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Items: 1 to 50 of 108

1.

Reprogramming of bone marrow derived mesenchymal stromal cells to human induced pluripotent stem cells from pediatric patients with hematological diseases using a commercial mRNA kit.

Sfougataki I, Grafakos I, Varela I, Mitrakos A, Karagiannidou A, Tzannoudaki M, Poulou M, Mertzanian A, Roubelakis G M, Stefanaki K, Traeger-Synodinos J, Kanavakis E, Kitra V, Tzetis M, Goussetis E.

Blood Cells Mol Dis. 2019 May;76:32-39. doi: 10.1016/j.bcmd.2019.01.003. Epub 2019 Jan 24.

PMID:
30709626
2.

The lysine-specific methyltransferase KMT2C/MLL3 regulates DNA repair components in cancer.

Rampias T, Karagiannis D, Avgeris M, Polyzos A, Kokkalis A, Kanaki Z, Kousidou E, Tzetis M, Kanavakis E, Stravodimos K, Manola KN, Pantelias GE, Scorilas A, Klinakis A.

EMBO Rep. 2019 Mar;20(3). pii: e46821. doi: 10.15252/embr.201846821. Epub 2019 Jan 21.

3.

A Female Patient with Xq28 Microduplication Presenting with Myotubular Myopathy, Confirmed with a Custom-Designed X-array.

Kosma K, Mitrakos A, Sofokleous C, Papadimas G, Fryssira H, Kitsiou-Tzeli S, Tzetis M.

Neuropediatrics. 2019 Feb;50(1):61-63. doi: 10.1055/s-0038-1676513. Epub 2018 Dec 12.

PMID:
30541163
4.

Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA.

Tsipi M, Poulou M, Fylaktou I, Kosma K, Tsoutsou E, Pons MR, Kokkinou E, Kitsiou-Tzeli S, Fryssira H, Tzetis M.

J Neurol Sci. 2018 Dec 15;395:95-105. doi: 10.1016/j.jns.2018.10.006. Epub 2018 Oct 4.

PMID:
30308447
5.

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

Farrell P, Férec C, Macek M, Frischer T, Renner S, Riss K, Barton D, Repetto T, Tzetis M, Giteau K, Duno M, Rogers M, Levy H, Sahbatou M, Fichou Y, Le Maréchal C, Génin E.

Eur J Hum Genet. 2018 Dec;26(12):1832-1839. doi: 10.1038/s41431-018-0234-z. Epub 2018 Aug 8.

PMID:
30089827
6.

Inducible nitric oxide synthase as a target for osteoarthritis treatment.

Leonidou A, Lepetsos P, Mintzas M, Kenanidis E, Macheras G, Tzetis M, Potoupnis M, Tsiridis E.

Expert Opin Ther Targets. 2018 Apr;22(4):299-318. doi: 10.1080/14728222.2018.1448062. Epub 2018 Mar 5. Review.

PMID:
29504411
7.

Dysregulated placental microRNAs in Early and Late onset Preeclampsia.

Lykoudi A, Kolialexi A, Lambrou GI, Braoudaki M, Siristatidis C, Papaioanou GK, Tzetis M, Mavrou A, Papantoniou N.

Placenta. 2018 Jan;61:24-32. doi: 10.1016/j.placenta.2017.11.005. Epub 2017 Nov 14.

PMID:
29277268
8.

Serum microRNA array analysis identifies miR-140-3p, miR-33b-3p and miR-671-3p as potential osteoarthritis biomarkers involved in metabolic processes.

Ntoumou E, Tzetis M, Braoudaki M, Lambrou G, Poulou M, Malizos K, Stefanou N, Anastasopoulou L, Tsezou A.

Clin Epigenetics. 2017 Dec 12;9:127. doi: 10.1186/s13148-017-0428-1. eCollection 2017.

9.

Potential sperm contributions to the murine zygote predicted by in silico analysis.

Ntostis P, Carter D, Iles D, Huntriss J, Tzetis M, Miller D.

Reproduction. 2017 Dec;154(6):777-788. doi: 10.1530/REP-17-0097. Epub 2017 Sep 15.

PMID:
28916718
10.

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

Tsoutsou E, Tzetis M, Giannikou K, Braoudaki M, Mitrakos A, Amenta S, Selenti N, Kanavakis E, Zafeiriou D, Kitsiou-Tzeli S, Fryssira H.

Pediatr Res. 2017 Aug;82(2):253-260. doi: 10.1038/pr.2017.65. Epub 2017 May 24.

PMID:
28422950
11.

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Syndrome: Additional Clinical Features.

Makrygianni EA, Papadimas GK, Vartzelis G, Georgala M, Tzetis M, Poulou M, Kitsiou-Tzeli S, Pons R.

Pediatr Neurol. 2017 Feb;67:e5-e6. doi: 10.1016/j.pediatrneurol.2016.11.001. Epub 2016 Nov 21. No abstract available.

PMID:
28041656
12.

Maternal epigenetics and fetal and neonatal growth.

Kitsiou-Tzeli S, Tzetis M.

Curr Opin Endocrinol Diabetes Obes. 2017 Feb;24(1):43-46. doi: 10.1097/MED.0000000000000305. Review.

PMID:
27898587
13.

A boy with conduct disorder (CD), attention deficit hyperactivity disorder (ADHD), borderline intellectual disability, and 47,XXY syndrome in combination with a 7q11.23 duplication, 11p15.5 deletion, and 20q13.33 deletion.

Kolaitis G, Bouwkamp CG, Papakonstantinou A, Otheiti I, Belivanaki M, Haritaki S, Korpa T, Albani Z, Terzioglou E, Apostola P, Skamnaki A, Xaidara A, Kosma K, Kitsiou-Tzeli S, Tzetis M.

Child Adolesc Psychiatry Ment Health. 2016 Sep 15;10:33. doi: 10.1186/s13034-016-0121-8. eCollection 2016.

14.

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

Galanos P, Vougas K, Walter D, Polyzos A, Maya-Mendoza A, Haagensen EJ, Kokkalis A, Roumelioti FM, Gagos S, Tzetis M, Canovas B, Igea A, Ahuja AK, Zellweger R, Havaki S, Kanavakis E, Kletsas D, Roninson IB, Garbis SD, Lopes M, Nebreda A, Thanos D, Blow JJ, Townsend P, Sørensen CS, Bartek J, Gorgoulis VG.

Nat Cell Biol. 2016 Jul;18(7):777-89. doi: 10.1038/ncb3378. Epub 2016 Jun 20.

PMID:
27323328
15.

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

Giannakopoulos A, Fryssira H, Tzetis M, Xaidara A, Kanaka-Gantenbein C.

J Pediatr Endocrinol Metab. 2016 Nov 1;29(11):1307-1311. doi: 10.1515/jpem-2015-0484.

PMID:
27235670
16.

Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases.

Tsipi M, Tzetis M, Kosma K, Moschos M, Braoudaki M, Poulou M, Kanavakis E, Kitsiou-Tzeli S.

Meta Gene. 2016 Feb 16;8:37-43. doi: 10.1016/j.mgene.2016.02.002. eCollection 2016 Jun.

17.

Compound heterozygosity of a paternal submicroscopic deletion and a maternal missense mutation in POR gene: Antley-bixler syndrome phenotype in three sibling fetuses.

Tzetis M, Konstantinidou A, Sofocleous C, Kosma K, Mitrakos A, Tzannatos C, Kitsiou-Tzeli S.

Birth Defects Res A Clin Mol Teratol. 2016 Jul;106(7):536-41. doi: 10.1002/bdra.23492. Epub 2016 Mar 11.

PMID:
26969897
18.

miR-15a and miR-24-1 as putative prognostic microRNA signatures for pediatric pilocytic astrocytomas and ependymomas.

Braoudaki M, Lambrou GI, Giannikou K, Papadodima SA, Lykoudi A, Stefanaki K, Sfakianos G, Kolialexi A, Tzortzatou-Stathopoulou F, Tzetis M, Kitsiou-Tzeli S, Kanavakis E.

Tumour Biol. 2016 Jul;37(7):9887-97. doi: 10.1007/s13277-016-4903-7. Epub 2016 Jan 26.

PMID:
26813564
19.

Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications.

Oikonomakis V, Kosma K, Mitrakos A, Sofocleous C, Pervanidou P, Syrmou A, Pampanos A, Psoni S, Fryssira H, Kanavakis E, Kitsiou-Tzeli S, Tzetis M.

Clin Genet. 2016 Jun;89(6):708-18. doi: 10.1111/cge.12740. Epub 2016 Feb 9.

PMID:
26777411
20.

TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations.

O'Rawe JA, Wu Y, Dörfel MJ, Rope AF, Au PY, Parboosingh JS, Moon S, Kousi M, Kosma K, Smith CS, Tzetis M, Schuette JL, Hufnagel RB, Prada CE, Martinez F, Orellana C, Crain J, Caro-Llopis A, Oltra S, Monfort S, Jiménez-Barrón LT, Swensen J, Ellingwood S, Smith R, Fang H, Ospina S, Stegmann S, Den Hollander N, Mittelman D, Highnam G, Robison R, Yang E, Faivre L, Roubertie A, Rivière JB, Monaghan KG, Wang K, Davis EE, Katsanis N, Kalscheuer VM, Wang EH, Metcalfe K, Kleefstra T, Innes AM, Kitsiou-Tzeli S, Rosello M, Keegan CE, Lyon GJ.

Am J Hum Genet. 2015 Dec 3;97(6):922-32. doi: 10.1016/j.ajhg.2015.11.005.

21.

Multi-allele genotyping platform for the simultaneous detection of mutations in the Wilson disease related ATP7B gene.

Amvrosiadou M, Petropoulou M, Poulou M, Tzetis M, Kanavakis E, Christopoulos TK, Ioannou PC.

J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Dec 1;1006:201-208. doi: 10.1016/j.jchromb.2015.10.036. Epub 2015 Oct 30.

PMID:
26580967
22.

Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD).

Destouni A, Poulou M, Kakourou G, Vrettou C, Tzetis M, Traeger-Synodinos J, Kitsiou-Tzeli S.

J Cyst Fibros. 2016 Mar;15(2):163-70. doi: 10.1016/j.jcf.2015.09.009. Epub 2015 Oct 19.

23.

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

Selenti N, Tzetis M, Braoudaki M, Giannikou K, Kitsiou-Tzeli S, Fryssira H.

Mol Cytogenet. 2015 Sep 30;8:73. doi: 10.1186/s13039-015-0174-z. eCollection 2015.

24.

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

Selenti N, Tzetis M, Braoudaki M, Gianikou K, Kitsiou-Tzeli S, Fryssira H.

Mol Cytogenet. 2015 Aug 12;8:64. doi: 10.1186/s13039-015-0169-9. eCollection 2015. Erratum in: Mol Cytogenet. 2015;8:73.

25.

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

Girardet A, Viart V, Plaza S, Daina G, De Rycke M, Des Georges M, Fiorentino F, Harton G, Ishmukhametova A, Navarro J, Raynal C, Renwick P, Saguet F, Schwarz M, SenGupta S, Tzetis M, Roux AF, Claustres M.

Eur J Hum Genet. 2016 Apr;24(4):469-78. doi: 10.1038/ejhg.2015.99. Epub 2015 May 27.

26.

BTNL2 gene SNPs as a contributing factor to sarcoidosis pathogenesis in a cohort of Greek patients.

Delaveri A, Rapti A, Poulou M, Fylaktou E, Tsipi M, Roussos C, Makrythanasis P, Kanavakis E, Tzetis M.

Meta Gene. 2014 Aug 31;2:619-30. doi: 10.1016/j.mgene.2014.07.009. eCollection 2014 Dec.

27.

Generation of human β-thalassemia induced pluripotent cell lines by reprogramming of bone marrow-derived mesenchymal stromal cells using modified mRNA.

Varela I, Karagiannidou A, Oikonomakis V, Tzetis M, Tzanoudaki M, Siapati EK, Vassilopoulos G, Graphakos S, Kanavakis E, Goussetis E.

Cell Reprogram. 2014 Dec;16(6):447-55. doi: 10.1089/cell.2014.0050. Epub 2014 Oct 29.

PMID:
25354259
28.

Are ALOX5AP gene SNPs a risk or protective factor for stroke?

Papapostolou A, Spengos K, Fylaktou I, Poulou M, Gountas I, Kitsiou-Tzeli S, Kanavakis E, Tzetis M.

Gene. 2014 Sep 10;548(1):56-60. doi: 10.1016/j.gene.2014.07.007. Epub 2014 Jul 8.

PMID:
25010723
29.

Association of MMP-1 -1607 1G/2G (rs1799750) polymorphism with primary knee osteoarthritis in the Greek population.

Lepetsos P, Pampanos A, Kanavakis E, Tzetis M, Korres D, Papavassiliou AG, Efstathopoulos N.

J Orthop Res. 2014 Sep;32(9):1155-60. doi: 10.1002/jor.22647. Epub 2014 May 16.

30.

Prenatal diagnosis for CF using High Resolution Melting Analysis and simultaneous haplotype analysis through QF-PCR.

Poulou M, Destouni A, Kakourou G, Kanavakis E, Tzetis M.

J Cyst Fibros. 2014 Dec;13(6):617-22. doi: 10.1016/j.jcf.2014.04.002. Epub 2014 Apr 29.

31.

Mesenchymal derivatives of genetically unstable human embryonic stem cells are maintained unstable but undergo senescence in culture as do bone marrow-derived mesenchymal stem cells.

Karagiannidou A, Varela I, Giannikou K, Tzetis M, Spyropoulos A, Paterakis G, Petrakou E, Theodosaki M, Goussetis E, Kanavakis E.

Cell Reprogram. 2014 Feb;16(1):1-8. doi: 10.1089/cell.2013.0040. Epub 2013 Dec 31.

PMID:
24380659
32.

Microduplication 3q13.2q13.31 identified in a male with dysmorphic features and multiple congenital anomalies.

Karavitakis E, Kitsiou-Tzeli S, Xaidara A, Kosma K, Makrythanasis P, Apazidou E, Kanavakis E, Tzetis M.

Am J Med Genet A. 2014 Mar;164A(3):666-70. doi: 10.1002/ajmg.a.36346. Epub 2013 Dec 20.

PMID:
24375959
33.

Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease.

Syrmou A, Tzetis M, Fryssira H, Kosma K, Oikonomakis V, Giannikou K, Makrythanasis P, Kitsiou-Tzeli S, Kanavakis E.

Pediatr Res. 2013 Jun;73(6):772-6. doi: 10.1038/pr.2013.41. Epub 2013 Mar 12.

PMID:
23481551
34.

Array-CGH revealed one of the smallest 16q21q22.1 microdeletions in a female patient with psychomotor retardation.

Tsoutsou E, Tzetis M, Giannikou K, Syrmou A, Oikonomakis V, Kosma K, Kanioura A, Kanavakis E, Fryssira H.

Eur J Paediatr Neurol. 2013 May;17(3):316-20. doi: 10.1016/j.ejpn.2012.12.004. Epub 2013 Jan 24.

PMID:
23352671
35.

Genotyping efficiency of 2 primer sets and an unlabeled oligonucleotide probe for the p.Phe508del in exon 10 of the CFTR gene as determined with high-resolution melting analysis.

Poulou M, Destouni A, Fylaktou I, Kanavakis E, Tzetis M.

Clin Chem. 2012 Oct;58(10):1490-2. Epub 2012 Aug 15. No abstract available.

36.

Further delineation of novel 1p36 rearrangements by array-CGH analysis: narrowing the breakpoints and clarifying the "extended" phenotype.

Giannikou K, Fryssira H, Oikonomakis V, Syrmou A, Kosma K, Tzetis M, Kitsiou-Tzeli S, Kanavakis E.

Gene. 2012 Sep 15;506(2):360-8. doi: 10.1016/j.gene.2012.06.060. Epub 2012 Jul 2.

PMID:
22766398
37.

An unusual case of Cat-Eye syndrome phenotype and extragonadal mature teratoma: review of the literature.

Tzetis M, Stefanaki K, Syrmou A, Kosma K, Leze E, Giannikou K, Oikonomakis V, Sofocleous C, Choulakis M, Kolialexi A, Makrythanasis P, Kitsiou-Tzeli S.

Birth Defects Res A Clin Mol Teratol. 2012 Jul;94(7):561-6. doi: 10.1002/bdra.23038. Epub 2012 Jun 22.

PMID:
22730277
38.

The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization.

Tzetis M, Kitsiou-Tzeli S, Frysira H, Xaidara A, Kanavakis E.

Expert Rev Mol Diagn. 2012 Jun;12(5):449-57. doi: 10.1586/erm.12.40.

PMID:
22702362
39.

Familial Pelizaeus-Merzbacher disease caused by a 320.6-kb Xq22.2 duplication and the pathological findings of a male fetus.

Kitsiou-Tzeli S, Konstantinidou A, Sofocleous C, Kosma K, Syrmou A, Giannikou K, Sifakis S, Makrythanasis P, Tzetis M.

Birth Defects Res A Clin Mol Teratol. 2012 Jun;94(6):494-8. doi: 10.1002/bdra.23015. Epub 2012 Apr 18.

PMID:
22511562
40.

Cystic fibrosis genetic counseling difficulties due to the identification of novel mutations in the CFTR gene.

Poulou M, Fylaktou I, Fotoulaki M, Kanavakis E, Tzetis M.

J Cyst Fibros. 2012 Jul;11(4):344-8. doi: 10.1016/j.jcf.2012.01.004. Epub 2012 Feb 11.

41.

Microdeletion and microduplication 17q21.31 plus an additional CNV, in patients with intellectual disability, identified by array-CGH.

Kitsiou-Tzeli S, Frysira H, Giannikou K, Syrmou A, Kosma K, Kakourou G, Leze E, Sofocleous C, Kanavakis E, Tzetis M.

Gene. 2012 Jan 15;492(1):319-24. doi: 10.1016/j.gene.2011.10.023. Epub 2011 Oct 20.

PMID:
22037486
42.

Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3.

Christopoulou G, Tzetis M, Konstantinidou AE, Tsezou A, Kanavakis E, Kitsiou-Tzeli S, Velissariou V.

Eur J Med Genet. 2012 Jan;55(1):75-9. doi: 10.1016/j.ejmg.2011.08.002. Epub 2011 Sep 9.

PMID:
21914491
43.

VPA-induced recurrent pancreatitis in a cystic fibrosis carrier.

Dinopoulos A, Karapanou O, Alexopoulou E, Tzetis M, Attilakos A, Fretzayas A.

Eur J Paediatr Neurol. 2011 Sep;15(5):453-5. doi: 10.1016/j.ejpn.2011.04.004. Epub 2011 Jul 20.

PMID:
21778093
44.

Quadruple-allele dipstick test for simultaneous visual genotyping of A896G (Asp299Gly) and C1196T (Thr399Ile) polymorphisms in the toll-like receptor-4 gene.

Litos IK, Ioannou PC, Christopoulos TK, Tzetis M, Kanavakis E, Traeger-Synodinos J.

Clin Chim Acta. 2011 Oct 9;412(21-22):1968-72. doi: 10.1016/j.cca.2011.07.001. Epub 2011 Jul 8.

PMID:
21763687
45.

Recommendations for the classification of diseases as CFTR-related disorders.

Bombieri C, Claustres M, De Boeck K, Derichs N, Dodge J, Girodon E, Sermet I, Schwarz M, Tzetis M, Wilschanski M, Bareil C, Bilton D, Castellani C, Cuppens H, Cutting GR, Drevínek P, Farrell P, Elborn JS, Jarvi K, Kerem B, Kerem E, Knowles M, Macek M Jr, Munck A, Radojkovic D, Seia M, Sheppard DN, Southern KW, Stuhrmann M, Tullis E, Zielenski J, Pignatti PF, Ferec C.

J Cyst Fibros. 2011 Jun;10 Suppl 2:S86-102. doi: 10.1016/S1569-1993(11)60014-3.

46.

Anton van Leeuwenhoek (1632-1723): father of micromorphology and discoverer of spermatozoa.

Karamanou M, Poulakou-Rebelakou E, Tzetis M, Androutsos G.

Rev Argent Microbiol. 2010 Oct-Dec;42(4):311-4. doi: 10.1590/S0325-75412010000400013.

47.

Rapid clinical-scale propagation of mesenchymal stem cells using cultures initiated with immunoselected bone marrow CD105+ cells.

Spiropoulos A, Theodosaki M, Stefanaki K, Paterakis G, Tzetis M, Giannikou K, Petrakou E, Dimopoulou MN, Papassotiriou I, Roma ES, Kanavakis E, Graphakos S, Goussetis E.

J Cell Mol Med. 2011 Sep;15(9):1983-8. doi: 10.1111/j.1582-4934.2010.01157.x.

48.

Cystic fibrosis conductance regulator, tumor necrosis factor, interferon alpha-10, interferon alpha-17, and interferon gamma genotyping as potential risk markers in pulmonary sarcoidosis pathogenesis in Greek patients.

Makrythanasis P, Tzetis M, Rapti A, Papatheodorou A, Tsipi M, Kitsiou S, Tsiamouri A, Poulou M, Roussos C, Kanavakis E.

Genet Test Mol Biomarkers. 2010 Aug;14(4):577-84. doi: 10.1089/gtmb.2009.0198.

PMID:
20722470
49.

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

Kaliakatsos M, Giannakopoulos A, Fryssira H, Kanariou M, Skiathitou AV, Siahanidou T, Giannikou K, Makrythanasis P, Kanavakis E, Tzetis M.

J Hum Genet. 2010 Nov;55(11):761-3. doi: 10.1038/jhg.2010.95. Epub 2010 Aug 5.

PMID:
20686492
50.

De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature.

Kitsiou-Tzeli S, Tzetis M, Sofocleous C, Vrettou C, Xaidara A, Giannikou K, Pampanos A, Mavrou A, Kanavakis E.

Am J Med Genet A. 2010 Aug;152A(8):1925-32. doi: 10.1002/ajmg.a.33447.

PMID:
20575009

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