Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Gregory, Papagregoriou"'
Autor:
Eleni M. Loizidou, Maria Kyratzi, Maria A. Tsiarli, Andrea C. Kakouri, Georgia Charalambidou, Stella Antoniou, Stylianos Pieri, Panagiota Veloudi, Michaela Th. Mayrhofer, Andrea Wutte, Lukasz Kozera, Jens Habermann, Heimo Muller, Kurt Zatloukal, Karine Sargsyan, Alexandros Michaelides, Maria Papaioannou, Christos Schizas, Apostolos Malatras, Gregory Papagregoriou, Constantinos Deltas
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract The Cyprus Biobank collects biosamples, medical and lifestyle information with the aim of reaching 16,500 Cypriots aged ≥ 18-years, by year 2027, as part of a multitasked EU funded project. Volunteers are both from the general population a
Externí odkaz:
https://doaj.org/article/e5470b8ee75847978735edb46beac09c
Autor:
Kaya Akyüz, Melanie Goisauf, Gillian M. Martin, Michaela Th. Mayrhofer, Stella Antoniou, Georgia Charalambidou, Constantinos Deltas, Apostolos Malatras, Gregory Papagregoriou, Charalambos Stefanou, Mariel Voutounou
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Introduction: Risk governance is central for the successful and ethical operation of biobanks and the continued social license for being custodians of samples and data. Risks in biobanking are often framed as risks for participants, whereas the bioba
Externí odkaz:
https://doaj.org/article/97683d6f97df424aa7f318e59a81502a
Autor:
Myrtani Pieri, Elena Theori, Harsh Dweep, Myrofora Flourentzou, Foteini Kalampalika, Maria‐Arsenia Maniori, Gregory Papagregoriou, Christos Papaneophytou, Kyriacos Felekkis
Publikováno v:
FEBS Open Bio, Vol 12, Iss 5, Pp 925-936 (2022)
Colorectal cancer (CRC) is the third most frequent human cancer with over 1.3 million new cases globally. CRC is a complex disease caused by interactions between genetic and environmental factors; in particular, high consumption of red meat, includin
Externí odkaz:
https://doaj.org/article/aa85aca7997845e8b6c7a9de8bb14005
Autor:
Athos Antoniades, Maria Papaioannou, Apostolos Malatras, Gregory Papagregoriou, Heimo Müller, Petr Holub, Constantinos Deltas, Christos N. Schizas
Publikováno v:
Frontiers in Digital Health, Vol 3 (2021)
Biobanks have long existed to support research activities with BBMRI-ERIC formed as a European research infrastructure supporting the coordination for biobanking with 20 country members and one international organization. Although the benefits of bio
Externí odkaz:
https://doaj.org/article/13bfebd609e14aea92b00de271eea680
Autor:
Christoforos Odiatis, Isavella Savva, Myrtani Pieri, Pavlos Ioannou, Petros Petrou, Gregory Papagregoriou, Kyriaki Antoniadou, Neoklis Makrides, Charalambos Stefanou, Danica Galešić Ljubanović, Georgios Nikolaou, Dorin-Bogdan Borza, Kostas Stylianou, Oliver Gross, Constantinos Deltas
Publikováno v:
Matrix Biology Plus, Vol 9, Iss , Pp 100053- (2021)
Alport syndrome (AS) is a severe inherited glomerulopathy caused by mutations in the genes encoding the α-chains of type-IV collagen, the most abundant component of the extracellular glomerular basement membrane (GBM). Currently most AS mouse models
Externí odkaz:
https://doaj.org/article/38be1c9bdd2b47dd9ba217ef68279c4b
Autor:
Konstantinos Voskarides, Gregory Papagregoriou, Despina Hadjipanagi, Ioanelli Petrou, Isavella Savva, Avraam Elia, Yiannis Athanasiou, Androulla Pastelli, Maria Kkolou, Michalis Hadjigavriel, Christoforos Stavrou, Alkis Pierides, Constantinos Deltas
Publikováno v:
BMC Nephrology, Vol 19, Iss 1, Pp 1-8 (2018)
Abstract Background About 40–50% of patients with familial microscopic hematuria (FMH) caused by thin basement membrane nephropathy (TBMN) inherit heterozygous mutations in collagen IV genes (COL4A3, COL4A4). On long follow-up, the full phenotypic
Externí odkaz:
https://doaj.org/article/60ea5110388c4002b20d58a5ee9ce72a
Autor:
Fezile Ozdemir, D Deren Oygar, Ahmet Behlul, Salahi Ataç, Simge Bardak, Meral Yükseliş, Constantinos Deltas, Gregory Papagregoriou, Apostolos Malatras, Daniel P Gale, Cemal Gurkan, Guy H Neild
Chronic kidney disease (CKD) is a global health priority with over 850 million people affected. The starting point for improving outcome must be to diagnose the primary renal disease and in low and middle income countries ‘unknown aetiology’ acco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ac5009b307e6f157f94f7e850b8a2be
https://doi.org/10.21203/rs.3.rs-2844330/v1
https://doi.org/10.21203/rs.3.rs-2844330/v1
Autor:
Despina Hadjipanagi, Gregory Papagregoriou, Constantina Koutsofti, Christiana Polydorou, Polichronis Alivanis, Aimilios Andrikos, Stalo Christodoulidou, Manthos Dardamanis, Athanasios A. Diamantopoulos, Anastasios Fountoglou, Eleni Frangou, Eleni Georgaki, Ioannis Giannikouris, Velissarios Gkinis, Pavlos C. Goudas, Rigas G. Kalaitzidis, Nikolaos Kaperonis, Georgios Koutroumpas, George Makrydimas, Grigorios Myserlis, Andromachi Mitsioni, Christos Paliouras, Fotios Papachristou, Dorothea Papadopoulou, Nikolaos Papagalanis, Aikaterini Papagianni, Garyfalia Perysinaki, Ekaterini Siomou, Konstantinos Sombolos, Ioannis Tzanakis, Georgios V. Vergoulas, Nicoletta Printza, Constantinos Deltas
Publikováno v:
Genes; Volume 13; Issue 12; Pages: 2203
Alport syndrome (AS) is the most frequent monogenic inherited glomerulopathy and is also genetically and clinically heterogeneous. It is caused by semi-dominant pathogenic variants in the X-linked COL4A5 (NM_000495.5) gene or recessive variants in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1a5b0461682d1d3d2660ba70464fb06
Autor:
Kostas Stylianou, Charalambos Stefanou, Myrtani Pieri, Constantinos Deltas, Kyriaki Antoniadou, Neoklis Makrides, Christoforos Odiatis, Oliver Gross, Dorin-Bogdan Borza, Gregory Papagregoriou, Pavlos Ioannou, Georgios Nikolaou, Isavella Savva, Petros Petrou, Danica Galešić Ljubanović
Publikováno v:
Matrix Biology Plus, Vol 9, Iss, Pp 100053-(2021)
Matrix Biology Plus
Matrix Biology Plus
Alport syndrome (AS) is a severe inherited glomerulopathy caused by mutations in the genes encoding the α-chains of type-IV collagen, the most abundant component of the extracellular glomerular basement membrane (GBM). Currently most AS mouse models
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9dede0573d325297111c28240dbf66d
http://www.sciencedirect.com/science/article/pii/S259002852030034X
http://www.sciencedirect.com/science/article/pii/S259002852030034X
Autor:
Louiza Papazachariou, Panayiota Demosthenous, Myrtani Pieri, Gregory Papagregoriou, Isavella Savva, Christoforos Stavrou, Michael Zavros, Yiannis Athanasiou, Kyriakos Ioannou, Charalambos Patsias, Alexia Panagides, Costas Potamitis, Kyproula Demetriou, Marios Prikis, Michael Hadjigavriel, Maria Kkolou, Panayiota Loukaidou, Androulla Pastelli, Aristos Michael, Akis Lazarou, Maria Arsali, Loukas Damianou, Ioanna Goutziamani, Andreas Soloukides, Lakis Yioukas, Avraam Elia, Ioanna Zouvani, Polycarpos Polycarpou, Alkis Pierides, Konstantinos Voskarides, Constantinos Deltas
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e115015 (2014)
Familial glomerular hematuria(s) comprise a genetically heterogeneous group of conditions which include Alport Syndrome (AS) and thin basement membrane nephropathy (TBMN). Here we investigated 57 Greek-Cypriot families presenting glomerular microscop
Externí odkaz:
https://doaj.org/article/3fce6fade7d6421f887f004d60da1484