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Items: 7


Genotype-phenotype correlation in X-linked Alport syndrome patients carrying missense mutations in the collagenous domain of COL4A5.

Tsiakkis D, Pieri M, Koupepidou P, Demosthenous P, Panayidou K, Deltas C.

Clin Genet. 2012 Sep;82(3):297-9. doi: 10.1111/j.1399-0004.2012.01849.x. No abstract available.


A miR-1207-5p binding site polymorphism abolishes regulation of HBEGF and is associated with disease severity in CFHR5 nephropathy.

Papagregoriou G, Erguler K, Dweep H, Voskarides K, Koupepidou P, Athanasiou Y, Pierides A, Gretz N, Felekkis KN, Deltas C.

PLoS One. 2012;7(2):e31021. doi: 10.1371/journal.pone.0031021.


Cyst formation in the PKD2 (1-703) transgenic rat precedes deregulation of proliferation-related pathways.

Koupepidou P, Felekkis KN, Kränzlin B, Sticht C, Gretz N, Deltas C.

BMC Nephrol. 2010 Sep 2;11:23. doi: 10.1186/1471-2369-11-23. Erratum in: BMC Nephrol. 2011;12:6.


Mutant polycystin-2 induces proliferation in primary rat tubular epithelial cells in a STAT-1/p21-independent fashion accompanied instead by alterations in expression of p57KIP2 and Cdk2.

Felekkis KN, Koupepidou P, Kastanos E, Witzgall R, Bai CX, Li L, Tsiokas L, Gretz N, Deltas C.

BMC Nephrol. 2008 Aug 25;9:10. doi: 10.1186/1471-2369-9-10.


The MTHFR 677TT and 677CT/1298AC genotypes in Cypriot patients may be predisposing to hypertensive nephrosclerosis and chronic renal failure.

Koupepidou P, Deltas C, Christofides TC, Athanasiou Y, Zouvani I, Pierides A.

Int Angiol. 2005 Sep;24(3):287-94.


Familial Mediterranean fever (FMF) mutations occur frequently in the Greek-Cypriot population of Cyprus.

Deltas CC, Mean R, Rossou E, Costi C, Koupepidou P, Hadjiyanni I, Hadjiroussos V, Petrou P, Pierides A, Lamnisou K, Koptides M.

Genet Test. 2002 Spring;6(1):15-21.


Germinal and somatic mutations in the PKD2 gene of renal cysts in autosomal dominant polycystic kidney disease.

Koptides M, Hadjimichael C, Koupepidou P, Pierides A, Constantinou Deltas C.

Hum Mol Genet. 1999 Mar;8(3):509-13.

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