs Defines Their Rejuvenated State and Conveys Them into a Novel Resource for Cell Therapy in Osteoarthritis
Author / Creator:Konteles, Vasileios ; Papathanasiou, Ioanna ; Tzetis, Maria ; Goussetis, Evgenios ; Trachana, Varvara ; Mourmoura, Evanthia ; Balis, Charalampos ; Malizos, Konstantinos ; Tsezou, Aspasia
Publisher:Switzerland: MDPI AG
Journal title:Cells (Basel, Switzerland), 2023-06, Vol.12 (13), p.1756
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Combined microdeletions and CHD7 mutation causing severe CHARGE/DiGeorge syndrome: clinical presentation and molecular investigation by array-CGH
Author / Creator:Kaliakatsos, Marios ; Giannakopoulos, Aristeidis ; Fryssira, Helena ; Kanariou, Maria ; Skiathitou, Anna-Venetia ; Siahanidou, Tania ; Giannikou, Krinio ; Makrythanasis, Periklis ; Kanavakis, Emmanuel ; Tzetis, Maria
Publisher:London: Nature Publishing Group UK
Journal title:Journal of human genetics, 2010-11, Vol.55 (11), p.761-763
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Prenatal Chromosomal Microarray Analysis: Does Increased Resolution Equal Increased Yield?
Author / Creator:Mitrakos, Anastasios ; Kosma, Konstantina ; Makrythanasis, Periklis ; Tzetis, Maria
Publisher:Basel: MDPI AG
Journal title:Genes, 2023-07, Vol.14 (8), p.1519
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Clinical Course of a Child With Cystic Fibrosis and the Genotype F508del/CFTRdup1_11: A Case Report
Author / Creator:Petrocheilou, Argyri ; Tzetis, Maria ; Loukou, Ioanna
Publisher:United States: Springer Nature B.V
Journal title:Curēus (Palo Alto, CA), 2024-08, Vol.16 (8), p.e67792
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Chronic p53-independent p21 expression causes genomic instability by deregulating replication licensing
Author / Creator:Galanos, Panagiotis ; Vougas, Konstantinos ; Walter, David ; Polyzos, Alexander ; Maya-Mendoza, Apolinar ; Haagensen, Emma J. ; Kokkalis, Antonis ; Roumelioti, Fani-Marlen ; Gagos, Sarantis ; Tzetis, Maria ; Canovas, Begoña ; Igea, Ana ; Ahuja, Akshay K. ; Zellweger, Ralph ; Havaki, Sofia ; Kanavakis, Emanuel ; Kletsas, Dimitris ; Roninson, Igor B. ; Garbis, Spiros D. ; Lopes, Massimo ; Nebreda, Angel ; Thanos, Dimitris ; Blow, J. Julian ; Townsend, Paul ; Sørensen, Claus Storgaard ; Bartek, Jiri ; Gorgoulis, Vassilis G.
Publisher:London: Nature Publishing Group UK
Journal title:Nature cell biology, 2016-07, Vol.18 (7), p.777-789
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The impact of preimplantation genetic testing for aneuploidies (PGT-A) on clinical outcomes in high risk patients
Author / Creator:Pantou, Amelia ; Mitrakos, Anastasios ; Kokkali, Georgia ; Petroutsou, Konstantina ; Tounta, Georgia ; Lazaros, Leandros ; Dimopoulos, Alexandros ; Sfakianoudis, Konstantinos ; Pantos, Konstantinos ; Koutsilieris, Michael ; Mavrou, Ariadni ; Kanavakis, Emmanuel ; Tzetis, Maria
Publisher:New York: Springer Nature B.V
Journal title:Journal of assisted reproduction and genetics, 2022-06, Vol.39 (6), p.1341-1349
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The Phenotypic Spectrum of 16p11.2 Recurrent Chromosomal Rearrangements
Author / Creator:Mitrakos, Anastasios K. ; Kosma, Konstantina ; Makrythanasis, Periklis ; Tzetis, Maria
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2024-08, Vol.15 (8), p.1053
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Therapeutic Effects of Mesenchymal Stem Cells Derived From Bone Marrow, Umbilical Cord Blood, and Pluripotent Stem Cells in a Mouse Model of Chemically Induced Inflammatory Bowel Disease
Author / Creator:Kagia, Argyro ; Tzetis, Maria ; Kanavakis, Emmanuel ; Perrea, Despina ; Sfougataki, Irene ; Mertzanian, Anny ; Varela, Ioanna ; Dimopoulou, Aikaterini ; Karagiannidou, Angeliki ; Goussetis, Evgenios
Publisher:New York: Springer Nature B.V
Journal title:Inflammation, 2019-10, Vol.42 (5), p.1730-1740
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Germline CNV Detection through Whole-Exome Sequencing (WES) Data Analysis Enhances Resolution of Rare Genetic Diseases
Author / Creator:Tilemis, Faidon-Nikolaos ; Marinakis, Nikolaos M. ; Veltra, Danai ; Svingou, Maria ; Kekou, Kyriaki ; Mitrakos, Anastasios ; Tzetis, Maria ; Kosma, Konstantina ; Makrythanasis, Periklis ; Traeger-Synodinos, Joanne ; Sofocleous, Christalena
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2023-07, Vol.14 (7), p.1490
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Estimating the age of p.(Phe508del) with family studies of geographically distinct European populations and the early spread of cystic fibrosis
Author / Creator:Farrell, Philip ; Férec, Claude ; Macek, Milan ; Frischer, Thomas ; Renner, Sabine ; Riss, Katharina ; Barton, David ; Repetto, Teresa ; Tzetis, Maria ; Giteau, Karine ; Duno, Morten ; Rogers, Melissa ; Levy, Hara ; Sahbatou, Mourad ; Fichou, Yann ; Cédric Le Maréchal ; Génin, Emmanuelle
Publisher:Leiden: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2018-12, Vol.26 (12), p.1832-1839
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A Novel Frameshift Variant and a Partial EHMT1 Microdeletion in Kleefstra Syndrome 1 Patients Resulting in Variable Phenotypic Severity and Literature Review
Author / Creator:Tzetis, Maria ; Mitrakos, Anastasios ; Papathanasiou, Ioanna ; Koute, Vasiliki ; Kosma, Konstantina ; Pons, Roser ; Michoula, Aspasia ; Grivea, Ioanna ; Tsezou, Aspasia
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2025-04, Vol.16 (5), p.521
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Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children
Author / Creator:Christodoulaki, Vasileia ; Kosma, Konstantina ; Marinakis, Nikolaos M. ; Tilemis, Faidon-Nikolaos ; Stergiou, Nikolaos ; Kampouraki, Afroditi ; Kapogiannis, Charalampos ; Karava, Vasiliki ; Mitsioni, Andromachi ; Mila, Maria ; Kanaka-Gantenbein, Christina ; Makrythanasis, Periklis ; Tzetis, Maria ; Traeger-Synodinos, Joanne
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2024-08, Vol.15 (8), p.1016
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Central precocious puberty in a boy with 22q13 deletion syndrome and NOTCH-1 gene duplication
Author / Creator:Giannakopoulos, Aris ; Fryssira, Helen ; Tzetis, Maria ; Xaidara, Athina ; Kanaka-Gantenbein, Christina
Publisher:Germany: De Gruyter
Journal title:Journal of Pediatric Endocrinology & Metabolism, 2016-11, Vol.29 (11), p.1307-1311
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Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly
Author / Creator:Tsoutsou, Eirini ; Tzetis, Maria ; Giannikou, Krinio ; Braoudaki, Maria ; Mitrakos, Anastasis ; Amenta, Stella ; Selenti, Nikoletta ; Kanavakis, Emmanouil ; Zafeiriou, Dimitrios ; Kitsiou-Tzeli, Sophia ; Fryssira, Helena
Publisher:New York: Nature Publishing Group US
Journal title:Pediatric research, 2017-08, Vol.82 (2), p.253-260
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Real-time PCR for single-cell genotyping in sickle cell and thalassemia syndromes as a rapid, accurate, reliable, and widely applicable protocol for preimplantation genetic diagnosis
Author / Creator:Vrettou, Christina ; Traeger-Synodinos, Joanne ; Tzetis, Maria ; Palmer, Giles ; Sofocleous, Christalena ; Kanavakis, Emmanuel
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2004-05, Vol.23 (5), p.513-521
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The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus
Author / Creator:Girardet, Anne ; Viart, Victoria ; Plaza, Stéphanie ; Daina, Gemma ; De Rycke, Martine ; Des Georges, Marie ; Fiorentino, Francesco ; Harton, Gary ; Ishmukhametova, Aliya ; Navarro, Joaquima ; Raynal, Caroline ; Renwick, Pamela ; Saguet, Florielle ; Schwarz, Martin ; SenGupta, Sioban ; Tzetis, Maria ; Roux, Anne-Françoise ; Claustres, Mireille
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2016-04, Vol.24 (4), p.469-478
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Association of Polymorphisms in the Promoter Region of NOS2A Gene with Primary Knee Osteoarthritis in the Greek Population
Author / Creator:Leonidou, Andreas ; Lepetsos, Panagiotis ; Kenanidis, Eustathios ; Macheras, George ; Tzetis, Maria ; Potoupnis, Michael ; Tsiridis, Eleftherios
Publisher:United States: Springer Nature B.V
Journal title:Curēus (Palo Alto, CA), 2020-01, Vol.12 (1), p.e6780
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An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4
Author / Creator:Selenti, Nikoletta ; Tzetis, Maria ; Braoudaki, Maria ; Giannikou, Krinio ; Kitsiou-Tzeli, Sofia ; Fryssira, Helen
Publisher:England: BioMed Central Ltd
Journal title:Molecular cytogenetics, 2015-08, Vol.8 (1), p.64, Article 64
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Synovial Fibroblast Extracellular Vesicles Induce Inflammation via Delivering miR-21-5p in Osteoarthritis

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Severe Hemophilia A and Moyamoya Syndrome in a 19-Year-Old Boy Caused by Xq28 Microdeletion

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Integration of Transcriptome and MicroRNA Profile Analysis of iMSCs Defines Their Rejuvenated State and Conveys Them into a Novel Resource for Cell Therapy in Osteoarthritis

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Combined microdeletions and CHD7 mutation causing severe CHARGE/DiGeorge syndrome: clinical presentation and molecular investigation by array-CGH

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Prenatal Chromosomal Microarray Analysis: Does Increased Resolution Equal Increased Yield?

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Clinical Course of a Child With Cystic Fibrosis and the Genotype F508del/CFTRdup1_11: A Case Report

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Chronic p53-independent p21 expression causes genomic instability by deregulating replication licensing

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The impact of preimplantation genetic testing for aneuploidies (PGT-A) on clinical outcomes in high risk patients

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The Phenotypic Spectrum of 16p11.2 Recurrent Chromosomal Rearrangements

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Therapeutic Effects of Mesenchymal Stem Cells Derived From Bone Marrow, Umbilical Cord Blood, and Pluripotent Stem Cells in a Mouse Model of Chemically Induced Inflammatory Bowel Disease

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Germline CNV Detection through Whole-Exome Sequencing (WES) Data Analysis Enhances Resolution of Rare Genetic Diseases

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Estimating the age of p.(Phe508del) with family studies of geographically distinct European populations and the early spread of cystic fibrosis

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A Novel Frameshift Variant and a Partial EHMT1 Microdeletion in Kleefstra Syndrome 1 Patients Resulting in Variable Phenotypic Severity and Literature Review

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Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children

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Central precocious puberty in a boy with 22q13 deletion syndrome and NOTCH-1 gene duplication

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Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly

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Real-time PCR for single-cell genotyping in sickle cell and thalassemia syndromes as a rapid, accurate, reliable, and widely applicable protocol for preimplantation genetic diagnosis

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The improvement of the best practice guidelines for preimplantation genetic diagnosis of cystic fibrosis: toward an international consensus

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Association of Polymorphisms in the Promoter Region of NOS2A Gene with Primary Knee Osteoarthritis in the Greek Population

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An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4

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